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November 1999 Cover
November 1999 Cover

 HIV Digest HIV Digest Archive  
November 1999 Email this to a friend
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When to Change Therapies

Doctors and PWAs are using recent research on viral load changes to fine-tune treatment decisions. But uncertainties remain about how to interpret and act on low levels of virus.

There is broad consensus on one point: The "gold standard" is a consistently undetectable viral load according to the most sensitive test available. "The steeper the decline in viral load, the more lasting the response," says Ben Cheng, an HIV treatment expert at Project Inform in San Francisco. One study has shown that failure to drop below 400 copies (the cutoff point of the standard test) by week 12, and below 50 copies (a level only measurable on an ultrasensitive test) by week 24, significantly increases the long-term likelihood of rebound to detectable virus levels.

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When to test and switch

Aggressive AIDS docs such as Steven Deeks of San Francisco and Douglas Ward of Washington, DC, monitor viral loads closely: Deeks tests patients undergoing treatment every month; Ward, every three months (and more often if viral load becomes detectable on the below-50 assay). Both see any increase as reason to immediately run a second test.

A confirmed increase to as low as 100 copies is enough to make them consider adding or substituting drugs-- especially for those patients on their first or second regimen, who have several treatment options left.

But some AIDS docs challenge this quick-change approach. "Treating a small increase as an emergency is an entirely inappropriate response," says Joseph Sonnabend, a longtime AIDS specialist in New York City. "Many of my patients have had viral load blips that later disappeared or stabilized. In fact, some patients are still doing well with a 5,000 count. What matters is the trend-- is it stable or steadily increasing? If you respond to each blip, you risk exhausting the limited available treatments, while needlessly terrorizing the patient for strictly theoretical reasons."

Is "failure" failure?

"For people who don't have options, the question is, once viral load becomes detectable, is it better to stop therapy to try to keep from accumulating more mutations?" says Cheng. The answer? "Nobody knows." Deeks' research at the University of California at San Francisco has found that a regimen can help even after most docs would say it has "failed." In his study, the CD4 cells of patients on a successful protease inhibitor regimen had an average half-life of 77 days, compared to only 24 days for those of untreated PWAs. But with PWAs who maintained their regimen even after viral rebound, their CD4 cells had a half-life of 43 days.

Some researchers theorize that the mutations required for HIV to escape protease inhibitors may have made it less deadly to CD4 cells.

Ballpark figures

Ward calls viral load "a real soft test" with varying results. "You could run the same tube of blood three times and get a variation of 5,000," he says. Plus, vaccinations or acute illnesses can skew the results. He urges patients to "look at the ballpark"-- the magnitude of the change in viral load. In the end, a viral load count is just one reading to consider along with other test results and treatment history.

For federal HIV treatment guidelines, go to www.hivatis.org/trtgdlns.html.

Editor's Note: from POZ


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