Page 177 - Journal of Special Operations Medicine - Spring 2017
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also drives a lot of marginal products, or products that   of the healthiest patient, the people who are the fittest
              don’t work. And the people who designed those trials   of the patients. On average, the age is almost 10 years
              are I think very clever. You can sort of tilt the playing   younger in pivotal trials for the FDA drug approval than
              field a little bit to favor your drug and the incentive to   in the real world. And then when you start to extrapo-
              do so is often tremendous—billions of dollars hinge on   late  drugs  that  have  real  side  effects  in  very  carefully
              one of these pivotal trials. And to some degree that’s be-  selected populations, and small benefits, in carefully
              cause it’s a human pursuit. But to some degree we could   selected populations, to the average patient that walks
              have policy changes that could more align the medical   into my clinic, who is older, who has other problems,
              research agenda with what really matters to patients   who is taking heart medicine. There was a paper that
              and doctors.                                       came out about one of those costly expensive drugs for
                                                                 liver cancer, and in the pivotal trial it had the benefit of
              DUBNER: Let me ask you: in your own field, in oncol-  about two, three months, something like that. But in the
              ogy and in the particular cancers that you treat, how   real world, in the Medicare data set, it had no improve-
              much more effective generally would you say the new   ment in survival over just giving somebody good nurs-
              cancer drugs are, than the ones that they are replacing   ing care and good supportive care. And I think that’s
              or augmenting?                                     the reality for many of these marginal drugs, when you
                                                                 actually use them in the real world, they start to not
              PRASAD: Let me say that there are a few cancer drugs   work so well, and maybe not work at all.
              that have come out in the last two decades that are re-
              ally wonderful drugs, great drugs. One drug came out   DUBNER: You’ve written and spoken about cronyism
              of work here, in the Oregon Health and Science Uni-  and conflicts of interest between drug makers and the
              versity, by Dr Druker, Gleevec, and that’s a drug that   doctors who prescribe drugs. I’m curious what happens
              transformed a condition where maybe 50 or 60 percent   when you go to an oncology conference. Are you an
              of people are alive at three years to one where people   unpopular person there?
              more or less have a normal life expectancy. So that’s a
              really wonderful drug. But I think if we’re honest with   PRASAD: Stephen, I always wear a bulletproof vest
              ourselves, we’ll have to admit that the majority of new   when I go. No, but this has really been sort of the way
              cancer drugs are marginal, that they offer sort of very   medicine has operated for many years. To some degree,
              small gains at tremendous prices, and to give you an   practicing doctors in the community having ties to the
              example of that, among 71 drugs approved for the solid   drug makers—that’s one thing—but increasingly, we see
              cancers, the median improvement in overall survival or   that the leaders in the field, the ones who design the
              how long people lived was just 2.1 months. And those   clinical trials, who write up the manuscripts, who write
              drugs routinely cost over $100,000 per year of treat-  the review articles, who sort of guide everyone in how
              ment or course of treatment.                       to practice in those fields, they have heavy financial ties
                                                                 to drug makers. And there’s a large body of evidence
              DUBNER: But that points to one of the tricks that   suggesting that biases the literature of towards finding
              works so well—which is if it’s 2.1 months extra, and   benefits, where benefits may not exist, towards more fa-
              if the expected lifespan was, just let’s pretend for a   vorable cost-effective analyses when drugs are really not
              moment, it was 6 months, then on a percentage basis   cost-effective. It’s a bias.
              that’s a massive improvement. So as the patient or as
              the pharma representative, I’m not talking about that   LISA BERO [professor of medicine and co-chair of the
              length of time—which might be lived under physical du-  Cochrane Collaboration]: Yes, well, we have a great
              ress and financial duress—but rather I’m thinking about   deal of empirical data showing that funding sources and
              goodness gracious, 33 percent life expectancy extension!  author financial conflicts of interest are associated with
                                                                 overoptimistic data.
              PRASAD: Right, a new drug improves lifespan 33 per-
              cent longer.                                       To find out more, check out the podcasts from which
                                                                 this text was drawn: “Bad Medicine, Part 1: The Story
              DUBNER: And who doesn’t want that, especially when   of 98.6” and  “Bad Medicine, Part 2: (Drug) Trials
              you’re sitting there with your loved one in a horrible   and Tribulations” (http://freakonomics.com/podcast/bad
              situation, facing the end?                         -medicine-part-1-drug-trials-tribulations/).

              PRASAD: The other thing that I’d point out is, those 2.1
              months, these clinical trials that are often conducted by
              the biopharmaceutical industry, they really choose sort




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