Timing of Antiretroviral Therapy for HIV-1 Infection and Tuberculosis

Diane V. Havlir(University of California, San Francisco), Michelle A. Kendall(Harvard University), Prudence Ive(University of the Witwatersrand), Johnstone Kumwenda, Susan Swindells(University of Nebraska at Omaha), Sarojini S. Qasba(Montgomery County Department of Health and Human Services), Anne F. Luetkemeyer(University of California, San Francisco), Evelyn Hogg(Social and Scientific Systems (United States)), James F. Rooney(Gilead Sciences (United States)), Xingye Wu(Harvard University), Mina C. Hosseinipour, Umesh Lalloo(University of KwaZulu-Natal), Valdiléa G. Veloso(Instituto Evandro Chagas), Fatuma Some(Moi University), N. Kumarasamy(Voluntary Health Services Hospital), Nesri Padayatchi(Centre for the AIDS Programme of Research in South Africa), Breno Santos(Hospital Nossa Senhora da Conceição), Stewart E. Reid(Centre for Infectious Disease Research in Zambia), James Hakim(Parirenyatwa Hospital), Lerato Mohapi(Chris Hani Baragwanath Hospital), Peter Mugyenyi(Joint Clinical Research Centre), Jorge Sánchez, Javier R. Lama, Jean W. Pape, Alejandro Sanchez(University of Southern California), Aida Asmelash(Botswana Harvard AIDS Institute Partnership), E. Moko(Botswana Harvard AIDS Institute Partnership), Fred Sawe(Kenya Medical Research Institute), Janet Andersen(Harvard University), Ian Sanne(University of the Witwatersrand)
New England Journal of Medicine
October 19, 2011
Cited by 538Open Access
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Abstract

BACKGROUND: Antiretroviral therapy (ART) is indicated during tuberculosis treatment in patients infected with human immunodeficiency virus type 1 (HIV-1), but the timing for the initiation of ART when tuberculosis is diagnosed in patients with various levels of immune compromise is not known. METHODS: We conducted an open-label, randomized study comparing earlier ART (within 2 weeks after the initiation of treatment for tuberculosis) with later ART (between 8 and 12 weeks after the initiation of treatment for tuberculosis) in HIV-1 infected patients with CD4+ T-cell counts of less than 250 per cubic millimeter and suspected tuberculosis. The primary end point was the proportion of patients who survived and did not have a new (previously undiagnosed) acquired immunodeficiency syndrome (AIDS)-defining illness at 48 weeks. RESULTS: A total of 809 patients with a median baseline CD4+ T-cell count of 77 per cubic millimeter and an HIV-1 RNA level of 5.43 log(10) copies per milliliter were enrolled. In the earlier-ART group, 12.9% of patients had a new AIDS-defining illness or died by 48 weeks, as compared with 16.1% in the later-ART group (95% confidence interval [CI], -1.8 to 8.1; P=0.45). Among patients with screening CD4+ T-cell counts of less than 50 per cubic millimeter, 15.5% of patients in the earlier-ART group versus 26.6% in the later-ART group had a new AIDS-defining illness or died (95% CI, 1.5 to 20.5; P=0.02). Tuberculosis-associated immune reconstitution inflammatory syndrome was more common with earlier ART than with later ART (11% vs. 5%, P=0.002). The rate of viral suppression at 48 weeks was 74% and did not differ between the groups (P=0.38). CONCLUSIONS: Overall, earlier ART did not reduce the rate of new AIDS-defining illness and death, as compared with later ART. In persons with CD4+ T-cell counts of less than 50 per cubic millimeter, earlier ART was associated with a lower rate of new AIDS-defining illnesses and death. (Funded by the National Institutes of Health and others; ACTG A5221 ClinicalTrials.gov number, NCT00108862.).


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