The importance of resistance to direct antiviral drugs in HCV infection in clinical practice

被引:340
作者
Sarrazin, Christoph [1 ]
机构
[1] JW Goethe Univ Hosp, Med Klin 1, D-60590 Frankfurt, Germany
关键词
Hepatitis C virus; Chronic hepatitis C; Direct-acting antiviral agents; Resistance-associated variants; Antiviral therapy; HEPATITIS-C-VIRUS; GENOTYPE; INFECTION; TREATMENT-NAIVE PATIENTS; NS3 PROTEASE INHIBITOR; TERM-FOLLOW-UP; REPLICATION COMPLEX INHIBITOR; SOFOSBUVIR PLUS RIBAVIRIN; DIRECT-ACTING ANTIVIRALS; INTERFERON-ALPHA; 2A; IN-VITRO RESISTANCE;
D O I
10.1016/j.jhep.2015.09.011
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Treatment of chronic hepatitis C virus (HCV) infection with direct-acting antiviral agents (DAA) is associated with high rates of sustained virologic response. Remaining factors associated with treatment failure include advanced stages of liver fibrosis, response to previous antiviral therapy and viral factors such as baseline viral load and suboptimal interaction of the DAA with the target based on viral variants. Heterogeneity within NS3, NS5A, and NS5B areas interacting with DAAs exist between HCV geno- and subtypes as well as HCV isolates of the same geno- and subtype and amino acid polymorphisms associated with suboptimal efficacy of DAAs are termed resistance-associated variants (RAVs). RAVs may be associated with virologic treatment failure. However, virologic treatment failure typically occurs only if other negative predictive host or viral factors are present at the same time, susceptibility to additional antiviral agents is reduced or duration of treatment is suboptimal. In this review geno- and phenotypic resistance testing as well as clinical data on the importance of RAVs for conventional triple therapies with sofosbuvir, simeprevir, and daclatasvir and available interferon-free DAA combinations are discussed. (C) 2015 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:486 / 504
页数:19
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