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Paths to long-term survival with CRC liver mets

Paths to long-term survival with CRC liver mets

DocTalk
2023
Dr. Hernandez-Alejandro
Ablation
Histotripsy
Liver
Stage IV
Transplant

Dr. Roberto Hernandez-Alejandro from the University of Rochester Medical Center discusses the range of treatment possibilities for bilateral liver metastases. Recorded in March 2023.

Betsy Post 0:00
We will go ahead and get started with this evening’s program. We are so excited to have all of you here watching live, and then for all of you that will be watching this recording, we’re very happy to make this available that way as well, because it’s all about educating patients and caregivers on the treatment options available. So just a couple of housekeeping items before I get into the introduction and turn it over to Dr. Hernandez. We will be taking questions at the end, so you can jot your questions down, or hold them till the end of his presentation, or you can put them in the chat – so please put them in the chat. You can chat to Julie. You can see Julie there, Julie Clauer, or you can send them to me. …Or you can send them to everyone. So there should be the chat feature. Please send the questions in the chat. Or you can write them down and hold them till the end. You don’t have to write them down if you have a better memory than I do, so if you think 20 minutes later, you’ll remember you can definitely do that as well. We have everyone muted just because we do want to make sure we have undivided attention for Dr. Hernandez and his presentation, but we will absolutely make time for Q and A at the end of the presentation. So I’m going to go ahead and share my screen with you, and hopefully you can see this okay. Don’t worry, it’s not “death by PowerPoint”. I’m just going to do a few slides with an introduction. So again, welcome everyone to our DocTalk this evening on “Exploring Paths to Long Term Survival With Colorectal Cancer, Liver Metastases”. Tonight’s presentation is going to be a focus for folks that have bilateral liver mets or extensive metastases. This is a little bit different than anything that we’ve offered previously with Dr. Hernandez. It really is focused on the community that has a lot of liver mets, so I just wanted to preface that up front, I think there is something for everyone here, whether you have a little or a lot, but we really wanted to impact patients and caregivers as they’re thinking about, “I’ve been told I’m inoperable, I can’t have a resection” – all of these things. “What are some different options, perhaps available to me? And how do I think about those options?” So again, we welcome everyone, but really we are trying to hear that this evening. So we’re really excited to have Dr. Hernandez with us. His resume is very extensive. I think a lot of you know him. He is active in COLONTOWN and so helpful to us. He comes to us from the University of Rochester Medical Center, where he’s the Chief of the Division of Transplantation. He has extensive training around the world, including in Canada and Japan. He has actually now over 130, not 110, (I need to update that) peer-reviewed publications in the area of liver transplantation and hepatobiliary surgery and he is on the editorial board of the Annals of Surgery. He is a pioneer in ‘donation: after cardiac death’ liver transplantation in Canada; the first to perform ALPPS in North America, and he did open the program on liver transplantation for colorectal cancer liver metastases in Rochester. He is well recognized as a team leader andinnovator and a mentor. If you know him, I know that does not surprise you at all, but my favorite thing about Dr. Hernandez is who he is as a person and what he does every day for patients and caregivers. So to us in COLONTOWN, he is, “Dr. H.”. We really appreciate and love you, Dr. Hernandez, thank you for everything that you do for our patients and our caregivers every day and for the impact that you make in their lives. We really appreciate you, and we’re really happy to have you here with us this evening. With that, I’m going to turn it over to you, and just remember to save your questions for the end. We will take those, put them in the chat or be prepared to answer live at the end. So thank you so much, and I will stop sharing and turn it over to you.

Dr. Roberto Hernandez-Alejandro 4:23
Thank you very much to all the members of COLONTOWN. Thank you very much, Julie and Betsy. Very nice introduction. It is a pleasure for me to be with all of you. I can see some familiar faces here, and I recognize also some other names. I think, before presenting, for some of you who don’t know who I am, I am very passionate about the field of of liver metastasis, since my early stages in my training. You know my title is in transplantation, and I use the hat of ‘transplanter’ but I want you to know that I do many liver resections. Perhaps, in my life, I have done more liver resections than liver transplants. Liver transplants are more complex. Liver resections are much more common. And the most common reason that we do liver resections is for liver metastasis. So I do a lot of liver metastasis resections and my presentation, I don’t want to be a bias on towards transplantation. I want to be fair with everything, and I don’t want to be moving things into the fields that I do, and before I decided to name the title of this presentation, I was thinking about, if I was a patient, if I would have one of my family members as a patient with colon cancer, what would I like to know and do, especially when the disease is advanced. And I try to be in your shoes on how stressful this could be, especially knowing all the options that are out there. And then you probably are scratching your head, where do I go? So with this, thank you again, for everybody that are opening the cameras and I’m looking forward to have questions. There are always great questions. And I am impressed with the participants, 64- that’s pretty great. So I’m going to share my screen. Let me know if this works. Can someone tell me if they can see me?

Betsy Post 7:03
Yes.

Dr. Roberto Hernandez-Alejandro 7:05
Perfect. Thank you, Betsy. All right, interrupt me if there’s a problem, Betsy and Julie. So this is titled “Exploring Paths to Long Term Survival With Colorectal Metastasis”, we have different options, on where we want to go, and I don’t think there’s a correct answer every time. There’s sometimes that there’s clear answers, but there’s a lot of times that there’s no clear answer. Seems to me that this group here, all of you know what’s happening with colon cancer, before the media. It’s impressive that years later, the media is putting in first page of Wall Street, and recently, I saw in CNN talking about a young population developing colon cancer. All of you guys know that this is happening since a long time ago. At least you, COLONTOWN, and the patients are making noise, and this is opening areas for research, and we need to work as a community on doing research and understand why colon cancer is happening more and is increasing in younger population. This graph represents what has been happening over the last few years. You can see here the year of birth in the bottom part, and this is a rate for 100,000. You don’t have to be epidemiologists to understand this graph, but you can see here from people that are 85 to around 50 years old that the rate of colon cancer, the detection, everything, is coming down. Why? Because we’re more aggressive. We have programs for doing colonoscopies. But the population from 45’s, 40’s, 30’s and 20s, we are not used to doing colonoscopies, and this is the area and the population where it’s increasing. Doesn’t mean that we shouldn’t be paying attention in this population, but this population requires a lot of work, and we need to do a lot of research to understand why, because this is a very silent disease, and many of the times when we diagnose the patients, which is 39-45 they have metastases and sometimes itgoes beyond the liver. Just to give some data, in 2021 there were in the US more than 150,000 new cases. And we know that half of the patients who have metastatic colon cancer will develop liver metastasis. So it’s not uncommon. Colon cancer is the third most common cancer in the world, after breast and prostate cancer is the most common cancer, and half of the stage IV population will develop liver metastasis. And I want to be very clear so far, until this moment, the only, and I will repeat it again, the only curative treatment is surgery. We haven’t been able to cure with other means at this moment. There’s no evidence. We help with other other treatments but the only thing that can potentially cure, not always, but many times, is surgery. So we need to try to focus and try to aim for: can we reach surgery? Sometimes there’s noway that we can reach surgery, so let’s go for other alternatives. But if we can reach surgery, how do we get there and how do we use the other alternatives as a bridge to surgery? This is very important, the concept of that. And the definition of cure that I want to be very clear about here, because a lot of you patients go to the oncologist or to the surgeon or to other specialists. When we say ‘cure’, it’s defined as five years, whether if you are in the field of oncology or transplant, we call it ‘cure’ at five years, if there’s no evidence of disease. There are some diseases that can come back after five years. Colon cancer, if we resect it, or we remove it, and it’s not coming back in five years, we call it cured. Still a little, little chance that it will come back, but probably not that much. However, there’s some data on follow up at 10 years or even more. So the goal of every patient that I personally think who has colorectal metastasis will be, I think they want to be cured. That’s the number one goal, or at least live longer with good quality of life, and also reduce the exposure to chemotherapy for as much time as possible. I think those are the goals when apatient has colorectal metastases, who is going to go for treatment. So how can we reach those goals?

Dr. Roberto Hernandez-Alejandro 11:48
Number one, you need a good medical and surgical team. That for me, is the most important part of this. You need a group or a liver surgeon, whether it’s in different fields, but a liver surgeon, you need a medical oncologist, you need a hepatologist – nowadays it’s a field that is working more on patients with colon cancer, the hepatologists are the liver specialists and they look at livers when they have fatty liver disease, other problems when the liver enzymes are going up. So it’s so important to involve them as well. Radiationoncologists, many of the times we need the interventional radiologists where, Y90 or TACE or other type of treatments, when we do portal vein embolization and those types of treatments, and we need to develop strategies to reach a surgical resection, as I mentioned a few minutes ago. Reaching resection, routine surgery will be the most important thing and the best potential outcome. And sometimes we have to be creative and innovative as professionals. If I’m a patient who has one or two liver metastases on the left side, I can tell you, you don’t have to be traveling and look for too many options. Probably close to you, there will be a person who will be able to do it, a good surgeon who’s going to be able to do a liver resection in the left side. They give you chemotherapy, and you have a good chance that probably to be cured, or if it has recurrence, to have follow up and to do something more. But when there are multiple spots – tumors, and you need someone to be creative and have strategies, then this is when you need this type of teams. When there are metastases in your lungs or in the adrenal glands, or when there is local recurrence, then we need to have a surgical team that is willing to push the envelope.

Dr. Roberto Hernandez-Alejandro 13:51
Resection of all the disease is something that is, …I call it ‘imperative’. We shouldn’t be doing a little resection here in the liver and then a little resection later on. Remember, liver metastasis, metastasize. What does that mean? If we have metastases in the liver, and we’re not treating those metastases, and we just leave them there. They’re going to send cancer cells to other places or to the other sites of the liver, and it’s going to come back. And I mean, with that living residual disease in colorectal metastasis shouldn’t be an option. This is what happens when we don’t have many options and we just give chemotherapy. And I think that this is complex and a difficult to understand, and a difficult pill to swallow. When we show this graph where we see that five year survival, it’s only 5 to 10% under chemotherapy, but it’s true, and this is what we’re facing. We want to be out of there. What happens when we use other types of treatment different than systemic chemotherapy? Many of you are aware about the hepatic artery infusion pump? Which I want to be very clear, I’m not against it. I think it has an impressive response. It’s great for patients who have advanced disease and perhaps for patients who are progressing. But this study here, it shows the group of hepatic artery infusion and those with systemic chemotherapy. So these two groups were patients who have unresectable liver disease, patients who we cannot go and resect them. And then they decided to go one went to systemic chemotherapy as a palliative treatment, and otherwise for the pump as a palliative treatment. And if you see, the dotted line is systemic and the solid line is hepatic artery infusion, and the survival at two years is practically the same. There was an increase of median survival of 24 months compared to 20 months in both of them. So definitely, there’s a little bit of benefit of hepatic artery infusion. But also we want to be very clear about what happened with with both of those things, and I’m going to make some comments about it.

Dr. Roberto Hernandez-Alejandro 16:11
I mentioned that ‘cure’ is defined at five years in the groups of transplantation and in the groups of cancer, but there’s some other groups that they really want to push and say, “Okay, let’s look at 10 years.”. So what happened when we resected the cancer? That means we removed it from the liver, the metastasis, the primary tumor, is removed. We resect it. What are my chances of being that patient and survive for 10 years or more? Well the chance is around 27%. So we know that a lot of patients during those 10 years, they will die from recurrence of the disease quite often. But remember, at five years, 5 or 10% when there’s only chemotherapy. So this is a huge benefit and a huge advantage to being able to go for resection, but the concept of resection is something that is very important, and that’s what I was mentioning about having a team that is willing to push the envelope. Many of you are familiarized with CT scans, hopefully not like this one, but well, there’s a lot of metastases. All those dark spots are metastases from colon cancer. So it’s difficult to be able to leave liver without cancer in this patient. So defining resectability many years ago, it was defined “arbitrary”. They said, if there’s less than four tumors, if we can leave good margins– that means that when we cut it, we stay far away from tumor, no evidence of disease outside the liver. And when the patient has a low clinical risk score– that is when there’s a single tumor or low CEA, which you know it’s a tumor marker, the nodes, etc, etc. — If I would be doing this in my life, I would be doing probably 10% of the surgeries that I do nowadays, only, or less than that. This has changed. And then in the early 2000s and later on, they started pushing the envelope and saying, let’s operate on patients, resect patients with more than four metastases. What happened to them? And this is a study that comes from Memorial Sloan Kettering center, almost 100 patients, and they started resecting and being more aggressive after receiving chemotherapy and resecting them, and it was an improvement of survival. So they were able to see, “alright, I think we can be more aggressive and push and operate on more liver metastases in the liver, not only four or less”. And this is a study that I want to show here, is what really changed in 2008 the management of colorectal liver metastases with chemotherapy. And I just want to let you know this journal, The Lancet, is very strong. It’s an extremely high impact factor. You publish there, you do very important research. And they analyzed 364 patients, all of them with less than four metastases. So a very simple study. And they said, “Okay, what happes if we give them chemo and then we operate on them compared to if we only operate on them without chemotherapy?”, and there was a 7% improvement of the disease-free survival. What does that mean? …That this patient, the recurrence, was later or more delayed compared to the patients who didn’t receive chemotherapy, showing a benefit of the chemotherapy. However, the chemotherapy didn’t have implications in the improval of overall survival, so the cancer came back later but at the end, patients survived at very similar rates. But there’s other benefits of the chemotherapy, which I think are more important which are learning thebehavior of the tumor, and it’s going to help us to decide what to do with the patients.

Dr. Roberto Hernandez-Alejandro 20:30
Now, let’s talk about what is one of the biggest problems that happen when we go and do resection, and what all the patients are afraid, is “oh, I’m going to have a recurrence”. So what happened with recurrence? In this study that is multi-institutional, many centers, more than 1600 patients: 947 patients had recurrence after resection. So they studied them, and they looked where the cancer came back. In 40%, only in the liver; in 20%, in the liver and outside the liver; and in 35% only outside the liver. So we know when it comes outside the liver in this population, the outcomes are not very good because the surgical treatment has to be different, especially those ones who are affected in several organs. But what happened with those ones who only came back in the liver? They went back for treatments, whether it was a resection or ablations or something that was going to remove them, and then when it came back again, there was 90%, so 372 patients that came back in the liver. So why am I showing you this road and this path? So there is a population of patients that we don’t know, but with time, we started learning that they only have liver disease, and these are the patients where we can even do much more and push the envelope and do big treatments, including liver transplantation in many of them. So what is this telling us? We need to identify clearly those patients that can be resected. But also we need to identify those ones who cannot be resected to be able to give alternatives, and maybe we can convert them to resection or other treatments. What other options do we have? Y90, microwave ablation, a lot of other centers they do RFA, or radio frequency ablation. The most common and advanced nowadays in the US is microwave ablation, external radiation and hepatic artery pump or other treatments that we’re seeing nowadays. So I was mentioning what is unresectable. In these slides, these slides that you can see, there’s a metastasis in this part. It’s the same one here, another one here. Well, maybe I can say, let’s go and do a big wedge here, and do a posterior right segmentectomy in this liver, and then hopefully the patient is cured. But perhaps other surgeons will think differently, they will say, “Oh, I will ablate this one here, and then I will do Y90, and then resect”. So which one is correct? Remember, surgery for most, if possible, will be the best. But of course, after chemotherapy to understand more the biology of the tumor in this patient, who has a lot of disease in the left side, and this is the same patient, a lot of disease in the right side, and you can see the amount of disease.

Dr. Roberto Hernandez-Alejandro 23:47
A lot of some colleagues that I know around the world, they will say, “No, this patient is unresectable”. Well, look at the segment 4 which has its own blood supply and own outflow. Maybe we can create growth there. Remember, the liver has regeneration. Maybe we can do a technique that makes thesegment to grow and have hypertrophy, and then we can go and do resection. What is that? It’s called ALPPS, right? And we were able to help this patient. This patient survived for seven and a half years and did very well. He was able to be with his grandchildren and enjoy life. The cancer came back later, but it was very different than surviving a few months or one year on. And this is what I was mentioning about in this paper, where a lot of surgeons from around the world – and I was invited to be part of these, from Switzerland, Norway, Brazil, United States, many other centers in Asia as well. We were asked and given tasks about, ‘would you resect these patients or not according to CT scans?”. And what it was, and this was more than 15 cases, and the conclusion was, there’s minimal agreement on therapeutic strategies. It’s inconsistent, and patients should consider going for second and third opinions. And this is very true. I think this paper shouldn’t go into a journal of medicine. This should go to magazines that people read. Because this is true, you need to be cautious on selecting your teams, because everything is going to be different, depending on where you go and wherever you feel comfortable, will be the best place to go.

Dr. Roberto Hernandez-Alejandro 25:39
What can we do nowadays when we see patients who have clearly unresectable disease, no place that we can do an ALPPS or a two-stage hepatectomy, what can we do with these patients? Well, this patient really received treatment here with us. Well, not necessarily with us, but long distance with us, under us, and impressively, the disease responded very well. And this is the same CT scans, but several months later, you can barely see those diseases. Patients get excited and say, “Well, my cancer is gone”. Wait a moment. No, it’s not gone. The cancer is going to be there the majority of time. And there’s evidence that it’s going to be there because it disappears in the CT scan or even in the MRI, it is still there at least 65-70% of the time the liver starts getting damaged. The cancer cell are there, and then they hide, and you cannot see them because the liver has already fatty disease in the liver, or some fibrosis, and we cannot see. The CT scan and the MRI are notmicroscopes. We can see around 3, 4, 5, 6, millimeters spots, but we cannot see microscopic spots, and they’re gonna come back. I think, with those patients, convert them with treatment and then we’ll check them.

Dr. Roberto Hernandez-Alejandro 27:19
Well, this is what happened: the recurrence it’s pretty high. It’s almost universal, and survival is around 30% for five years. And the majority of the patients, around 81-82% of them, will have cancer back by five years. It’s better than not having a resection, but definitely there’s an improval in the survival of these patients who are converted to resectable, but sometimes there could be other options. And, I have talked about this previously, but for the people who are new or that are new today, towards the right side, and we need to remove all the right side and the left side is small, we can do a portal vein embolization with interventional radiology or for patients who have several tumors, but we find there’s an area where we can resect these tumors, and after resecting these tumors, then we can embolize or, get the right portal vein, similar to the wall. We will wait several weeks until the left side of the liver where there’s no tumors, will grow. That’s called ‘hypertrophy’, or regeneration of the liver. And then we can go back to the operating room for a second operation, remove the right side of the liver and the patient is free of cancer. There’s also the ALPPS procedure, which is a very similar situation, but that thing is different, because in the first stage, we divide the liver and the liver will grow very quickly and very accelerated. I had the opportunity of being a pioneer on the ALPPS in North America having good outcomes. But unfortunately, the vast majority of the patients with the two stage hepatectomy with the ALPPS the vast majority of them will have recurrence, and this is disease-free survival. That means, how many of the patients are free of cancer at three years? 80%, the cancer has come back in this study of 459 patients. In these 65 patients, 80%, and in this group, 74% of the patients will have. This is from France, this is from MD Anderson, and this is a systematic review that means that …(extended internet connectivity interruption)…

Dr. Roberto Hernandez-Alejandro 29:49
…we have better chemotherapy, we know. We have better treatments, and if you compare different eras, so in the 2000’s and the late 1990’s, we have seen an increase in the survival of patients after resection. And I think, better surgeons we’re understanding more therapy. We were talking about recurrence. What happened when there is recurrence after resection? The line that is color yellow, it’s a line where it’s showing when the patients have liver disease only, and when they only have lung disease only, when it comes back in the lungs, these patients have a better survival. I’m talking here about resection. So patients who had colon cancer, liver metastases, they go for chemo, they are resected, the tumor is removed, the liver is doing well, and unfortunately, they have lung metastasis, if there’s only lung metastasis, they have better survival, compared to those ones who have liver recurrence. So liver recurrence, why it’s coming often the liver, those “ghost” metastases, those disappearing liver metastasis. I mentioned it a few minutes ago. They disappear. It doesn’t mean that they disappear. There has been, until a few years ago, evidence that radiologically, there’s nothing in the right side. They were metastasis in the right side, we give chemo. They disappear. We can only see the left side. We go and operate on the left side, and then in few months or one year, there they are on the right side. What does that mean? Are these recurrence or is this residual disease? Most likely residual disease. Studies show that around 83% of the patients clear on develop metastases is when we look at new CT scans or MRIs. Now, I will show you some data now with tissue, not necessarily with radiology. But what do we know, and I mentioned about the behavior of the tumor to understand how the tumors behave, and that’s the biology of the tumor, the size and the number of the tumors is important, the tumor markers, the level. Nowadays, a lot of people are asking, “What about Signatera or the new Guardant360?”. Our center is working on this and understanding more, it might be a good tool for decision making, before a decision of surgeries or transplantation, and to follow up with the patients. We call it liquid biopsies, or circulating tumor DNA. How much time has the patient had the disease? If the patient is stable and has one year, two years, probably we could be more aggressive to be able to do something. The fact that a patient is responding to chemotherapy, or to systemic chemotherapy, or to hepatic artery pump infusion, that is a good sign that the tumor is behaving and that justifies us to be aggressive. So all of these, the presence or not of lymph nodes, the evidence of extrahepatic disease, the genetics of the tumor, all of these are tools that for us as physicians who dedicate time for cancer patients, help us to decide what we can do for these patients.

Dr. Roberto Hernandez-Alejandro 33:41
And the next slide is just to show you, I know this is not a medical talk, but this is just to show you that the patients who have — the bigger the tumors, the more of the metastases, the outcome is going to be more complex. So you don’t have to really understand this. This is, I took it from a presentation that I gave to physicians and but what this slide is showing is the more tumor load, the worse the outcome. We need to help and find ideas on how to help these patients and what to do. The higher the CEA, the worse the outcome. And these are patients if we do liver resections with high CEA, with high tumor load, the presence of lymph nodes. We know that the outcome is going to be worse if there’s cancerous lymph nodes around the liver than if they are not cancerous lymph nodes around the liver. If a patient is progressing on their chemotherapy, that means that the tumors are growing, and then we go and resect, the outcome is worse than if the patient is responding to chemotherapy. The more mutations the patient has, if we compare it to the patients who have no mutations or only one mutation on the genetics, the more complex outcome the patient is going to have oncologically as well.

Dr. Roberto Hernandez-Alejandro 35:02
So let’s put together these cases’ time. Imagine that we have a 53 year old patient who has liver metastases from colon cancer, the primary is located in the right side. The patient has four liver metastases in the right side of the liver, and there’s no evidence of disease outside the liver, then what are we going to do? Okay, well, clearly we should give systemic chemotherapy. We will understand more about the biology of that tumor, maybe three months, and then we restage. We do a lot of CEA again. We do CT scans again, and the patient is responding. All right, let’s go to surgery. What are we going to do? Are we going to remove both of the tumors together, the liver and the colon? Well, we have to see if the patient is fit enough. We have a good team that communicates with colorectal surgeons and the liver surgeons. We can do simultaneous resection. What about if it’s a very big liver surgery and the tumor is located in the rectum, right? One very low, the other one, very high. Can we do that? And maybe the patient has a very high BMI? It’s a patient who has some obesity? Well, that’s going to be a more complex surgery. Should we do it all in one stage? Well, we have to decide and talk inthe tumor board. What are we going to do first? If the liver has more disease, then we go first for the liver, and then for the rectal tumor, the colon. Or sometimes we can do minimally invasive surgery, we can do the colon, and then we can do the liver with minimally invasive surgery, or we can combine.

Dr. Roberto Hernandez-Alejandro 36:45
So that is where the strategy of a team to develop what is the best for the patient comes in. What about if the patient is not responding? The same patient that I mentioned to you three months later, we do the CT scan and the tumors are growing. Now, I’m not going to tell the patient, “well, there’s nothing more to do”. No, that’s not an answer for me. Well, hepatic artery infusion could be a good option for these patients here. Why? What do we know about hepatic artery infusion? One of the good things is the conversion rate. It has a stronger conversion rate than the systemic chemotherapy, right? And we know that. I showed you at the beginning there’s no benefit to comparing both at the end, but in this situation, we know that systemic is not working. I totally justify going for surgery and getting the pump, and let’s see, hopefully this will work, and hopefully we can do something later. But you might ask yourself, so why not use the pump from the beginning? Well, to be honest, there’s some advantages, as I mentioned, and some disadvantages of the pump that I see. Let’s start with the advantages I mentioned, very good response and high rate of conversion, but you won’t necessarily have that with the systemic. The systemic can’t give you this as well. But the disadvantages, some of you know this, the travel arrangement, if you don’t live in a city or in a place where it has it financially, the pump has many times these functions. There’s an increased incidence of biliary and vascular complications. Some of the patients that maybe are here will be able to talk about it, some vascular complications that can happen aneurysms, bleeding or dysfunctions and biliary toxicity, which I really think is a little bit higher, perhaps, is underreported. But a lot of patients develop these biliary problems. It responds very well, and the tumors decrease. But you pay for these. And also here, I’ve seen some patients who have dislodgement, the pump flipped and needs to be reoperated on, and high risk of technical surgery complications could be happening.

