Latest / Becker’s Healthcare Podcast / Dr. Ajay Goel on Blood-Based Screening and the Next Frontier of Cancer Prevention
Transcript
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- 0:58- Hello. Thank you so much for tuning in
- 1:00- to the Becker's Oncology Leadership podcast.
- 1:04- I'm Elizabeth Gregerson, a reporter here at Becker's,
- 1:07- and today, I'm talking to doctor Ajay Goel.
- 1:10- Doctor Goel is a professor and chair of
- 1:13- the department of molecular
- 1:15- diagnostics and experimental
- 1:17- therapeutics at City of Hope. Doctor Goel, thank
- 1:20- you so much for time. Before I dive
- 1:22- into my questions, questions, I would love if
- 1:24- you could share just a bit about your
- 1:26- background and your role at City of Hope
- 1:29- for our listeners.
- 1:30- Absolutely happy to do so. So I'm Jay
- 1:33- Guel.
- 1:34- I wear multiple hats at City of Hope.
- 1:36- One of those you introduced already. I'm I'm
- 1:39- a department chair for the department of molecular
- 1:41- diagnostics and experimental therapeutics.
- 1:44- So within this department, we do a lot
- 1:46- of work around,
- 1:48- cancer diagnostics
- 1:49- and developing new treatments and therapies for this,
- 1:53- for different cancers. So that's one role. In
- 1:55- addition to that,
- 1:57- I also serve as
- 1:59- associate director
- 2:01- for
- 2:02- basic sciences
- 2:03- within the CDF Hope comprehensive
- 2:06- cancer center. So so I I participate in
- 2:09- all the basic,
- 2:10- basic sciences program within the institution.
- 2:14- And then the third title I wear is
- 2:16- I also serve as
- 2:17- director of biotech innovations
- 2:20- at the at this,
- 2:21- City of Hope Hospital.
- 2:23- So
- 2:25- so I've we had multiple roles,
- 2:27- but my own lab, my own research
- 2:30- team focuses heavily
- 2:33- on gastrointestinal
- 2:34- cancers only, which means cancers starting from
- 2:37- esophagus, stomach, colon, pancreas, liver, rectum.
- 2:42- So we do
- 2:43- a variety of things,
- 2:45- within the gastrointestinal
- 2:46- cancers or GI cancers in brief. Mhmm. But
- 2:50- a big emphasis of my research is on
- 2:52- cancer prevention.
- 2:53- And that's part of the reason we are
- 2:54- here together to discuss one of the recent
- 2:56- studies we have published today.
- 2:58- But we do a lot of work around
- 3:00- developing
- 3:01- molecular
- 3:02- minimally invasive, noninvasive
- 3:04- diagnostics
- 3:05- for the early detection of these cancers.
- 3:09- Perfect. Thank you for kind of setting the
- 3:10- stage for where you're coming from and and
- 3:13- teasing where why we're talking today.
- 3:15- So, yes, a study did come out,
- 3:19- for a blood test,
- 3:20- and your study found
- 3:22- roughly eight and ten
- 3:24- precancerous
- 3:25- lesions. So if you could go into, you
- 3:27- know, the background of this study, just briefly
- 3:29- for our listeners,
- 3:31- but I'd love to point out the distinction
- 3:34- that the test was able to catch precancerous
- 3:37- lesions, not just cancers that have already formed,
- 3:40- especially through that lens of prevention
- 3:43- and why that distinction matters so much for
- 3:46- how health systems should be approaching
- 3:48- cancer screening.
- 3:50- Yes. So I think this is what gets
- 3:52- us very excited about this particular study. So
- 3:55- this was essentially the key
- 3:58- central message of the study.
- 4:00- So early cancer detection and cancer prevention are
- 4:04- not the same thing.
- 4:06- Finding a colorectal cancer at stage one
- 4:09- versus stage three
- 4:11- can make a big difference because if you
- 4:13- can find a stage one cancer,
- 4:15- it can clearly improve
- 4:18- the opportunity for successful treatment.
- 4:21- But if you can identify
- 4:23- advanced adenomas
- 4:25- or advanced polyps, which are essentially the precursors
- 4:29- which eventually can become into cancer, and if
- 4:31- you can treat them in
- 4:34- time, we can essentially prevent the disease from
- 4:36- happening in the first place. So it's a
- 4:38- big distinction.
- 4:39- Finding precancerous polyps, you treat them, you take
- 4:42- them out. These people will never ever probably
- 4:45- develop colon cancer to begin with. So it's
- 4:47- a big deal. So we have essentially prevented
- 4:49- the cancer. If you take out stage one
- 4:52- cancer versus stage three,
- 4:54- these people can live
- 4:56- probably their full lives. So it's not just
- 4:58- about early detection. It is
- 5:00- early detection at what stage. So that's why
- 5:03- it's important. So in other words, this is
- 5:06- distinction
- 5:07- is especially important in colon cancer because
- 5:10- screening already gives us a powerful opportunity for
- 5:15- prevention. Finding advanced adenomas
- 5:17- are clinically actionable lesion lesions.
