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Change in Official "When-To-Start" Recommendations

February 22, 2001

A note from TheBody.com: Since this article was written, the HIV pandemic has changed, as has our understanding of HIV/AIDS and its treatment. As a result, parts of this article may be outdated. Please keep this in mind, and be sure to visit other parts of our site for more recent information!


On the same day as the opening of the 8th Annual Retrovirus Conference, the National Institutes of Allergy and Infectious Disease (NIAID, a division of the National Institutes of Health [NIH]) issued revised HIV treatment guidelines. The prior guidelines advised that anti-HIV therapy should be considered, even when a person had no symptoms, if she or he has a T-cell count less than 500, or a viral load above 10,000 by bDNA, or 20,000 by PCR.

A growing awareness of the long-terms side effects of anti-HIV therapy, the evident inability of current medications to eradicate HIV, and the better-than-expected immune recovery observed in people who begin therapy with T-cell counts between 500 and 350 have led to the latest change in the guidelines. The guidelines now suggest that therapy be considered when the T-cell count is below 350, or the viral load is above 30,000 by bDNA, or 55,000 by PCR.

At Retrovirus, there were three presentations evaluating the impact of when anti-HIV therapy is begun. One presentation from the Swiss HIV Cohort purportedly showed a beneficial effect from initiating anti-HIV therapy when the T-cell count was above 350 (LB 6). However, this was a very poor study which retrospectively compared two very different groups of people, those who began therapy during a one year period when their T-cells were above 350, to a group who did not start therapy during that year, and the majority of who (82%) never received therapy. Obviously, the first group had fewer adverse clinical events such as AIDS-defining illness and death. The more appropriate comparison group would have been people who started anti-HIV therapy after more than a year, with T-cells below 350, but before they got sick. There was an interesting observation in this study that of the people who started therapy, 60% changed at least one drug in their regimen (29% due to side effects), and 20% stopped therapy completely. These findings illustrated the problems of tolerance and adherence with the regimens used during the time period of this study.

There were two other presentations (Abstracts 519 and 520), also retrospective cohort studies, which showed that there is a definite survival advantage for people to be on anti-HIV therapy if their T-cell count is below 200. They also showed a trend towards better clinical outcomes in people starting therapy with T-cell counts between 200 and 350, but no difference in people on or off therapy when their T-cells are above 350.

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In the study presented by Timothy Sterling, from Johns Hopkins University, it was observed that once you accounted for CD4 cell count, viral load did not predict clinical outcome. That study also showed that disease progression rates were worse in men, compared to women, in the group with under 200 T-cells. Dr. Sterling concluded that more emphasis should be placed on the T-cell count in determining when to start therapy and that it appears that anti-HIV therapy can be deferred until the T-cell count is "substantially lower than 500" (Abstract 519).

The other study was from the CDC's Adult and Adolescent Spectrum of Disease Project, which includes data from over 5,000 people, from 11 cities in the US, including Seattle (Abstract 520). They found that when anti-HIV therapy was deferred until after the T-cell count was below 200, there were more deaths. They also saw a trend, which did not reach statistical significance, for better outcomes in the group that started therapy when the T-cell count was between 200 and 350. There was no benefit observed for the group that began therapy with T-cell counts above 350. The bulk of the findings from these studies provide support for the change in the HIV treatment guidelines, but each one also shows the limitations in data acquired from retrospective analysis.

At the Retrovirus press conference, STEP asked Dr. Fauci, Director of NIAID, if he was concerned that insurers and HMOs might try to deny coverage for people who choose to begin anti-HIV therapy, or continue on therapy, when they have T-cell counts above 350. He said that the guidelines panel tries to make their recommendations on the best available data. They are aware of the possible misuse of the guidelines, but the guidelines clearly state that the decision to begin anti-HIV medications is a complex one and must be made on an individual basis, in consultation with a person and their healthcare provider.

Coincidentally, the week before Retrovirus, NIAID has apparently decided that it is not feasible to conduct a large, prospective, randomized "when-to-start" trial in the U.S. at this time. Rather, the NIH will be investigating the feasibility of gathering data from observational cohorts.

These groups of people will be followed closely, over a long period of time (5 or 10 years), and evaluated based on the when they initiated anti-HIV therapy and any clinical events, such as opportunistic infections or medication side effects, that occur.

To read the press release from the NIH regarding the change in guidelines, go to www.thebody.com/niaid/guidelines_update.html.


A note from TheBody.com: Since this article was written, the HIV pandemic has changed, as has our understanding of HIV/AIDS and its treatment. As a result, parts of this article may be outdated. Please keep this in mind, and be sure to visit other parts of our site for more recent information!



  
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This article was provided by Seattle Treatment Education Project. It is a part of the publication STEP Ezine.
 
See Also
Read the Guidelines for the Use of Antiretroviral Agents in HIV-1-Infected Adults and Adolescents (PDF)
More News and Analysis on HIV Treatment Guidelines

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