JAMA Forum: The Risks and Benefits of Expedited Drug Reviews

Image: Waldemarus/Thinkstock

The US Food and Drug Administration (FDA) oversees several programs that expedite approval of certain drugs that treat serious conditions and address unmet medical needs. On average, a drug in an expedited program reaches market almost a year sooner than other drugs. However, expediting drug approvals raises concerns that important safety or effectiveness information will be missed, potentially heightening risk of patient harm.

Most new drugs are approved with relatively little data about long-term outcomes. More than two-thirds of approvals are based on studies lasting less than 6 months. The FDA approves novel therapeutic agents more quickly than do similar regulatory bodies in Europe and Canada, with the median time for cancer drug approval of 6 months. Expedited reviews have increased in the last 2 decades, driven by drugs that are not first in their class, implying that they do not address unmet needs, according to a study by Aaron Kesselheim, MD, JD, MPH, of Harvard Medical School in Boston, and colleagues.

Greater Risks Than Benefits?
These facts suggest that the FDA’s expedited review programs may invite greater risks than benefits. The idea that doing something more quickly means it is not done as well has considerable face validity. Nevertheless, it is an empirical question whether the benefits conferred by drugs that receive expedited FDA approvals outweigh their risks to a greater or lesser extent than drugs approved with standard reviews.

A recent study by James Chambers, PhD, MPharm, MSC, of Tufts Medical Center in Boston, and colleagues sheds some light on this issue, albeit with many caveats. They compared the average quality-adjusted life-year (QALY) gains conferred by drugs with accelerated FDA approvals to those of drugs that underwent the standard approval process. The researchers’ sample of drugs included all of those approved by the FDA between 1999 and 2012. They obtained drugs’ QALY gains relative to prevailing treatment options from the research literature, excluding studies with pharmaceutical industry sponsorship to eliminate that source of financial bias. To be conservative, for studies that compared a drug with multiple alternatives, the authors selected the most effective comparator (that is, the one resulting in the highest QALY gain). In total, they analyzed 135 drug-indication pairs, 76 with accelerated approvals, 59 with conventional approvals.

The study found that drug-indication pairs with expedited approvals had higher median QALY gains than those with conventional approvals: 0.182 vs 0.003 QALYs, respectively. Drug-indication pairs in multiple expedited reviews had an even higher median QALY gain of 0.307. These results suggest that the FDA’s expedited drug review programs include drugs that provide greater benefits than those undergoing conventional review. Indeed, to the extent the expedited programs handle drugs for conditions for which there is unmet medical need, relatively larger QALY gains are to be expected.

Limitations
Naturally, the study has some limitations. A major one is that not all drugs could be analyzed, because of lack of QALY data. In total, the sample included only 30% of all FDA-approved drugs in the 1999-2012 study period (57% of approved drugs that underwent expedited approval and 79% of approved drugs that underwent conventional approval were not included in the analysis). It is therefore possible that the results do not generalize to all FDA-approved drugs.

Another significant limitation is that drugs approved with expedited programs are done so based on surrogate end points, as are the studies used to attribute QALY gains. Surrogate end points are usually biomarkers that indicate improved health that can be measured more quickly than the outcomes we care most about, like survival. Basing FDA approval on surrogate end points is controversial because they may not have strong predictive power for the outcomes of interest. For example, a systematic review found that most surrogate end points used in cancer drug trials don’t correlate strongly with survival. Another study found that a majority of cancer drugs approved based on surrogate end points in recent years have unknown or no beneficial survival effects. The extent to which QALY gains based on surrogate end points reflect true QALY gains is uncertain.

QALYs have other, well-known limitations. For instance, they may not fully capture all our preferences for treatments. An extreme manifestation of this point is exhibited by the “rule of rescue,” which is the tendency for people to prefer to expend greater resources to aid patients close to death, even if greater QALY gains could be achieved by using those resources for others.

It is also possible that with more time, safety concerns will arise for drugs with expedited approval. Drugs subject to less FDA scrutiny are more likely to exhibit safety problems, be withdrawn from the market, or carry black box warnings. We should therefore continue to monitor these drugs and update the performance of expedited approval programs as more information is available. Of concern, over the 2009-2013 period, only a minority of drugs with expedited approval had their efficacy tested in a postmarket trial within 3 years. Regardless of one’s view of the quality of FDA review or any particular study of a drug, we should agree that the outcomes of FDA policies in general and of particular drugs with expedited approvals based on surrogate end points warrant additional scrutiny.

Because expedited review programs are intended for drugs that treat serious conditions and address unmet medical needs, accepting greater risk may be reasonable and more consistent with patients’ preferences. However, because many of these drugs also come with high price tags, financed with public funds through Medicare, Medicaid, and other programs, the patients’ point of view is not the only one of relevance. A consideration of cost is also reasonable from the point of view of taxpayers.

***

About the author: Austin B. Frakt, PhD, is the Director of the Partnered Evidence-based Policy Resource Center, Veterans Health Administration; an Associate Professor at Boston University’s School of Public Health; and an Adjunct Associate Professor with the Department of Health Policy and Management at the Harvard T.H. Chan School of Public Health. He blogs about health economics and policy at The Incidental Economist and tweets at @afrakt. The views expressed in this post are that of the author and do not necessarily reflect the position of the Department of Veterans Affairs, Boston University, or Harvard University.  (Image: Doug Levy)

About the JAMA Forum: JAMA has assembled a team of leading scholars, including health economists, health policy experts, and legal scholars, to provide expert commentary and insight into news that involves the intersection of health policy and politics, economics, and the law. Each JAMA Forum entry expresses the opinions of the author but does not necessarily reflect the views or opinions of JAMA, the editorial staff, or the American Medical Association. More information is available here and here.

 

 



Categories: Adverse Effects, Drug Therapy, Health Policy, Patient Safety/Medical Error, The JAMA Forum

Tags: , , , ,