Abstract

IntroductionCo-infection with Hepatitis C (HCV) and HIV is common and HIV accelerates hepatic disease progression due to HCV. However, access to HCV treatment is limited and success rates are generally poor.MethodsWe conducted a systematic review and meta-analysis to assess HCV treatment outcomes in observational cohorts. Two databases (Medline and EMBASE) were searched using a compound search strategy for cohort studies reporting HCV treatment outcomes (as determined by a sustained virological response, SVR) in HIV-positive patients initiating HCV treatment for the first time.Results40 studies were included for review, providing outcomes on 5339 patients from 17 countries. The pooled proportion of patients achieving SVR was 38%. Significantly poorer outcomes were observed for patients infected with HCV genotypes 1 or 4 (pooled SVR 24.5%), compared to genotypes 2 or 3 (pooled SVR 59.8%). The pooled proportion of patients who discontinued treatment due to drug toxicities (reported by 33 studies) was low, at 4.3% (3.3–5.3%). Defaulting from treatment, reported by 33 studies, was also low (5.1%, 3.5–6.6%), as was on-treatment mortality (35 studies, 0.1% (0–0.2%)).ConclusionsThese results, reported under programmatic conditions, are comparable to those reported in randomised clinical trials, and show that although HCV treatment outcomes are generally poor in HIV co-infected patients, those infected with HCV genotypes 2 or 3 have outcomes comparable to HIV-negative patients.

Highlights

  • Co-infection with Hepatitis C (HCV) and HIV is common and HIV accelerates hepatic disease progression due to HCV

  • A recent systematic review of clinical trials assessing HCV treatment outcomes in HIV co-infected patients reported that around 37% of patients achieve a sustained virological response (SVR) with pegylated interferon and ribavarin, with a lower success rate observed in patients infected with HCV genotypes 1 and 4 [6]

  • Clinical trials are appropriate for determining drug efficacy, outcomes may differ under programmatic conditions where adherence to treatment, patient and provider motivation and available resources may be limited [8]

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Summary

Introduction

Co-infection with Hepatitis C (HCV) and HIV is common and HIV accelerates hepatic disease progression due to HCV. A recent systematic review of clinical trials assessing HCV treatment outcomes in HIV co-infected patients reported that around 37% of patients achieve a sustained virological response (SVR) with pegylated interferon and ribavarin, with a lower success rate observed in patients infected with HCV genotypes 1 and 4 [6]. These outcomes are poorer than those seen in HIV negative patients [7]. We conducted a systematic review to assess the outcomes of HCV treatment in HIV co-infected patients in programmatic settings

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