What’s in a Name? A Lot, When It Comes to ‘Precision Medicine’

important molecularly targeted cancer drugs, like Roche’s vemurafenib (Zelboraf) or Pfizer’s crizotinib (Xalkori), that are a whole lot more precise than old-fashioned chemo drugs. I’ve also used the term to describe powerful new kinds of molecular diagnostics that can guide treatment decisions, like Genomic Health’s Oncotype Dx, CardioDx’s Corus CAD, or Nodality’s Single Cell Network Profiling test.

What the “precision medicine” movement argues, correctly, is that these types of innovations allow for more precise diagnosis and treatment of patients at the molecular level.

Here’s what the NRC committee said about its choice of term:

“As used in this report, ‘Precision medicine’ refers to the tailoring of medical treatment to the individual characteristics of each patient. It does not literally mean the creation of drugs or medical devices that are unique to a patient, but rather the ability to classify individuals into subpopulations that differ in their susceptibility to a particular disease, in the biology and/or prognosis of those diseases they may develop, or in their response to a specific treatment. Preventive or therapeutic interventions can then be concentrated on those who will benefit, sparing expense and side effects for those who will not. Although the term ‘Personalized Medicine’ is also used to convey this meaning, that term is sometimes misinterpreted as implying that unique treatments can be designed for each individual. For this reason, the Committee thinks that the term ‘Precision Medicine’ is preferable to ‘Personalized Medicine.’”

What the committee doesn’t say in writing—but which many surely were thinking—is that the new term also provides a way to give this concept a fresh start. Leading biomedical researchers and companies have been talking up personalized medicine for a decade now, and there’s still not a very long list of successful products you could file under this header. Personalized medicine, with so much promise unfulfilled as of yet, has picked up a lot of negative baggage in research and clinical circles.

Last week, when I visited Stanford University and Caltech on reporting trips, the negativity toward the personalized medicine movement was striking. Three biomedical researchers shooke their heads at me when I said I had attended the Personalized Medicine World Conference earlier in the week in Mountain View, CA.

“I think [precision medicine] is fine,” says Stephen Friend, the president of Seattle-based Sage Bionetworks, a nonprofit building an open-source biological database for researchers and physicians. “The old term is not yet delivering as soon as hyped.”

Momentum for this renaming effort came from Stephen Galli, the chair of pathology at Stanford University, according to fellow NRC committee member Maynard Olson of the University of Washington. Olson, one of the leaders of the Human Genome Project, says he was quickly persuaded by Galli’s argument. The gist is that personalized medicine has largely been associated with single anecdotal success stories. Those kinds of advances are extremely valuable if they happen to a member of your family, and they can make for great experiments that generate new scientific hypotheses, like the work Mike Snyder has done at Stanford.

But “N of 1” experiments make a weak foundation for physicians who want their decisions to rest on medical evidence. Physicians are more likely to join the movement if they see a way to get more and more data on patients to help sharpen up their sometimes shaky attempts to diagnose disease. Precision, basically, is the opposite of ambiguity. Physicians are bound to listen closely to something that can help them out of the ambiguity zone. Think for a second, about “flu-like symptoms.” How valuable would it be for a physician if someone had a quick, cheap, super-accurate blood test that could say someone’s “flu-like symptoms” were actually from H5N1 “bird flu” or malaria?

“When (Galli) first brought up the idea, I think most committee members thought ‘precision medicine’ sounded odd, but he won everyone over quickly as we considered the suggestion,” Olson says. “The gist of the idea is to distance genomic medicine from any suggestion of a retreat from evidence-based to anecdotal medicine. If you think about it, nearly all high-profile claims of success in ‘personalized medicine’ have been n = 1 anecdotes. Medicine has been there—we do not want to go back.”

There are other arguments that personalized medicine has struggled with, particularly cost and data-sharing. Especially during a time of healthcare cost-control, it will cost way too much to get everybody’s genome, transcriptome, metabolome, proteome and other ‘omes socked away in electronic health records. Cost needs to keep coming down. And big medical institutions also need to figure out how to play in the same sandbox with biomedical researchers. Today, most physicians don’t have a clue of what to do with the precious information they might get from the genome of, say, a tumor sample. Even if they did know how to use it, they’d probably be afraid to share their samples and data with other physicians and researchers, because of patient privacy concerns and legal liability fears.

These are tough issues. They are social, economic, and political barriers not easily broken down by exponential technology progress.

Personally, I like the term “personalized medicine” and all of the long-term grandiosity it conveys. Precision medicine, to my ear, sounds more incremental, less inspiring. But if Galli and his fellow clinicians see value in the term “precision medicine,” and they recoil at some limited definition of “personalized medicine,” then maybe it’s time to let the clinicians have their way. The clinicians need to contribute samples, and data, that researchers can use, and the researchers need to send back the insights and data they get to the clinicians and drug companies. While egos may be wrapped up in personalized medicine, the movement will never coalesce without physicians and physician/scientists in leading roles. A switch in vocabulary is a pretty small sacrifice to make on the road to more custom-tailored healthcare.

Author: Luke Timmerman

Luke is an award-winning journalist specializing in life sciences. He has served as national biotechnology editor for Xconomy and national biotechnology reporter for Bloomberg News. Luke got started covering life sciences at The Seattle Times, where he was the lead reporter on an investigation of doctors who leaked confidential information about clinical trials to investors. The story won the Scripps Howard National Journalism Award and several other national prizes. Luke holds a bachelor’s degree in journalism from the University of Wisconsin-Madison, and during the 2005-2006 academic year, he was a Knight Science Journalism Fellow at MIT.