SF AIDS Ward 86 - 25 years of saving lives San Francisco Chronicle, USA - HIV is a particularly agile virus, said Havlir, but a medical watershed occurred in 1996 with the introduction of combination anti-retroviral therapy, ...
Researcher to lecture in Palm Springs on AIDS therapy The Desert Sun, CA - Rossi will be one of the featured speakers Thursday at the City of Hope's Research Advances in HIV/AIDS Community Forum at Hotel Zoso in Palm Springs. ...
New Data Shows HIV Therapy Tipranavir (Aptivus) Is Effective And ... Medical News Today (press release), UK - Aug 5, 2008 ... study show that Aptivus? enabled the children to achieve sustained virologic and immunologic responses and was a well-tolerated antiretroviral therapy. ...
Why Treatment Isn't Effective For HIV Science Daily (press release) - 7, 2008) ? University of Minnesota researchers have answered a key question as to why antiretroviral therapy isn't effective in restoring immunity in ...
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Source: Google Scholar
HIV/AIDS trial: continuous antiretroviral therapy superior to episodic therapy
The enrollment into a large international HIV/AIDS trial comparing continuous antiretroviral therapy with episodic drug treatment guided by levels of CD4+ cells has been stopped.
Enrollment was stopped because those patients receiving episodic therapy had twice the risk of disease progression ( the development of clinical AIDS or death ), the major outcome of the study
The trial, known as Strategies for Management of Anti-Retroviral Therapy, or SMART, was designed to determine which of two different HIV treatment strategies would result in greater overall clinical benefit. HIV-positive volunteers were assigned at random to either a viral suppression strategy, in which antiretroviral therapy ( ART ) was taken on an ongoing basis to suppress HIV viral load; or a drug conservation strategy, in which ART was started only when the levels of key immune cells, called CD4+ cells, dropped below 250 cells per cubic millimetre. Volunteers in the drug conservation group were taken off ART--with the aims of reducing drug side effects and preserving treatment options--whenever their CD4+ cells were above 350 cells/mm3.
The trial involved an international collaboration of 318 clinical sites in 33 countries.
It began enrollment in January 2002 and had successfully recruited more than 90 percent of its target of 6,000 participants: as of January 11, 2006, when enrollment was stopped, 5,472 volunteers had joined the study.
At the time of the DSMB review, the average follow-up was approximately 15 months. The analysis revealed that participants on CD4+ cell-guided episodic treatment faced more than twice the risk of disease progression relative to participants on continuous ART.
Furthermore, there was an increase in major complications such as cardiovascular, kidney and liver diseases in the participants on the drug conservation arm.
These complications have been associated with ART, and it was hoped that they would be seen less frequently in those patients receiving less drug.
Although the risk-to-benefit ratio of drug conservation over the longer term remains uncertain, the DSMB recommended that enrollment into the trial be halted in light of the findings to date, and the SMART Executive Committee and NIAID ( National Institute of Allergy and Infectious Diseases ) agreed with the recommendation. Upon reviewing the results, the Executive Committee also conveyed to local study investigators its recommendation that it would be prudent to re-initiate therapy in ART-experienced patients in the drug conservation arm. All study physicians and participants are being notified of the findings and recommendations.
Follow-up visits will continue for all participants in the SMART trial while the study team considers plans for longer follow-up.
The investigators will analyze the SMART study data in detail to gain insights into the reasons for the increased risk.
" This trial was designed to help physicians and their HIV-positive patients identify the best approach to treatment management," adds Wafaa El-Sadr, of the Harlem Hospital Center and Columbia University in New York City, one of the principal investigators for the trial. " We were surprised to learn that in the short term, episodic antiretroviral therapy carries such an increased risk without evidence of sparing patients the known side effects associated with ART."
The SMART study was coordinated by four international centers: the Medical Research Council Clinical Trials Unit in London; the Copenhagen HIV Program in Denmark; the National Centre in HIV Epidemiology and Clinical Research at the University of New South Wales in Sydney, Australia; and the Terry Beirn Community Programs for Clinical Research on AIDS ( CPCRA ) in Washington, DC.
