Pop Quiz: Which Cholesterol Pill Is Better? Answer: Depends Who Funded The Study!

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duh.jpgIn head-to-head trials of two drugs, the one deemed better appears to depend largely on who is funding the study, according to an analysis of 192 statin-drug comparisons carried out between 1999 and 2005 by researchers at the University of California at San Francisco. They examined 192 published results of trials comparing one cholesterol drug to another, or a non-statin.

Two links stood out. If the reported results favored the test drug, the trial was about 20 times more likely to be funded by the manufacturer, rather than the company that made the comparison drug. And if the conclusions or interpretation of the trial favored the test drug, the trial was about 35 times more likely to be funded by the maker of that drug rather than the comparison drug.

The results of the new analysis are reported in the June 7 edition of the journal “PLos Medicine.”

“Many people are concerned about the growing proportion of drug trials funded by the drug’s manufacturers,” says Lisa Bero, a UCSF professor of clinical pharmacy and health policy studies, who is a senior author of the study. “Results of drug trials affect what drugs are covered by medical plans, and so what drugs physicians will prescribe. If drug trial outcomes are largely determined by who pays for the trial, we don’t really know what the best drug is.”

The UCSF study examined the links between reported outcomes of the statin trials and such factors as study design, sample size, thoroughness and type of analysis, as well as funding source. They examined only published randomized controlled trials, which involved seven different statins overall, all studied in head-to-head comparisons.

The analysis found that about half of the trials were funded by industry, and about a third didn’t disclose any funding source. Among those declaring industry funding, about one fifth explained the role of the sponsor, such as data analysis, or writing and preparing the manuscript. Trials with no disclosed funding sources were less likely to have conclusions favoring the test drug, compared to trials with industry funding, the researchers report.

The researchers note that a number of factors can result in results favoring a sponsor. Drugmakers could selectively fund trials on drugs that are likely to produce a statistically significant result, the researchers explain. This can be accomplished, they say, by selecting non-equivalent doses of drugs for esting. Also, sponsors may choose not to report results that don’t favor the drugs they sell, or they may report positive results in more than one journal, skewing the number of positive articles about a drug.

In addition, almost half of the trials lacked adequate blinding assuring that study scientists don’t know which drug the patients were taking until the end of the trial. The researchers found that those studies with adequate blinding were less likely to report results favoring the test drug. This finding was independent of who funded the study - in other words, funding source was a stronger predictor of outcome than blinding, but both had independent effects on outcome.

The most important weakness found in most of the trials was a lack of clinical measures of outcome, such as heart attacks or mortality - considered better indicators in trial design than less direct measures such as lipid levels. “The studies don’t give us
the best information we need to choose one statin over another,” Bero says.

The study also differed from most other assessments of influences on drug trials by examining 11 different factors, and how they may interact to affect trial results. Most previous studies examined the link of results to one factor alone, such as funding source. But this analysis adjusted for “confounders” - study aspects that can influence the results, such as study design, including randomization, blinding, sample size, even choice of comparison drug in the study. Including the confounders still pointed to industry sponsorship as the most influential factor related to positive results and conclusions.

The study examined trials by all funding sources, as well as a subset of studies that were only industry funded. Favorable results and conclusions were associated not so much with industry sponsorship, but with the specific company that funded the study, Bero points out.

“The data available on choosing between statins based on head-to-head drug comparisons appears to be influenced by financial conflicts of interest,” Bero says. “So decision makers - those choosing drugs for a formulary or insurance plan - should be skeptical about these kinds of trials. We need to know if a newer, more expensive drug is really better compared to older, less expensive drugs.”

The research was funded by a California Tobacco Related Disease Research Program grant.

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  1. The clinical implications of this are enormous. Patients can stop taking their statins and instead use their co-pays to fund a study. In a few months, they will be feeling terrific.

  2. Hi Hank,

    That’s an interesting way of looking at it. I should have thought of that. Oh well.

    Thanks for writing
    Ed

  3. I’ve only had a chance to skim this, but it seems a little unreasonable to criticise trials for not being outcome studies (i.e., looking at CV or mortality endpoints). Those are huge, lengthy (and expensive) trials. It has pretty much been conclusively shown that use of statins is associated with mortality benefits, and LDL reduction is a reasonable surrogate. I’m not totally familiar with all of the large outcomes studies, but HPS, SSSS, AFCAPS, WOSCOPS were all placebo-controlled. I’m not sure AstraZeneca, Pfizer, or Merck really want to undertake a head-to-head statin CV outcomes study. For a study like that, I suspect the NIH/NHLBI will need to undertake something like that if someone wants an answer on the most effective CV mortality reduction.

    I’m also somewhat comforted that of the blinded trials (which I think is an important aspect of this review), results were significantly less likely to be positive for the test drug, even though funding stayed significant in the multivariate model.

  4. A more serious response than my last. Unless there is new data, I don’t think any of the statins have shown a mortality benefit in _primary prevention_ except for men under 65 with very high risk factors (of which being a man is one).

    As John Abramson has shown in some of his recent work, a number of the studies that are cited to support wider use of statins in national guidelines - including some of noted in the last post - actually included none of the relevant pt. groups (i.e., no women, no one over 65, etc.) which the guidelines embraced.

    Initially, of course, it was the _lack_ of a clear reduction of mortality (depite reduced CV events) that led to concerns about associations between statins and cancer. Those concerns appear not to be supported as of now. But they do demonstrate the importance, I think, of still keeping mortality the endpoint of endpoints (in all relevant senses).

  5. While I appreciate your emails and your concerns. At this moment Americans are in danger of unrelieable medical supervison of medications that doctors are prescribing. One of the most used medication, statin drugs for cholesterol is silently killing people. Doctors, the medical profession, pharmaceutical companies are not telling the the truth and Congress and The present administration allows this. The qualituy of healthcare is most important, but Americans are not receiving ethical healthcare. What is the answer? I have researched tons of information and I am coinvinced that our helthcare system and government is most corrupt. As an indvidual that would like to see truth and honesty in goivernment but do no know how to accomplish this HELP!

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