JAIDS Journal of Acquired Immune Deficiency Syndromes · 2008 · 28 citations · 28 references
MedicinePharmacokineticsPharmacologyBioavailabilityClinical PharmacologyMolecular VirologyAntiretroviral TherapyAntiviral AgentsAntiviral PharmacologyAntiviral PharmacotherapyAntiviral ResistanceAntiviral TherapyAntiviral Safety AssessmentClinical Pharmacology EvidenceHiv Antiretroviral TherapyNucleoside Reverse Transcriptase InhibitorsProtease Inhibitor ResistanceProtease InhibitorsProtease Resistance ProfilesReverse Transcriptase Inhibitor Resistance
OBJECTIVE: When to start hepatitis C treatment in HIV/hepatitis C virus (HCV)-coinfected patients remains unresolved. Our objective was to determine if a baseline CD4 count >/=350 cells/mm predicts a sustained HCV response to pegylated interferon plus ribavirin. METHODS: We conducted a multicenter cohort study of HIV/HCV-coinfected patients treated for HIV in hospitals in Nice, Tourcoing, and Marseille (France). Sustained viral response (SVR) was defined as undetectable HCV RNA 24 weeks after treatment. The relation between CD4 cell count and SVR was examined separately for patients with HCV genotype 1 or non-1. RESULTS: One hundred seventy-five patients were included. In patients with HCV genotype 1, the rate of SVR was 13% and was not related to baseline CD4 cell count (odds ratio [OR] = 1.0, 95% confidence interval [CI]: 0.1 to 9.3). In patients with HCV genotype non-1, the rate of SVR was 46% and was not significantly increased by a baseline CD4 count >/=350 cells/mm (OR = 1.8, 95% CI: 0.6 to 5.9). CONCLUSIONS: Higher CD4 cell count at treatment initiation with pegylated interferon plus ribavirin did not improve treatment success probability, regardless of HCV genotype.
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Gilbert Greub, B Ledergerber, Manuel Battegay et al. · The Lancet · 2000 · 903 citations
Raymond T. Chung, Janet Andersen, Paul A. Volberding et al. · New England Journal of Medicine · 2004 · 873 citations · Full text