Retreatment of patients with chronic hepatitis C, subtype 3a, and cirrhosis, who previously failed a regimen containing second-generation NS5A inhibitors with sofosbuvir + glecaprevir/pibrentasvir and ribavirin for 16-24 weeks.

IF 3.8 2区 医学 Q2 VIROLOGY Journal of Virology Pub Date : 2025-02-25 Epub Date: 2025-01-22 DOI:10.1128/jvi.01843-24
Sergii V Fedorchenko, Zhanna Klimenko, Tatiana Martynovich, Iryna Solianyk, Tatiana Suprunenko
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引用次数: 0

Abstract

The outcomes of retreatment patients infected with hepatitis C virus genotype 3, cirrhosis, with velpatasvir may be affected by treatment failure with velpatasvir. The efficacy of SOF+GLE/PIB+RIB 16-24 weeks of treatment has been shown. The presence of NS5A resistance-associated substitution mutations, including Y93H, and the number and regimens of the past failed therapy do not influence the likelihood of achieving sustained virological response. When velpatasvir treatment fails, pibrentasvir should be used as the first choice for retreatment.

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慢性丙型肝炎,3a亚型和肝硬化患者,先前失败的第二代NS5A抑制剂sofosbuvir + glecaprevir/pibrentasvir和利巴韦林治疗16-24周。
3型丙型肝炎病毒感染、肝硬化患者再用维帕他韦治疗失败可能影响其预后。SOF+GLE/PIB+RIB治疗16-24周的疗效已得到证实。NS5A耐药相关替代突变(包括Y93H)的存在,以及过去失败治疗的数量和方案不影响实现持续病毒学应答的可能性。当维帕他韦治疗失败时,应首选吡布伦他韦进行再治疗。
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来源期刊
Journal of Virology
Journal of Virology 医学-病毒学
CiteScore
10.10
自引率
7.40%
发文量
906
审稿时长
1 months
期刊介绍: Journal of Virology (JVI) explores the nature of the viruses of animals, archaea, bacteria, fungi, plants, and protozoa. We welcome papers on virion structure and assembly, viral genome replication and regulation of gene expression, genetic diversity and evolution, virus-cell interactions, cellular responses to infection, transformation and oncogenesis, gene delivery, viral pathogenesis and immunity, and vaccines and antiviral agents.
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