Kwo Paul Y, Badshah Maaz B
Department of Medicine, Division of Gastroenterology/Hepatology, Indiana University School of Medicine, 975 W. Walnut, IB 327, Indianapolis, IN, 46202-5121, USA,
Curr Gastroenterol Rep. 2015 Oct;17(10):462. doi: 10.1007/s11894-015-0462-0.
The addition of the first direct-acting antiviral agents, the NS3 protease inhibitors boceprevir or telaprevir, to peg interferon and ribavirin was a major advance in the treatment of genotype 1 hepatitis C individuals with sustained virological response (SVR) rates of 63-75 %. Those who did not achieve SVR had high rates of resistance-associated variants against NS3 protease domain. Retreatment options for those who have failed first-generation protease inhibitors generally are guided by retreatment with direct-acting antiviral agents from other classes. Phase 2 and phase 3 data have demonstrated that retreatment with 12-24 weeks of a NS5B inhibitor (sofosbuvir) in combination with a NS5a inhibitor (daclatasvir or ledipasvir) with or without ribavirin can achieve SVR at high rates comparable to treatment-naive individuals.
在聚乙二醇干扰素和利巴韦林的基础上添加首批直接作用抗病毒药物——NS3蛋白酶抑制剂博赛匹韦或特拉匹韦,是治疗基因1型丙型肝炎患者的一项重大进展,持续病毒学应答(SVR)率达到63%-75%。未实现SVR的患者中,针对NS3蛋白酶结构域的耐药相关变异率很高。第一代蛋白酶抑制剂治疗失败患者的再治疗方案通常以使用其他类别的直接作用抗病毒药物进行再治疗为指导。2期和3期数据表明,使用NS5B抑制剂(索磷布韦)联合NS5a抑制剂(达卡他韦或来迪帕司韦)治疗12-24周,无论是否联合利巴韦林,均可实现较高的SVR率,与初治患者相当。