Dr. Roberto Hernandez-Alejandro 39:04
Let’s move to the case 2 study. Imagine a 46 year old patient that we removed the primary. The CEA is in 42. The patient has a KRAS mutation, one of these mutations, but there’s no evidence of extrahepatic disease, and this patient has all these multiple tumors. What do we want to do? Systemic chemo, HAIP infusion? Do we go for resections? Do we do an ALPPS? Do we take the patient for transplant? So we can have many options for these patients. I don’t think there is one correct answer at this moment. We need to remember to understand how that tumor behaves. I will go for systemic chemotherapy. Let’s go for systemic chemotherapy, and the patient received FOLFOX and FOLFIRI. And look at these, a lot of calcifications, and those tumors got smaller. Now are we going to do resection and ablation? Are we going to give Y90? Remember, I mentioned to you the patient… — I will go back… look at the many lesions that this patient had. Now it’s here. For me, it will be very easy to say, “Oh, I do a resection, a wedge here, maybe ablation here, and a wedge here”. But I know that all of these are hiding, they are sleeping, and they’re going to come back. So those are the ghost metastases, and we know that there’s a high recurrence rate. Wait and see, hepatic artery pump infusion. What should we do? I think we need to talk and understand the patient, what they need, in my opinion, in this case that I created, resection, perhaps not ideal due to the high recurrence. Ablation, the same thing, higher recurrence, of course, it’ss not as invasive as a surgery, but it will have high recurrence. And I think the benefit is questionable. Y90 probably, maybe if the patient is not tolerating more chemotherapy, or maybe combined with chemo as a bridge for some bigger operation. Should we wait and see? I don’t think it’s ideal, if there’s no other treatment options, and the patient’s family are in agreement, maybe we can do it. The hepatic artery pump, I think is a good option if there are no other plans for a bigger operation, and if the patient doesn’t want to continue with systemic chemotherapy, such as FOLFIRI. So you can see that it also depends a lot on what the patient wants and where does the patient want to go? In my situation, I will continue. The patient is tolerating chemo that FOLFIRI is more tolerated. I will continue more time with the FOLFIRI and the low CEA had no evidence of progression. Well, guess what? That patient got transplanted and was successful. 1.5 years of chemotherapy, no evidence of disease, and a good quality of life. Some issues on bile duct structures, but the patient is out of chemotherapy and enjoying life.

Dr. Roberto Hernandez-Alejandro 42:13
And this is where it comes from, my field of transplantation, where all these data were coming from, from Norway, but not anymore. This data now, it’s coming from North America. This is the first paper that comes from North America. This is also one of the very high impact factor journals, JAMA surgery, where we published this showing the first 10 patients with living donor liver transplantation and unresectable liver metastases that fulfilled the criteria, showing very similar outcomes as the group of Norway. They have been doing this for more than 10 years. We just started doing this close to four years ago. And here is the United States. This is a study that also we recently participated, Dr Tommelyama. It’s here as well from our center, some of the groups from Stanford and Cleveland. And we published this together. 48 liver transplants at that moment, last year, around the end of the summer, went in the United States for liver transplants for colorectal metastasis. So it’s not only 10 or 15; – 48. So probably by this moment, there are 60 or probably more, and we were able to see that it has a pretty good outcome, similar to patients in Norway.

Dr. Roberto Hernandez-Alejandro 43:42
What is that? Imagine having an outcome that this population of patients with unresectable disease, where they have a five year survival of 5%, then, now in five years, they have a 60% survival. That is pretty impressive. Now, some of the patients got living donor. Some of the patients got a diseased organ. Disease organ means it’s coming from someone who was brain dead, someone who died in the ICU and the family decided to donate the organ. So how do those patients receive a diseased organ? The reason that they were able to receive an organ is because they have a sick liver, not only because of the cancer, because all the multiple treatments with chemotherapy, Y90, hepatic artery infusion, and this liver was burnt out liver, and the patient has liver dysfunction, and the patient received a liver transplant, and those are the ones who didn’t do very well, the outcome was more complex on these patients, unfortunately. So what I want to see here, and the message that is very important for those patients for transplant, transplant shouldn’t be the last option. Transplant should come early in the algorithm because the outcome would be much, much better if we transplant the patient in the early stages. If we wait for the patient to not have more options and to be a burnout liver, we may be able to do a transplant, but the outcomes might not be the best. Technically, they won’t be doing very well. So this is an important message. We receive patients who are at the end, and we help them. And if we can do it, we do it. But if it comes earlier, I tell you the story is completely different. This is my institution protocol that we have been modifying after we have been learning in the last four years. We go for something that is called the Oslo score, that was developed in Norway. But we also added more things here that makes us more strict to be sure that things go in the right direction.

Dr. Roberto Hernandez-Alejandro 45:57
One of our research fellows was working on this project, and we have 138 referrals, that was until, I think, January, patients that came to assess for being a transplant candidate. And from those patients, 53 were men. 46 were women. This is the location of the primary tumor, majority of the patients have the tumor in the left side or in the rectum, 20% of the states have been referring patients were situated here, and there were three patients that were international. The stars are centers that are in cities or states from where more patients have come to us. And from those evaluated, many of them drop out in the beginning, because I mentioned to you it is very strict, but there are still around 26 candidates, and we are monitoring them, hopefully they come into this field and are the ones who have liver transplantation. I have here 13, just a few days ago we did number 14. And this is what will happen, those ones who dropped out, many of them were disease progression. Many of them had other centers. But what I think is most important here is the referral was made an average of 10 months after the diagnosis. So again, the (internet connectivity dispruption) earlier the referral, the earlier we see them, we can come and work. Perhaps of those 112 patients, they will refer earlier, maybe, and this is speculation, but maybe around 15% of those patients maybe will have the chance of being transplanted. I might be wrong, and there’s no evidence of this, but that is my feeling just looking at the way that the disease progresses. I want to show you, and I hope you don’t mind, this is a real liver. This is a donor, and that’s what we do, and this is something that helps us. We use something that is called green indocyanine, where we have to divide the liver. The patient is going to donate the right side, and the left side of the liver will stay in the donor. And this is how we mark. (internet connectivity dispruption) And we know where we are going to be cutting with something that is called a hydro jet and you can see here we’re dividing –

Julie Clauer 48:59
Dr Hernandez, sorry, when the video was playing, it was hard to hear your voice. So do you mind just describing what was in the video again?

Dr. Roberto Hernandez-Alejandro 49:12
Can you hear me now?

Julie Clauer 49:14
Yes.

Dr. Roberto Hernandez-Alejandro 49:15
Okay, so you saw the liver getting green, right? And this is with a special lamp. We inject something that is called green indocyanine. We are blocking the right side, the artery and the vein, and this is helping us to decide where exactly we have to divide the liver. And I think it’s pretty impressive to see that, and it’s a lot of advanced technology that is helping us for doing the correct operation. Nowadays, these green indocyanine is also used to detect sometimes liver metastases. Some centers in Asia are using it and they inject it one week before doing the liver resections in these patients. But while if you were able to see the green, indocyanine part. I will skip that one. The next slide here, if you are still seeing me, is how we divide the liver, and I will play it and I will talk. But this is with a water jet. With water we divide the cancer cells. You can see in the right side here, it has already divided all the liver, and this is the left side that stays in the donor. I will play it and I will talk.

Dr. Roberto Hernandez-Alejandro 50:45
Okay, so that’s how we divide the liver, and we try to maintain like minimal blood loss in these patients, despite the fact that the liver is an organ that receives a lot of blood supply. In our experience doing living donor liver transplantation on these 14 patients, that is our survival: 80% survival at three years, and recurrence-free survival, only 90%. So this is, I would say, a little bit better than what is happening in Norway. But I think a lot of the patients, maybe some of them, will have recurrence at some moment. But the thing is, if it comes back and it comes back in the lungs, we can do a lot of other things.

Dr. Roberto Hernandez-Alejandro 51:24
What are the advantages of having living donor liver transplantation compared to other options? Well, there’s a risk to the donors, definitely, but we try to decrease as much as possible the risk in the donors, doing a very good selection of these patients; Problems of bile ducts or vascular complications, we have been fortunate that we haven’t had any biliary or vascular complications in all our donors. And the advantages is that we remove patients from the waiting list. We do this in patients with cirrhosis, right? That’s a very good way of helping patients on the waiting list, that we transplant the patients prior to the recipient becoming very sick, it’s elective and non emergency, and what I call here, minimal cold ischemia time, is that the liver stays in the ice for a short period of time. And probably a lot of benefits that we can talk about more in other moments. Do we transplant patients after the pump? What happened? They can have very good response, as you know. We use the same criteria as those patients who have systemic chemotherapy. However, patients need to understand that there’s a higher surgical challenge. The hepatic artery where they put the catheter of the pump gets very damaged, and the damage is because of the same chemotherapy that is going through that artery. And that artery cannot be used for putting back together. And the liver needs that artery to get oxygenated blood. So we need to come up with a strategy. And our expert here, Dr. Tomiyama, myself, and other surgeons that work together, like Dr. Piena, Dr. Nair, and all the team together, we find arteries that are behind the spleen that we will need to dissect and flip it over to the liver to be able to do this, or something that is called a conduit, that we use, coming from the artery to provide blood supply to the liver. So definitely, it’s a more complex operation. There are some patients, for some reason, that have less complications or less complexity of the operation, but there are other ones that have a higher complication rate.

Dr. Roberto Hernandez-Alejandro 53:44
This is a new study that I don’t think I have shown here, and this is pretty impressive, because this is a 10 years follow-up on the Norway patients. This is the first time that I’m showing a slide of Norway, right? Because now we have a lot of data from from the US, but we don’t have this data in the US yet, because this is our 10 years follow up from 60 patients of data, 10 year survival of 50%. These are patients who have unresectable liver metastases, stage four, who were going to have only palliative chemotherapy. They responded, they did a liver transplant, and at 10 years, 50% of them are alive. So this is pretty impressive, but this is only those ones who have an Oslo score of two, one or zero, which is strict, as I mentioned to you. I mentioned about pulmonary recurrence. When it comes in the lungs, we can treat these patients. We can resect it, and they do pretty well. When it comes in the liver, the outcome is not that good after transplantation. Just to mention about recurrence: Recurrence after resection is pretty high, that takes place in the liver, when in the liver after transplantation is pretty, pretty small, and the survival rate at five years, as I mentioned, 10 years, 50% at 10 years compared to 20% at 10 years on resection. I want to be very clear here: I’m not saying that instead of doing a resection, we should do a transplant. A patient who is resectable, we should do resection. A patient who is unresectable, which we hopefully, we can do a transplant, a patient who is unresectable and responded very well to chemotherapy, transplantation will have a huge benefit, in my opinion, on these patients. This study from our center, very recent study. We analyzed all the liver ‘explants’. That means what we removed, and those patients have a very good response, and we analyzed all the studies with the permission of the patients, and the analysis of the patients, and they signed the consent, and we analyzed how many metastases they had, and we compared to the CT scan or the MRI before the transplant, and they have —

Julie Clauer 56:17
Dr. Hernandez, I’m sorry this is such a good slide, can you put it on full screen, just because it’s so deep? It’s so detailed, I want to make sure people can see it. It’s such a good study. I’m so sorry.

Dr. Roberto Hernandez-Alejandro 56:27
All right. So these are the patients. They explant – that means that the liver, when it came out, went to pathology, and the pathologist sliced it and analyzed it centimeter by centimeter, and these are the amount of tumors that they found at the moment. The brown livers right? This one that is a partial liver is because this patient had a left hepatectomy, or these patients had a right hepatectomy. But they analyzed, and as you can see, the vast majority of the livers in pathology have more tumors than what the CT scan, which is the one in the middle the CT scan, or the MRI before the transplant. What is this telling us? That 64% of the time, we were able to find more disease of what we were able to see in the scans. I showed you that with radiology, but this is the first time that we have the entire liver that we’re able to prove it. So this is, I think, a very important information to give. And I think this is showing us why, when we do liver resection after a lot of liver metastases disappear, why we see a very high recurrence rate. I have to be fair, right? It’s not, “Okay. Let’s go for transplant, and you’re done”, and then you go and play in the park. Well, some of them can do that, but for some of them, life after transplantation, there could be some complications. You have to be on immunosuppression. It’s not like chemotherapy at all. It’s pretty well tolerated. Sometimes there could be some things, especially in the first year, that you have to be measuring and knowing the levels of your immunosuppression, but it’s pretty well tolerated and low side effects in the vast majority of the times. There can be some acute complications, such as vascular complications that probably in the artery that sometimes we need to put a stent or something like that, to to avoid the artery to close, because it’s very small vessels that we use. Unfortunately, biliary complications is more common.

Dr. Roberto Hernandez-Alejandro 58:38
What are those biliary complications? There could be leaks or strictures when we put together the donor and the recipient’s bile duct, sometimes we have to put those stents. And in some patients, we can remove it at one year, six months. And some of the patients require it for long term. And some of them, they require a metallic stent for life. Retransplantation could be an option for some patients. We have a patient that was transplanted and hasn’t had recurrence, but the liver developed some complications later on because of some biliary complications, and now the patient is listed for retransplantation. And also I put that with chemotherapy, the patients normally do not receive chemotherapy after transplant, but in case there’s recurrence, the patients can tolerate chemotherapy. And just to finalize here, I just want to show something that I know that one of the patients who came here with us, and I think it was in the group of COLONTOWN and decided to go to Germany, because this patient has some roots in Germany, went for a live donor liver transplantation with this concept that is called the ‘Rapid Concept’, and it’s using a live donor, but they use a small portion of liver instead of using the right side. They keep the right side with cancer but they wait for this growth in a few weeks, and then they come back when this left side is bigger, and remove it. And this is a new concept. There hasn’t been any center in the US or Canada doing this yet. I think it might happen at some moment. I think we have other options in North America. But this is a new concept that I just want you to know about the rapid surgery, which I think it’s a pretty impressive surgery, but perhaps is, there’s no need of doing it in that many patients. I want to leave this because this is for me, giving hope. This is hope for a lot of patients who are unresectable, or patients who perhaps have liver disease and lung disease and maybe disease in other places that are unresectable because there’s metastasis outside the liver. And I am not getting paid for it, nothing like that. I just wanted to, I asked them if they can share with me this short video. And I think some people have seen this. This is histotripsy. It’s an ultrasound that liquefies, destroys the tissue, creating dead cells. So imagine that we can use this. …I don’t think it’s going to run, so I apologize that it’s gonna… I have to do it this way.

Dr. Roberto Hernandez-Alejandro 56:29
Can you hear my voice?

Julie Clauer 1:01:50
Yes, yes.

Dr. Roberto Hernandez-Alejandro 59:56
Okay, so this is liquifying so it’s through an ultrasound with water, and it’s going to destroy the tumor in the liver, and it’s going to have an immediate reaction. So I’m really looking forward to doing this, and we don’t have to open the patient. This can be done from outside, but we need to anesthetize with general anesthesia, the patient in the operating room. General anesthesia, the patient gets intubated, so the patient is not moving. We rotate the patient, we put this machine and this area will go down to the abdomen of the patient, and there’s going to be a big bubble of water coming out here, like a balloon that incorporates to the skin of the patient. And we can assess the tumors in this ultrasound, and we can target the tumor and start decreasing it. Is this going to cure the patients? I’m not sure, but probably, and we need to develop more studies. The trials were done in the US and in Spain, in patients who were palliative the outcomes, it’s going to be helping all a lot of this, is going to be for trying to downsizing the tumor and to make the patient resectable, or to be able to bring those patients to transplant in different types of tumors, and a lot in colorectal liver metastases. And with that, I think I’m done.

Dr. Roberto Hernandez-Alejandro 1:00:38
Well, conclusions. Let’s let’s say, you need a good team. You need to feel comfortable with them. Chemotherapy is very important to understand the behavior of the tumor. There are different modalities that can be helped, and patients need to know about them. And also the field of liver transplantation in those patients with stage four advanced multiple metastases, they should know about that, and surgeons should be in their toolbox. Transplant shouldn’t be the last option. It’s not the last option. Liver transplantation in selected patients is providing great results, and it’s important to have a multidisciplinary team approach. We need to collect more data, and that’s what we’re doing here, and we are doing a lot of research in our institution and taking tissue and understanding more about the molecular phenomena that are happening in those tumors that hopefully we can help patients in the future. And with this, I would say thank you very much, and I will stop sharing.

Betsy Post 1:00:38
Great. Thank you. Julie, do you want to do some of the questions? I think just scroll to the top. Or do you want me to do them?

Julie Clauer 1:04:39
You’re so good at it. I’ll do it if you want me to, but you’re so good at doing it,

Betsy Post 1:04:45
I’ll start it off. So thank you so much. Thanks everyone for hanging in. We are going to go in order for some of the questions that were sent through chat. So the first question that I’m seeing is, you mentioned Fatty Liver. Is this a common thing to occur after you have liver surgery?

Dr. Roberto Hernandez-Alejandro 1:05:06
No, it’s not a common thing to have after surgery. Is not an uncommon thing to happen after receiving chemotherapy. Fatty Liver is very common nowadays, in the US, in a lot of us, we can develop fatty liver just because our the way that we eat and our sedentary lives can create that. But if we receive chemotherapy, that creates fatty liver as well. So it’s more common with chemo, not necessarily because of the surgery. The surgery itself do not create fatty liver.

Betsy Post 1:05:42
This one, I actually think you addressed but it’s on your thoughts on doing the hepatic pump with the goal of resection. But I think you addressed that a little bit later after that question came through.

Dr. Roberto Hernandez-Alejandro 1:05:54
I’ll just, to go quick, Betsy – is yes, pump, and surgery after pump. It’s a great thing that happens, and it has a very good response rate and conversion rate with the pump. Definitely. We know that there could be some hiding ghost metastases, in some of those patients. But it’s a risk that can happen, but it it makes it a little bit more complex, a bigger operation in the liver. Definitely, it’s a little bit more complex to do after the pump.

Betsy Post 1:06:32
So there was a paper that you showed from, I’m going to probably say this incorrectly, ‘brouquet’, ‘brocketts’, the 2011 paper where you showed the rate of disease-free survival, was there a rate of overall survival?

Dr. Roberto Hernandez-Alejandro 1:06:51
So what is the question?

Betsy Post 1:06:54
So she was saying that when you talked about that, or you referenced that particular paper, you showed the rate of disease-free survival. What was the rate of overall survival?

Dr. Roberto Hernandez-Alejandro 1:07:08
The one for brokette, let me see if it’s the one from Northern Europe, …I don’t know if which one is the one from Brockette, but what I can tell you is, disease-free survival after resection in patients who have response it’s disease-free survival. That means that patient, that won’t have disease at five years, right? It’s going to be around, generally, around 30% of the patients, depending on the amount of disease. So the majority of the patients, we know that they’re going to have recurrence of the disease after resection. Of course, as I mentioned, the more metastases we have and then going for resection, then the higher chances of having recurrence. So size matters for sure.

Betsy Post 1:08:10
Do we have data on outcomes for patients who get FOLFOX, then the hepatic pump, as compared to patients who get FOLFIRI and then the hepatic pump?

Dr. Roberto Hernandez-Alejandro 1:08:21
So, I’m not a medical oncologist, but I can tell you that the rate of response of FOLOFOX and FOLFIRI, is very similar. A lot of the time some of the initial studies, were done with FOLFOX. So that’s why they start with FOLFOX. The problem with FOLFOX is that many of you know that the side effects are neuropathy, and they can create problems with your fingers, with your toes, with your lips. So it’s not uncommon that the patient at six months does not tolerate so then they switch you to FOLFIRI. That is more tolerated than FOLFOX. So there’s no data which one of them will work best. I think both of them do have a very similar response rate, and normally when patients use a pump, they also receive systemic chemotherapy. So, many of them, they go on FUDR, which is the chemotherapy that is used in the pump, plus systemic chemotherapy, because, remember, the pump is only attacking the liver, but there is also systemic disease that the patients still need some chemotherapy for the systemic disease. We want those lymph nodes to be without cancer, so they need to attack from both sides.

Betsy Post 1:09:40
Do you think surgeons are on board with using CtDNA testing, and what actions could a patient take if there’s a positive ctDNA?

Dr. Roberto Hernandez-Alejandro 1:09:50
That’s a great question. A positive ctDNA, is something that is telling us there are circulating tumor cells. A lot of the times, the liver sheds DNA from the cancer, quite often, and we do CT scans and we cannot see it, and we do CT scans from head to toes, and we cannot see it, but later on, it’s going to come back. I think it’s difficult at this moment to justify if we resect the patient or we transplant the patient, and there’s no evidence of disease in the imaging, but the circulating tumor DNA is positive, it’s going up. It’s difficult to justify starting chemotherapy in that patient if we haven’t seen it, but I think collecting the data is going to be able to give us that answer in the future, because this is probably, I want to be cautious, probably better than having CEA measurements. A lot of the times the CEA is low and it never moves too much, and probably it’s more sensitive than circulating DNA. But we need to collect more of these data.

Betsy Post 1:11:00
Do you have an approximate percentage of people with colorectal cancer who will only develop a solitary liver met? I saw a video from a liver surgeon made a couple years ago, who said it was around 50%.

Dr. Roberto Hernandez-Alejandro 1:11:17
That only developed liver Mets?

Betsy Post 1:11:19
One liver met.

Dr. Roberto Hernandez-Alejandro 1:11:24
It happens. I don’t see that often, perhaps because my practice has turned into seeing patients with advanced and multiple liver metastases. One of our surgeons, Dr. Nair, just recently, did a robotic single resection of a met. And yeah, I think there are many of them, but I don’t know a percentage or a number that I could say. And though any patient who has one or five and they are resected, they need to have a close follow up, those patients, because recurrence can happen, and we need to have a close follow up.

Betsy Post 1:12:04
Is transplant an option if a stage four patient has recurrence in the liver after five years of being NED?

Dr. Roberto Hernandez-Alejandro 1:12:11
Definitely, the answer is yes, transplant could be an option for those patients who have recurrence of the disease, even after resection or after ablation, as long as we see that they fulfill the criteria that you know they are responding to any type of treatments, whether this is a local, regional therapy or surgery or ablation or chemotherapy. If they are responding and there’s no disease outside the liver, those patients could be candidates for transplantation.

Betsy Post 1:12:44
What are the common reasons that insurance companies deny coverage for a living-donor liver transplant?

Dr. Roberto Hernandez-Alejandro 1:12:51
I don’t think this is just for living-donor liver transplant. It’s for liver transplant because liver transplant for colorectal metastasis is not authorized or in the United States in insurance, and even if you live in a country where you know there’s a social system, like in Canada or in Norway or in France, you need to come with an idea on saying why you’re going to take a liver, like a cadaveric liver, and put it in a patient who is not normally on the waiting list. So you need to justify, very clearly that, – so here in the US, the insurance says, “Well, this is not an indication for liver transplantation”. And our team, what we have been doing, and we have turned to be, I would say, experts in this field, is fighting with insurance companies first in a polite and nice way, talking to them peer to peer and sending a lot of data and documentation. Initially, they were saying there’s no American data. Now we can provide that American data that I showed to you, and that helps us trying to get approval for these patients. And sometimes we need to use other medias, not necessarily the peer to peer. Sometimes, if it’s denied, denied, denied, sometimes, social media helps the patients a lot, and the insurance in the end, they accept. So far, we have been successful, but to do this, you need to have a team that is willing to move the needle.

Betsy Post 1:14:28
So many of us who come from rural areas have little support for determining a bridging strategy to get to transplant. Some of us might progress during this time when donors are being screened. How can we solve this problem and ensure people feel they have an appropriate bridging strategy?

Dr. Roberto Hernandez-Alejandro 1:14:50
Well, access to transplant… This is a big problem in the entire country, in the world, about access to healthcare systems, to different complex treatments. And this is not only for colorectal metastases. I think it’s also for other areas where I work in the field of complex liver surgery, complex cancer in the pancreas. You know, a lot of the patients, they are able to reach treatment because they have a better social media, they have a better/good insurance, or they live in a city that can provide different types of treatments, but not having access to these options, a lot of patients are in a disadvantage. I personally think that having places like on social media, like COLONTOWN, for example, or other groups that help support patients, and being able to provide this education exactly like what you’re doing today, it helps patients within the community, and you are the ones who have a voice and then spread it, and people who are able to reach out to you, and you can guide them and provide them the opportunities, right? It’s difficult, and hopefully it continues opening. And I think, making a voice, it’s so important to help different communities, people who have to live in small places, minorities that are disadvantaged, it’s really important to be able to provide this education.

Betsy Post 1:16:31
Definitely, I know we have at least one patient that’s kind of taking some of that on, so I can connect on that later with this person. Is there any comparative data comparing the hepatic pump versus Y90 therapy and converting nonresectable to resectable disease for surgical intervention?

Dr. Roberto Hernandez-Alejandro 1:16:55
I’m not aware that there’s a study comparing Y90 with the pump. I can tell you that I have a lot of experience with Y90 because as a transplanter, we do treatment of the most common primary tumor that is called HCC in liver. Nobody here, I think, is associated with the HCC. But this tumor is quite common, and we treat it very often in the US with Y90, and many of those patients later on go to transplant, and we see how they respond. Y90 works very well in HCC and in other cancers that is cholangiocarcinoma, it also is pretty helpful. But now using Y90 in liver metastases is not the norm. It’s not in very common use. We have used it very few times, but a lot of the patients that we see, some of them, they have been treated already with Y90. But those are the patients who’re going to go for liver transplant, the ones that I’m telling you that received some Y90, but comparing hepatic artery infusion with Y90, I’m not aware of any study comparing them. It’s a different strategy, and I think the indication is very different, because what the Y90 could be more located for a specific area of the liver, and the pump is more in an entire liver with a blood supply.

