Big Data and the Individual Patient
You call it personalized medicine, I call it precision medicine—at least we can probably agree that the aim of healthcare is to provide each patient with
the best possible treatment. Beyond this starting point, though, we head straight into another area of disagreement, namely, What do you or I mean by “best
treatment”: Is it the treatment that works best on average, or the one that’s most likely to work in a specific individual? And how will we be able to tell
the difference, when each patient has so many unique characteristics that can affect the risk level of the outcome and the potential benefits of therapy?
entered this roiling debate a few years ago with an article by two eminent clinical researchers who were also practicing physicians. David Kent, then at
Tufts Medical Center, and Rodney Hayward, at the University of Michigan VA Medical Center, proposed a shift in the way we think about clinical
trials: “Because many factors other than the treatment affect a patient’s outcome, determining the best treatment for a particular patient is fundamentally
different from determining which treatment is best on average.”
Fair enough, except that once you start taking each patient’s unique physiological state into account, the questions multiply into a medical hall of
mirrors. It’s almost enough to bring on nostalgia for the good old days of “Feed a cold, starve a fever.”
But let’s not go back there just yet, because there may be a forum in which reasonable people can come together, plow through masses of data from
innumerable clinical studies, and sort out which specific treatment tends to succeed under which particular circumstances, for which individual patients.
As it happens, one of the lesser-known articles of the Affordable Care Act provides for just such a forum, the Patient-Centered Outcomes Research
Institute. PCORI reviews and funds clinical studies to gauge the relative effectiveness of various treatments. A hypothetical example might be, say,
research to determine how badly clogged a patient’s carotid artery must be in order to justify plaque-removing surgery—a procedure that can greatly reduce
the risk of a stroke but that also carries significant risks of its own—rather than some other form of intervention that might be less drastic but also
PCORI also endorses another kind of initiative, “supporting not just clinical effectiveness research itself but the dissemination of the
research,” says Kent, a professor of medicine at Tufts Medical Center and director of its Predictive Analytics and Comparative Effectiveness (PACE) Center.
PCORI’s reasoning is that many different groups of people can benefit from hearing about such research: patients, healthcare providers, insurance
purchasers and payers, drug and medical-device manufacturers, and policy makers, as well as other researchers.
To this end, an upcoming symposium will bring together members from each of these “stakeholder” groups (including me, representing American Scientist as part of the push toward dissemination along with patient advocacy groups, policy makers, clinicians, and others). I look
forward to reporting on some lively back-and-forth: With presentations from experts in the analysis of evidence-based medicine, measuring quality in
healthcare, preventing secondary stroke, and the application of genomics in public health, no one should be at a loss for data. Even better, with about an
hour allotted for open discussion—including questions submitted online by people participating remotely—any and all viewpoints will be welcome. The
symposium, scheduled for Thursday, June 4, 8:30 a.m. to 12 noon EST, is free and open to the public at the the Jaharis Building of the Tufts University
School of Medicine, in Boston; anyone may register to attend in person or online.
Afterwards, “we hope to continue the conversation,” says Kent, so the symposium will be archived and made available afterwards. And of course I’ll offer my own take on the event as well. Stay tuned!
This post is published in From the Staff
Connect With Us:
Oct 30, 2015
Ten costume ideas that look smart and start conversations about our favorite subject: science.
Mar 16, 2015
Decades of research into genetic disorders have scrutinized but a tiny part of the human genome—the part with the code for making proteins. This tiny part yielded the causes of sickle-cell disease and hemophilia and inspired a slew of labs to seek causes for more diseases in protein-coding DNA. But those labs’ quests returned surprising results...read more.
Mar 30, 2016
An evolutionary anthropologist thinks there are three particular ways that natural selection has made our sleep different from that of other great apes.
Receive notification when new content is posted from the entire website, or choose from the customized feeds available.