- 5:20- So a blood test that does not remove
- 5:22- them but can find them can help
- 5:26- trigger
- 5:27- a preventative approach means if their test turns
- 5:30- positive, somebody has advanced polyp, now they can
- 5:33- go see their gastroenterologist,
- 5:35- and they can treat them very effectively.
- 5:37- So in this particular study, we call as
- 5:41- DANAB study. So in this particular study we
- 5:43- just published, we found that we could
- 5:46- identify
- 5:47- eighty one percent of advanced ad adenomas or
- 5:50- polyps
- 5:51- in addition to ninety one percent of colorectal
- 5:54- cancers
- 5:55- and almost ninety two percent of stages one,
- 5:58- two, three cancers.
- 6:00- So what makes this study more important? Because
- 6:02- we can find advanced adenomas and stage one
- 6:05- cancers at a very high degree of sensitivity
- 6:08- and specificity,
- 6:09- which is a game changer in a way.
- 6:12- From a health care system perspective, I think
- 6:15- the change that changes the question.
- 6:17- We should be asking for future screening technology.
- 6:20- We should not evaluate them only by how
- 6:23- many cancer does this find, but we should
- 6:25- also ask how many cancers
- 6:28- might this screening strategy ultimately help prevent. So
- 6:32- I think that's a biologically or clinically more
- 6:34- important question that how many cans cancers not
- 6:37- only we can find, but how many we
- 6:38- can prevent.
- 6:40- I love that kind of rephrasing of the
- 6:43- of the question. I think almost got goosebumps
- 6:45- when you said it, but, yeah, that is
- 6:47- such a a needle kind of moving,
- 6:50- statistic to think
- 6:51- you're not catching cancer, you're catching it before.
- 6:56- A key point of the study too is
- 6:58- the fact that this screening test is a
- 7:00- blood test.
- 7:02- Nationally, colorectal cancer screening rates, you know, have
- 7:05- been stuck well below the goal for years.
- 7:09- And
- 7:10- anyone who, you know, reads news about cancer
- 7:13- knows that incidence is growing with young adults.
- 7:18- Where do you see a tool like blood
- 7:20- based screening,
- 7:22- you know, actually moving screening numbers?
- 7:25- Is it able to?
- 7:27- Is it their cautious optimism?
- 7:29- Will they be will blood based tests, you
- 7:31- know, become as standard as colonoscopy? What's your
- 7:34- kind of
- 7:35- strategy or mindset when you're watching these types
- 7:38- of tests become more and more
- 7:41- used?
- 7:42- Yes. I think this is a very relevant
- 7:44- question. So I think blood based screening has
- 7:47- a real potential to increase
- 7:49- participation
- 7:50- in screening. Mhmm. But I would view this
- 7:53- as an additional doorway to screening
- 7:57- Mhmm. Rather than replacing the doors we already
- 7:59- have. By that, what I mean is we
- 8:01- have colonoscopy. We have some other test. All
- 8:03- of them are there, but the participation, just
- 8:05- like you said, is lower. So what blood
- 8:08- test do is they open another opportunity for
- 8:10- us to increase
- 8:12- the cancer screening, bring more people into the
- 8:15- fold, and help more people participate. And there
- 8:18- are decades of data that any kind of
- 8:21- cancer screening tool we can use. Whatever that
- 8:24- might be, every one of them help. So
- 8:26- the goal is bottom line is, yes, it
- 8:29- will help participation.
- 8:31- So
- 8:32- our manuscript highlighted an important
- 8:35- operational problem. Just like you said, despite having
- 8:38- very effective screening methods, participation has not consistently
- 8:41- reached the approximate target of eighty percent, you
- 8:44- know, screening,
- 8:46- population level,
- 8:47- wide.
- 8:48- Blood testing offers a different type of access
- 8:51- because it can potentially be incorporated
- 8:53- into an encounter that is already happening. People
- 8:56- are already going to the clinics. They are
- 8:57- going for different reasons.
- 8:59- So if a patient may come in for
- 9:01- annual physical, for example, a patient may be
- 9:03- coming in for diabetes monitoring. They may be
- 9:05- coming in for cholesterol testing or some other
- 9:09- blood draw.
- 9:10- And
- 9:11- they it presents the opportunity. Because once they're
- 9:13- already in the clinic doing some other workup,
- 9:15- they can the doctor can now
- 9:17- ask, hey. Would you be interested in getting
- 9:20- your risk for colon cancer estimated? And from
- 9:22- the same tube of blood, now we can
- 9:24- measure that as well. So, certainly, the patient
- 9:26- who did not come into the clinic for
- 9:28- colorectal cancer screening got screened for that particular
- 9:32- cancer,
- 9:33- and now they don't have to make a
- 9:35- special visit,
- 9:36- to get colon cancer screening. So it's very,
- 9:39- very important.