Betsy Post 1:18:28
Is liver transplant only available to patients that have cancer only in the liver?

Dr. Roberto Hernandez-Alejandro 1:18:37
To be very clear and orthodox, I have to say yes, but I have to tell you that, for example, we have a patient who had a lung metastasis, and that patient, they removed it, and the patient, one year later, after removal of the lung metastasis, came and said, “Can you transplant me?”, and there’s no evidence of recurrence in the lungs. And then the patient was a candidate because of liver, and we couldn’t find any other disease outside the liver. Am I going to say no? It was hard for us. We discussed it in our team, and we did a transplant, and the patient is doing well and there is no evidence of disease, I think more than two years now, or even two and a half, maybe a complex case, but the patient did very well. So I think there’s space for pushing the envelope in some specific patients. But to be very orthodox, if there’s disease outside the liver, it’s not in the best interest for the patient to have a liver transplant.

Betsy Post 1:19:46
When should a liver mets patient consider a second opinion or other opinions on their treatment?

Dr. Roberto Hernandez-Alejandro 1:19:58
That’s a tricky question. But I would say, if you go the first time and you feel very comfortable, and you know this person or this group or this team knows what they’re doing, and they’re giving you hope and opportunities to get treated and they’re looking for, ‘okay, this is the way that we’re going to get you to resection’. I would stay there. I wouldn’t move. If I feel that there’s something that I don’t feel very good, I will look for second, third opinions, fourth opinions. It’s not complex nowadays, especially, having virtual visits, the vast majority of the patients that my team says is with this disease are patients who we do telemedicine, right? We don’t ask the patient to be traveling to see us and spend thousands of dollars on a plane ticket and keeping them in the waiting room for a long time. They come here once, we’re going to treat them. But we manage the patient from a distance using telemedicine. So that is helpful, but if you don’t feel comfortable, or also if your disease is very complex, then probably you need to hear second, third opinions. And it doesn’t matter if you are with what you think is the best. A lot of the times, patients come with us for the first time. And if there’s complexity, I tell them, “Listen, go and talk to another one, the other person, other surgeon. And I want you, if you’re going to come to us, I want you to be sure that you are comfortable with us with the decision making”, so it’s important, it creates a better bonding with/ between the group, the surgeon and the patient and the family.

Betsy Post 1:21:51
Is a liver transplant preferable to multiple liver resections due to recurrences, or have liver resections as long as it is possible?

Dr. Roberto Hernandez-Alejandro 1:22:02
If I understand the question very well. So if you come, if your patient has a liver section, and then recurrence, and then resection, and then recurrence, is that something similar to having a liver transplant?

Betsy Post 1:22:15
So I think, I think he’s saying if you’re having multiple recurrences, should you then, be looking at transplant, or should I continue down this path of multiple liver resections?

Dr. Roberto Hernandez-Alejandro 1:22:29
Well, what I will be concerned with that patient that is having recurrence and recurrence and recurrence is that there’s going to be a moment that the recurrence is not going to be in the liver, it’s going to be outside the liver, and then that will change the plan and the strategy completely, and then transplantation is not going to be an option. Or also there’s going to be the moment that the tumors are going to mutate, and it’s going to change, and it’s not going to be responding to chemotherapy. So definitely the multiple recurrence, I think transplantation plays a very important role if we’re able to prove that there’s no disease outside. Hopefully that responds your question?

Betsy Post 1:23:19
Yes, that did. You were talking about the timing of transplantation and not to wait too long in people with liver-limited disease, when is a good time to start thinking about transplantation?

Dr. Roberto Hernandez-Alejandro 1:23:34
I think at any moment, you know, it’s March right now, and we recently saw a patient who was diagnosed with sigmoid cancer and multiple liver metastases, and the patient was going to the first session of chemotherapy. Before going to the first chemotherapy treatment the patient contacted us. I could say, “Well, there’s no problem. I can see the patient in six months”. No. Meeting with the patient, talking, meeting each other, connecting, creating a plan. I know it’s going to be a long term and probably the patient will drop off, hopefully not but guiding, talking to them and making connections with their oncology team from here, sometimes we connect with oncology teams from other centers. We talk to them, we explain what we’re doing. Some of them, they are aware of what we’re doing. Some of them, they are not aware about transplantation, for example, especially these complex cases. And sometimes we see patients that they were told that they were unresectable, and we say, “Wow, we think you’re resectable”. I can tell you a surgeon close to your place that maybe we’ll be able to do, or you want to come here, or something like that. So those things happen sometimes. So if the patient is in the early stages, we think it’s good to talk to the to the transplant team, they don’t have to wait for months or years ahead.

Betsy Post 1:25:12
Is there anything one can do to prevent developing fatty liver? You know, after having chemo or with chemo?

Dr. Roberto Hernandez-Alejandro 1:25:20
Not that I know, not that I know. I know that there was a study done in small animals about avoiding fatty liver with chemo, and I know that it was done with green tea. Green tea protected, but the amount of green tea that you will need to drink, you will need to be swimming in a big swimming pool and drinking all of it. So it was very high levels of green tea. That’s the only thing that I know that has help for decreasing fatty liver. But the amounts will have to be very high. And I think probably you will get intoxicated with green tea. Exercising, also watching the diet might be helpful, or at least decrease or delay the fatty liver, but the chemo will damage the liver.

Betsy Post 1:26:16
I’m going to mess this name up, just FYI. You can laugh at me, but it’s the new machine that you showed at the end that new technique. Are there any institutions that might be the first to jump on the histotripsy? See, I don’t know how to say it… technology!

Dr. Roberto Hernandez-Alejandro 1:26:33
Yeah, it’s called histo-trip-sy.

Betsy Post 1:26:36
See, that’s easy. I can say that now, okay.

Dr. Roberto Hernandez-Alejandro 1:26:39
I told them to change the name, because, but I cannot say names but there are two institutions, one, you know, which one that is, and the other one is not that far from here, that are pretty advanced, but these companies are working in many other places, trying to get these placed out there. So I think it’s going to take a couple of years to be out there strong in the market. But I think they’re going to start with, 3, 4, 5, centers, starting to do it, and hopefully by the end of this year or in the Fall, I’m looking forward to being able to use that here.

Betsy Post 1:27:32
You mentioned we don’t have too many questions left. You mentioned one of the patients you presented data on received remote care under your team? Can you clarify what that means, and how would one involve your team remotely from you? And he said, I’m seeing Dr. Kooby, and Dr. Mitel from Emory in Atlanta, whom you might know.

Dr. Roberto Hernandez-Alejandro 1:27:55
Yeah, well, what we do is, we invest a lot in the patient. We follow the patient pre-operatively, in the surgery, and sometimes the complexities that post op, and some patients clearly are concerned, especially because sometimes they want to have a very quick answer, right? We have been able to place a team of navigators that are helping all these patients. We have a coordinator on living-donor, one of the nurse practitioners helps us directly with patients with colorectal liver metastases. We need a nurse practitioner that was working with us that left, and we’re hiring a new one that is coming soon, so there’s a full team that follows these patients, and we’re going to put more resources in to follow these patients. What we do is we communicate with them and contact them, and then if it’s needed, if we there’s something surgically that is needed, we contact a liver surgeon or a hepatobiliary surgeon or a transplant surgeon in their place in Atlanta there, that’s the case that we do it. I know Dr. Kooby extremely well. We’re friends, we’re colleagues and a lot of other places that we know, and that’s what we’re trying to do, and connect with the patients pre-op as well, for the chemotherapy, and if it’s needed later on, to connect with the oncologist. That’s what we try to do as well.

Betsy Post 1:29:27
I can connect also with you, if you message me: the person that asked that question, so I can help you with that also. We just have a couple left. What are the chances of a stage three rectal cancer patient currently on FOLFOX to develop liver mets?

Dr. Roberto Hernandez-Alejandro 1:29:45
Wow, that’s a great question. So the patients who have a stage three, that’s a reason that they go for chemotherapy to decrease the chance of the patients to develop liver metastases. Those patients need to have follow up CT scans and CEA every six months, depending on the timing for the next five years, because we know that there can be some some recurrence rate. And I think it depends, also it’s not only stage three. There are different stage threes. There are A, B, and different depending on the amount of lymph nodes that were found in the rectal cancer. And it can go as high as 40% it can go as high as 60%, the chances of having liver metastases. The good thing is, the patient knows that there’s a risk, and there’s going to be a close follow up, and if they catch it earlier, then things can be done in an early stage. You don’t have to wait to have 10, 12, 15, metastases, and then, then there’s a complexity to this. So it’s terrible to have colon cancer, but you have, in earlier stages, you can be watching very closely for the metastasis and catch them in an early stage.

Betsy Post 1:31:24
And I think we just have one more: does the hepatic pump, those treatments cause significantly higher amounts of fatty liver?

Dr. Roberto Hernandez-Alejandro 1:31:34
Yes, but I think the fatty liver, it gets a little bit burnout. By burnout, what I mean, is it creates more fibrosis. Fibrosis creates scar tissue, and one of the problems of the pump is what I mentioned about the biliary damage. The liver produces bile, and it runs through little bile ducts, like a tree in the in the winter, right? No leaves. That’s exactly how a bile duct is inside of a liver. Those little branches and middle branches start getting damaged, and the bile cannot come down. And then this is when the patients start having the elevation of the bilirubin, or the liver enzymes elevated a little bit. So then they have to decrease the amount of FUDR, or they delay it, or they say, let’s stop it. And then it’s giving only systemic chemotherapy. So that’s the toxicity. It’s what happens. I’m not saying that this is bad, don’t use it. No, it has its benefits, it’s better to attack the cancer. But these are side effects that happen that creates, what’s called, fibrosis scar tissue. You saw those pictures that I put there with healthy livers from donors. If I would show you a liver after multiple treatments with the hepatic artery pump, you couldn’t recognize the liver. Of course, I will be putting the ones that we ended doing transplant because they got a lot of damage. There might be many that are not that damaged, but that could be created by too many treatments.

Betsy Post 1:33:09
I’m going to take this one last question. Is fatty liver irreversible? And what are the symptoms? Are there symptoms of it?

Dr. Roberto Hernandez-Alejandro 1:33:23
I think fatty liver is not irreversible. Fatty liver can be improved, especially when it’s not created by chemotherapy. And really, when we have a fatty liver with no chemotherapy, it can be changed in two, three months, in a patient who changed their habits of how they eat, how they work, how they do things in life that can be changed. Now, if it’s chemotherapy, that is creating the fatty liver? And if the chemotherapy is stopped, the patient will have improvement of the fatty liver and the liver definitely will. But I will be worried about,okay, if the patient had cancer and now stopped the chemotherapy, now what is the patient getting, right? So definitely, that will be a little bit of a concern. If the patient has fatty liver and went for resection, and there’s no evidence of recurrence, and it’s of chemotherapy, that liver is going to recover for sure.

Betsy Post 1:34:28
Do we have time for one more? There’s one more that just came in. I want to have to – it’s 9:35 – you’ve been so generous with your time, we’ll just take one more. Is the chance that the hepatic liver pump causes damage to the liver reduced for individuals who tolerated eight or 10 sessions of chemo FOLFOX without too much damage to the liver.

Dr. Roberto Hernandez-Alejandro 1:34:51
Oh, well, it would be difficult for me to answer that. And probably, you know the experts on maybe the Dr. Kemmeny in MSK, who is the person in the world who knows more about this will be able to answer that question. So I don’t feel I have the knowledge for you being able to answer that. I think there’s no association between if you tolerate a lot of FOLFOX, that means that you’re going to be able to tolerate a lot of FUDR in the pump. I don’t think it’s that. I think it must be something different, because the mechanism of action of FUDR in the pump is different than the systemic FOLFOX. It’s a different mechanism of action. So I don’t think they are associated. But don’t feel expert to answer this question.

Betsy Post 1:35:43
So I just want to thank you, Dr Hernandez, for all of your time, your amazing presentation, taking all of the questions, and, just being so generous with all of us, so thank you so much, and thanks everyone for attending. This was great, and we really appreciate it.

Dr. Roberto Hernandez-Alejandro 1:36:13
Well, yeah, thank you very much, Betsy. Thank you very much, Julie and everybody for being here. I think I probably prolonged too much my talk, sorry about that, and maybe was too much information. But I just wanted to be clear and showing that panorama about what is out there.

Betsy Post 1:36:23
Someone just said that three years ago this week, she was recovering from stage one ALPPS in Toronto. Her liver is clean to this day from that surgery.

Dr. Roberto Hernandez-Alejandro 1:37:02
I’m very happy about that.

Betsy Post 1:37:03
Yeah. I thought you’d like that. Lots of thank yous in the comments.

Dr. Roberto Hernandez-Alejandro 1:37:07
So thank you very much. And also I want to thank – because I wouldn’t be able to do this without the team – that the amazing team that I have surrounding myself, and the institution that is supporting me. So thank you everybody. I think there’s few members of my team that are in this talk, but well, thank you very much again.

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2023
Dr. Hernandez-Alejandro
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Histotripsy
Liver
Stage IV
Transplant

Dr. Roberto Hernandez-Alejandro from the University of Rochester Medical Center discusses the range of treatment possibilities for bilateral liver metastases. Recorded in March 2023.

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Histotripsy for mCRC liver mets

Histotripsy for mCRC liver mets

DocTalk
2023
Dr. Hernandez
Liver
Stage IV
Histotripsy

On December 20, 2023, Dr. Hernandez discussed the newly FDA-approved treatment of Histotripsy in the treatment of mCRC liver metasteses within a week of performing the first time use of this novel therapy after FDA-Approval in the US. He describes the history of the therapy, what it entails, why and for what conditions it is applicable and future research ideas.

Warning: Graphic surgical images at 13:00 minute mark.

 

Betsy Post 00:01
Welcome, everyone. Thank you so much for joining us this evening for our latest DocTalk. I’m so pleased tonight to be with us here for our COLONTOWN DocTalk. Dr. Louise Connell from Memorial Sloan Kettering Cancer Center. Dr. Connell, I think is very well known in COLONTOWN. So if you’ve been around for a while, you definitely know her name. If you are familiar with liver Mets, and especially if you’re interested in the hepatic pump, I know that you definitely have seen her name. And our groups such as Liver Lovers Lane and HAI Pump People, I’m sure that we have some of her patients here tonight to support her as well. So we are so thankful for your time, Dr. Connell, especially for doing this after hours so that we could get maximum participation from our patients and our caregivers. So thank you, again, for agreeing to do this, we’re really excited to hear from you on how you treat patients specifically with the pump. I know that you have some things about the future about the pump, which is really exciting. I’m very excited to hear that. And then we did have patients and caregivers submit questions in advance. So we will get to those questions at the end of Dr. Connell’s presentation. So at the end of her talk, she will, we’re going to do some Q&A based on some questions that we received in advance. As she is presenting, we would ask that you please stay muted so that we can make sure we’re being respectful of her presentation her time, but do put your questions in the chat. So please do use the chat feature to submit your questions. And we will get to those live questions at the end of the presentation and the pre-submitted Q&A. So with that again, Dr. Connell, thank you so much for being here. The floor is yours.

Dr. Connell 01:55
Okay, thank you, Betsy. And first of all, I just want to say thank you very much for the invitation to speak here tonight to you all. COLONTOWN is is a resource that I hear so much about from my patients, and a platform that I think provides so many of you with information that you bring to the clinic, to advocate for yourselves and to, you know, advance your care. And I think, you know, it’s been such an important resource that, you know, if there’s any way that I can help provide additional information, particularly about the liver pump. This is an honor to be asked to do this. So tonight, my slides section is small on purpose, because I really wanted to give you all an opportunity to ask questions. And I would encourage you to submit any questions that you have for me. I did just want to provide some background on you know where we are today, today in terms of metastatic colorectal cancer treatments, and in particular, the role for HAI therapy. I think many of you already know much of this information. But in particular, for patients and caregivers who perhaps are new to this or maybe considering a pump, I did want to provide just some background slides on the pump treatment.

Dr. Connell 03:15
I’m going to just advance my slides here. So first of all, I just wanted to put up this disclaimer to acknowledge some of my consulting work. But truly the presentation today is purely for informational and educational purposes. And it’s really based on my clinical experience with patients and my knowledge in terms of pump management.

Dr. Connell 04:16
And at diagnosis, we see approximately 20% up to a third of patients will have liver Mets at diagnosis whereas the majority of patients will go on to develop liver metastatic disease during their follow-up. The question is what are our treatment options nowadays for metastatic colorectal cancer and, I’ll just briefly run through this on this slide on the next slide. But essentially we have or our cornerstone standard of care chemotherapy treatments, and we combine these drugs with biologics. I think increasingly we’re hearing about biomarker-driven approaches and I’ve highlighted here are the four key targets that we look for in patients who are newly diagnosed being microsatellite status. Their RAS status, BRAF status and HER2 status. 

Dr. Connell 05:00
And, of course, you know what I think I’ve always in patients because of the work that I do is the role for local regional approaches and particularly in patients who have liver only disease or liver dominant disease and looking to intermix this and combine it with my chemotherapy drugs and with biomarker-driven approaches to get the best outcomes for patients. So in terms of patients with liver dominant or liver only disease, you know, I consider resection, ablation, of course, hai therapy and also y 90 as well as I should mention radiation treatments to the liver. And also, I think local regional approaches have a role to play in patients who have lung metastases or illegal metastatic disease which is out where you may have an isolated tumor or a small tumor. And you know, maybe you can be more localized with your treatment approach and for the lung that would include ablation resection and also stereotactic radiation. D=So the progress that has been made in the last you know, 50 years is phenomenal. Unfortunately, a long time ago, when patients were diagnosed with metastatic colorectal cancer, and there were no drug options, the recommendation was for best supportive care and, then over time, really, it was single agent 5FU. And this slide shows where we are today in terms of drug treatments. On the left hand column, you really see our cornerstone drugs, which is the Fluorouracil, Capecetibine have been being the oral version Irinotecan and oxaliplatin, and this is what we all know, as, you know, fall Folfox, Folfirir, the combinations of these drugs, looking at VEGF inhibitors such as Bevacizumab, EGFR inhibitor, centuximab, or, or panitumumab in patients who are RAS Wildtype and then on the right column, we see the newer drugs that are out there, right. 

Dr. Connell 07:01
So with patients who have BRAF mutated colorectal cancer, the combination of NRAS and Centuximab, HER2 is now you know, very to the fore in terms of drug therapy, which a centuximab and trust panitunamab. And then there’s been a lot of focus recently in terms of MSI, high disease and Immunotherapy options. And what I always say to my patients in clinic is that this is very important to determine for patients, but it’s such a small group of patients that we see.

Dr. Connell 07:21
And then the third line drugs you know what I would say briefly about these drugs Regorafenib Taz 102, which I typically combined with Bevacizumab, or for Fruzaqla is that these are drugs that, you know, have limited clinical benefit, and they have a high side effect profile. And I’m very selective in terms of which patients I decide to use these drugs for. More commonly, I would personally use TAZ102 with Bevacizumab and but that differs from patient to patient. And what I’ve highlighted on the far right is what I consider the star of the show which is liver directed treatment. And I think it’s so important to think about it in our patients and the core drug that we have is fluoxetine, and then we use Mitomycin you know, further and, you know, down the line for patients or if they’ve, you know, beginning to develop progression on fluoxetine, and I can talk about that a little bit more in the question and answer section.

Dr. Connell 08:52
So what is a Hepatic artery infusion treatment so traditional chemotherapy is delivered through through a vein. You know, in colorectal cancer, we typically have a meta port in place because of the fight through fluorouracil being given in an infusional form. The drug travels through the body’s bloodstream to reach the liver, and only a small portion of the drug will ultimately reach tumors in the liver. And as many of us who are patients and on treatment know, and it comes with side effects and typically, you know, issues such as diarrhea, mouth sores, you know, low blood counts such as neutropenia has. The benefit of hepatic artery infusion therapy is that it’s delivered through a pump first of all, which is implanted just below the skin in the abdomen. The drug is administered through the hepatic artery, directly to tumors in the liver, and it delivers up to 400 times a higher drug concentration to tumors in the liver. So we’re really getting to directly to the problem. And this is just a graphic showing. You know how that works with the pump.

Dr. Connell 10:13
Basically that the liver is a unique organ in that it has a dual blood supply. And we manipulate this information through the use of hepatic artery and fusion treatment. So there’s essentially two vessels which supply the liver, the hepatic artery and the portal vein. And liver metastases are perfused by the Patek artery, whereas what we call normal parenchyma, or normal liver tissue is perfused, primarily by the portal vein. So with hai therapy, we’re delivering the fluorouracil, which is a prodrug of 5FU or so into the hepatic artery, and we get very high concentration of the drug to the liver. And as I mentioned in the previous slide, it’s almost 400 times higher than those achieved by intravenous administration. And, and the important thing here is that essentially, the drug is entirely soaked up by the liver around 97% of the drug, it has a very short half life. So there’s minimal systemic exposure for patients and toxicity from the drug.

Dr. Connell 11:42
So I have two very brief slides just looking at some of the clinical evidence. And on this slide, we see the clinical evidence for HAI therapy in patients who have unresectable colorectal liver metastases. So the first study highlighted here was published in 2017. And basically, this was a case control study, which looked at the use of HAI with modern systemic chemotherapy combinations compared to systemic chemotherapy alone. And you can see even from the bar charts, there’s a there’s a difference there that’s quite visible between the purple bar, which is essentially the combination treatment and the orange colored, which is systemic treatment alone. And what was seen in this case control study is that median overall survival was doubled in patients, when they received combination treatment at around 32.8 months compared to our modern systemic chemotherapy options, which was 15.3 months. And this was even when conversion to resection was not achieved in patients. And this was statistically significant.

Dr. Connell 12:43
On the on the right side, then we see another paper and this was published in 2018. And this looked at like long term results from a prospective trial, and which again, looked at the response to hai therapy, and with systemic treatment, and basically, the overall tumor response rate to the combination of HAI with systemic chemotherapy was 73%. And there was a very high response rates in patients who were chemo naive. So when it was given in the first line, it was 86%, whereas in patients who were previously treated, it’s still very high, it’s 67%. And what we saw here is that 52% of patients were converted to resection with the combination treatment, despite the fact that the majority of these patients had what we would consider a high disease burden within the liver, and many of them had had previous chemotherapy.

Dr. Connell 15:19
I just briefly put up here, and this is really to January questions, you know, what’s the future for HAI therapy? Or how can we further advance what we know? And I think there’s two very important points to bring up here. And I know, these are questions that come up for me in the clinic is, you know, can we combine hai therapy with other systemic treatment options? One that’s very topical, you know, is kind of get it with Immunotherapy. And another would be, you know, some of these other newer drugs that are out there, you know, in particular for a patient to perhaps is her2 positive, BRAF mutated patients. So, you know, can we give them and right now, the honest answer is we don’t have the safety data to combine these drugs together. But it’s something that we do need to consider going forward in terms of trials. And, and also, I would like to highlight the HAI Consortium, and I think that’s a very important group. And it’s essentially a group of centers within the United States and also outside the United States, where we’ve come together, and we’re trying to generate trials. And there is a trial, which has been activated, which I know has been previously discussed here. And I think this is going to be a group that’s going to help propel forward future trials on hai therapy and and help all of you as well as patients in the future going forward. And it’s a very important collaboration to be able to replicate. I think what we’ve seen achieved at Memorial Sloan Kettering in particular with HAI treatment, and can we, you know, replicate that throughout the United States and more globally for patients.

Dr. Connell 17:01
So, what does it mean for a patient then to live with the palms, so just to get to some practicalities, so it does require a surgery to place the pump. And that’s important to say to patients and the majority of patients it’s placed at the time of an open surgery. In some patients where, for example, the colon primary, or the rectal primary has already been removed, and there is going to be no liver resection. There are some newer techniques such as robotic, placement and minimally invasive which are done by some of our surgeons. In terms of recovery. The honest answer is you can you can travel. And you can also continue to do most of the activities that you’ve enjoyed doing before. And during active treatment, the pump has refills every two weeks, you do not get drug every time it alternates between fluoxetine with heparin saline. And it is important to be mindful of the travel schedule. And I do say that to my own patients, because there is a residual within the pump, but you do not want the pump to run dry. So it’s very important to you know, mention any travel to your your treating physician and to try to accommodate that for patients as well. And otherwise, what I also want to highlight, and I mentioned this a little bit with the consortium, but there’s been a huge increase in terms of the number of centers since 2019, that are able to put in a level upon number one, and also for local refill centers. And this is something that is continuing to gain momentum. I think this is something that I learned, I’ll be honest with you during the COVID pandemic was so important for patients because there was huge difficulty in in people being able to commit to coming here every two weeks to New York at for pump refills and, and there’s a lot more physicians out there, and who who can now help assist with local refills. And that can be huge for patients, even if they’re not able to get the flux your dean locally, for example. But coming to coming to New York once a month is much better than having to commit to traveling every two weeks for example. And, and you know, it is important to also to mention that and we are trying to help train local oncologists also who maybe don’t have experience with the pump, but to be able to help some of some of you and some new patients who really want to commit to this to have refills locally. And then just to briefly mention, you know, some of the safety elements with fluoxetine. So, the anterior pump is indicated for the use of fluoxetine and it is contraindicated to the use of this and patients who have extensive extrahepatic disease or if you have limited liver function. And then always important to mention, you know some of the adverse events that can occur with the pump which are rare but serious and we can discuss them a little bit further in the q&a section.

