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Unrevealed Analysis Weakens Claim of AIDS Vaccine "Success"
 
 
  October 5, 2009
Science Mag
by Jon Cohen
 
When the U.S. Army and its collaborators in Thailand announced at press conferences on 24 September that a large clinical trial of an AIDS vaccine had lowered the rate of new HIV infections by about one-third, researchers were surprised and encouraged. Although it was only a modest reduction, it was the first positive result from any AIDS vaccine trial.
 
Now some researchers who have seen more of the data in confidential briefings are complaining that a fuller analysis undermines even cautious claims of success, and they are raising questions about the way the results were announced.
 
The press conference and press releases discussed an analysis that included all 16,000 people who participated in the trial, except for seven who were infected before receiving any doses of the two vaccines that were used in combination. Seventy-four people in the placebo arm of the study became infected with HIV, while the similarly sized vaccinated group only had 51 infections-a 31.2% efficacy. The analysis indicated that there was about a 96% level of confidence that the effect was real and not due to chance-just above the 95% cutoff that is widely used as a measure of statistical significance.
 
In the private briefings, researchers learned that a second analysis, which is usually performed in vaccine studies and was part of the Thai study's design, also found that vaccine recipients had fewer infections, but the reduction was not statistically significant and the level of efficacy was slightly lower. This analysis eliminated people in both groups who did not rigorously follow the protocols. "Anything that really works, you'll have enough robustness in results to be significant with both analyses," says Douglas Richman, an AIDS researcher at the University of California, San Diego, a longtime critic of the study. Richman did not discuss the specific results with Science.
 
"The press conference was not a scholarly, rigorously honest presentation," said one leading HIV/AIDS investigator, who like others asked that his name not be used. "It doesn't meet the standards that have been set for other trials, and it doesn't fully present the borderline results. It's wrong." Two biostatisticians who specialize in HIV prevention trials and have not seen the data, said that the results from all participants are the more important data, but they were puzzled that the press conference did not include the analysis that excluded those who didn't follow the protocols. "I think if people saw [the two analyses] diverging in a vaccine study, they'd have a lot of questions," says David Glidden, a biostatician at the University of California, San Francisco.
 
Colonels Nelson Michael and Jerome Kim, researchers with the U.S. Army who helped run the study, strongly objected to the assertion that they gave the data a positive spin. "We needed to get enough information out so we could give the world community a fair glimpse of what we've learned," said Michael. He notes that in addition to showing select researchers a fuller presentation of the data, a paper under review at the New England Journal of Medicine describes both analyses, and all the findings will be discussed on 20 October at an open AIDS vaccine meeting in Paris. "We tried very carefully to make sure that message was crystal clear," said Michael. "There's now hope. But that said, we've tried to be very careful not to oversell this."
 
Several researchers wonder why the data were even released publicly before the Paris meeting. People running the trial learned the results on 10 September, and Michael said there was concern that the information would leak before 20 October. Thai collaborators asked for the 24 September date, Mahidol Day, which commemorates the passing of the current king's father, a clinician who studied public health at Harvard University.
 
The debate over the way the results were presented will have no immediate practical impact because even under the most optimistic assessment, the vaccine offered too little protection to be a serious candidate for widespread use. But a modest success, even one that is marginally significant, may point the way to new vaccine strategies. "I think that the field is energized," said Kim. "Everyone should wait until the data are out."
 
Several critics point out that a press conference 2 years ago about another AIDS vaccine efficacy trial-which was prematurely stopped because the product clearly was not working-researchers reported both analyses (subs. req). What is more, the AIDS Vaccine Advocacy Coalition, a nonprofit that issued a report about interpreting the Thai results before the data were unveiled at the press conference, stressed the importance of both. "The safest route is to report both ... and to analyze any difference," the report states. "Advocates' take-home message: no matter what the headlines say, a single number is not the full result."
 
 
 
 
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