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Interferon‐α/β for treatment of chronic hepatitis C infection in the era of direct‐acting antiviral agents
Author(s) -
Enomoto Masaru,
Tamori Akihiro,
Murakami Yoshiki,
Kawada Norifumi
Publication year - 2014
Publication title -
hepatology research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.123
H-Index - 75
eISSN - 1872-034X
pISSN - 1386-6346
DOI - 10.1111/hepr.12289
Subject(s) - ribavirin , medicine , hepatocellular carcinoma , regimen , interferon , hepatitis c , hepatitis c virus , drug resistance , immunology , antiviral drug , drug , combination therapy , virology , pharmacology , virus , biology , microbiology and biotechnology
Type I interferons ( IFN ‐α/β), with or without ribavirin, have been the only agents that can eradicate the hepatitis C virus ( HCV ). An IFN ‐free regimen combining oral direct‐acting antiviral agents ( DAA ) will be approved soon for genotype 1 patients. Here, we discuss the role of IFN ‐α/β in the forthcoming “era of DAA ” with consideration of limitations and concerns about IFN ‐free therapies. First, the therapeutic efficacy of first‐generation DAA varies among the different subtypes. While the rate of sustained virological response ( SVR ) is 60–90% among patients with genotype 1b, the rate often falls short of 50% in patients with genotype 1a. IFN and ribavirin can still be indicated for patients with genotype 1a as a platform for combination with DAA . Second, there is concern about the emergence of drug‐resistance resulting from inappropriate use of DAA . The clinical significance of pre‐existing resistant variants has not been elucidated. Drug resistance may affect the efficacy of next‐generation treatments. An IFN and ribavirin backbone in combination with DAA is an effective measure to prevent the emergence of drug resistance and/or to suppress pre‐existing resistant viruses. Third, it remains unknown whether the incidence of hepatocellular carcinoma ( HCC ) will be reduced in patients who achieve SVR with IFN ‐free regimens. In contrast, there are many reports in J apan demonstrating the preventive effects of IFN on the development of HCC . When patients do not achieve SVR with first‐generation DAA , low‐dose IFN maintenance therapy is a treatment option until the next‐generation therapy with pan‐genotypic potency and high genetic barrier become available.