Journal article
Abacavir/Lamivudine Versus Tenofovir DF/Emtricitabine as Part of Combination Regimens for Initial Treatment of HIV: Final Results
The Journal of infectious diseases, Vol.204(8), pp.1191-1201
10/15/2011
DOI: 10.1093/infdis/jir505
PMCID: PMC3173503
PMID: 21917892
Abstract
(See the editorial commentary by Hull and Montaner, on pages
1154–6
.)
Background.
AIDS Clinical Trials Group A5202 compared blinded abacavir/lamivudine (ABC/3TC) to tenofovir DF/emtricitabine (TDF/FTC) with efavirenz (EFV) or atazanavir/ritonavir (ATV/r) in human immunodeficiency virus (HIV)-infected treatment-naive patients, stratified by screening HIV RNA (< or ≥10
5
copies/mL). Due to higher virologic failure with ABC/3TC in the high HIV RNA stratum, blinded treatment was stopped in this group, but study follow-up continued for all patients.
Methods.
Primary endpoints were times to virologic failure, regimen modification, and safety event.
Results.
In the low HIV RNA stratum, time to virologic failure was similar for ABC/3TC vs TDF/FTC with ATV/r (hazard ratio [HR] 1.25, 95% confidence interval [CI] 0.76, 2.05) or EFV (HR 1.23, 95% CI 0.77, 1.96), with significantly shorter times to regimen modification for ABC/3TC with EFV or ATV/r and to safety events with EFV. Prior to stopping blinded treatment in the high stratum, higher virologic failure rates were seen with ABC/3TC with EFV (HR 2.46, 95% CI 1.20, 5.05) or ATV/r (HR 2.22, 95% CI 1.19, 4.14).
Conclusions.
In the low HIV RNA stratum, times to virologic failure for ABC/3TC or TDF/FTC were not different with EFV or ATV/r. In the high stratum, virologic failure rate was significantly higher for ABC/3TC than for TDF/FTC when given with either EFV or ATV/r.
Details
- Title: Subtitle
- Abacavir/Lamivudine Versus Tenofovir DF/Emtricitabine as Part of Combination Regimens for Initial Treatment of HIV: Final Results
- Creators
- Paul E Sax - Division of Infectious Diseases, Department of Medicine, Brigham and Women’s Hospital, Harvard Medical School, andCamlin Tierney - Department of Biostatistics, Harvard School of Public Health, Boston, MassachusettsAnn C Collier - University of Washington School of Medicine, Harborview Medical Center, SeattleEric S Daar - Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center, the University of CaliforniaKatie Mollan - Department of Biostatistics, Harvard School of Public Health, Boston, MassachusettsChakra Budhathoki - Department of Biostatistics, Harvard School of Public Health, Boston, MassachusettsCatherine Godfrey - The Division of AIDS, National Institute of Allergy and Infectious Diseases, Bethesda, MarylandNasreen C Jahed - Social & Scientific Systems, Inc., Silver Spring, MarylandLaurie Myers - Frontier Science & Technology Research Foundation, Amherst, New YorkDavid Katzenstein - Stanford University, Palo Alto, CaliforniaAwny Farajallah - Bristol-Myers Squibb, Plainsboro, New JerseyJames F Rooney - Gilead Sciences, Foster City, CaliforniaBelinda Ha - GlaxoSmithKline, Research Triangle Park, North CarolinaWilliam C Woodward - Abbott Laboratories, IllinoisJudith Feinberg - University of Cincinnati, Cincinnati, OhioKaren Tashima - Brown University, Providence, Rhode IslandRobert L Murphy - Northwestern University, Chicago, IllinoisMargaret A Fischl - University of Miami School of Medicine, FloridaAIDS Clinical Trials Group Study
- Contributors
- Jeffery L Meier (Contributor) - University of Iowa, Internal MedicineJack T Stapleton (Contributor) - University of Iowa, Internal Medicine
- Resource Type
- Journal article
- Publication Details
- The Journal of infectious diseases, Vol.204(8), pp.1191-1201
- DOI
- 10.1093/infdis/jir505
- PMID
- 21917892
- PMCID
- PMC3173503
- NLM abbreviation
- J Infect Dis
- ISSN
- 0022-1899
- eISSN
- 1537-6613
- Publisher
- Oxford University Press
- Language
- English
- Date published
- 10/15/2011
- Academic Unit
- Microbiology and Immunology; Infectious Diseases; Epidemiology; Internal Medicine
- Record Identifier
- 9984094330802771
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