Hepatitis C Virus Resistance to Direct-Acting Antiviral Drugs in Interferon-Free Regimens

被引:418
作者
Pawlotsky, Jean-Michel [1 ,2 ]
机构
[1] Univ Paris Est, Hop Henri Mondor, Dept Virol, Natl Reference Ctr Viral Hepatitis BC&D, Creteil, France
[2] Hop Henri Mondor, INSERM, Unite 955, 51 Ave Marechal Lattre Tassigny, F-94010 Creteil, France
关键词
Resistance; Resistance-Associated Substitutions; Treatment Failure; Retreatment; DACLATASVIR PLUS ASUNAPREVIR; GENOTYPE; INFECTION; TREATMENT-NAIVE PATIENTS; TERM-FOLLOW-UP; BASE-LINE; GRAZOPREVIR/ELBASVIR PLUS; PEGYLATED INTERFERON; 1-INFECTED PATIENTS; VIROLOGICAL TOOLS; CLINICAL-TRIALS;
D O I
10.1053/j.gastro.2016.04.003
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Treatment of hepatitis C virus (HCV) infection has progressed considerably with the approval of interferon-free, direct-acting antiviral (DAA)-based combination therapies. Although most treated patients achieve virological cure, HCV resistance to DAAs has an important role in the failure of interferon-free treatment regimens. The presence of viral variants resistant to NS5A inhibitors at baseline is associated with lower rates of virological cure in certain groups of patients, such as those with genotype la or 3 HCV, those with cirrhosis, and/or prior nonresponders to pegylated interferon-based regimens. DAA-resistant HCV is generally dominant at virological failure (most often relapse). Viruses resistant to NS3-4A protease inhibitors disappear from peripheral blood in a few weeks to months, whereas NS5A inhibitor-resistant viruses persist for years. Re-treatment options are available, but first-line treatment strategies should be optimized to efficiently prevent treatment failure due to HCV resistance.
引用
收藏
页码:70 / 86
页数:17
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