Hepatology. 2011 Mar 3. doi: 10.1002/hep.24262. [Epub ahead of print]
Pawlotsky JM.
National Reference Center for Viral Hepatitis B, C and Delta, Department of Virology, Hôpital Henri Mondor, Université Paris-Est, Créteil, France; INSERM U955, Créteil, France. jean-michel.pawlotsky@hmn.aphp.fr.
Abstract
Current treatment of chronic hepatitis C virus infection is based on the combination of pegylated interferon-α and ribavirin. The recent development of direct-acting antiviral molecules active on hepatitis C virus, together with in vitro and in vivo studies showing that these drugs may lead to the selection of resistant viruses if administered alone, has raised concerns that resistance may undermine therapy based on direct acting antivirals. A new standard-of-care treatment will soon be available for both treatment-naïve and -experienced patients infected with hepatitis C virus genotype 1, based on a triple combination of pegylated interferon-α, ribavirin and a protease inhibitor, either telaprevir or boceprevir. With this therapy, most failures to eradicate infection in treatment-adherent patients are due to an inadequate response to pegylated interferon-α and ribavirin, in the context of a low genetic barrier to resistance of first-generation protease inhibitors. This article reviews patterns of resistance to hepatitis C virus direct acting antiviral drugs in development, the mechanisms underlying treatment failure when these drugs are combined with pegylated interferon-α and ribavirin, the consequences of treatment failure, and possible means of optimizing therapies using direct acting antivirals in the future. (HEPATOLOGY 2011.).
Copyright © 2011 American Association for the Study of Liver Diseases.
PMID: 21374691 [PubMed - as supplied by publisher]
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