Showing posts with label research ethics. Show all posts
Showing posts with label research ethics. Show all posts

Thursday, February 3, 2011

Equipoise: No Help for Ethical Deliberation

This post might seem a bit off the wall for this blog, but I'll defend it by noting that we discuss ethical issues at the medicine-Pharma interface, and so unavoidably touch on the ethics of drug research more generally. The article I will discuss here (subscription required) makes some excellent points that have not previously been a part of that ethical discussion.

Frank Miller, a philosopher-bioethicist at NIH, and Steve Joffe, pediatric oncologist with the Dana-Farber Cancer Institute, write on the question of "equipoise." The standard view today of the ethics of randomized clinical trials takes off from the apparent dilemma of a physician enrolling subjects in a randomized experiment. Traditional medical ethics says that the physician's duty is to advise the patient with regard to therapy, according to the doc's best clinical judgment. This seems inconsistent with allowing a patient of yours to get a treatment, or not, at the toss of a coin. The solution, according to ethical thinkers back in the 1980s, was that a randomized trial is ethical only in a state of clinical equipoise--when the relevant community of physicians considers it a toss-up as to which of the two treatment arms is superior.

First thing to note is that the equipoise rule would prohibit the vast majority of placebo-controlled trials. Yet the FDA routinely requires placebo-controlled trials for most of the meds they approve. So tons of supposedly unethical trials are conducted to win FDA approval. Is the FDA unethical, or does this signal a flaw in the equipopise theory?

A few years back, Frank Miller and I argued that it's the equipoise end of the stick that has the problems. (Not that the FDA doesn't have problems, but that's another post.) We relied at that time heavily on a set of arguments that claim that clinical medicine and clinical research are two quite different enterprises and require different ethical rules. To argue that the clinician trial investigator has the same duty to the research subject as the physician has to the patient mixes up those different sets of rules.

Miller and Joffe here expand that argument considerably by arguing that it's not just a matter of conducting research according to the ethics of the individual physician-patient relationship, erroneous as that may be. There's another issue at stake. The equipoise argument is based on the idea that the only "consumer" of the research findings is the individual doc trying to make treatment decisions for individual patients. If that doc is in a fog about which of two treatments is superior for any given patient, then it's presumably ethical to do a randomized trial. But as soon as that doc becomes unfogged, and has a clear preference for one treatment over the other, then scrap the trial. (Ending trials early, before they allow definitive conclusions, is one deleterious consequence of equipoise that Miller and Joffe list.) Or in the case of clinical equipoise, stop the trial when the relevant community of docs becomes unfogged to a sufficient degree (whatever that is, yet another problem with equipoise).

This view, say Miller and Joffe, is fundamentally incomplete. There are other important consumers of this research, namely policymakers, including those often-derided folks at the FDA. And policymakers don't have the luxury, or the burden, of dealing with patients one at a time. These folks are duty bound to adopt a population perspective, asking what the impact of a drug (for example) is on the entire patient population. To get such data, randomized trials are usually needed (not always), and the trial may have to go on often beyond the stage at which individual physicians have reasonable preferences for one treatment over the other. The policy need for these data is legitimate and ethically sound, and so it's shortsighted to invoke "equipoise" as a reason to rule out those trials, or to stop them too early.

Bottom line--ethics is important in research and the rights of subjects must be adequately protected, but the concept of equipoise is quite a wrong-headed way to go about that task.

Miller FG, Joffe S. Equipoise and the dilemma of randomized clinical trials. New England Journal of Medicine 364:476-80, Feb. 3, 2011.

Miller FG, Brody H. A critique of clinical equipoise: therapeutic misconception in the ethics of clinical trials. Hastings Center Report 33(3):19-28, 2003.