Dr. Connell 19:59
So with that, I’m going to hand it over to Betsy, and we’ll go through the questions. So I’ll stop sharing here.

Betsy Post 20:08
Great, thank you so much. And then please, as we go along, if you do have questions, actually, I have one, two for the end, please do put those in the chat and we will get to those shortly. So the first question we have Dr. Connell is Why is HAI therapy generally done at the same time as systemic chemotherapy?

Dr. Connell 20:31
Yeah, so, you know, this question comes up a lot. And I think the important thing here is the there is a synergy between fluoxetine through the pump and giving it with systemic treatment in particular arena Tekin, and our EGFR inhibitors, but also importantly, we have to protect against the risk of extra hepatic disease, right. So if I have a patient and they’re on track to try to get to a liver resection, what is absolutely devastating for a patient is to get to a surgery. And the procedure is aborted because extra hepatic diseases detected and or for something to develop on a scan prior to surgery. So it’s really to help protect outside the liver, to allow us to focus on the treatment of the liver metastases with the flexibility and treatment.

Betsy Post 21:23
Thank you. How do you determine which systemic regimen that you’re going to use with the metastatic colorectal cancer liver met patients? And how does having a pump alter that?

Dr. Connell 21:35
Yeah, and so the first thing to say is that, while we typically and in the majority of patients give systemic chemotherapy with the HAI therapy, the dosing is automatically lower than it would be if a patient was receiving systemic chemotherapy alone. Because we have to balance the toxicities from using the two in combination. And so there is a different standard dosing of this systemic FOLFOX, for example, as opposed to somebody who’s on FOLFOX own in terms of what to use for patients. So there’s a few things to look at. I think the first thing is, in a patient who is previously untreated, the standard would be to use Folfox.

Dr. Connell 22:19
With the liver pump, and in somebody who possibly comes and they’ve had both treatments, what I take into consideration is I look and see, you know, what response, did the patient get to each individual systemic treatments previously, right? Did their cancer previously progress on Folfox? Do they maybe have stable disease on full theory, but they didn’t get enough of a response, and also the side effects that patients have had from previous treatment. So if somebody comes into me in clinic, and they have very severe neuropathy from previous oxaliplatin, I’m not going to jump to using that drug. So I think what’s important to consider is how the patient’s cancer has responded to previous drugs before the time interval that they’ve had from a particular regimen to perhaps another recurrence or something else developing and also the side effects for the patients from previous treatment.

Betsy Post 23:13
Thank you. The next question is, are there any situations where the HAI therapy might be done without systemic chemotherapy at the same time,

Dr. Connell 23:27
Um, very, very rarely, I have one patient since I began practicing here that I’ve done it in so I very, very select patients. In general, the preference is to give with systemic chemotherapy. Again, you know, in, in the scenario where I decided not to do it, it was a very detailed discussion with the patient about why we were not doing it and the risks of of not doing it together. But in general, it’s given. It’s given with some form of systemic chemo. And, you know, what I prefer for my patients is at least we give a single agent even if a doublet such as you know, 5FU with oxaliplatin or 5FU with Ironotecan is too much. And but as I said, it’s very rare that I do it. I’ve only done it once since I’ve been practicing here and had very real reasons for not doing systemic side effects may be possible in the liver area during HAI therapy.

Dr. Connell 24:28
Yeah, so the side effect profile is very different to systemic chemo. The two main things that I say to patients is we learned early on and many of the studies that were done with the liver pump the the risk of ulceration in the gut in the GI tract, so all patients are put on a medication to help prevent reflux. So pantoprazole protonix, and in patients who say to me that they’re having increasing reflux symptoms, for example, or they’re having some pain or discomfort, you know, just under the chest, and I’d have a very low threat To get an endoscopy to look for an ulcer, so that’s the first thing. But it’s much less common nowadays because we’re routinely giving protonix with it. I think what the big thing is, you’ve got to watch the delivery of blood work very closely. And in the majority of patients, you don’t come to clinic with any symptoms, right? You feel fine, you feel well, in general, patients feel better than they felt on previous systemic chemotherapy because okay, I’m still giving it but I’m giving a little bit less than you would have had previously. And what I always say to people, actually, when they come to me is it can be a little bit frustrating, right? If you fly to me from San Francisco, or you come from Canada, and you feel great, and then I see the liver enzymes, and I say, sorry, I can’t give the drug today or you know, we’ve had to give a few weeks holding off on the drugs. So the honest answer is we’ve learned from experience that we do have to be very mindful of the liver bloodwork, and then the majority of patients picked up on the bloodwork and the patient doesn’t have any symptoms themselves. However, in some patients, if you begin to develop any symptoms, such as jaundice, you know, anything like that, then a very low threshold to get your liver enzymes checked. And even if you’re local, to check them to see because that’s the biggest thing that we have to watch for is liver toxicity.

Betsy Post 26:16
How long does active treatment last? And what is the average number of treatments? And does this change? Does this change if the HAI therapy is being done before or after liver resection?

Dr. Connell 26:30
Yeah, yes. So the answer to the final question is yes. So if somebody has had a liver resection, and we’re using this as an adjuvant treatment, it’s six months of treatment. And then we stop. And in the majority of patients, we’ll get four doses in of the fluoxetine of the liver drug in the six month period, when we look at, you know, liver enzyme alterations, but we stop automatically at six months, and however many doses the patient has managed to successfully get that’s it. And in a in a person who is not resected, or I’m trying to convert to resections, when unresectable disease or in the conversion setting, there really isn’t a limit in terms of the number of doses that a patient can get. And the it really depends on how their liver is tolerating the drug, you know, what kind of response that we’re getting, you will have to make a change to the to the drug dosing. And what I’ve seen in practice is that typically, that happens around two to three months into treatment. It’s not uncommon, that it could happen even after the first dose, but there will be some dose modification. And patients can still respond on low doses. And that’s also important to say, because again, I also acknowledge that, you know, really, you’re committing to come in here for these treatments or to hai center. And it’s very disappointing, if you hear you’re getting a quite a significant dose reduction. And but you still respond to this. And it’s different to what we know about the dose reductions that are done with systemic chemo.

Betsy Post 28:04
Thank you. Is it possible to do treatment again, with the pump later on, if needed? 

Dr. Connell 28:14
Yes, exactly. Yes, you can. And this is why, you know, our, our preference is for patients to keep the pump, right, because particularly, what I would say to patients is, if you are using it as adjuvant therapy after liver resection, or you’ve been converted to resection from the pump, at the time of surgery, the recommendation, so your NED at that point, right is at least two years. Ideally, we prefer patients to keep the pump in longer. But the highest risk period for recurrence is the first two years and the rationale behind that is because the pump is not something that can be put back in right a little bit like a metal porch, right? So we want to keep that option open. Particularly if, if it’s helped you get to your surgery, number one, and you know, so that we can use it again. So absolutely, yes, you can use the drug again.

Betsy Post 29:11
Thank you already answered the next one, which was does the pump stay in when active treatment is done? And for how long?

Dr. Connell 29:18
Yes. Yeah. Yeah. And so yeah, and this question comes up and the honest answer is as well what I would say is i i Never tell someone to take a pump out I wait for them to tell me that they’re ready for it to come out because I think it’s a very personal decision. I think it’s something that for many patients has been you know, revolutionary, I guess and and I think, you know, we can educate and guys and that but it has to feel right to you as a patient to know when is the right time to remove it. If somebody really wants it out within six months. I’m like, please keep it for two years but beyond that, I really leave it up to the patient’s decide

Betsy Post 29:59
Are there other drugs ever used in the pump like oxaliplatin?

Dr. Connell 30:05
Yeah, so, oxaliplatin has a very low extraction rate into the liver. It is used in Europe because they have a slightly different device there. We don’t routinely use it here. But we do use Mitomycin and that’s something I referred to briefly during my talk. And I have seen patients who perhaps are beginning to develop some resistance to Flox your deen or maybe are beginning to run into more issues with their liver enzymes. And I’ve used Mitomycin in those patients and seen you know, some very good responses with the middle myosin what I would just say about that is you can give it in combination with fluoxetine. So you can give both drugs at the same time if your liver enzymes are good. So if the liver bloodwork is good, if the liver enzymes are high, tickling the outsource or perhaps the bilirubin, and that it’s safer to give Mitomycin on its own, but that’s typically our second drug that we use. We don’t give oxaliplatin.

Betsy Post 31:09
What are the causes for the mitomycin following HAI therapy with the traditional treatment?

Dr. Connell 31:19
Why would we give it right?

Betsy Post 31:21
I think you already spoke to that. 

Dr. Connell 31:24
So yeah, yeah. So I think if you’re getting a slowing down in response, possibly to flux, your routine, maybe you are getting some response, but you’re beginning to run into some of these liver toxicity issues. And so they would really be the main reasons that we do it. And really, I would use it in a situation where it’s liver only progression, of course, like I wouldn’t use it if there was signs of anything happening

Betsy Post 31:47
Um, and then since I’m not an oncologist, I might mess up these names. But what are the views on the use of Bev, which I know is Avastin. So we’ll take that one first. The new third line or a drug that was just FDA approved for colorectal cancer, liver Mets, or the EGFR inhibitors. So what are the views on those three and maybe address them separately? Because I know it could be different after the HAI therapy when the pump is running glycerin.

Dr. Connell 32:18
Okay, so I’ll start with EGFR inhibitors first, because that’s probably the easiest ones you can give EGFR inhibitor is at the same time that you give fluorouracil safe to do works very well with the liver pump.

Dr. Connell 32:32
And you can also give it after liver treatments. So there’s no limitation at all with EGFR inhibitors and actually works very well with with FUDR, or Avastin is something that we’d urge early on, that should not be used the same time that we’re giving fluoxetine. So it’s it’s a combination, so it should not they should not be used together. And but a patient can have Avastin or Bevacizumab later on, if you’re simply just getting glycerol through your pump. And so, if for example, I have somebody who the liver is still no evidence of disease, there’s, you know, issues arising outside the liver in the lung, perhaps or lymphnodes. Have I given Avastin? Absolutely I have, I generally prefer to try to delay the use of Avastin further out from using the liver drug because I have seen in some patients some delayed issues with billary complications if I’ve tried to use the Bevacizumab a little bit too quickly after stopping the liver pump treatment. And but yes, you can use them separately but not together and then forget never the honest answer is we don’t know yet. Because it’s such a new drug definitely would not use them together. And I think you know, you would think along the same lines as you know, what we do with Stivarga, etc. You know, they can be given but not together. And the honest answer is and I kind of led to this during my sliders, I really reserved the use of any of these drugs too much, much later on for patients. I think if you can do something like long ablations or radiate, I think you’re helping the patient more than jumping to any of these newer, third fourth line drugs that are approved.

Betsy Post 34:17
Thank you. And these are questions that we see in Colin town all the time, and these were the most frequent questions that I received for you. So these have to do with Y90 So if a patient has had Y90 How does this affect their ability to receive HAI therapy after?

Dr. Connell 34:38
Yeah, okay. So this comes up quite a lot. The honest answer is if I see a patient before a Y90 Maybe they come with a second opinion we usually prefer to give the pump before Y90 that’s the honest answer. So usually what I say to patients is, you know, pump first and any of these proceed procedures like Y90 or radiation I would reserve for later on. And have I had patients who’ve had y90 And I’ve given pump treatment to absolutely, I think we have to look at those cases individually. And it’s something that we would show at our tumor board. And we would really look at the extent of the Y90, for example, how the blood vessels in the liver look after the Y90.

Dr. Connell 35:24
Often you need to dose reduce the flux your routine a little bit faster in those patients so I can get the drug in for the patient, but I can’t get as much drug in. And but I’ve had people respond after y 90 I think our preference is to do pump first.

Betsy Post 35:45
If a patient has HAI therapy, and then does Y90? Would the patient be able to use the HAI pump again, if it is still functional?

Dr. Connell 35:56
Yeah, and so this is an interesting one. I haven’t personally ever done that myself. I think from a technical point of view, it would come back to what I said previously, is that you’d have to really look structurally at the liver and see, you know, there’s there’s newer Y-90 techniques out there. And I know whether our interventional radiologists here they do more selective Y90 So if perhaps, you know, there was a regional Y90 And then you’re trying to treat the rest of the liver. Technically, you could. I think just with with my own practice, and the way that I view it, because I keep Y90 for Later on, it just hasn’t worked out that way with the patients that I’ve seen. But again, I think this is something that you would have to have the right imaging, it would have to be viewed as a multidisciplinary team, whether that’s the right thing for the patient, you know, including an interventional radiologist, including a radiation oncologist right, is radiation safer than Y90 A surgeon and a medical oncologist to decide what’s the right thing for that particular person.

Betsy Post 36:56
Some additional questions have to do with transplants. This is something that we’re hearing more and more about, especially for unresectable disease, obviously, and we have patients a lot of times that are making a decision, sometimes between the pump or transplant, but something that we’re hearing now is the question first, could the pump be used as a bridge to liver transplant?

Dr. Connell 37:18
Yeah, so this is very typical? I think without intentionally setting out that way. And I’ve had some patients who’ve done very well with transplantation after pump treatment, I think the tricky thing about the transplant process is that it’s a long process for patients. Right. So my own experience with my patients has been is that sometimes they’re waiting like 12 to 18 months. And I’m trying to control everything with the pump at the same time. So I have used it but not intentionally. I’m on discussions with transplant centers. And speaking with surgeons here, this is something that I think we’re going to need to study. And we’re going to need to collaborate on to see if we can help more patients by combining the two techniques.

Betsy Post 38:37
Another question, how do you consider the option for liver transplant as part of your overall treatment plan or approach for patients?

Dr. Connell 38:47
Yeah, so. So when I see patients, you know, this can often come up. And I think with transplant, what I say to people is we got a real sense of how the pump is helping a patient in unresectable disease, like, you know, about six months in, you know, look, and you’re talking back and forth with the surgeons, you know, do we think that we’re going to be able to convert to resection here? Do we have any of these options like why nine tear or radiation? And I think it’s always appropriate to get an opinion from a transplant center, and particularly if it’s something that the patient themselves is questioning, right, because you want to hear directly. And there’s a little bit of bias right between different different specialties and obviously I’m very Hai and but I’ve certainly collaborated with transplant centers, and then you know, when somebody is listed for transplant in practice, what I do is I follow what they want me to do, so I don’t change any treatment, you know, they tell me what they want to do. The important things about transplant is a few things. So you cannot have any extra hepatic disease obviously so there can be no evidence of extra hepatic disease. And the second thing is that the primary tumor has to be removed.

Dr. Connell 40:03
So, you know, they would be the two things. But if you have liver only disease and and resection is not feasible, and you’ve heard that from the liver surgeon and you’ve heard that from your medical oncologist then then I do think transplant is something that needs to be considered. And they removed the pump at the time of transplant as well. 

Betsy Post 40:26
So is there data available to show how successful ATI therapy is? And I know that we did talk? You talked about that earlier, but I didn’t know if you wanted to elaborate on that a little bit more.

Dr. Connell 40:39
Yeah, so we do have data. And I’ve shown some of the data here, I think what’s important is that we need more randomized to data. And I think, you know, that’s what the consortium is going to help with and why we’re trying to collaborate with other institutions. And I think trying to address this question of, is the pump so successful? Because it’s given here in New York or you know, Kansas, can I get the same level of care? Or in Chicago, or, you know, Atlanta? And I think the honest answer is there’s so much more knowledge out there about the pump. And we do need to do more trials. And also, I also mentioned this as well, there’s so many newer drugs out there, right. And patients want to know can kind of get them together, is it safe to get them together? And this has to be done in a trial setting.

Betsy Post 41:27
So another question we get quite a bit. So now that Dr. Kemeny has retired, how was care being distributed for patients that are being seen at Memorial Sloan Kettering?

Dr. Connell 41:39
Yeah. And so what I would say about that is, honestly, all of us can can can do pump treatment, I think a huge part of Dr. Kennedy’s legacy. What’s visible to patients and caregivers is is what she did for you, right? Understandably, a huge part of her legacy for us at Memorial is the teaching and training that she gave to us. And, you know, she was a phenomenal mentor to me. And to many of my colleagues.

Dr. Connell 42:10
All of our practices differ a little bit. So some of us do more pump than others. But honestly, all of us can do pump in terms of her practice. And it’s been divided between Athol I think for for active patients, understandably, because I was mentored under her I have many of her patients. I think, what’s also important to say, though, is that, for any of you who have, you know, some complex decision making, there’s something to be to be, you know, figured out, you know, is it now the right time to think about y 90, you know, have I achieved what I can with the pump, that’s never a decision that’s made in isolation by an individual, whether that’s a medical oncologist, it’s our tumor board is a huge resource for people and, and that’s often what I what I see myself as like, You’re not coming here to memorial for me, you’re coming for the expertise from the whole group. And never think that a decision a very important decision like that, look, will I say to this patient that you should go and get a transplant opinion, you’re not going to hear that just for me, I’m going to speak with my surgeons I’m going to speak with with them, and we’re going to show your case at the tumor board. And I think that’s very important to know, is that there’s huge collaboration amongst us as medical oncologists, and also multidisciplinary team involvement in any major decisions for patients.

Betsy Post 43:31
I know that you spoke about the Consortium, and that all the pomp programs, especially since my team that have opened up, but How can patients across the country get good access to HAI therapy?

Dr. Connell 43:44
Yeah, so I think there are more centers, who are implanting the pumps, number one, and also so many more centers where, you know, they’re able to assist with with local fields, I think the consortium is really helping with that. I would also say that there’s a huge collaboration between us, you know, I definitely speak with medical oncologists at other institutions. You know, I relied on mentoring, when I started off with this, and I try to share what I’ve learned in the nuances, you know, with oncologist with other centers, I think, when you start off, you know, what I always say to people is, you have to be comfortable with the person that’s treating you, right. And whether that’s having a pump or not having a pump, I think, number one, you have to be comfortable. So, you know, and you also have to think from a practical point of view, you know, look, if financially and with my family or my work commitments, is it feasible for me to fly up and down to New York every two weeks? And for many patients, it is for others. It’s not. Do I have a local doctor who can do this? Did I did We did our personality match? You know, and but I think there is so much more knowledge out there nowadays and there’s also huge camaraderie between us and sharing of knowledge. And, I think the consortium and the trials and everything that’s going to come out of that is going to further reinforce that for patients.

Betsy Post 45:11
One more question, and then we’re going to take the live questions, we have quite a few. How does the start of that new pump trial impact the ability of new patients to receive HAI therapy?

Dr. Connell 45:23
Yeah, so it’s a very relevant question. And you know, what I would say about the pump trial, it’s a very, very select group of patients, right? It’s a very important study, right to help answer this question, in a randomized setting of, you know, conversion to resection for patients with HAI versus modern systemic chemotherapy. So it’s for patients who’ve had more than three months, but less than six months of systemic chemotherapy in the first line. So it’s a very small group of patients. And the honest answer is the reason that we’re doing that is because we don’t know the question, right, we are the answer, we wouldn’t be doing it if we already knew that one was better than the other. And that’s important to say about any trial. If you’re a patient who is untreated, you had no chemotherapy, you can have a pump off trial, if you’ve had more chemotherapy, like you’ve had a year of chemotherapy, you don’t, you don’t qualify for the trial. So it’s a very, very select group of patients. And that will be explained to you as well, in the in the in the clinic setting.

Betsy Post 46:30
So moving on to some of our live questions, we have one, is there a certain temperature that you have to keep your body under while you have a pump?

Dr. Connell 46:42
Yeah, so this question comes up quite a bit, you know, I think you have to be sensible, right? So he will speed up the rate of infusion of the drug. Hot tubs are a no, no, you can get in a swimming pool. And so body temperature can affect us, I don’t give anyone like a specific number. But I just say like, you have to be mindful of it. And I have a patient who said they have a hot tub with that, put it on regular temperature. So you know, swimming, and all of that is fine. But sitting in heat, you don’t want to put heat pads directly on the pump. If you have pain in your back for another reason, you can put heat out there, but you just want to do want to put it directly over the pump.

Betsy Post 47:25
Is it true that you can’t lift more than 10 pounds when the pump isn’t?

Dr. Connell 47:31
Yeah, so again, this comes up quite a bit. So usually I say around 15 pounds to patients. In the beginning, I think you have to be very mindful of that similar with any surgery to be honest with you. Over time, honestly, what happens is you have a very good sense of your pomp and also scar tissue forms. And so I tell patients that, you know, using a binder, you know, be sensible. But a lot of people say, Well, you know, my toddler is 30 pounds, you know, and I’m never gonna say to somebody, you can’t lift your child up, you know. So I think within reason, and I think if you’re, you know, the further out, you get the sense you have your palm, the binder, scar tissue, and, and, you know, for lifting children in the beginning, I usually say to people, you know, sit down and lift them up onto your knee, you know, things like that. So I try to be creative with how you do things. But I do think we have to be practical in that regard. And the concern about the weight lifting is the connection between the catheter and the pump, and also the risk of, you know, the pump flipping, and the more secure it is over time that the lower the risk of that

Betsy Post 48:39
Um, there’s a question about the drug and mutations. And I know specifically, we do have some BRAF patients here. So question, there’s a question about, is the HAI therapy equally effective for all mutations?

Dr. Connell 48:56
Yeah, so it’s a very good question. I think what I would say to you is, is that we do use the pump and in all patients, I certainly have myself patients who have BRAF mutations, and I’ve used the pump, and I’ve seen some very good results with it. So I wouldn’t discriminate based on that. And but I think it’s something that we’re going to need to study a little bit further to see how we best serve people going forward. But I definitely have patients who’ve done well. And you know, maybe later on I’ve used the combination I mentioned earlier, such as graphics to toxic map, and but if they have liver only disease, we still put pumps and we still get flux your routine and I’ve definitely seen good responses. I have a patient who was probably an outlier but from from early 2019, and still NED

Dr. Connell 49:47
and had, you know, resection, had liver pump to get your resection and as BRAF mutated, you know,

Betsy Post 49:55
right. I think you answered this, but I’ll ask it for those pursuing liver resection, is there a recommended number of fudr treatments from the pump before considering surgery?

Dr. Connell 50:10
And so the honest answer is there isn’t a set number per se, if somebody has unresectable disease. So what we do is we scan every two months because we want to keep a close eye on the response that we’re getting and how the liver is tolerating it, right? So you’re scanned every

Dr. Connell 50:29
which is a little bit different to the adjuvant in the adjuvant setting, you’re scanned every three. But what I usually say to people is that honestly, at two months, it’s it’s not very common that patients are ready for surgery, it’s typically around the four to six month mark, but there isn’t a set number is really depends on the location of tumors, the technicality if somebody has liver, you know, bi lobe disease, so both the right and the left side involves the surgeon will say to me, Look, we need to do these portal vein embolization, you know, certain procedures to help get to a second stage liver surgery. So the some of those factors to come in. But there’s no hard and fast rule with the number of doses that a patient has to have

Betsy Post 51:13
HAI pump decisions require very close coordination between the medical oncologists and surgical oncologist Are there any best practices from that cross specialty communication that you would highlight is beneficial to apply? Even beyond the HEI application?

Dr. Connell 51:31
Yeah, so, you know, what we’ve learned to serve patients best is that multidisciplinary involvement is so so important. Right? And, and I kind of, you know, said that earlier on, like, any major decision point you need to think about, you know, how am I helping the patient right now? And also, how is this going to affect what I want to do in the future for the patient? Right. So in my own practice, here, I do my clinics alongside the surgeons at for that reason. And you know, when I asked some of these questions, we also have very heavy input from our interventional radiologists. And I think that’s very important is to try to get the different options there. And sometimes there is there’s two options, right maybe let’s say for the liver, it could be resection or it could be ablation, and then we can see both and help make the decisions by getting the input from from both specialties for example.

Betsy Post 52:32
Are there restrictions on jogging and working out?

Dr. Connell 52:37
Okay, so what I would say about that is if you put 20 of us in a room, a mix of surgeons and medical oncologists, everybody would say something different and it’s very controversial. And I allow my patients to light jog and the the concern again is really the connection of the catheter to the pump. And again, what I say to people is exactly what I said weightlifting you know, if someone comes in to me and you know jogging is your is your your cam time, you know, your therapy so to speak. You know, it’s very hard to say to somebody, you know, don’t jog and but I say you know, try to be sensible about it, have a binder on Wait a while and I do allow patients to do like jogging. The surgeons do lap people jog and there’s other medical oncologists who say no, and we love stationary bike. We love the peloton. That’s, that’s probably the safest thing that you can do and the best thing and a good form of workout. But yes, I do say to patients, they can jog.

