Current therapy for chronic hepatitis C: The role of direct-acting antivirals

被引:124
作者
Li, Guangdi [1 ]
De Clercq, Erik [2 ]
机构
[1] Cent South Univ, Natl Clin Res Ctr Metab Dis,Xiangya Hosp 2, Metab Syndrome Res Ctr,Key Lab Diabet Immunol, Dept Metab & Endocrinol, Changsha 410011, Hunan, Peoples R China
[2] KU Leuven Univ Leuven, Rega Inst Med Res, Dept Microbiol & Immunol, Minderbroedersstr 10, B-3000 Leuven, Belgium
关键词
Direct-acting antivirals; NS3/4A drugs; NS5A drugs; NS5B drugs; VIRUS GENOTYPE 1; SOFOSBUVIR PLUS RIBAVIRIN; TREATMENT-NAIVE PATIENTS; TREATMENT-EXPERIENCED PATIENTS; NS3/4A PROTEASE INHIBITOR; HCV NS5A INHIBITOR; PREVIOUSLY TREATED PATIENTS; FIXED-DOSE COMBINATION; IN-VITRO ACTIVITY; SUSTAINED VIROLOGICAL RESPONSE;
D O I
10.1016/j.antiviral.2017.02.014
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
One of the most exciting developments in antiviral research has been the discovery of the direct-acting antivirals (DAAs) that effectively cure chronic hepatitis C virus (HCV) infections. Based on more than 100 clinical trials and real-world studies, we provide a comprehensive overview of FDA-approved therapies and newly discovered anti-HCV agents with a special focus on drug efficacy, mechanisms of action, and safety. We show that HCV drug development has advanced in multiple aspects: (i) interferon-based regimens were replaced by interferon-free regimens; (ii) genotype-specific drugs evolved to drugs for all HCV genotypes; (iii) therapies based upon multiple pills per day were simplified to a single pill per day; (iv) drug potency increased from moderate (similar to 60%) to high (>90%) levels of sustained virologic responses; (v) treatment durations were shortened from 48 to 12 or 8 weeks; and (vi) therapies could be administered orally regardless of prior treatment history and cirrhotic status. However, despite these remarkable achievements made in HCV drug discovery, challenges remain in the management of difficult-to-treat patients. (C) 2017 Published by Elsevier B.V.
引用
收藏
页码:83 / 122
页数:40
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