| Literature DB >> 12001042 |
Milos Opravil1, Bernard Hirschel, Adriano Lazzarin, Hansjakob Furrer, Jean-Philippe Chave, Sabine Yerly, Leslie R Bisset, Marek Fischer, Pietro Vernazza, Enos Bernasconi, Manuel Battegay, Bruno Ledergerber, Huldrych Günthard, Colin Howe, Rainer Weber, Luc Perrin.
Abstract
This randomized study evaluated the efficacy and tolerability of continued treatment with protease inhibitor plus nucleoside-analogue combination regimens (n=79) or a change to the simplified regimen of abacavir-lamivudine-zidovudine (n=84) in patients with suppressed human immunodeficiency virus type 1 (HIV-1) RNA for > or = 6 months who did not have the reverse transcriptase 215 mutation. After a median follow-up of 84 weeks, virologic failure was 6% in the continuation and 15% in the simplified group (P=.081). Previous zidovudine monotherapy or dual therapy and archived reverse transcriptase resistance mutations in HIV-1 DNA at baseline were significant predictors of failure. Study treatment was discontinued because of adverse events in 20% of the continuation and 7% of the simplified group (P=.021). Simplification to abacavir-lamivudine-zidovudine significantly decreased nonfasting cholesterol and triglyceride levels; however, this switch strategy carries a risk of virologic failure when treatment history or resistance testing suggest the presence of archived resistance mutations to the simplified regimen.Entities:
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Year: 2002 PMID: 12001042 DOI: 10.1086/340312
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226