Betsy Post 53:41
So if there is a patient that has, for example, ovarian or peritoneal disease, but the patient was potentially able to have all of that removed. Could they still get pumped?

Dr. Connell 53:56
Um, so for over a yes. So if you have liver and ovary because we know that colorectal metastases to the ovary, are quite resistant to chemotherapy, so in general, the bias is to lean towards surgery in that situation anyway. So you would often do if you can do a liver and you would also remove the ovaries at the same time. So yes, with peritoneal disease, there’s a little bit of pause. I’ll be honest with you. The tricky thing about peritoneal disease is that you often can’t fully appreciate peritoneal disease on scans. And and it’s only at the time of surgery that you really have an understanding. And I’ve had some patients where perhaps there’s been like limited peritoneal disease, you know, a year ago it was removed and maybe they come looking for a pump. And and usually if there’s, you know, a period of time, typically a year, year and a half, not thing happening in the parish name again, then, you know in select cases we’ve put pumps in. And but I wouldn’t say to you upfront that I’ve put a pump in for a patient when they have active peritoneal disease at the same time.

Betsy Post 55:14
For every two to three months scans, do you do CT MRI, and I’m gonna throw in there you PET scan stew? Might as well add it in.

Dr. Connell 55:24
Yeah, and, okay. Um, so in that regard, what I would say to you is I started off using CT and patients. So I do routinely, CT chest, abdomen and pelvis. Over time. From looking at the CT scan, you understand with the individual patient, whether you’re seeing things clearly in the liver or not, if not, particularly in patients who maybe have, you know, a lot of chemotherapy prior to the pump being placed, because the chemotherapy changes the texture of the liver, what we call like fatty liver change, or sclerosis. So in those patients in MRI may give additional information. So the honest answer is, my starting off rule is CT only, I’ll involve an M or liver if I feel like I’m not seeing things clearly with a CT. And I really don’t routinely use a PET scan, unless I get to a point in a patient where a specific question has come up on a on a CT, for example, I do a patch, and I see that the patch is giving more information than the CT has. Similarly, if I do a patch on a patient, and I see that I’m not getting anything different from it, then I don’t routinely follow with Pat. And I think that would be the standard approach. For most patients. The tricky thing with PET scans is there can often be you know, false positive things on a PET scans and something lights up. And it’s it’s not anything related to the cancer and then it causes, you know, a lot of concern, understandably. Yeah, so that’s how I would view it. But I do have some patients where I know that only MRI shows that are only pet shows that and then once I learned that with the patient, then I continue to use that imaging modality. But I still always do my CT as well.

Betsy Post 57:12
We have one more question about I think exercise I see here. What about horseback riding? I’m a serious equestrian.

Dr. Connell 57:21
Yeah, so this came up for me recently. The issue with with horse riding is the bouncing activity. Right and the concern for the catheter? Again, I don’t think it’s a complete contraindication I think, and I know I’m repeating myself a lot but wearing the binder, a similar lead to what I’m seeing with light jogging. I mean, you can I don’t even know the word for isn’t trotting. for horse riding, you know, you have to be mindful of that. And but I wouldn’t, you know, I wouldn’t say you can’t do it again, if that’s something that a patient is passionate about, and it’s their form of relief, or escape from what’s going on, then I think that’s important to consider. So have a binder be mindful. That’s what I would say.

Betsy Post 58:07
We just have two or three more. So how would you know if there’s a problem with the connection from the pump? Perhaps from over lifting, etc?

Dr. Connell 58:19
Yeah, the honest answer with that is that most patients don’t know. And it’s picked up on scans. That’s the most common scenario. And that’s really where we see it. If somebody has, you knows, for example, they’ve had a trauma, you know, so So I had a patient a few years ago, and they were in there on a regular bicycle, and they flipped over the handlebars, and they were like, This doesn’t feel right, you know, so I scanned and you know, there you knew there was some incident proceeding, and you would check for it or they had pain afterwards. But the honest answer is in the majority of patients picked up on scans and you don’t feel any difference.

Betsy Post 59:03
Let’s see, I know I’m gonna mess this this word up.

Dr. Connell 59:08
So what are the thoughts around using the capecitabine with the pump while receiving radiation to treat the primary replacing traditional systemic treatment? Okay, yeah, so this comes up quite a bit. So when patients have a rectal tumor and you know, you can treat them with chemo radiation. So we do, you know, and you know, that’s in terms of a rectal tumor, the surgery is much more life altering. So if you can effectively get a complete clinical response or fully treat the rectal tumor than chemo radiation is recommended. What do I do in my patients? So the issue with Capacetibine Xeloda is that it causes more increase in liver enzymes, and it can affect the dosing of the fudr. So what I do for patients is if

Dr. Connell 1:00:00

We have a rectal primary and we’re doing chemo radiation. And we’ve just put a pump in for liver disease, you can give the fudr you can give the liver treatment during the chemo radiation. But instead of using the Xeloda and or capecitabine of being I use fluorouracil which is sort of the old way that they that they used to do chemo radiation. And because again, I want to try to maintain the higher doses in the pump and keeps it being tends to interfere with that more. So.

Betsy Post 1:00:36
I think I got to almost every question, one of my questions that I have, if I can just sneak one in I know it’s 802. But with all the centers opening up, I feel like we’re seeing some oncologists are using the Urso dial and some are not. And I don’t know if you feel comfortable speaking to that, and how you use it in your practice and how the decisions made to use that or not?

Dr. Connell 1:00:59
Yeah, it’s a very good question. I mean, I think what I would say to you as well is there’s even differences in the practice here at Memorial as well. I, I use it quite early on in patients, because I think, you know, the two ways we manage the liver inflammation are the steroids through the pump at the time of the flush as well as versatile. And, and in the long term for patients being on steroids continuously. You know, there’s this kind of late side effects with that there’s the weight gain that comes from steroids, there’s a few patients where versatile can be a little bit tricky. So sometimes patients can notice the very loose stool. So if I have a patient who’s struggling with, you know, diarrhea issues or anything like that, from arena Tekin, or even five floor yourself, I kind of hold off on the earth a dial, but I tell them why I’m not doing it, you know, but I do tend to use it early on. And I also tend to keep it on board longer, even after I’ve weaned down the steroids in the pump, and I have someone off treatment, because I think it helps with the liver inflammation, I typically start off on twice a day in some patients, you may have to go up to three times a day. But again, if you even select 10 oncologists here at Memorial, everyone would do something a little bit different. But I give the options to patients. And I also explain, as I said, when I don’t use it and what my concerns are for that particular person.

Betsy Post 1:02:31
Well, it’s 8:04. And I think we have gotten to most of the questions. There is one here that I’m not sure we may have to get back to because it’s you know, the top centers for ATI. And with so many new centers that have opened up since 2019. I think by volume, we’d have to kind of look into that to see who they are. I know Duke is one of them. I know they’re very, they’re a high volume center now. But with the opening of the consortium, I know we have a lot more centers throughout the US. So I can take that offline. And definitely I can talk to the folks at inteiro on that as well. Just about the volume at the other centers. But yeah, so I just wanted to say again, thank you so much for your time, I learned a lot. And it was so good to hear just from a medical oncologist. So in addition to Dr. Kemeny and hear how you’re using it, your practice, and I learned a lot of just about the trial and other things. And your take on that. And I really appreciate it. I know you were so generous with your time and answering all of these questions for the patients. And we really all appreciate it. So thank you so much. And I know we’ll be in touch if we have additional questions. So thanks for everybody that attended tonight and thanks for all your participation. We really appreciate it. So have a great evening. Thanks again. And we’ll see you soon.

Dr. Connell 1:03:46
Thank you everybody. Bye

DocTalk
2023
Dr. Hernandez
Liver
Stage IV
Histotripsy

On December 20, 2023, Dr. Hernandez discussed the newly FDA-approved treatment of Histotripsy in the treatment of mCRC liver metasteses within a week of performing the first time use of this novel therapy after FDA-Approval in the US. He describes the history of the therapy, what it entails, why and for what conditions it is applicable and future research ideas.

Warning: Graphic surgical images at 13:00 minute mark.

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Multimodal Management of Liver Mets

Multimodal Management of Liver Mets

DocTalk
2025
Dr. Rocca
Ablation
HAI
Histotripsy
Liver
Radiation
Stage IV
Surgery
Transplant
Y90

In this video, Dr. Rocca delves into the Multimodal Management of Colorectal Liver Metastases, exploring innovative therapeutic options and strategies to improve patient outcomes. Recorded in January 2025.

Betsy Post 0:00
(Video begins mid intro sentence) ….Histotripsy. But when I was speaking with him and preparing for the talk, he had mentioned that he really thinks it’s important for patients to understand not just histotripsy by itself, but all of the different liver directed treatments that are available, so patients can really make wise, informed decisions be part of their care. So I really want to thank him, on behalf of COLONTOWN for being here tonight, and I’m going to turn it over to him in just a second. I want to make sure everyone knows how it’s going to work. So Dr. Rocca is going to speak to us, present to us, give us his wisdom, and if you have questions for him at the end, there will be a time for questions. Please use the chat feature here in Zoom; You just click “chat” and add your question to the chat. The questions will be held to the end of the presentation, and then at the end, when we have time for Q and A, I will read the questions to him, and he will answer those questions. So without further ado, I’m going to turn it over to Dr. Rocca. Again, thank you for being here – we’re so excited to learn from you.

Dr. Juan Rocca 1:09
Thank you so much Betsy for inviting me to speak, and I hope that I can help you figure out different treatment options. I think that you know, here at Cornell, we are a division of surgeons that do liver surgery, liver transplantation, histotripsy. We work hand in hand with our oncologists and interventional radiologists with ablation, our radiation oncologists with radiation. And once a week, we have a meeting, which is called a multi disciplinary tumor board, where we bring our cases, and we have the input of absolutely every physician that is involved in the care of colorectal cancer. I think it’s an amazing meeting, because it really tries to bring the best treatment option for each individual patient. And this is the purpose of this talk today. I think that it’s important to try to clarify – I have no conflicts, – but I just wanted to clarify the purpose of the talk. I think that many of you may know about one or two options that were presented to you, but not all of the options. Maybe you feel you’re being boxed in, the care you’re getting, where you went to get your first consultation about the treatment of your situation. So the main purpose of this talk is to — you geta lot of different treatment options but then, many of you also may know about all the different options, and may be really confused about what is the best option for you, or if you want to know more about the benefits and the risk of each of the treatments or combination of treatments. And finally, I hope in the different situations I’m going to be presenting, I hope that you can relate to those situations, and you can decide what of these options may be working best for you.

Dr. Juan Rocca 3:38
The outline of the presentation has multiple components. First, we’re going to do a quick overview of the treatments that are available for colorectal liver metastasis. This is only metastasis to the liver, which is the main focus. Then we’re going to be discussing what is the gold standard in the treatment of colorectal liver metastasis, which today is a combination of systemic treatments, which is mainly chemotherapy and targeted therapies and surgery. That’s what weconsider the gold standard. From there, we have a lot of data about how that works, and from there, we can move on to other combinations of therapies when surgery is not a good option. For that, we need to discuss, what is resectable disease. That is disease that can be treated with surgery, versus unresectable disease. And then we are also going to be discussing the role of ablation. You’ve probably heard about ablation, different types of ablation, but ablation can be done with microwaves or radio frequency, and this can be used with surgery or can be used for resectable disease, but also can be used on unresectable disease. Then we’re going to go over the role of other local, regional therapies and the different combinations of them. We’re going to discuss the role of liver transplantation. It’s a very strict criteria for liver transplantation, but we’re going to go over that. And finally, we are going to discuss how histotripsy, can contribute to this multimodal management of colorectal liver metastases. It’s a new technology, it’s quite promising in many aspects, and everybody’s embracing it now. We don’t have too much data to really put it against the other treatments, and so it’s important to disclose that. It is promising, it is exciting, I do it quite often, it’s just that sometimes it’s hard to offer something that we don’t have complete proof that it works in the long term. So that’s why I left it for the end.

Dr. Juan Rocca 6:10
Okay, so let’s go with the treatments available for colorectal liver metastasis, starting with what we call the systemic therapies, which today is a mix of different regimes of chemotherapy. All of these sound familiar to you: Folfox, Folfoxiri, Folfiri, Capox; and different targeted therapies like Avastin, Cetuximab, Panitumumab, Pembro. And all these regimens can be combined depending on the different type of mutations that the tumors may have, like the MSI status, the RAS mutations, the BRAF mutations that are of worse prognosis. But now there are more trials and treatments for BRAF mutations, HER 2 mutations as well. The systemic therapies are the backbone of colorectal liver metastasis. In the past, we used to probably use it only in some situations. Now it’s pretty much in every situation. Now for locoregional therapies, I always include surgery as a locoregional therapy, because at the end of the day, when we do liver surgery, even liver transplantation, we are treating the disease in one spot in one region, so it’s a locoregional therapy. So it probably is better to divide it in those locoregional therapies that require an operation, require surgery like resectionwhich is surgery, with or without ablation. We do ablation at the time of an operation, an open operation, a robotic operation. We can do ablation on a laparoscopic operation. We can do ablation together with resection. We’re going to also touch on the role of the Hepatic Arterial Infusion pump and liver transplantation. All these require operations. And then some therapies that do not require an operation is also ablation, which can be done percutaneously with the interventional radiologist. Y-90 radioembolization, which is an injection of material with radioactive activity into the liver, radiation- external radiation and histotripsy.

Dr. Juan Rocca 8:36
So first, the management of colorectal liver metastasis in the last 20 years has improved significantly. The survival of patients who have colorectal liver metastasis improved for three reasons, mainly because we have much better chemotherapy and immunotherapies and different targeted therapies. We have been a lot more aggressive with the surgery that we perform for colorectal liver metastasis, and we also have better locoregional treatments that we’re going to go into in a little bit. But if you look at the last 20 years, the number of operations we’re doing for colorectal liver metastases has increased significantly, and when you divide those patients that made it to surgery versus those that could not have surgery, that’s a striking difference in the survival. So that’s why today, being able to say that we have resectable disease is really very important, because it impacts the prognosis, it impacts the survival and most of the survivors, we’re going to try to put it at the five year mark, which is what most of the papers are usually able to measure or compare survival of different combinations of techniques.

Dr. Juan Rocca 10:02
Let’s try to define resectable disease first. So, resectable disease is that, the tumor in the liver, or the tumors in the liver can be removed or treated with liver surgery. The goal of resectable disease is to get to a condition called NED, which is “”no evidence of disease”, because this is associated with the longest survival. If we can bring you to NED, even knowing that the tumor may come back later, each time we bring you to NED we are giving you the best chance of having the longest survival. Now, resectable disease may require systemic therapy before surgery more and more. In the past, we used to discuss that some situations were benefited, first with surgery and then chemotherapy. But now the data is moving more towards trying to do systemic therapy and then surgery in the liver, mostly when you have a higher number of tumors in the liver. Sometimes they require more than one operation. We call this staged hepatectomy, or staged operations, or a combination of an operation with a locoregional treatment afterwards, in order to get you to the NED status, and one of the conditions is that the patient has to be able to go through an invasive procedure and surgery.

Dr. Juan Rocca 11:31
Now, on the other hand, unresectable disease is the opposite of this. The tumors cannot be removed or treated with liver surgery, or we can, but by removing them, we are not going to be able to bring you to NED. We cannot get rid of all the disease, and this is usually conditioned by the number, the size and the location of the liver tumors. Sometimes you have small tumors that are in a poor location inside the liver that require a major operation of the liver. So that’s when other techniques may really be able to bring you closer to resectable. Sometimes due to the condition of the liver, the chemotherapy can be toxic, can give you fatty liver, can give you fibrosis, can give you some scarring on the liver, so the liver may not be able to tolerate a big operation. Sometimes, when we do systemic therapy, it’s a good test of time to understand the biology of that tumor, and if the tumor progresses while on chemotherapy it’s telling us that doing surgery on that liver tumor is probably not going to help too much, so that could be a reason for being unresectable. Technically, we can do the operation, but the biology of the tumor is telling us that it’s not going to help the operation. Sometimes you have disease outside the liver that dictates the survival more than the disease in the liver. And you can have disease outside the liver, for example, in the lungs. The disease in the lungs is quite indolent and easy to manage. The disease in the peritoneum, it’s difficult to make it respond to chemotherapy,…bone disease, etc. So there are different situations which require a multi disciplinary decision about what the best treatment option is. I want to highlight this, because again, in the past, and not long ago, we were discussing if pre-operative, systemic therapy before liver surgery was a good thing to do. And yeah, maybe for a single lesion that came years after removing the colon, and has a slow progression, maybe you can argue that you could do an upfront resection and then do chemotherapy later. But more and more data is coming out that the use of systemic therapy, mostly when you have a bigger number of lesions, is really important in making disease more controllable for surgery, and that improves the recurrence after the surgery.

Dr. Juan Rocca 14:50
So this is a nice study: It’s about 1000 patients that were matched between those that had only chemotherapy versus those that have had chemotherapy and surgery, but they were much based on the size of the tumors and the number of the tumors. And there are different scores that are standard, the CRS score, the TB score, the Game score. These are different scoring systems that we have to assess risk of liver metastasis and the risk of recurrence. And clearly, those that received chemo before the surgery did better in the overall survival, and did better if you look at the recurrence free survival for the first two, three years. The two groups were about the same, but then, after three years, they started spreading again. And those that didn’t receive chemo before surgery had less recurrence free survival than those that received chemo. So I think this is a one of the many studies that now are showing the benefit of having systemic treatment before surgery.

Dr. Juan Rocca 16:06
Now, a few other concepts of surgery in colorectal liver metastasis. First is, we want to resect the tumor with clear margins. That means that we want to cut the liver where there is no tumor, but we also want to leave enough liver volume. Clear margins for colorectal, liver metastasis can be as little as one millimeter. That’s enough, even when a tumor is sitting in a blood vessel near the liver, if we peel it off, that’s enough, too. So it’s not that we need to do a lot of surgery around the tumor. And this is important. The type of surgeries that we usually do, any liver surgery, we can have what we call the West Resection, where we take a little piece where the tumor is sitting. Or we can start taking segments of the liver. The liver has eight segments. And we can take, for example, this will be 25% of the liver. This will be almost a 35-40% of the liver, the left hepatectomy, the extent the left hepatectomy is almost 70% of the liver. We have different sections of the liver. So typically for colorectal liver metastasis, we try to avoid doing anatomical hepatectomies. We try to go around the lesion. The type of surgeries that we usually do for colorectal liver metastasis here in the first column, the Type A, is what we call the parenchyma sparing liver surgery. That means that, knowing that we need to have at least one millimeter of margin, we go around the lesion as many times as we can. Not always we can. Sometimes the lesions are too big, like you can see in the B column. And if the lesions are too big, either we are forced to cut the right side of the liver, for example, and remove maybe 60% of the liver. Or sometimes, if we feel that the rim on the liver is not enough, we might need to do some intermediate steps like what we call portal vein embolization, to deprive blood flow to the site of liver we’re going to remove and let the other side grow before doing the operation. Sometimes we do the two stage liver surgery when we have multiple lesions on both sides, we first do an operation on one side and we remove, for example, here, these two small lesions on the left side. We remove them, we wait for the liver to grow, and then maybe six weeks or eight weeks later, we can go back and remove the entire right side with all the lesions. But these are goals of surgeries with the goal of bringing the patient NED, without evidence of disease.

Dr. Juan Rocca 19:07
And this is the “ALPPS” procedure, which is another two stage procedure where we cut the liver halfway, we don’t cut it all, and we remove the tumors, and that will accelerate the growth of the liver. Instead of in six to eight weeks, we can go back in two weeks and remove the other side of the liver. Again, as you can see, the complexity of these operations increases when you have a bigger size of tumor, or a bigger number of tumors, or both sides of the liver. But these are all techniques that we use to be able to bring the disease to zero, at least with the method that we have today to see disease, which is CT scan and MRI or PET scan.

Dr. Juan Rocca 19:54
Now, why is it important to save as much liver as we can is because when you have multiple tumors, 70% end up coming back at some point. And if our goal is to prolong the survival as much as we can, we need to have enough liver to keep treating that liver. We sometimes do a second surgery in the long term, like two years later, or even a third operation to take care of new lesions that are coming back after a while.

Dr. Juan Rocca 20:37
But then also, it’s important to understand that ablation has a big role here because those patients that – when the tumor comes back, they could have a second operation or an ablation to treat the tumor, they have a better survival in the long term. Those are the ones that we manage to bring to the five year mark. I think it’s important to understand that sometimes patients that have resectable disease have the best prognosis for a five year survival, but many times may require more than one operation, more than one procedure, while still receiving systemic therapy. Okay, this is how we get you there.

Dr. Juan Rocca 21:14
This is just a study to show that the difference between doing a measures hepatectomy, like cutting half of the liver, versus doing a parenchymal sparing hepatectomy and ablation to take care of many lesions. And this is an important study that show that when you compare those strategies, they have the same survival, and the patients that have a parenchyma sparing hepatectomy and ablation have less complications than those who have a major hepatectomy, which is important. This is an important number here, back in 2014 only 31% of the cases were being done with parenchymal-sparing surgery and ablation. And that rose to almost 50% in 2022 which is is an important trend. We really use ablation a lot when it comes to colorectal liver metastasis. And this is a study that came out this week, actually another multicenter study that compares the role of ablation or surgery. When you are talking about tumors that are three centimeters or less in size, they have the same outcome. Okay, it’s not inferior to do ablation versus resection. Resection is a gold standard, but now ablation, up to tumors of three centimeters, is equivalent. And this is really important, because sometimes, if we do an operation, we clear your tumor, and in a year or two later, you have a new tumor coming back, you might be able to get away with ablation, without surgery.

Dr. Juan Rocca 23:01
Or if I do an operation and to treat three tumors, and I can safely remove two, but the third one is in a tough spot, or I may require to remove more liver, I can do an ablation of that tumor. That is equivalent, as long as the tumors are three centimeters or less, this is another important thing, as we have a higher number of tumors in the liver, we have less chance of surviving in the long, long term, or a higher size of tumors. This is the liver met survey registry. It’s the largest registry in colorectal liver metastasis. I wanted to show you that these are the things that we always consider for puttingsomeone in the category of being resectable or being unresectable. If sometimes, technically, we can remove all these lesions, but they tend to come back, resectability is not only a matter of a technical surgery, it’s also had to do with the tumor biology and the number, the size, but also how long it takes for that tumor to come back. Sometimes when we do operations and we have what we call the very early recurrence after we do an operation, we get the patient to NED, and then in about three months, we have a new new tumor that is telling us that the biology of the tumor is aggressive, and that usually is associated with the number of lesions that we have, or if there’s any extrahepatic disease, or if there’sany mutation, and it’s sometimes important to the surgery. The outcome after the surgery will tell us a bit more about the biology of that tumor, and that will guide our decisions about what to do next. So, in summary, liver surgery for resectable scenarios, I think it’s always important to understand that surgery always has risk. Liver surgery is always complex, even if we do it small, as small as we can. But you know, it offers really good long term outcomes. 50% can achieve long term survival after a successful resection, always, in my opinion, combined with systemic therapy, and it’s also important to understand that many of these tumors are going to come back in five years-60 to 70%, and that’s why we need to keep treating it as aggressive as we can.

Dr. Juan Rocca 25:44
Now, what happens for those that we consider that we cannot resect, that it’s beyond all these different scenarios that I just showed you where we can do an operation or an ablation? Well, first, I think if you do systemic therapy alone, chemotherapy and now with targeted therapies, the survival at five years is about 20%. But still, it’s important to understand that this is the backbone of the multimodal treatments. Over that backbone of systemic therapy, we can add the benefit of other locoregional therapies that can improve the survival. And those other locoregional treatments can be ablations that a non surgical ablation, percutaneous ablation, Y-90 radioembolization and external radiation. So a brief description of each of these. Ablations can be done with radio frequency or microwaves. We put a needle inside the tumor in the liver, and pretty much we burn the tissue. So that pretty much burns the tumor tissue and the liver tissue that is around with the margin. So the same thing we would do in surgery to make that tumor cells dead. That can increase, maybe 10% more the survival at five years if we combine it with systemic therapy. Now we don’t have a lot of data about Y-90 radioembolization at five years. But yes, we use it when we have tumors that are more than threecentimeters where ablation doesn’t really do a good job. And we inject the tumor inside with radioactive particles, and the tumor slowly gets radiated and becomes non-viable or dies. These injections can be done very focal at the level of the tumor or in different segments. Sometimes for liver transplantation, we use it in the whole liver to keep the tumor at bay until we get to a transplant. I think it’s really an important treatment, and it’s always important to consider.

Dr. Juan Rocca 28:13
And then we have the external radiation or SBRT, which, again, we don’t have long term data. We usually reserve for those patients that cannot receive other treatments. But yes, we do know that it’s able to achieve good local control of the tumor, at least in the first two years when we radiate a tumor in the liver. So I want to bring to the discussion also the role of the hepatic arterial infusion pump, which nowadays is not just that. It’s combined also with systemic therapy, but you’ve probably heard about this usually for unresectable disease, when you have tumors that are on both sides of the liver and multiple tumors. It’s a good method to downstage tumors to decrease the size and the number and sometimes convert them to resectable. So what it does is, because the chemotherapy is usually toxic to the entire system, we give only some specific chemotherapy into the liver, and that first passage into the liver will make the chemotherapy concentrate in the liver only and not give toxicity to the rest of the body. It does have survival benefits, because about 50% of those that receive a hepatic infusion pump may be able to be downstage to the point that they can be converted to surgery.

