Dissemin is shutting down on January 1st, 2025

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Public Library of Science, PLoS ONE, 3(11), p. e0151703, 2016

DOI: 10.1371/journal.pone.0151703

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Impact of Safety-Related Dose Reductions or Discontinuations on Sustained Virologic Response in HCV-Infected Patients: Results from the GUARD-C Cohort

Journal article published in 2016 by Study Group Guard-C., Lee Yn, Kr Rajender Reddy, Gentian Shabanaj, Arjan Harxhi, Mitchell L. Shiffman, Filip Van Der Meersch, Nawal Guessab, Nadir Mahindad, Hassene Mahiou, Alessandra Orlandini, Mulkay Jp, Hans Van Vlierberghe ORCID, Pierre Laukens, Veronique Lefebvre and other authors.
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Data provided by SHERPA/RoMEO

Abstract

BACKGROUND: Despite the introduction of direct-acting antiviral agents for chronic hepatitis C virus (HCV) infection, peginterferon alfa/ribavirin remains relevant in many resource-constrained settings. The non-randomized GUARD-C cohort investigated baseline predictors of safety-related dose reductions or discontinuations (sr-RD) and their impact on sustained virologic response (SVR) in patients receiving peginterferon alfa/ribavirin in routine practice. METHODS: A total of 3181 HCV-mono-infected treatment-naive patients were assigned to 24 or 48 weeks of peginterferon alfa/ribavirin by their physician. Patients were categorized by time-to-first sr-RD (Week 4/12). Detailed analyses of the impact of sr-RD on SVR24 (HCV RNA