- 9:40- I think the greatest near term opportunity is
- 9:43- among people who are eligible for screening but
- 9:45- repeatedly do not complete colonoscopy
- 9:48- or stool based testing. They just
- 9:51- don't participate.
- 9:52- So I think that may be particularly relevant
- 9:54- for screening eligible adults
- 9:57- in their late forties, early fifties who have
- 10:00- recently
- 10:01- become eligible but have not participated
- 10:03- in this kind of screening. So our study,
- 10:06- the DANF study
- 10:07- itself does not establish that offering this test
- 10:10- will
- 10:11- increase participation. Everyone in our study underwent colonoscopy.
- 10:15- However, the question has to be answered prospectively.
- 10:19- Prior evidence, like I said, supports that any
- 10:22- kind of blood testing will help rescue can
- 10:25- function as a rescue strategy for screening
- 10:28- avoidant individuals, people who just don't feel the
- 10:31- need for it. So
- 10:32- will blood testing become as standard as colonoscopy?
- 10:36- I think it could eventually become a standard
- 10:38- component of colon cancer screening for sure, but
- 10:41- I would not frame these two as competing
- 10:44- technology. Colon colonoscopy remains unique because it can
- 10:48- diagnose
- 10:49- and remove precancerous lesions.
- 10:52- A positive blood test leads to colonoscopy. So
- 10:55- they both work
- 10:56- in hand hand in hand in that way.
- 10:59- So if I have to sum up, the
- 11:01- answer would be the future may not be
- 11:03- about choosing between colonoscopies,
- 11:05- stool testing, or blood testing.
- 11:07- It may be about making every patient has
- 11:09- a screening pathway that are actually willing to
- 11:13- complete. So one way or the other, we
- 11:15- need to bring people who are not participating
- 11:17- into the screening programs.
- 11:19- Absolutely. And I'd love to kind of pick
- 11:22- your brain as well. When we're looking towards
- 11:25- the future and seeing all these different screening
- 11:27- options that will be available,
- 11:29- what should health system and hospital leaders know
- 11:32- about the current state of kind of coverage
- 11:34- and reimbursement
- 11:36- when it comes to these types of screening
- 11:38- tools?
- 11:39- So this is an extremely important issue because
- 11:42- the screening technology
- 11:43- cannot
- 11:44- have population level impact
- 11:47- if it is scientifically impressive but financially or
- 11:51- logistically inaccessible. So it's in it's very important
- 11:54- that we keep that in mind.
- 11:56- For Deneb specifically,
- 11:57- we are not at the reimbursement stage, so
- 12:00- I would like to clarify that. The essay
- 12:02- remains in a research setting. The current study
- 12:05- establishes
- 12:06- diagnostic potential, but we still need large prospective
- 12:10- phase four validation study before we consider routine
- 12:14- clinical implementation, but that's where we are heading
- 12:17- now. Mhmm. Our study also did not perform
- 12:20- a formal
- 12:21- cost effectiveness analysis.
- 12:23- We did note that Deneb uses very simple
- 12:26- PCR
- 12:27- based essay,
- 12:28- which can which is routinely available in almost
- 12:31- every diagnostic lab,
- 12:33- and they could ultimately
- 12:36- help in scalability
- 12:38- and reimbursement
- 12:40- should be fairly straightforward.
- 12:42- However,
- 12:44- all of the reimbursement framework
- 12:46- emerging from this category,
- 12:49- exist because we do this kind of PCR
- 12:52- based approach for many other things. Medicare currently
- 12:55- covers
- 12:55- qualifying blood based biomarkers for colon cancer
- 12:59- screening once every three years for eligible
- 13:02- asymptomatic
- 13:03- average risk beneficiaries
- 13:05- ages between 45 to 85. So the the
- 13:08- the the reimbursement
- 13:09- program is already in place, and Medicare also
- 13:12- covers follow-up colonoscopy
- 13:15- as a screening service after a positive blood
- 13:18- based biomarker
- 13:20- has been tested.
- 13:21- So
- 13:22- CMS's national coverage framework also includes requirements related
- 13:26- to FDA authorization and test performance. So coverage
- 13:29- should not be assumption
- 13:30- simply because it essays a blood test. So
- 13:33- so in other words,
- 13:35- all the elements are in place for health
- 13:37- care system leaders. I think the bigger point
- 13:39- is to
- 13:40- look beyond the price of the lab test
- 13:42- yourself. The relevant economics includes
- 13:46- entire screening pathway.