Dr. Juan Rocca 30:04
When you put it all together, the latest studies the overall five year survival for unresectable disease with the pump is about 50%. But then if you divide into those that responded to the pump and the systemic therapy and were able to have surgery, those had a survival of about 70% at five years. But then the other ones didn’t respond. It’s about 50/50. The other half that did not respond didn’t make it to the five years. But again, these are not only therapies that allow you to downstage treatment, but also to be able to understand the biology of the tumor. And those tumors that respond, they have a shot at having surgery or even transplantation, and those tumors that do not respond, at least we try very aggressive therapy, and if they do not respond, biology wasn’t clear.

Dr. Juan Rocca 31:09
All right, so now liver transplantation. Liver transplantation is the most radical treatment for liver disease from colorectal liver metastasis, and that’s why we call it the ultimate liver correctional treatment. Because what we do is, we take care of some cases of unresectable disease, liver transplant should not be offered to those that have resectable disease, because they have very good survival. But those who have unresectable disease, and they have a five year survival below 50%, below 30% some of them, they could benefit from having a complete removal of the liver, and by removing the entire liver, we’re not only removing the tumors, but also we’re removing the factors that are in that specific liver that allow the tumor to come back. Okay? So that’s the rationale behind it. But of course, for that, you need to be able to have a disease that is well controlled, right? So it’s kind of a long pathway to get to transplant, and many times all these different techniques that I told you beyond surgery, like ablation, like a radioembolization, or Y-90 radiation, or even the hepatic arterial infusion pump, are methods that we use to keep the disease at bay so we can make it to transplant. We use a lot of time, as a test of time, to tell us that the biology of that tumor is manageable to the point that we can do a liver transplant and not have an immediate recurrence, Okay?

Dr. Juan Rocca 33:08
So this is the latest study that we have in transplantation. We have some data from the United States. We have data from Norway, which were the pioneers on this more than 10 years ago, but this is the study that came out last year in 2024 and it’s a multicenter study in different countries of Europe. They show that if you tranplant patients with unresected liver metastases under central criteria of the stability of disease and the disease has to be restricted only to the liver. You cannot have peritoneal disease, you cannot have bone disease, you cannot have lung disease. So with that criteria, when they looked at the intention to treat, this is all the patients that were recruited to the trial. The five year survival was 56% for those that received a liver transplant, versus 12% for those that only received chemotherapy. Now, when you start tweaking a little bit the criteria to make it stricter, then the five year survival – that’s what they call the “per protocol” survival – the five year survival went up to 73% when you did liver transplant and chemotherapy, versus 9% for chemotherapy alone. So this is important, because this 73% is beyond what we consider the survival benefit of a liver transplant, which is about 60% at five years. Remember that liver transplant is a standard practice for many other diseases. It started with liver cirrhosis and many other diseases that are not related to cancer or some diseases that are related to liver cancer from primary liver tumors, and they have a high standard of survival. The survival of the liver transplant at five years nowadays is about 80% for most of the indications, and for some cancer indications about 70%. so it’s hard to really start doing liver transplants for colorectal liver metastases if you are going to be having a five year survival that is be below that benchmark of about 60%.

Dr. Juan Rocca 35:38
Now the other thing I wanted to show you about this data is that, as you can see, on the progression-free survival “per protocol”, those that received a liver transplant, with the red dotted line, they did have recurrence. They have a fair amount of recurrence, but by two years, 50% have some sort of recurrence, and we’re going to talk about that. Much of that recurrence could be treated. So if you can treat the recurrence after liver transplant, you have this concept that we have here, is the secondary progression-free survival. That is how you prolong the survival after treating the recurrence. So we’re going to go a little bit deeper into this and talk about the recurrence patterns after liver tranplant, and the difference with the liver surgery. If I do liver surgery for colorectal liver metasteses, the primary site of recurrence will typically be the liver because the liver that I did surgery on still has the conditions for a new tumor, and is harboring microscopic tumor or new tumor to be seeded and grow back and recur. Okay? When we do a liver transplant, not only are we removing the tumor, but we’re removing that liver with those factors, and we’re putting in a different liver that may not have those factors. So the recurrence pattern after liver transplant is not in the liver, it’s mostly in the lungs. And as I told you before, the lung metastases are indolent, usually they take a long time to progress, they are not as life threatening as a metastasis in the liver or the bones, or the brain. So it is important to consider this when we know that some patients have lung metastases after liver transplant, but they can be treated with surgery.

Dr. Juan Rocca 37:51
This is an example that I want to show you. This was done last year in Chicago. I trained in Northwestern Memorial, actually, many years ago, and a young patient that received a liver transplant for colorectal liver metastases was 8 years out from that liver transplant without problems, except for some lung metastases that had recurred and was stable, but they kept coming back after different treatments. So for the first time, it was decided to do a lung transplant for metastases in the lung, 8 years later after a liver transplant. So this is way far from what we consider standard of care, but at least it’s giving us a glimpse of what we could achieve by having a long term survival for unresectable, colorectal liver metastases.

Dr. Juan Rocca 38:52
Of course, we have to be very cautious with all this, and unfortunately, the patients that can be eligible for a liver transplant, the patients with colorectal metastasis, about 1 or 2% of all the patients that are there. So this is an important figure that can give you a sense of all the patients that have colorectal cancer, half of them have colorectal liver metastasis, about 30 to 50% of them have no evidence of extrahepatic disease, which means that we could consider liver transplantation. But you know, 70% of them are technically resectable, so we should resect them. And then there’s the 10% that, if we consider all the selection criteria, may be able to be considered for transplantation. But then, in the end, through the pathway of transplantation, which requires a wait time or requires treatments, requires them to go through a transplant evaluation and to receive an organ transplant from either a live donor, or a diseased donor, only 1 or 2% may be able to receive it. This is encouraging to be able to come with liver transplant, but still, it doesn’t have the scale to impact everyone. This is just to show you the protocol that we have at Weil Cornell for transplantation of colorectal liver metastases. We have a trial that is listed in the clinical trials.gov site. We did transplant five patients, but we did evaluate, (this is a bit old), more than 35 patients. The definition of unresectable is made at the tumor board. We look at the imaging, and we have surgeons, we have oncologist, we have interventional radiologists, and we come up with different strategies to decrease the tumor burden and see if there is a way to resect this patient and make them NED. If we don’t find a way, then that patient, if they only have disease limited to the liver, that patient may be able to go into liver transplantation. For that, we need to have different tests of the lungs, the liver, a PET CT, we usually do six months of chemotherapy, and we have to make sure that the disease remains stable or responds. And then sometimes we have to remove the primary tumor. If the colon tumor was still there, we had to remove it and wait and give another treatment session. And then closer to the transplant, we typically give lobar Y-90 which is this radioembolization to the both sides of the liver, because at some point we need to stop the immunotherapy before the liver transplant, and we need to wait about six to eight weeks for that immunotherapy to go away. We want to have some control in the tumor with with the Y-90. That’s why we usually give it. The product Y-90 is quite toxic to the liver, so we have a little window there to stop the immunotherapy with the effect of the Y-90, and then do the liver transplant.

Dr. Juan Rocca 42:13
This is a summary of the outcomes of different scenarios for colorectal liver metastases. So starting with the easier scenario, single liver metastasis, you can have a five year survival up to 60% with surgery and systemic chemotherapy. If you have multiple liver metastases that are resectable, you have a combination of different treatments and as I told you, you can have survival rates that go between 40 to 50% at five years. If you have multiple liver metastases that are unresectable, your five year survival can go from 10 to 20% if chemo only, up to 30% if you add ablation or chemoembolization or radiation to it. If you have a hepatic arterial infusion pump, your overall survival can stretch to 50% or more. It depends on if you respond to the arterial infusion pump. If you don’t respond, your five year survival won’t get to five years. It’s going to be hard, but you might be able to respond and become eligible to either having surgery or a transplant, for some cases, we do consider patients that are being downstaged with a hepatic infusion pump, we do consider for transplant in some situations, and then liver transplantation, if you make it to liver transplantation again, 1 to 2% only can make it there. You can get up to 75 to 80% of five year survival. It doesn’t have the scale, but yes, it’s very promising for those that can meet the criteria.

Dr. Juan Rocca 44:10
So now let’s put this into the right context. I think this is a great picture to tell us what the scale of all this is. Okay, so unresectable here at the bottom, if unresectable are in the 10,000, resectable is about 10% of that, in the 1000s. Okay, so the resectable disease as we define it, that we can do surgery, combined with chemotherapy, maybe with ablation, the tumor comes back, we do surgery again or ablation. That is in the proportion of the 1000 compared to the 10,000 of those that cannot have resection or cannot become NED. Then those that may be considered for liver transplantation are in this grey zone. Yes, they are not resectable, but the burden of disease is not too much, or the biology of the tumor is not too aggressive, like, for example BRAF mutations are not being accepted for liver transplantation because they are too aggressive, but some other RAS mutations are being accepted. And of course, there’s a test of time, etc. So, liver transplantation would be in the 10’s of transplants, okay. So this is just to give scale to, or to give a good context of the different treatment options.

Dr. Juan Rocca 45:45
Okay, now let’s talk about histotripsy now, and I gave you all the data about what the other options can accomplish in terms of survival. Histotripsy, because it’s a new method, and we’ve only been doing it for one year in the United States and in the world, we know we won’t have five year survival data. But how does it work? So first, it’s a non- invasive tumor treatment. It does not require surgery, it does not require a needle to be inserted into the liver. It’s just ultrasound, so in that regard, it’s very novel. It could be compared to external radiation therapy. But external radiation therapy is a lot more toxic. So, what it does is the ultrasound, the shock waves from the ultrasound, induces cavitation, that is, bubbles that expand and collapse so rapidly that it destroys the tissue and the cells, and makes them explode. It’s like an implosion. And that area that is being destroyed turns into what we call a lysate or a liquid, a liquid that only has proteins or different components of the cells, but has no viable cells. Now, the important thing is that these cells that are being mechanically disrupted are cells that are usually either cells like liver cells or tumor cells, but some cells that make blood vessels or bile ducts or scaffolding structures of the liver are not being destroyed because they have high collagen, so that allows the liver to regenerate back in that area. Once that lysate or that fluid is being reabsorbed by the lymphatic system of the liver, the liver will eventually regenerate in that area. This is a little video that you probably saw. But just to give you an idea, how the setup is for histotripsy: We do histotripsy in the intervention radiology suite. Some other centers to it in the operating room, some other centers are doing it in an intervention room that is not specific to anything, but we need to have the patient under general anesthesia. That’s important to understand. So you know patients that have severe heart disease or severe lung disease, some diseases that are not related to the cancer, but you know that they are unsafe for general anesthesia. Those patients cannot qualify for it. But we would put the patient under general anesthesia, and then we use a special water bath that has to be put over the the abdomen in the region of the liver to be able to transmit the ultrasound waves into into the liver. And we use a regular image in ultrasound that is coupled to it so we can see the lesions.

Dr. Juan Rocca 49:05
So this is how the device looks. This is pretty much how we set it up. And then this is a closer view of what happens inside the liver. If this is the tumor, these shock waves start creating these bubbles of implosion and expulsion, and with that, start destroying the cells and creates a bigger bubble. It’s like a chain reaction. And that bigger bubble starts going around. We usually have a very focal targeting of the beam, and we move it in around the the size of a golf ball, if you want, until we create that size. Here you can see what happens when you have this fluid or the lysate. The blood vessels are usually preserved and the lymphatics are usually preserved. So that would allow the liver to regenerate in the coming weeks after the destruction of the tissue.

Dr. Juan Rocca 50:23
This is a representation of once the lymphatic system absorbs the tissue-the lysate, the liver tissue, can grow back into the area. Let’s look at the difference between histotripsy and ablation, because they in some regards are comparable, because histotripsy can be used for lesions that are about three centimeters or less in order to treat the entire lesion. The difference between ablation and histotripsy is that, because ablation pretty much hits the area and cooks the tumor cells on the liver tissue, the regeneration of the liver is not as much. It takes a long time to reabsorb the tissue because it’s pretty much not liquid, it’s solid and it’s is like a burnt tissue instead. You can see the defect there. Here, that beginning is very similar to ablation. But then over time, the normal liver tissue starts growing already, until you have a minimal scar there. So this is one aspect of histotripsy. The other one is that there’re some areas that we can preserve blood vessels and bile ducts after doing histotripsy in areas of the liver.

Dr. Juan Rocca 51:50
The final one that maybe many of you have heard is what we call the abscopal effect, which is an effect that by treating one or two lesions, and by allowing the liver to reabsorb that lysate, with antigens of the tumor that unmasked for the immune system tumor antigens, and allows the immune system to be more active against other tumors that were not treated. That’s a very exciting, exciting effect. However, we don’t see it too often. We see it in about 20% of the cases. And we still don’t have a good way to take which cases are going to have that effect and which cases are not. It’s kind of a hit or miss. But I think it’s important to remark that this is another potential benefit, and I think with more data, we may be able to determine which type of tumors or which type of genetic mutations or what type of liver or location or size can really respond with this immunologic synergistic effect. This is another example of what we do prior to liver transplant for other disease, which is hepatocellular cancer, but hepatocellular cancer is a tumor from liverdisease that we transplant. But many times before transplant, we have to do different treatments of the tumor to keep it at bay. And these are very sick patients, and we are being able to do this treatment now, instead of doing invasive treatments like ablation. We can do histotripsy to reduce the tumors or even knock out that tumor until the patient gets into transplant.

Dr. Juan Rocca 53:41
I just wanted to remark the abscopal effect is a systemic immune response that is triggered by the tumor destruction, and it can expose the tumor antigens and that can potentially enhance the immune surveillance. Now this is observed not very frequently, but it’s something that is under investigation, and hopefully we can find a way to make it happen more often. We believe that keeping chemotherapy and immunotherapy while doing histotripsy, can really help synergize the effect of histotripsy. This is just to show you how in one year only, historipsy was embraced by many centers in early state, a total of 28 centers now have it, many here in New York. And this is the number of tumors that were treated in 2024. You can see that colorectal cancer is the majority of them, about 260 cases, neuroendocrine tumors, pancreatic cancer, cholangiocarcinoma. These are all metatsteses in the liver. Cholangiocarcinoma, HCC, which is a primary tumor of the liver, that we do transplants for and other types of tumors. The specialties that do this can be interventional radiology, in some centers radiation oncology does it as well, hepatology or surgery. There are different trials that led to the approval of this technology for treatment of liver tumors. Some initial trials a few years back. – But the trials that really led to the FDA approval was this Hope4Liver trial, which is a multicenter trial in the US and Europe that was able to demonstrate effective treatment once you target and you can go around the tumor and destroy the tumor and the tissue around it. That’s the effectiveness. It didn’t come back within 30 days, which is not long term, but at least within 30 days, and then that it is safe. That there were only a few adverse effects because it’s non- invasive. There were minimal cases of serious adverse events that we call, like infection, like liver failure or death. In those 44 there were a total of three cases only.

Dr. Juan Rocca 54:00
Now this is the important study, the BOOMBOX trial. The BOOMBOX trial is a prospective trial, where we enroll all the patients that are receiving histotripsy, and we follow them up for five years. This is why it’s so important, because we really need to get the five year data to be able to compare to all the existing tools that we have to treat liver tumors. We are participating in this study where we actually enrolled three patients already. And I think it’s it’s important that if you are the receiving histotripsy, you’re very likely going to be enrolled in the BOOMBOX trial, or you may be even enrolled in some other specific trials that are using historipsy in different contexts. For example, in the contexts of certain chemotherapy, certain immunotherapy, or associated to other treatments.

Dr. Juan Rocca 57:21
I have a clinical case that is a transplant case. Just wanted to highlight that there was a woman that had a diagnosis in 2020 and had surgery for the colon in 2021 January, and then had liver metastases and a year later had surgery in the liver in 2022 where they removed different lesions, they removed seven lesions. Okay, so there was resectable, but in the high risk end, and had ablations, then had chemo later, and then five months later, as soon as they stopped the chemo, there were some tumors that came back, they recurred. So she had another surgery in January of 2023 one year later, with resection of three lesions and ablation again, and then was followed by chemotherapy again. And so this is a colorectal cancer operated in 2021 liver surgery. In 2022 liver surgery in 2023, and every time that they stopped the chemotherapy, the tumors were coming back into the liver. The patient was sent to us to discuss different options of treatments. She had no mutations that were of concern for us. And then I just want to show you a little bit, at the top of presentation, the tumors that were active. There was one here, one here, one here, and another here, four liver tumors, and there was an area that was also non-viable of liver. So we did a first intake. We did a PET scan that showed us that the the metabolic volume of the tumors were not that big. A metabolic tumor of almost 90. Best survival is 70 or less, but 90 is quite acceptable. You can see here, 1-2-3-4- 4 tumors, and there was a question of a fifth tumor. In this case, we could say that there’s enough liver. And there are only four tumors, why don’t we go back and resect it again? Yes, but this is when the concept of biology and resectability can come together. Anytime you stop the chemotherapy after resection, the tumor came back, and it was the third recurrence. So, we were a bit skeptical about doing again a resection, and we presented this case at the tumor board. We looked everywhere, the chest, the the bones, and there was no evidence of disease anywhere else. So we presented this as different treatment options. One was to start the chemotherapy of course, to repeat resection and ablation. We could refer her to another center. -We don’t do the hepatic arterial infusion pump, but she could go to receive hepatic arterial push pump, then resection. The problem here was she already had multiple resections. We could include her on the transplant pathway. And so we reinitiated the chemotherapy. And then after three months later, after chemotherapy, she got stable disease, we decided to do a periportal lymphadenectomy to make sure that the lymph nodes around the liver were negative. These were negative, and then we continued again, chemotherapy for another three months, while we gave Y-90 to keep the tumors at bay,after stopping the chemotherapy. And we were able to restage again, we didn’t see any evidence of disease outside the liver. Disease in the liver was better. There was less tumor burden. Here you can see the lymphadenectomy. So after we did a final run of patient, and we find that it was controled liver disease with those four lesions that were smaller, the tumor volume on the PET scan went from 90 to 64, under 70, we considered that she was a good candidate for liver transplantation, and we were able to give a live donor liver transfer from her son. That was in May, and so far, at this point, she has no evidence of disease. So I think this can illustrate all the different therapies that we talk about, except for histotripsy for this case. But we would consider histotripsy in some cases that are going to transplantation, to show you that we always need to find a way to either make someone resectable, or someone that can have aggressive treatments like ablation, like a hepatic artery infusion pump, to see if they can respond and they can become resectable, or they can become transplantable and ultimately prolong the survival more than 50% at five years which is evolved. I’m going to open the floor for questions.

Betsy Post 1:03:16
Thank you so much. I’ve learned a lot. This was great. I think it really talks to all the different treatments and how they can be used together. And a great introduction on histotripsy. I know we appreciate it. So I’m gonna go through some of the questions, we have a question on transplant. Is it always best to have a transplant if one is a candidate for that and not resectable. So I think, sort of looking at that pathway.

Dr. Juan Rocca 1:03:45
I think it’s worth to have an early consultation if the diagnosis is unresectable and no evidence of disease outside the liver, I think it’s worth it to have a consultation. Remember, anytime you go to a transplant center to inquire about transplantation for this, they will put you on a protocol that will require at least one year of wait time from the time you get a diagnosis, and maybe six months after removing the colon and having chemo for about a year, at the very least, to show that you have stable disease. And then we do all this testing to make sure that there’s no disease outside the liver. Many centers do this surgery before the transplant to remove the lymph nodes to make sure that there’s no lymph nodes that are positive around the liver. So it really is a process. So if there is any question about eligibility for transplant, I think it’s important to go to a transplant center that has a protocol for that and inquire.

Betsy Post 1:04:56
We have a question about general anesthesia. So I think it’s obvious that a transplant liver resection are going to be done under general anesthesia. But I think as far as histotripsy, Y-90, the ablation, SBRT, some of those treatments, does a patient have to be under general anesthesia, or how would you handle that?

Dr. Juan Rocca 1:05:15
Yeah, that’s a great question. Any surgical procedure, of course, is under general anesthesia. Ablation – it depends on the center for percutaneous ablation. Some centers do it with sedation only, depending on the location. Some centers prefer to do it with anesthesia because they have a better control on the movements of the patient. With histotripsy it’s the same thing. Histotripsy requires anesthesia because when you target the lesion and you treat it, the respiratory movement has to be predictable. So with anesthesia, we can control the movement of the of lungs and how the liver moves, and we can decrease the amplitude of the movement to the minimum to try to stay in the area and not burn. For example, when we’re doing it, histotripsy or ablation, but mostly with histotripsy we don’t want that area to move too much, because maybe then the ultrasound beam can go into the colon or to the stomach or to the duodenum, to areas that are not liver, and can damage those areas. So that’s why it requires general anesthesia. Now, if we find a way to do a less invasive treatment, like with ventilation that doesn’t require general anthesthesia, that’s in discussion. But so far to my knowledge, none of the centers that do histotripsy are avoiding general anesthesia. Everyone is using general anesthesia so far. For radioembolization you might not need general anesthesia. That’s sedation only. For radiation, you don’t need anything.

Betsy Post 1:07:14
Is it logical to pursue partial histotripsy with the intent of down staging before other therapies such as SBRT or Y-90? In other words, is it logical to target one part of a tumor with histotripsy and then use another therapy to finish the areas that were not treated? For example, in cases where Y-90 or SBRT would not get all of the tumor alone or would be too risky?

Dr. Juan Rocca 1:07:42
Yes. So that’s a very important question, and this highlights the role of multimodal treatments, right? Yes, histotripsy can be done for what we call complete treatment or partial treatment. So if histotripsy can be done, let’s say, the liver has three tumors. The three tumors are under three centimeters, and they’re in spots that are safe to burn around the tumor or burn. Just do the histotripsy to lysate the tissues, so that will be a complete treatment. There were three lesions, the three lesions were completely treated with the histotripsy. That’s a complete treatment. Okay. Now, for most of the cases, we do histotripsy in situations that we have more tumor burden, multiple lesions, different sizes. And what we do is we try to do a stage histotripsy. We treat two or three tumors at a time. And sometimes, for example, if there’s a tumor that is five centimeters, we may treat three centimeters once, and then come back and treat the remainder two centimeters and to try to clear the entire tumor. Or sometimes we have multiple tumors. Some of them, we can target them with histotripsy, but some others may be in a difficult location for histotripsy, either because it’s close to the colon, close to the stomach, or high up, or surrounded by lung, and it’s hard to get the ultrasound beam to get there. So sometimes we use combined modalities of histotripsy with ablation or histotripsy with radiemobilization in order to treat all the tumors that are in the liver.

Betsy Post 1:09:39
Thank you. Could you provide your thoughts on getting a hepatic pump with replaced right hepatic artery abnormality?

Dr. Juan Rocca 1:09:50
Yeah, so the the arterial anatomy is an issue, and the eligibility of the hepatic infusion pump depends on different variations. But the problem would be, when you’re trying to inject, the catheter of the pump has to be in an artery that’s only to the liver and not anywhere else. So many times when you do this procedure, I don’t do this procedure, but Memorial Sloan is located across the street. They do it, and so they are very detailed about the different branches of the arteries where the catheter is to make sure that that chemotherapy goes only into the liver and doesn’t go into the stomach or into the pancreas, into the duodenum. Many times, when you have a right replaced hepatic artery it may be very difficult to control the flow, or can even reflux. And that could be a contraindication. That’s right. So if you were turned down because of having a right replaced hepatic artery, this could be a contraindication, yes.

Betsy Post 1:11:11
For tumors that are under three centimeters, is radiation equally as effective as ablation? I think you talked a little bit to that, but I did want to ask you that.

Dr. Juan Rocca 1:11:23
Yes. So this is the COLLISION study. The study that I showed was a multi center study in Europe. The research came out with the final results. Actually, the study was stopped earlier. So the study was designed as a non inferiority trial. This is the gold standard, was resection for tumors less than three centimeters. And they started comparing ablation for those same tumors, same size, and they couldn’t see any significant difference. They recruited 300 patients, 150 and 150, pretty much. And they stopped it early because there was no difference in the outcome. So this validates ablation as an equal treatment to resection for tumors under three centimeters. Of course, the devil is in the details, and that doesn’t mean that in your specific case, you should have an ablation, another resection. That depends on the location of the tumor. Sometimes the access with the ablation, sometimes we do it with surgery, but sometimes percutaneously, it’s not as easy to access every tumor in the liver than with a surgical ablation, or sometimes a resection makes more sense. No, that depends on the specifics of the case.

Betsy Post 1:12:49
Thank you. And this is from a patient that actually had the histotripsy procedure done to three lesions in the liver. The patients had two CT scans since the histotripsy, and is just wondering, other than comparing the size of tumors of those treated lesions on the CT scans, how would the patient know if histotripsy-induced abscopal effect has taken place?

