So why is this such a contentious subject?
Whether Tamiflu is useful has become an issue that is about much more than just the drug's ability to fight flu.At first, manufacturer Roche, which is headquartered in Basel, Switzerland, refused to allow independent researchers access to all its data on clinical trials of Tamiflu. This made the drug a rallying point for those campaigning for more openness in clinical trials. Some scientists, notably the Cochrane group of medical reviewers and the journal BMJ, feel that the pharmaceutical industry has distorted medical research to portray its drugs as more beneficial than they actually are, and that this case is an example of this. Others say that the work from the BMJ and the Cochrane group unfairly downplays the drug's real benefits.
What does the latest study add?
The research, published in The Lancet1,
is based on individual patient data provided by Roche — which provided
some funding for the work but was not otherwise involved, according to
the authors. It combines data from different trials in a process called
meta-analysis, and is, according to a press release from The Lancet, the “most thorough analysis” of Tamiflu so far.Led by epidemiologist Arnold Monto of the University of Michigan in Ann Arbor, the team looked at data from 9 clinical trials, which included 4,328 participants. People given a placebo saw their influenza symptoms pass in a little more than five days on average, whereas those given Tamiflu felt better after four days. The team also found that among those infected with influenza, Tamiflu reduced the risk of ending up in hospital by 63%.
This result sounds familiar, somehow…
An analysis from the Cochrane group, published in the BMJ last year2,
also aggregated data from multiple trials. That study found that
compared with a placebo, Tamiflu reduced the duration of symptoms from 7
days to 6.3 days — or by about 17 hours — on average. But it found no
difference in admissions to hospital.
So Tamiflu is useful?
Neither
published paper makes an explicit recommendation for or against using
Tamiflu to treat influenza. Both teams found significant side effects,
including nausea and vomiting. The Lancet paper concludes that
the drug does offer benefits, but it adds that whether these outweigh
the side effects is something to be “carefully considered”.Media reports have sometimes characterized the BMJ study as showing the drug to be useless, and study co-author Carl Heneghan, director of the Centre for Evidence-Based Medicine at the University of Oxford, UK, said last year that money spent on stockpiles had been “thrown down the drain”. The study itself said only that the results “provide reason to question the stockpiling of oseltamivir … and its use in clinical practice as an anti-influenza drug”.
Is the latest study really independent?
That depends on whom you believe. Tom Jefferson, a reviewer with the Cochrane group and a co-author of the BMJ meta-analysis, says that the Lancet study
should be viewed in the light of the fact that it was funded by Roche
and that some of the authors have links to the pharmaceutical industry.
Two of the four authors have accepted money from Roche separately from
the study, and one of these also serves on the board of pharma company
Gilead Sciences, based in Foster City, California, which invented
Tamiflu and licensed it to Roche.“These authors are not neutral,” says Jefferson.
Stuart Pocock, a medical statistician at the London School of Hygiene and Tropical Medicine and one of the authors of the Lancet paper, disagrees. He stresses that Roche had no involvement in the study design, and that although his co-authors may have links to the company, their experience is crucial for good science. “One needs co-authors who really know about influenza,” he says. “There’s a great danger independence becomes ignorance if you push it too far.”
Where do we go from here?
Jefferson says that the Lancet
paper adds nothing new to the science on Tamiflu. “What they say there
has been said before,” he says. Pocock counters that the study is the
first to use the “totality of data” from trials, so it should “greatly
defuse any uncertainty” about the risks and benefits of the drug. Now it
is up to policy-makers and health economists to decide how this
evidence should be turned into policy, he says.Pocock adds, “There tends to be an antagonistic arrangement that can occur between, on the one hand, defensive companies wanting to promote their drugs and, on the other, extreme activists who wish to claim that anything a company finds is nonsense. In reality, objective evidence lies between those two extremes.”
- Nature
- doi:10.1038/nature.2015.16820