'The Most Progressive Health System on the Planet'

Geisinger: 'The Most Progressive Health System on the Planet'

Geisinger CEO David Feinberg Talks Genetics and Refunds With Eric Topol

; David T. Feinberg, MD, MBA

Disclosures

October 05, 2018

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Eric J. Topol, MD: Hello, I'm Eric Topol, editor-in-chief of Medscape, and I'm really delighted today to talk with Dr David Feinberg, who heads up the Geisinger Health System. David, it's great to have you with us.

David T. Feinberg, MD, MBA: Thanks so much, Eric. I'm excited for our conversation.

Topol: I'd first like to give a little background. Make sure I've got it right: You went to UC Berkeley, [then] Chicago Medical School; you got an MBA from Pepperdine University, and eventually became the CEO of the UCLA Health System. Then you made a big switch moving from UCLA to Geisinger about 3.5 years ago. What was that like to make this big move from Los Angeles to Danville, Pennsylvania?

Feinberg: Well, first of all, UCLA is an amazing organization. I did my residency and fellowship there. I didn't think I was ever leaving UCLA, but I'd sent a team of guys [to Danville] a couple of years before because everyone was talking about "Geisinger, Geisinger." And when that team came back, it really changed how we provide neurosurgical services at UCLA. Then, a couple of years later, Geisinger calls and says, hey, we're looking for a chief executive.

I thought I would just go to learn more about Geisinger so I could bring it back to UCLA. What I found during that exploration phase was that I could get all the "stuff" that Geisinger had over to UCLA, but it would take 10 or 15 years, and then it would be the end of my career. Or, I could go to a place that already had all the tools and see what could happen. So, my wife and I probably did 10,000 steps every night, talking about why are we moving, why should we do this, should we do it or not do it? I had never had another job other than UCLA!

And then I came to Geisinger. I made that decision and I've got to tell you, it's amazing.

First of all, I feel liberated in that Geisinger has only one mission, unlike an academic medical center that's worried about research and academics and teaching and clinical care. At Geisinger, our only focus is the community; it's the people that we serve, so you have the freedom from that academic medical center piece. We now have a medical school, an insurance company, and a very strong clinical delivery system, and we have 33,000 people who get up every morning and try to make it better for our friends and neighbors.

It's been incredible also from a personal standpoint. After being in the echo chamber of West Los Angeles—we were living in Beverly Hills—we now live in "the other America." It's very rural and it's very poor, and things that are happening in our country make much more sense to me now than had I not had this opportunity. So it's been a privilege to move to the middle of Pennsylvania.

Topol: That's fantastic. We're going to talk about some of the things you're doing there that are truly unique on the planet, at the most progressive health system I know, so that is a real credit to what you've been doing. But before we do that, I want to read a quote I have of yours that I love:

"I think our industry is so screwed up and is ripe to be disrupted; either we do it or some Stanford drop-out in a black turtleneck is going to." That one really hit me as being from a person who truly gets it.

Let's talk about your extraordinary effort with genomics, not just the collaboration that you did with Regeneron, but also your announcement of expanding it to all patients at Geisinger who are interested.

Our doctors said to us, 'I want to do this on all my patients!'

Feinberg: There are some organizations that are way ahead of us in sequencing a cancer gene and understanding what medicine to use, or are looking at genetics and saying to patients, "You should be on this medicine or on that medicine."

Our approach is based on asking, "What if we did whole-exome sequencing on our entire population?" We started this to see whether we could find medically actionable genetic conditions that we could do something about. We are 200,000 patients into it—or I should say, research subjects, because we started with research—and we have found that 3.5%-4% of those people have something actionable: BRCA, malignant hyperthermia, Lynch syndrome, genes associated with cardiac arrhythmia.

We saw a 16-year-old girl in our emergency department who came in dehydrated from soccer. We gave her some fluids, and she participates in the MyCode study. It turns out she has two genes associated with fatal cardiac arrhythmias in young athletes. Because of where we are and the fact that most people don't move, there are 30 people in her family whom we care for that we have in our electronic records. We get all the genetics, and it turns out 15 of that 30 have the gene. Now, many of them have pacemakers or are on beta-blockers, or both, that are literally saving their lives.