Dr. Juan Rocca 1:13:17
Yeah, so far the way to tell is with imaging. This could be MRI or a CT scan that has contrast. And with that between two to four weeks after the procedure, you could see the abscopal effect is, if you got treated three tumors, but there are three tumors that were not treated. You should see a rim enhancement in the tumors that were not treated, like there’s some inflammatory activity around the tumors. If you do it early, maybe two weeks later, and if you do it later, like four weeks later, if that already happened, you should see a reduction in the size of the non-treated tumors. The only way to document abscopal effects nowadays is, like we did mention so far.

Betsy Post 1:14:13
Can you comment on the HAI pump for patients after resection to help prevent recurrence, so, when a patient would get a pump to help prevent recurrence. I think you did comment some on that, but I just wanted to ask that.

Dr. Juan Rocca 1:14:27
So the pump has benefits. It’s an aggressive therapy. It’s like two stage hepatectomy or even liver transplantation. These are aggressive therapies, and it has benefits, but also has some drawbacks or toxicities. The benefit is if you respond to the pump and you can downstage the tumors to make them resectable, which 50% can respond? Good news. You’re in a good spot if you respond and you can have resection. For example, the chances of recurrence is a lot less after using the hepatic arterial infusion pump. So not only it can reduce the burden of disease and make it resectable, but also it will prolong the amount of the recurrence-free survival. Okay, so that’s important. On the other hand, sustained treatment with the pump can lead to liver toxicity, and in some cases, can lead to some irreversible liver damage on the bile ducts. It is reported to be 1 to 3% but when it happens, it’s a real deal. So as part of an aggressive treatment that can be very effective, it’s always important to discuss the potential risks of having liver injury or having to interrupt the treatment because there’s liver toxicity. Not every patient can continue the treatment, and sometimes it has to be interrupted. The management of the pumps requires a multidisciplinary team that is not only the surgeon, but it’s very specific oncologists that know how to manage the dosing in order to manage the toxicity in the liver and to try to mitigate the potential injuries to the liver.

Betsy Post 1:16:36
In your opinion, how many times can you perform resection and targeted therapies on the liver before you would consider that transplant path would be the best path forward.

Dr. Juan Rocca 1:16:49
Yes, well, the clinical example I showed you was two times resected, and the third time that it recurred, we decided to do a liver transplant. It depends on the presentation. If someone presents with unresectable disease, but in that gray zone that is unresectable, but the size of the tumor is no more than five centimeters, there can be multiple tumors. The metabolic volume on the PET scan is not high. It’s not more than 90. Of course, that kind of patient has to be on chemotherapy. So if they are stable on chemotherapy, or responding on chemotherapy, and we see that there are more than six seven lesions, it could be considered for trouble, because we know that resecting six or seven lesions with surgery, the chances of recurrence is very high. And the long term survivors are showing one of the curves, of resection, chemotherapy, of seven or more lesions, the five year survival is about 25%. So some cases that present like they could be considered for transplant from the get-go based on how they present, in the number of lesions, the number and the type of mutations we would consider transplantation up front. But clearly resectable cases with low risk of recurrence, or a lower risk for recurrence, we would resect first.

Betsy Post 1:18:38
Does Weill Cornell have different criteria for transplant than Columbia?

Dr. Juan Rocca 1:18:45
Not too different. But Columbia just started doing this. I think that they just listed a patient so they’re trying to use the more recent criteria from the transplant trial. We have our own criteria. Our trial has been around since 2021, and we evaluated 35 patients. We transplanted five. So we actually work together. We are under New York Presbyterian we are two different universities, or two different types of faculty under the same hospital system. We work on two protocols together, and we are actually working on a common protocol based on our experience with transplantation and their experience.

Betsy Post 1:19:39
Does the liver regenerate in areas where you receive Y-90?

Dr. Juan Rocca 1:19:44
Not so much. No. The areas that were not affected by Y-90 will regenerate. But the liver areas that receive Y-90 will not. It depends on the doses of Y-90. They are very variable. It depends on some mapping studies to make sure there’s no — dosage chance into the lungs, depending the goal of the of the Y-90 if it is to destroy a specific area of the liver or to give lobar Y-90 like before transplant, to kind of keep the tumor at bay. But lobar Y-90 is very toxic too. So sometimes, if we give the lobar Y-90 too early before transplant, we may have some liver failure. So I think it’s important to understand, at the timing of the transplant, if you have a live donor, it’s a lot easier to really have a good timing and be able to to schedule the Y-90 3 months before transplant, knowing that at that time, if the liver has failure, it can be rescued with a transplant. When you go into the disease donor wait-list, and it’s more unpredictable when the transplant is going to happen so that we can run into liver decompensation or liver failure from the lobar Y-90 that was already beaten up by the chemotherapy too and prior resections, etc.

Betsy Post 1:21:15
Is histotripsy an option for patients with the BRAF mutation, and then, as well, a RAS mutation, such as NRAS or KRAS?

Dr. Juan Rocca 1:21:25
Yes, there’s no contraindication based on mutations for histotripsy. The limitations on histotripsy are certain size of tumors or certain locations where, we may not be able to clean the entire tumor from the liver. But if there’s no other therapy available,I think histotripsy is totally indicated, yeah.

Betsy Post 1:21:55
I just want to make sure.

Dr. Juan Rocca 1:21:56
We do histotripsy in patients that we would not be doing any other therapy because they have disease. We know that the liver disease is the one that really dictates survival. Many patients that present to us with liver metastases, but they have lung metastases, bone metastases, and they are generally doing well, and the liver disease is threatening their survival we do histotripsy on those patients.

Betsy Post 1:22:30
Is it possible if you have a tumor right next to the IVC?

Dr. Juan Rocca 1:22:35
With what technique?

Betsy Post 1:22:37
With histotripsy, sorry.

Dr. Juan Rocca 1:22:39
Yes, yes, the IVC is a big vessel, same as the hepatic veins. We usually anticoagulate for that, because even if the vessel is preserved, the skeleton of the vessel is preserved at the endothelium, which is the the cellular lining that is very delicate on the blood vessels. That one gets destroyed, but the structure remains. So the endothelial lining gets repopulated very quickly. But to prevent clotting, we give anticoagulation. So for the hepatic veins and the IVC, the venacava, it is safe to do it with anticoagulation. For the portal vein,t hough, it’s a bit trickier because the portal vein is a different type of flow. Sometimes despite anticoagulation, we can have clotting on the portal vein. And that’s something you have to be careful about. So lesions are very close to the center of the liver, where there’s a lot of portal branches, we try to avoid them.

Betsy Post 1:23:55
And I apologize if I missed this one. We just have a couple questions left. One is, what is the largest size that can be treated with histotripsy?

Dr. Juan Rocca 1:24:05
In different sessions, you can treat larger lesions. It all depends on the location. And sometimes large lesions, you may be able to access with the ultrasound being an area of the lesion, but the other area is too high, there’s too much lung that doesn’t let you deliver energy. But by six centimeter lesion, if there’s no other good option to treat it, I would try histotripsy. Now we should consider, usually, for lesions that size, we also consider Y-90 because Y-90 is very effective at reducing large size lesions if they are not resectable.

Betsy Post 1:24:47
Let’s see. I think all the liver-related questions are pretty good. I think we’ve got some people saying they’re going to make an appointment with you. I think you had your email on that prior slide, that last slide, so I just want to make sure that as part of the recording, everyone can see that. So if you do have questions specific to your case especially, and you want to seek a consult, this is the email with follow up questions, I feel like we got everything we could.

Dr. Juan Rocca 1:25:25
I’m not very reliable with emails. Some days I’m in the operating room all day, and I get many patients that send me emails. I think it’s probably better to leave an office number, because at least someone can be more accountable for replying, but yes, I can send the office number, and we have a free assistant that usually take all the calls.

Betsy Post 1:25:55
Perfect. If you send that to me, I’ll make sure that everyone gets it. And I appreciate that. I appreciate all of your time. You’ve spent an hour and a half with us tonight, late in the evening, and we are so appreciative. I learned a lot. This was great. I know that the patients and families here tonight got a lot out of this, and I just can’t thank you enough. So thank you so much, and there’s a lot of thank yous in the chat.

DocTalk
2025
Dr. Rocca
Ablation
HAI
Histotripsy
Liver
Radiation
Stage IV
Surgery
Transplant
Y90

In this video, Dr. Rocca delves into the Multimodal Management of Colorectal Liver Metastases, exploring innovative therapeutic options and strategies to improve patient outcomes. Recorded in January 2025.

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Histotripsy: New Technology for Liver Tumor Treatment

Histotripsy: New Technology for Liver Tumor Treatment

DocTalk
2024
Dr. Miller
Histotripsy
Stage IV

In this panel DocTalk, Dr. Burns breaks down histotripsy — an exciting, noninvasive technology that uses sound waves to destroy liver tumors without heat or radiation. Recorded in July, 2025.

Betsy Post 0:27
Welcome everyone to this evening’s DocTalk. We’re really excited to have Dr. Kevin Burns with us. A lot of you in the LIVER LOVERS group requested him, and you talked about how much you respect his work in histotripsy. So I reached out to him and asked him if he could present to us on this DocTalk. And he said, “Sure”. So we feel very fortunate to have him with us this evening to talk to us about histotripsy. I’m going to go over just a little bit about how this is going to work in just a second. But I also wanted Dr. Burns to see a few anonymous comments about him. These are just three that I pulled just so you could see what your patients are saying about you. So I hope that the positive feedback is something that is encouraging to you. You’re very well respected and we’re really excited to have you here, just so everyone knows. If you’ve not attended a DocTalk with me before, or if you’ve forgotten, I’ll ask politely that you stay muted throughout the presentation and put questions for Dr. Burns in the chat. Use the chat feature to ask questions, and then at the end, we will answer questions as much as we have time for. I will go over those questions at the end with him. So without further ado, I will turn it over to you. I will stop sharing and let you share. And again, we really thank you so much for being here with us tonight. We’re excited to learn from you.

Dr. Kevin Burns 1:51
Thank you for having me. I’m Dr. Kevin Burns. Thank you for having me. This will just be like an informational thing. I’m not going to show any cases necessarily, of how this is used, but kind of just what is the technology; How does this compare to any other sort of technology that’s out there; And I think one of the important things to know is, obviously, this is a new procedure. There are a lot of things we’re going to be learning over time. And, we learned something from every case. There’s probably been almost 2000 procedures now performed worldwide. So, people are learning things as we go. We had our first international historipsy summit, it was actually about six weeks ago, that was held in Minnesota. We had doctors from all over the US, and then as well, some of the international sites. So there’s physicians from Hong Kong, some from Europe, that were all there, and we were discussing how we all do these cases differently, and how we can learn from each other. So I think there’s a lot to learn, and this procedure is going to get better and better over time, as you can see here on this slide. So this on the right, is the Edison machine. So this is the, basically, the machine that currently delivers histotripsy. So histotripsy is basically a mechanism, and this company, HistoSonics, makes this machine called Edison. I will disclose I am a consultant for this company, but in this regard, I’m speaking as myself, and I don’t represent the company during this talk, so anything I say will just be my personal opinion. So they’re the only ones that commercially make a platform for this. On the other side of the screen here is what we call the ‘bubble cloud’. This is what is happening inside, just a pictorial, and so histotripsy creates this bubble cloud which can go in and dissolve tissue. So hisotripsy, so it’s a novel mechanism of action. That means it’s a new way to destroy tissue compared to anything we had before, and it’s a mechanical disruption.

Dr. Kevin Burns 4:13
As you can see in this depiction over on the right, this is a kind of a phantom, and histotripsy is happening. And you see it really just completely takes out the center of this phantom here. And you can see how precise the margins are. It’s very, very, very very precise, meaning you can get right up to a critical structure without entering it. And so this causes instant tissue liquefaction and cell death. And it’s very precise and controlled. And I think important too is you can see that there’s no damage in the tissue, around this lesion. This is what a treatment head would look like. And so this would be positioned inside of the water bath on you, and we’d use this to localize the tumor. There’s an ultrasound probe built in, so we can use live imaging to see and then just think about this like a satellite dish and setting all these beams, and it’s only where they meet at this one focal point. Think about it like the size of a grain of rice, where this histotripsy happens, and if there’s not enough power, histotripsy doesn’t happen. Also importantly, as you can see, that histotripsy doesn’t happen on any of the way into the tissue. And so that means that we can treat through structures and it doesn’t damage them. So we could treat through the gallbladder, through the ribs, potentially through the stomach, but as long as the lesion is safe, then we’re able to treat it.

Dr. Kevin Burns 1:51
This is just another depiction. It’s what would be happening on a microscopic level. And this is that bubble cloud. Basically the histotripsy creates this intense negative pressure, it rapidly expands and contracts all the air that is present in the cells, and it uses this to instantly destroy the cell. So as you’ll note, too, histotripsy either is on or off. There’s no gradient. So when we talk about other therapies like microwave ablation, cryoablation, other therapies like that, there’s different levels of ablation, so the center of the lesion will generally get to a hotter temperature or colder temperature, depending on the device. And then as you spread out, there’ll be areas that may not be completely dead, but when you look with histotripsy, it’s all histotripsy or it’s not and so that’s another differentiating factor as well. There’s going to be some videos that we’re going to play here. So this is a demonstration video. I’ll let this play through, and this will simulate what would happen during a procedure if you were there.

Dr. Kevin Burns 1:51
This is the machine that the physician would be controlling, and this is how the procedure room setup is. Generally, this is going to be done in an operating type of room. It’s the procedure, I think, importantly, it’s not sterile. So there’s no incisions. Nothing breaks your skin anywhere. We are doing these under anesthesia in almost all situations now, and so that’s why, most commonly it’s going to be done in a procedure room. But I think as we learn more and more, I think this is going to move to the outpatient setting, where we can do this in a surgery center so we can get you in and out faster because of this procedure, it’s non invasive. So this would be to set up. There’s an ultrasound here that we can use to ultrasound you as well as provide the signal of the ultrasound. This is the water bath that sits on you. This is put on after you’re asleep, and the treatment head goes inside of this water. So if you think about ultrasound waves, if you ever had an ultrasound, they put that ultrasound gel on that’s to get rid of any air that’s between the ultrasound probe and your skin, because the sound waves don’t really transmit through air. And so this water bath will create a consistent water from the treatment head all the way to your skin. And so the treatment can successfully be delivered. This water bath can be positioned in different ways. In this example, the patient is lying face up, but we can put people on their side to move things around, or get to tumors that are in other locations. We’ve got many liters of water in here. So this is actually quite heavy, and so it takes a couple people to get this all positioned for you. – I’ll continue this video. – and so this is, again, what the treatment head would look like. And so this was going to simulate a procedure of treating one tumor inside of a patient. Here’s the treatment head inside of the water bath and here’s the simulated ultrasound waves coming down. And then at the center, this is the targeted tumor. And so the doctor can basically decide how big in all of the dimensions we wanted to do this. This is showing some fusion imaging. So in certain situations, we can take your pre-existing CT or MRI, and we can try to fuse it with the ultrasound, so that can help us find locations that maybe are hard to see or we’re not confident we’re in the correct location. So this fusion can help us localize more difficult to reach tumors and then after we program everything out, we basically set all the voltages. That just means, how much power does it take to kill your tumor? And that’s personal to every patient. Then we start this process. The robotic arm will move the treatment head through our pre program path in order to deliver that histotripsy throughout the tumor, including a margin. Next, we’re going to see what this would look like internally. So again, this is a simulation of what this will look like. This bubble cloud is going to go through, and it’s really liquefying everything in the treatment field.

Dr. Kevin Burns 9:21
And so if you had one tumor that was small that we are going after, this procedure can be fairly quick. I would say it’s pretty common that we’re going to be treating multiple tumors, and multiple tumors can be treated in one session. So that’s just kind of an overall of what the procedure would look like while you’re asleep, if this was something you were going to go through. Again, this was another demonstration here. I’ll pause this here. This is just more about how this works. So this is the treatment head again, and in the bottom corner, you can see there’s a number turning up. That’s the physician dialing the voltage up. Once you hit the critical voltage for your tissue and your body, histotripsy will happen. And then you could keep turning it up and nothing else happens. So we try to calibrate that for every patient to use the least amount of power in order to enable histotripsy to happen. And then if we look at what happens here, this would be what the physician would be doing. This is a simulation, again, of what would be happening. I think it’s helpful to actually see what would be happening inside, to visualize this. This is a piece of animal liver that’s sitting in this phantom, and this is very sped up, but this is what would be happening to the tissue internally. And I think it’s also important to know that there’s no damage anywhere else in the structure. It’s only in this treatment volume and where the histotripsy is happening. And then we’ll see that we’re actually going to cut this open, and you can see that this liver tissue is actually turned into a liquid, so basically, completely liquefied. So inside of your body, your body’s natural repair processes and lymphatic system would go through and reabsorb this and the cavity would decrease over time.

Dr. Kevin Burns 11:26
Now, if you did histotripsy, and then you immediately removed a tumor, and then you gave it to a pathologist, they would be able to do the staining. This would be similar to any biopsy you would have, and they would see that the histotripsy area is this acellular lysate, meaning that on the outside, we can see all these cells. They’re perfectly preserved, not damaged at all. So, very thin margin here, but you can see that it’s completely killed and then completely alive. So you can get very close to critical structures without damaging them. And you can also preserve more liver parenchyma than other therapies, potentially. And so this is that acellular lysate. This is something where the pathologist can’t actually tell what tissue this is from, and that means this is basically completely destroyed. Another important feature of histotripsy is kind of some tissue selectivity. So if the type of tissue has a lot of collagen in it, it’ll be resistant to the damage from histotripsy. In the liver, that would be the bile ducts, the portal vein, the hepatic arteries. You can see these are examples inside of animals where you can see histotripsy was performed, and then the liquid was washed out. And you can see that these vessels still run completely through the treatment zone. And in this video here, you can see that they’re actually washing everything out. And you can see the stroma and the structure of the liver remains, but all of the tissue is completely destroyed. This allows us to treat potentially in some more dangerous areas, in the hilum or the center of the liver, maybe a tumor that’s right on a vein or right on a bile duct. And we can maybe do this a little bit more safety than other therapies could, compared to microwave ablation or radiation.

Dr. Kevin Burns 12:50
This would be an example of a preserved vessel. This patient was treated with histotripsy and then they had an MRI. And this big black cavity is the histotripsy zone, and then this is a portal vein branch running through. You can see that this vessel is still open, even though it was completely inside of the treatment zone. If this patient had a microwave ablation here, likely this whole area would get scarred down, or potentially there could be a recurrence, because the vein would keep flowing in blood, and it wouldn’t allow enough temperature here to destroy the tumor right along the vein. And so histotripsy gives us a way to instantaneously and completely destroy a tumor so it’s a for a lesion that’s an appropriate size this is a one-time procedure to go in to try to kill it. We can potentially alter the microenvironment and immune system, we’ll touch on this in a moment. In certain patients, we can reduce the disease burden, and we can improve patient’s quality of life. If you have a tumor, let’s say you have many tumors, and we know that the chemotherapy is not working anymore, if you have a lot of pain, we’ve been able to treat tumors in patient that have pain, and that’s reduced their pain, or maybe it’s pressing on a bile duct, and you need to have a drain placed. So there can be ways to use histotripsy, even if we’re not curing the disease, in order to make you have a better quality of life with very minimal side effects related to the procedure.

Dr. Kevin Burns 14:16
There’s a lot of literature, again, this is all in animals on “immune modulation”. That means that doing histotripsy is doing something to alter the immunologic response to the tumor. This does not happen in most patients. This happens in some patients but obviously we study things in animals, so there’s many animal models kind of showing that this does happen. And so I think with all the data we’re collecting now, especially in the BOOMBOX study and other studies, we’re trying to learn who is benefiting from this the most, which tumor types, which mutations, and which therapies may augment this because I think this will be an important part of histotripsy’s future. So, this would just be an example of immune infiltration. So, if you look at a control animal versus a tumor that was treated with histotripsy, you can see that there’s a lot more immune cell infiltration into this non-targeted tumor. Looking at other modalities, so external beam radiation, radio frequency, those weren’t really much different than controls, but a mouse model treated with histotripsy had a much higher percentage of tumor infiltrating lymphocytes, and that’s one of this markers of having an immune response. And then looking at the tertiary lymphoid structures, or tumor infiltrating cells in other models, you can see that again, more papers show that in non-treated tumors, there’s some immune cell infiltration which does not exist in the controls. And again, a lot of this data is available if it’s something that you want to do further research on. And then in humans, hopefully we have some more answers for this in the next coming years.

Dr. Kevin Burns 15:54
So again, the procedure is non-invasive, and so that’s one of the hallmarks here. We are generally putting everyone under general anesthesia, so it’s non-invasive, but we’re still getting put to sleep so there are some risks related to anesthesia. I would say most patients have mild pain. There are some patients who have more severe pain, and that’s going to be based on the tumor location, and generally, your physician will be able to tell you that ahead of time. So if I’m going to treat something on the edge of the liver or right under one of the ribs, I’m going to let the patient know ahead of time that that that lesion is probably likely going to hurt afterwards, just so when you wake up, you don’t think something’s wrong because you’re having pain. So I would say, “You know what? The maximum pain can go up to a five or six, usually that’s right after the procedure, and then it can die down after that”. There are definitely some people who have no pain. They walk out of the procedure like nothing happened. It is again, a single session procedure for an appropriate lead, and that means one that we can completely cover at one time. Again, here’s just another setup of what the room would look like if you were there.

Dr. Kevin Burns 16:52
These are just some general things, in case you want to come back and reference a video. So, just some things about the procedure. Oftentimes, we will give you some dietary restrictions prior that helps reduce the amount of gas that’s in the abdomen. As you can imagine, you can have gas in the colon and the small bowel, and if that moves around or gets near the liver, that may eliminate a window in order to see some of the tumor. So oftentimes, we will do a bowel preparation, and you usually will be provided instructions on that by your physician that’s performing the procedure. A closer look up here, so you can see that this is a simulated patient here. There is some kind of oil on the patient, you actually get castor oil rubbed on your skin, and that helps, again, create this contact between this membrane here. This is a very pliable surface, we fill this with water, and this conforms to your body well, and then the treatment sits right in here. So this is really all that contacts you, and this is a disposable part, it gets changed out with each patient here. So this would be a simulation of what the physician would be seeing during the procedure. So again, this is in a phantom, but during the therapy we can monitor this live. Once we turn it on, we can monitor live if something changes, if the breathing changes, or the tumor moves in location, we’ll see that live. We can pause the therapy. We can replan and move things out. We’re monitoring this live here. And so this little crosshairs here is the histotripsy happening. You can see on ultrasound, we can already see that this tumor area is much more dark than the surrounding area. And so that we can see that we gave histotripsy into that area. So this is just an overview of what the console looks like when your physician is performing the procedure.

Dr. Kevin Burns 18:30
After the procedure, you can definitely have some pain. Most patients, at least in my practice, are discharged the same day, a couple hours after the procedure. Some patients may stay overnight for certain reasons, but I would say, 95% of patients will go home the same day. And there’s definitely normal things that happen after this. The following day, it’s fairly common that you would have a fever, a flu-like illness. If you’ve had other therapies like microwave ablation or an embolization, they can be very similar to that. And you can also have some fatigue, and that can last for several days. Looking at some of the data that helped get this procedure accepted, and the first was the THERESA trial. This was conducted in Barcelona, Spain, and this was a safety study, to make sure this works and make sure it’s safe. And so just an example of a tumor that would have been treated in there. This is an MRI showing this white spot here. This is a tumor that they did histotripsy on it, one week afterwards. You can see it’s larger, that’s very important to note, if you have histotripsy or any therapy, and then you get an image a week two weeks later, most likely it’ll be much larger than it was, because oftentimes we treat a tumor, plus a margin, that means we’re treating the tumor plus some of the normal liver around it to make sure there’s no cell that’s trying to escape already, to make sure we encompass all of that. And then in this patient, for example, once you get out to eight weeks, you can see that it really has a dramatic size decrease compared to that one month imaging.

Dr. Kevin Burns 20:02
Next was the HOPE4LIVER trial. Up. So again, this was basically a technical success and safety trial, and this had a total of 44 subjects that were both in the in the EU and in the US, and looking at the breakdown of tumors that were treated. Most of them were not primary liver cancer so the most common would be metastasis from the colon, rectum, breast and pancreas, and then the others were hepatocellular carcinoma. So really, in all comers to compare this, and this is really a safety trial and efficacy and the one year data was just published from this, and this showed that the success rate was about 95%, meaning that in 95% of the patients, the tumor was correctly targeted and treated. And this is based on the immediate imaging, and the safety showed that there was only about 7% of patients who had any sort of complication- related – and one patient had pain. There was one patient of note, that did have liver failure after this procedure. So this is just something to note, and your doctor would likely discuss this with you if they thought you were at risk for this. This patient had greater than 20 tumors, and this patient unfortunately passed away about one month after the procedure, likely due to just the progression of the remaining tumors in the liver.

