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Efficacy and Safety of Danoprevir-Ritonavir plus Peginterferon Alfa-2a–Ribavirin in Hepatitis C Virus Genotype 1 Prior Null Responders

机译:Danoprevir-Ritonavir加上Peginterferon Alfa-2a-Ribavirin在C型肝炎病毒基因型1先前无效反应者中的疗效和安全性

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摘要

Danoprevir (DNV) is a hepatitis C virus (HCV) protease inhibitor that achieves high sustained virologic response (SVR) rates in combination with peginterferon alfa-2a–ribavirin in treatment-naive HCV genotype 1 (G1)-infected patients. This study explored the efficacy and safety of ritonavir-boosted DNV (DNVr) plus peginterferon alfa-2a–ribavirin in G1-infected prior peginterferon-ribavirin null responders. Null responders (<2-log10 reduction in HCV RNA level at week 12) were given an open-label combination of 100 mg of ritonavir and 100 mg of DNV (100/100 mg DNVr) every 12 h (q12h) plus peginterferon alfa-2a–ribavirin for 12 weeks. All patients achieving an early virologic response (EVR; ≥2-log10 decrease in HCV RNA by week 12) continued treatment with peginterferon alfa-2a–ribavirin; those without an EVR discontinued all study drugs. Twenty-four prior null responders were enrolled; 16 patients (67%) were infected with HCV G1b, and 8 (33%) were infected with G1a. Ninety-six percent of patients had an IL28B non-CC genotype. A sustained virologic response at 24 weeks posttreatment (SVR24) was achieved in 67% of patients, with a higher rate in G1b-infected (88%) than G1a-infected (25%) patients. Resistance-related breakthrough occurred in 4/8 G1a and 1/16 G1b patients through the DNV resistance-associated variant (RAV) NS3 R155K. NS3 R155K was also detected in 2/2 G1a patients who relapsed. Treatment was well tolerated. Two patients withdrew prematurely from study medications due to adverse events. Two serious adverse events were reported; both occurred after completion of DNVr therapy and were considered unrelated to treatment. No grade 3 or 4 alanine aminotransferase (ALT) elevations were observed. DNVr plus peginterferon alfa-2a–ribavirin demonstrated high SVR24 rates in HCV G1b-infected prior null responders and was well tolerated. (This study has been registered at under registration no. .)
机译:Danoprevir(DNV)是丙型肝炎病毒(HCV)蛋白酶抑制剂,在未接受过治疗的HCV基因型1(G1)感染患者中,与聚乙二醇干扰素alfa-2a-利巴韦林联用可达到较高的持续病毒学应答(SVR)率。这项研究探讨了利托那韦增强的DNV(DNVr)加聚乙二醇干扰素α-2a-利巴韦林在G1感染的先前聚乙二醇干扰素-利巴韦林无效反应者中的疗效和安全性。空反应者(第12周时HCV RNA水平降低<2-log10)每12小时(q12h)给予100 mg利托那韦和100 mg DNV(100/100 mg DNVr)的开放标签联合加聚乙二醇干扰素。 2a–利巴韦林治疗12周。所有达到早期病毒学应答(EVR;到第12周HCV RNA降低≥2-log10)的患者均继续接受聚乙二醇干扰素α-2a-利巴韦林治疗;没有EVR的患者停用所有研究药物。已有二十四名无效应答者参加; HCV G1b感染了16位患者(67%),G1a感染了8位(33%)。 96%的患者患有IL28B非CC基因型。 67%的患者在治疗后24周(SVR24)达到了持续的病毒学应答,感染G1b的患者(88%)高于感染G1a的患者(25%)。通过DNV耐药相关变异(RAV)NS3 R155K,在4/8 G1a和1/16 G1b患者中发生了耐药相关突破。在2/2 G1a复发患者中也检测到NS3 R155K。治疗耐受性良好。两名患者因不良事件而提前退出研究药物。报告了两个严重的不良事件。两者均在DNVr治疗完成后发生,并被认为与治疗无关。没有观察到3级或4级丙氨酸氨基转移酶(ALT)升高。 DNVr加上聚乙二醇干扰素α-2a-利巴韦林在HCV G1b感染的既往无效应答者中显示出较高的SVR24发生率,并且耐受性良好。 (本研究已在注册号。处注册。)

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