We did that for our research enterprise, and Regeneron helped fund this to use that information in a deidentified way for their drug discovery. But we felt we couldn't wait to turn this on [more broadly]. It was actually our doctors saying to us, "I want to do this on all my patients!"

I think it's now been about 2 months since we said that for any of our patients, we'll do whole-exome sequencing for free. We get the results in about 2 weeks. When we get a positive result, the first thing we do is notify your primary care doctor, who then gets a 30-minute continuing medical education course on BRCA or Lynch [syndrome] or whatever the disorder their patient has—essentially, a refresher course.

Five days later, the patient is notified that they have a genetic mutation and is asked to come in to see the doctor. That way, the doc is prepared for the visit, the patient is prepared, and they have a discussion—because all it is, is a genetic mutation. The real thing is, should we go to the breast clinic? What do we need to do differently on the basis of this information? We've built it into our electronic health record, so it's very easy to have the ongoing surveillance.

Topol: Have you noticed that the doctors are getting "genomified"? That is, are they really getting more up to speed because of this program?

Feinberg: No question! There are certain health systems where doctors say, "I won't meet with you if you come in with 23andMe results." Ours is the opposite. Our doctors said, "We want this now in routine clinical care." They didn't buy in until they had their first patient with return results, and we prepped them with the right information and they had a positive experience. Then they became ambassadors for the program.

The other thing we saw that we didn't anticipate was, when we give somebody a genetic result back, that doctor the next day gets calls from six brand-new patients who want to see that doctor. The patient went home and told their friends, "I have a genetic mutation," and now their friends want to go see that doctor.

Topol: Amazing. As you know, David, there was a recent review in the New England Journal of Medicine[1] that basically pointed out that everyone with colon cancer should be screened for Lynch syndrome. Very few actually get that screening. But you're proactively doing this in patients, and not just in patients—I saw that you were the first one to enroll in the program.

Feinberg: I've had my genome done so many times now because I'm interested in the user interface. It always comes back with the same things: I've got male pattern baldness, but Rogaine® is working, and I'm actually protected against celiac disease, so I could practically bathe in wheat. But yes, it's actually the fifth time I've done my genome.

We see it as [leading to] a cost decrease. In routine clinical care today, if your parents had colon cancer at an early age, the gastroenterologist would say that all offspring should start colonoscopies at age 30 because of the family history. We know, though, that only one half of those offspring actually have the Lynch syndrome mutation, and the others shouldn't get their colon screen until age 50 or so.

It's the same with BRCA; 50% of people who have BRCA-positive breast cancer have no family history. We know it's a genetic disorder, but maybe mom died of something else or there's no sister and they don't have the family tree in their mind, so if they went to a doctor, no one would order a BRCA test.

We're finding those 50% BRCA-positive people without the family history, so we think if you live in central Pennsylvania and you're a young woman, your chances of getting breast cancer are lower here than anywhere in the United States because we know who's BRCA-positive.

The same way that we sequence your DNA, we sequence your ZIP code. We know everything about where you're living.

Topol: For people who are not as familiar with your health system, you have mentioned some 33,000 employees, but how many patients are you serving in the whole region?

Feinberg: We take care of about 3 million folks; it's about a $7.5 billion organization. We have 12 or 13 hospitals, helicopters, clinics, an insurance company, a medical school, and research focused on genetics.

Topol: Now I want to go from genetics to another topic that you've been pioneering, and that's the food pharmacy. Can you enlighten us about that program?

Feinberg: We think that the most important thing for you to live a long life, and to have a lot of life in your years, is not what takes place in the hospital, not what takes place in the clinic; medical care probably accounts for only about 20% of health outcomes. We think it's your genetic code, and we also think it's your ZIP code. So the same way that we've sequenced your DNA, we sequence your ZIP code. We know everything about where you're living.

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