- 13:48- Who gets offered the test? I think that's
- 13:50- very important. How many additional pause previously onscreened
- 13:53- patients
- 13:54- are can participate in such a testing program?
- 13:57- What proportion of tests are turned positive? How
- 14:00- many follow-up
- 14:01- colonoscopies are generated? What is the completion rate
- 14:04- for those colonoscopy? So there's so many other
- 14:05- questions, but I think this is exactly the
- 14:08- point where we need to be. The issue
- 14:10- is particularly relevant because the specificity of the
- 14:13- test we just published is very high. It
- 14:16- is almost eighty five percent specific
- 14:19- for finding advanced neoplasia or advanced polyps in
- 14:22- our cohort, which is really import impressive because
- 14:25- in a true population screening strategy
- 14:28- where advanced polyps is relatively uncommon,
- 14:31- that could generate meaningful number of follow-up colonoscopies.
- 14:35- We explicitly identify that as a issue. This
- 14:38- is a issue,
- 14:39- requiring prospective and health economic evaluation. So so
- 14:44- we are there, but we still need to
- 14:45- do a stage four test, stage four clinical
- 14:48- trial to answer some of the questions. But
- 14:50- I think these are all relevant things, and
- 14:53- and the value proposition will depend upon whether
- 14:56- such a blood test can bring more people
- 14:58- into a screening,
- 14:59- program and ultimately help prevent cancers, which will,
- 15:02- in the end, you know, trump the cost
- 15:06- for managing these patients if they were missed
- 15:08- during screening and have advanced cancer.
- 15:12- Absolutely. Thank you for kinda laying that out,
- 15:15- as well. I think it's such crucial information
- 15:17- to have, especially as, you know, these types
- 15:20- of studies
- 15:21- continue to come out showing, you know, how
- 15:24- different tests can screen and and change numbers
- 15:26- like you said.
- 15:28- Before I let you go, I always like
- 15:30- to end my conversations with oncology leaders about
- 15:34- what's exciting them the most
- 15:36- when it comes to the future of cancer
- 15:37- care. And feel free to take this in
- 15:39- any direction if you don't, you know, just
- 15:41- wanna talk about the blood test, if you
- 15:42- wanna talk about something else as well, but
- 15:44- I always love to end with that kind
- 15:45- of note of optimism
- 15:47- about the future. So what's exciting you right
- 15:50- now, doctor Goel?
- 15:52- Yes. I think what excites me most is
- 15:54- the possibility that we are now beginning to
- 15:56- move from a model centered primarily on treating
- 15:59- cancer after it has happened to the one
- 16:03- that increasingly helps in earlier interception of the
- 16:06- biological process where we can possibly
- 16:10- prevent the cancer
- 16:11- or maybe cure it if we can find
- 16:14- it at a early enough stage. So I
- 16:16- think this is very, very important. For decades,
- 16:18- most of the cancer medicine has
- 16:20- focused on developing better treatments for established disease.
- 16:25- And as advances in therapy,
- 16:28- you know, targeted therapy, immunotherapy, precision oncology
- 16:31- have improved, but still, I think there's a
- 16:34- big window of opportunity there
- 16:36- to to intercept these cancers at much earlier
- 16:39- biological stage. So technologies such as liquid biopsies
- 16:43- for blood test and others,
- 16:45- they can help
- 16:46- overcome that
- 16:48- challenge that we cannot only find these cancers
- 16:51- early, but possibly we can find them much,
- 16:54- much, much, much earlier where we can either
- 16:56- prevent or possibly cure these patients from having
- 16:59- these diseases.
- 17:00- So I think the next frontier in cancer
- 17:03- care is simply
- 17:04- not treating the cancer more precisely
- 17:06- once it has developed,
- 17:08- but it is learning
- 17:09- how to recognize the biological process early enough
- 17:12- that for some patients,
- 17:14- we can prevent cancers from happening,
- 17:17- from becoming their diagnosis
- 17:19- at all. So, essentially, this is gonna be
- 17:21- the next frontier. This is gonna be the
- 17:22- future of cancer care.
- 17:25- Amazing. Well, thank you so much. I I
- 17:27- love leaving it on that note, and I'm
- 17:29- excited to see
- 17:30- what comes out next, from City of Hope.
- 17:34- Doctor Guell, thank you so much for coming
- 17:36- on the podcast, taking the time to share
- 17:37- your insights. I know our audience really appreciates
- 17:40- it. Thank you so much for having me.
- 17:42- Enjoyed it.
- 17:43- And thank you to our listeners for tuning
- 17:45- in to Becker's Oncology Leadership podcast.
- 17:48- I invite you all to check out even
- 17:50- more of Becker's Healthcare podcasts
- 17:52- at beckerspodcast.com.
- 17:55- Thank you again to doctor Goel for joining
- 17:57- me today and to our listeners. Have a
- 17:59- good one.