Dr. Kevin Burns 9:21
And so again, looking at some example images. This top image would be a small tumor here that was treated. So you can see on the first day afterwards, tumor is much larger, but you see it’s kind of black now, so it doesn’t take up any of the contrast dye. And then at one month, you see it’s getting smaller. And then by six months, one year and two years, you really see that you can barely tell anything was there. So that’s another powerful attribute of histotripsy, is that we get reabsorption of the cavity, so over time, they shrink down a lot. If we were to treat this with a microwave ablation, you would just see a big area of scar tissue, of all dead tissue around it, and that would pretty much just stay the same size forever. Sometimes that can be similar with radiation so it can be helpful with histotripsy that this really gets reabsorbed. And so it can be helpful for follow up because if we see that it’s getting smaller, and then maybe you’re out two, three years, it starts growing again, then we can be concerned that there could be a recurrence, and we may need to address that. Looking at the one year data, they showed that there was basically a 90% local tumor control at one year. So in 90% of the tumors that were treated at one year, there was no evidence of recurrence. So this is pretty comparable to other local therapies, and this is considered a very good effect. And again, in these, 96% of these had complete tumor coverage immediately post procedure. Again, very overall safe procedure.

Dr. Kevin Burns 22:41
And then if you look at the survival rates here, so about 73% of the patients with primary liver cancer were still alive at one year, which is very favorable with current data. And then in liver metastatic disease, about half the patients at one year were still alive. Again, this is a very sick patient population that was in this trial. These patients had to progress through all lines of systemic therapy, and so these are much sicker patients than somebody who’s still able to get chemotherapy or still has other options. We also published as part of this, this study of some of the first nine centers that came online. We looked at the first 230 cases treated clinically. So this means not part of a trial, this is a real-world user. So we participated, and you can see the other sites that participated here. We, overall, showed that this was a very safe procedure. That was the the point of this. We’re doing something new. We need to make sure that it’s safe. And so this looked at a total of 230 patients again, across these nine centers. Looking at these, almost half were colorectal liver metastasis. So that’s a very common patient population that we’re treating. And then you look at these, 95% of these patients had no complications. That means 5% of patients had some minor complications and there was one major complication in this as well, again, that was a patient who, unfortunately did pass away from progressive disease elsewhere, outside of the treatment zone, but overall, a very safe procedure. And so whenever you have a new procedure, we need to prove that it works, and so this is the hardest part.

Dr. Kevin Burns 9:21
The company is sponsoring a study, and you may be asked to participate in some studies. When you get your procedure done, there are a lot of individual doctors looking at very specific things, and there’s a lot, I think, that we’re going to learn over the next coming year. One of the ones is called BOOMBOX. This is a study that we’re just going to collate the results from multiple sites in order to get a large number of patients with each kind of tumor type and see how patients are progressing over time. So when we talk about liver-directed therapies, there are a lot of options for colorectal liver metastasis. One of them is surgery, which I didn’t put on this slide, but surgery is definitely an option if you have all your disease confined to one lobe of the liver, potentially, you could have that lobe removed. You can even get liver transplants now. You can have hepatic arterial infusion pumps. And so those are some of the things I won’t mention here, because I’m just talking about some targeted therapy. So we have histotripsy. We have Y-90, which I’m sure you guys are familiar with as well. We have microwave ablation and SBRT. We can also mention chemoembolization on here as well. And so if you kind of compare the mechanism of these – so histotripsy is non-invasive, and it’s ultrasound based, and it mechanically lyses the tissue. Y-90 uses radioactive beads that emit this very strong radiation in order to kill the tumor with radiation, microwave ablation uses intense heat in order to coagulate the tissue and kill it, and then SBRT, or external mean radiation, again, uses highly focused external radiation that can be delivered over the course of many sessions in order to give critical radiation to kill a tumor. So some of the benefits of these procedures, histotripsy and external beam radiation are both non invasive. Histotripsy generally will require anesthesia, whereas SBRT will not. Histotripsy in general is a single session procedure, whereas SBRT has multiple procedures that you would have to come back for. Another benefit, histotripsy doesn’t damage any of the tissue on the way in or the way out. When you get treated with radiation, although it’s very precise now, and it’s much more tolerated than it was before, there is some radiation that is affecting the organs on the way in and so that can be of a concern in lesions that are in a certain location.

Dr. Kevin Burns 9:21
Y-90 or radioembolization is very minimally invasive, all done through a small catheter that’s in the artery. It’s very effective if you have a larger tumor or you have multiple tumors all in the same area of the liver. And again, this is also an outpatient procedure. And microwave ablation is also a very fast procedure. So microwaves can be very fast. It’s well established. It’s been around for over a decade, and so we have a lot of evidence showing for microwave ablation that it’s equivalent to surgery, based on a trial called the COLLISION trial that came out for lesions under under three centimeters. Histotripsy is new, so there is still some limited availability. There’s spotty insurance coverage so that’s one of the other things we deal with and the ideal candidates for these procedures. So histotripsy kind of opens up… There’s some more patients who can be treated but in general, we’re thinking about someone who has oligometastatic disease. That means you can count the number of lesions, and you think there’s a chance you might be able to get all of them. In some cases, we’re just debulking patients, so let’s say you’re trying to get to a transplant, and your CEA has to be under a certain level. Histotripsy could be beneficial to start debulking some of the tumor to see if we can get the CEA level down, or if you’re having pain, or if there’s a tumor in one location that’s causing a problem, that may be a reason to go after that one as well. Again, once we get more data on the immune effects of this, this could get into more widespread practice as well. So these are just the different therapies, and if there’s questions about these later, we can talk about these.

Dr. Kevin Burns 15:46
When we talk about histotripsy, when people ask, can my tumor be treated with histotripsy it’s a very complex question, because we have to, one – be able to see the location of the liver. And so this is just a depiction of what the liver segments are. The liver is divided into eight segments based on their blood supply. And the liver is also different in every patient. Some people’s livers are bigger, some are smaller, some are higher in the chest. And so if you tell me you have a tumor in segment four, that’s one centimeter, can you treat it with histotripsy, you still need to see the pictures, but pictures, because everybody is different, really, on the inside. If you’ve had surgery before, that will also alter where your liver is and so it’s really important to review these images to make sure that it’s something that can be treated. If you consult with someone who does histotripsy, and I don’t think it’s good for histotripsy, we’re going to let you know what some of the other options are, in case you haven’t been told about them. But I think point of the slide is that every segment is currently being treated. At the beginning, we were not treating segment eight, segment seven, and now those are much more common for us to be able to treat.

Dr. Kevin Burns 15:46
And so some of the strengths of histotripsy really, is that it preserves the liver parenchyma. It can preserve the hepatic veins, the portal veins, the bile ducts. This means that we can treat the more dangerous tumor locations. We have good radiologic results. That means over time, the tumors get smaller, and so they can be easy to follow on imaging. It’s also non-invasive, and you get immediate results. The tumor is dead before you wake up from the procedure. So looking at histotripsy in general right now, we’re really focused on the liver, but this is a technology that will probably come to a lot of other organs in the future. The kidney trial called HOPE4KIDNEY, that one just closed, so we’re waiting on the results for that, and that would be to treat primary kidney cancer. The trial to treat pancreas tumors is underway. A safety trial is underway in Europe, and so that will hopefully come to the US soon. And then, as you can imagine, this technology may be able to be adapted to other areas throughout the body. So I will stop here, and if anyone has questions, I can check the chat as well.

Betsy Post 30:22
Yes, we have a lot of questions. Okay, I can read these off. And if any of these regarding insurance are not something that you can speak to, that’s fine. So just let me know because we do have a couple about that. If you have knowledge if histotripsy is covered by the VA, and if not, do you have any idea on the timeline to getting it covered?

Dr. Kevin Burns 30:46
Sure, yeah we have treated VA patients, and we’ve had referrals from the VA directly. I can’t say it would be covered 100% of the time, but I know that I think the VA is supportive of this technology now. So I would say that I would go to your doctor at the VA and see if they can get a referral to try to get a review approved, because I know we have treated patients with VA insurance. That wasn’t the case at the beginning, but I would say, since this year, we have been able to do that. I don’t know the specifics of that, but, but we have treated VA patients or with VA insurance.

Betsy Post 31:18
Well that’s great. Now this question I’m really interested in, too, so I’m glad someone asked it: what was the biggest breakthrough or learning that happened at the recent conference you mentioned?

Dr. Kevin Burns 31:33
I think it’s just that there’s so much people have come up with a technology and then doctors will figure out the best way to use it. So there’s a lot of different use cases. So, when this first came out, we were just going to treat tumors that are in the left liver that are very easy to see. And you’ll see that now we’re doing using different anesthesia tricks. We can get the liver to move around, and we can treat these very tough locations that maybe when this technology was thought of, that wasn’t really something that was thought to be possible. And so as doctors are doing more and more cases, they’re getting more experience in how this works. And so I think that’s one of the things, and it’s also to see that a doctor in Hong Kong learned to do the same thing, and we’re all doing the same thing. And so it’s nice to see that the worldwide community is really participating in this.

Betsy Post 32:31
Great and I know you talked about this a little bit, but we have a big following of histotripsy, a lot of interest in it. We did have a prior talk, but that was a while ago. So if you could speak to this question, it sounds like you can go through ribs safely now, so the right side is on the table, because we did have a prior talk on that, and they said that would be sort of a no go. So I’d love to hear more about that.

Dr. Kevin Burns 32:55
Yeah, that was at the beginning where they thought that this was all going to have to do what’s called subcostal, meaning under the rib cage, and so that really limits the liver. I would say, pretty quickly into treating – so all the trial patients, those are all subcostal treatments. All the initial treatments were generally subcostal. Pretty early into our experience, we started doing transcostal treatments, meaning that we put you on your side, so you generally your left side down, and we could treat through the ribs. And so as an I’m an interventional radiologist, we do a lot of procedures in the liver, transcostal, meaning between the ribs. That’s how we put in biliary drains. That’s how we do microwave ablations, that’s how we do biopsy. So that’s a very common way for us to access the liver. And so we’re really familiar with that anatomy. And so now I would say most of our treatments are probably right sided and through the ribs now, so that’s probably the most common things that we treat now the there’s a newer histotripsy machine, and so anyone that gets a machine now gets the new one, and all the other ones are being replaced, so everyone’s going to have the same one, and it does allow maybe some deeper lesions to get treated. There’s some subtle differences between it. histotripsy still happens on either one, but I think the point of that is treatment times are faster now. Treatments are about 40% faster than they were a year ago, and that’s through software improvements as well as hardware improvements. At the beginning, when we were treating transcostal, it was through the ribs. There’s a lot of pain associated with that. I think there’s a little bit, potentially some less pain now with this new treatment, and just because the procedure time is a little bit faster.

Betsy Post 32:41
In the portal vein picture that you showed, how long does it take for the liver to repair itself?

Dr. Kevin Burns 34:16
So generally, when we have a patient and we’re out one month from the procedure, the tumor will likely be around the same size, but it’ll be hopefully dead as long as we are able to deliver effective histotripsy. But once you get out to three months, that cavity is a lot smaller. And then at six months, sometimes it’s just a little speck. So the liver can repair pretty quickly and process that dead tissue in there.

Betsy Post 34:58
We do serve an international community in COLONTOWN so I was happy to see some of that information. And we do have a question here. I’m curious if any Canadian doctors joined the international conference you mentioned earlier, or maybe if you know of anyone in Canada that’s doing this now, or any information on that? This patient had had ALPS, so an aggressive extended in 2020, recently, facing recurrence. And would histo be something worth exploring?

Dr. Kevin Burns 35:26
Yeah. So currently, there’s no one practicing this in Canada. I know there’s a lot of interest in bringing it there, and I think every country has its own regulatory bodies that have to approve these things. So I think it will get there soon. I don’t have any knowledge of when that would actually happen, and I’m sure it will get adopted there as well. But there are many Canadian patients who seek medical care in the US, and many of them travel down to have this procedure. I would say, in a patient who’s had a liver resection hisotripsy, for an appropriate lesion would be a very good technology, because you’ve had surgery before. That means that likely, you’re probably not going to go through surgery again. And so you’re looking at probably microwave ablation, potentially, Y-90 or TAS radiation. So I think histotripsy does offer a unique advantage. You’ve been through surgery, so we can avoid needles to go through. And since you have probably less liver, although the liver is probably hypertrophy, we can, we can not damage as much liver as you could in another procedure. So I would say recurrence after a resection is a very common indication for histotripsy currently.

Betsy Post 36:37
Thank you. How long is one under general anesthesia?

Dr. Kevin Burns 36:41
I would say, depending on the number of lesions and the size the procedure it can take anywhere from one to three hours.

Betsy Post 36:50
How many tumors can be treated in one session?

Dr. Kevin Burns 36:53
There’s not realy a limit on number of tumors, more of some volume limitation. So if you think that there’s going to be a lot of tissue getting destroyed, your body has to process that. We didn’t speak to this earlier, but it’s very rare, some patients can have some kidney issues after this procedure. That’s extremely uncommon, and we think that may be due to potentially high volume treatment. So it’s also going to be a lot for your body to process. You probably have very severe side effects as well. And so if you had five small tumors, those could be all treated at the same time. But if you had one large tumor, that may be all that the physician or myself would be comfortable going after at one time just due to the volume of the lesion.

Betsy Post 37:34
What about histotripsy triggers an immune response? I think you spoke a little to this that.

Dr. Kevin Burns 37:39
Yeah. So again, in humans, we still have a lot more to learn on this. There are definitely case reports. That means it’s not a peer reviewed study, but case reports of patients who have had this response. That means that, because this is not thermal and not radiation it doesn’t just necose everything, and so the cells are completely destroyed, but there may be some protein or antigen that is left in the acellular lysate, and as your body cleans that up, it may learn to recognize something that was hidden from the body. So cancer generally progresses because it can escape the body’s natural processes. So if we can show it some antigen or some way to recognize the tumor, then potentially, I say potential, because we still need to prove this out in humans, that you could help stabilize disease elsewhere in the liver.

Betsy Post 38:28
What would be some of the more common things that would disqualify a patient from being able to receive histotripsy?

Dr. Kevin Burns 38:35
I’d say most common would be size and location of the tumor. A tumor that’s on the liver dome, if you’ve heard that, it’s probably not a great location to treat, because there are some better options; and size, if you had a single six centimeter tumor, this is probably not the best option for you. This could be combined with other things. And so I think those are the most common things. If you have very bad liver function, that would be another discussion we do. There are people who we do treat with poor liver function, but and there are people who get better after this procedure. So it’s a case by case basis with that. So I would say those are the most common things. Or if for some reason, you can’t have anesthesia, that would be one of the other disqualifying factors. There have been cases done not under general anesthesia. But I would just say in general, the reason we use general anesthesia is so that we can control your breathing. So if you imagine, the liver is going to move, it’s right under the diaphragm, so it moves every time you take a breath. So if we put you under anesthesia, we can augment that, make it less or more and we can make it predictable, meaning it’s the same every single time we take a breath. And so that we can make sure we can treat a tumor that might be right next to the stomach or right next to the pancreas, and nothing’s going to move and injure any other organ.

Betsy Post 39:46
How many procedures have you performed?

Dr. Kevin Burns 39:49
I — hundreds. I don’t know the exact number. One of my practices is myself and my two partners performing it. I think we’re almost 300 cases here. I work at another facility as well, and I know we’re over 100 cases there, yeah. So something like that.

Betsy Post 40:15
Can histotripsy be used for lymph nodes?

Dr. Kevin Burns 40:20
Yes. Speaking not for the company, talking about this, histotripsy is a technology, so think about it like radiation. If you’ve ever had radiation, you might have had, let’s just say you had rectal cancer. You might have radiation to your rectal area. You might have radiation to a lesion in the bone, to the liver. So you can have radiation anywhere in the body, as long as it’s something that’s safe. So histotripsy is a technology that can be applied to other organs in the body. Right now, in practice, it’s in the liver. The kidney trial just ended. The pancreas trial is starting. And so if you fast forward, you can think that this is probably going to move to a lot of other organs throughout the body, and mainly be ‘can the lesion be seen and safely treated without injuring another organ?’. I would say this, treating lymph node now would not be something that’s like an approved therapy, and it wouldn’t have any sort of insurance coverage at this point.

Betsy Post 41:16
Is there any risk of histotripsy causing metastasis via tumor cells not being destroyed and becoming dislodged?

Dr. Kevin Burns 41:23
That’s a common question that we do get and I understand the question. It makes sense. I’ll speak at this histotripsy summit we were just at. The scientists who helped discover this, and this question was brought up, and basically what they had said is, they tried to make this happen in animals, and they couldn’t do it again. Animals may not always apply to humans, but it’s something that hasn’t really been seen. And so that’s all I can say on this right now.

Betsy Post 41:51
Do you have to stop chemotherapy for a certain amount of time before getting this procedure, or can it be done while getting chemotherapy?

Dr. Kevin Burns 42:04
Great question, I usually mention this. I forgot to mention that. In general, we do not stop any systemic therapy for this so that is another advantage for a patient who may have very good control on a systemic therapy and they don’t want to stop. You know, to have surgery is one of the most common ones where you need to stop for quite some time. And so we generally treat patients on their therapy. If you have very severe side effects right after you get your chemotherapy, it’s probably not the best time to schedule your procedure, but it can be done around the therapy. And we like to think this is going to be synergistic, kind of with the chemotherapy. I would say in a future state, we may learn that there are certain immunotherapies that may augment or enhance the effects of this, and that’s something that’ll take years to tease out. But in general, you do not need to stop your chemotherapy. I’ll mention, if you’ve had a hepatic arterial infusion pump, you can still be treated. That’s another question that I commonly get. And we don’t need to stop the pump or anything like that.

Betsy Post 43:02
Can patients with underlying health conditions qualify to receive histotripsy?

Dr. Kevin Burns 43:08
Yeah, I think it’ll be dependent on whether or not you’re a candidate to have any procedure. First, would you be able to have anesthesia? If you have really bad cardiac disease, that may be a disqualifying factor, or whether your liver, we think is healthy enough to take any sort of procedure.

Betsy Post 43:27
I think you probably talked a little bit about this, but can this be done on a patient who has multiple tumors, such as 10 plus?

Dr. Kevin Burns 43:35
Yeah, so if 10 plus tumors, it’d probably be quite hard to get all of them. We have to make sure that the treatment goal is aligned but it definitely can be done on patients with that many tumors. I would classify that was probably going to be a debulking procedure, or, let’s say, maybe you have nine tumors in the right liver, and there’s one on the left. If the left sided one could be treated, maybe you could qualify for some other procedure for the right, and so every patient is different. There are a lot of patients who are seeking this procedure out to see if they can have any immunologic benefit from this, because they know they’re not really a candidate for anything else.

Betsy Post 44:14
I’ve been told Medicare covers histotripsy. Has this been your experience?

Dr. Kevin Burns 44:19
Yes, yeah. Medicare seems to be covering this as far as we’re aware.

Betsy Post 44:28
Are you aware of any centers offering or planning to offer histotripsy in Australia?

Dr. Kevin Burns 44:35
No one currently. I think there’ll be more news to come on that, maybe later in the year. But I know there’s a lot of advocacy trying to bring this to a lot of countries. I think this is very patient driven so if you live in Australia, or if you are in another country trying to bring this, I think it’s going to be very patient driven at this point to bring it up to the appropriate people. Probably get a doctor involved that maybe you think would be a person to advocate for this and then try to bring that into the system. I think it’s going to depend a lot on regulatory bodies in those countries. This is available in Hong Kong, outside of the US, this is available in Hong Kong and in Dubai or in UAE. I think it’s in Abu Dhabi.

Betsy Post 45:19
I don’t know if you can answer this so it’s okay if you can’t, but how much would it cost if you paid out of pocket?

Dr. Kevin Burns 45:29
It changes, I’m not going to answer that on a video, because this changes in every site is going to have different prices. What I’ve learned in this, is medical costs are very complicated, and so this can change frequently, and it can vary by site. So I would say it’s not steep, but it’s cheaper than other things that I know of that can be done as well.

Betsy Post 45:56
Yeah, I think that this patient has said she’s tried four different insurance approvals and all of that, and been denied, which is unfortunate.

Dr. Kevin Burns 46:05
Yeah and I would say, just speaking to this there, I’m sure people know who Jenny Stein is. She’s somebody who works trying to get approval. So a lot of hospitals, and we use her. She basically, all she does is try to get histotripsy patients approved. And so just know that if you see somebody for histotripsy and then we submit your stuff, there’s this SWAT team of really good people, really working behind the scenes, trying to get all these approved. And no matter what your insurance is, they’ll try to get everything approved. We’re doing peer to peers. We’re doing appeals. I’ve had to go on, I’ve had to go on a telephone court case to argue my case. So there’s a lot that’s being done for this. It’s a new therapy, and so it is expected, and I think over time, there’ll be more acceptance from this. Main thing is we just need to publish more data and so we can support. I did a peer to peer. They got overturned because I sent the person the new one year HOPE4LIVER data, and she said, that’s long term evidence. I think this is appropriate for the patient. I’ll approve it. So as we get more data, we’re going to get more approvals for patients.

Betsy Post 47:13
Is there a size limit for treating a tumor? I heard you mentioned a six centimeter tumor was too large.

Dr. Kevin Burns 47:20
There’s no size limit for the tumor, but if you had a single tumor, there could be a better option. And so I think that’s why it’s appropriate to speak with a physician. I’m an interventional radiologist. This is done by interventional radiologists as well as liver surgeons. There’s also a radiation oncologist that does this, so they can probably discuss with you what the other options are, and make sure you choose the appropriate thing for your tumor. If you had a six centimeter tumor in the hilum of the liver, and there’s no other option, then, yes, this can be a therapy where we’re going to try to treat as much of the tumor as possible, prevent, and potentially relieve a biliary obstruction. Maybe you have a biliary drain that you’re trying to get out. So there can be other reasons why we would still go after a tumor that’s larger. You know, this is a colon cancer forum, but there’s a lot of patients with cholangiocarcinoma that are these very large, aggressive tumors, and so this can be used to start kind of debulking those tumors, maybe allow a patient to get to another procedure, potentially a resection. So there can be reasons to go after a larger tumor.

Betsy Post 48:17
Are you aware of any ongoing histotripsy trials for lung mets?

Dr. Kevin Burns 48:22
No. The only trial currently enrolling is the pancreas safety trial in Barcelona, Spain. I think lung is going to be a long ways off. As you can imagine, this therapy doesn’t work there. And so you can imagine that that may have a lot of factors that would make this much more complicated to treat something in the lung. So I think that that is going to be probably quite far off into the distance. There are a lot of other procedures for lung mets, so I would say SBRT, or radiation, which we mentioned later, is fairly common for that. And then if you speak with an interventional radiologist, there’s a lot of ablation modalities that can be done for lung mets as well.

Betsy Post 48:58
I should have asked this earlier with the chemo question I knew it was going to be asked, Can this be used with Avastin?

Dr. Kevin Burns 49:04
Yes, we are not stopping Avastin with this. So that is also what differentiates this from from some other therapies. I’ll speak to, kind of related to Avastin. Avastin, we know, impairs wound healing and may mess with vessels. So if you’re having a TAS or a Y-90, that can make the vessels more friable, and obviously it impairs wound healing. So we haven’t seen any issues with Avastin. We talked about this procedure being extremely safe, now that we have done more procedures total, there are some patients who have some very rare complications, so there definitely have now been patients that have had some bleeding related to this, but that’s still going to be very, very small compared to any other therapy that we offer and so far, I haven’t seen that associated with Avastin.

Betsy Post 49:49
That is the last question that I see. So I just wanted to thank you again for being with us this evening, and if there’s anything you’d like to add before we sign off. This has been enormously helpful. I have learned a ton. So I truly appreciate it. And of course, everyone in the comments is agreeing, just saying how helpful it was. So this is truly a huge update from the last DocTalk we had on histotripsy so I really appreciate it, and I’ll turn it over to you to say anything else that you’d like to.

Dr. Kevin Burns 50:19
Yeah if you can still see my screen, this is just the contact information for Mission Hospital, which is one of the sites I operate at, just in case you want to get in contact with our nurse navigator to ask any questions or try to get into our system. This is the contact information, so I’ll leave that there. So I think, in summary, this is a new procedure. This is not magic. It’s still a procedure that requires a lot of skill and learning in order to treat these tumors and first decide, should we treat the tumor? That’s one of the other important things. And so when you consult with either a surgeon, interventional radiologist, or another physician performing this, you can ask, what are the other alternatives? And we can decide, or help you decide, what you think is best for you to do. There’s lots to learn with this. So every patient we treat, we are learning. When we treat a patient, we treat a lot of patients who travel to us. We’re going to want to see you back virtually. We do a lot of virtual consultations. We’re going to want to see you back at one month, three month, potentially six months, depending on how things are going. Because we want to see what is happening to these lesions over time so that we can learn, we can improve our techniques, and we can offer even better therapies over the course of years.

Betsy Post 51:33
Thank you so much, and thanks for everyone for attending and all of your great questions and participation. So have a great night. Thank you, bye, bye.

Dr. Kevin Burns 51:40
All right. Thank you, everyone, bye.

DocTalk
2024
Dr. Miller
Histotripsy
Stage IV
Doc Talks

In this panel DocTalk, Dr. Burns breaks down histotripsy — an exciting, noninvasive technology that uses sound waves to destroy liver tumors without heat or radiation. Recorded in July, 2025.

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