Auckland Clinical Studies, Auckland, New Zealand.
Antimicrob Agents Chemother. 2014;58(2):1136-45. doi: 10.1128/AAC.01515-13. Epub 2013 Dec 2.
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 ClinicalTrials.gov under registration no. NCT01185860.).
达诺瑞韦(DNV)是一种丙型肝炎病毒(HCV)蛋白酶抑制剂,与聚乙二醇干扰素 alfa-2a-利巴韦林联合用于初治 HCV 基因型 1(G1)感染患者时可实现高持续病毒学应答(SVR)率。本研究探讨了利托那韦增强型 DNV(DNVr)联合聚乙二醇干扰素 alfa-2a-利巴韦林在既往聚乙二醇干扰素-利巴韦林无应答的 G1 感染患者中的疗效和安全性。无应答者(第 12 周时 HCV RNA 水平降低<2log10)接受开放标签的 100mg 利托那韦和 100mg DNV(DNVr 100/100mg)每 12 小时(q12h)联合聚乙二醇干扰素 alfa-2a-利巴韦林治疗 12 周。所有获得早期病毒学应答(EVR;第 12 周时 HCV RNA 降低≥2log10)的患者继续接受聚乙二醇干扰素 alfa-2a-利巴韦林治疗;未获得 EVR 的患者停止所有研究药物。24 例既往无应答者入组;16 例(67%)患者感染 HCV G1b,8 例(33%)感染 G1a。96%的患者携带 IL28B 非 CC 基因型。24 周治疗后持续病毒学应答(SVR24)在 67%的患者中实现,G1b 感染患者(88%)高于 G1a 感染患者(25%)。通过 DNV 耐药相关变异(RAV)NS3 R155K 发生耐药相关突破的患者在 4/8 例 G1a 和 1/16 例 G1b 中出现。在 2/2 例 G1a 复发患者中也检测到 NS3 R155K。治疗耐受性良好。由于不良事件,有 2 例患者提前退出研究药物。报告了 2 例严重不良事件;均发生在 DNVr 治疗完成后,被认为与治疗无关。未观察到 3 级或 4 级丙氨酸氨基转移酶(ALT)升高。DNVr 联合聚乙二醇干扰素 alfa-2a-利巴韦林在既往无应答的 G1b 感染患者中显示出高 SVR24 率,且耐受性良好。(本研究已在 ClinicalTrials.gov 注册,注册号为 NCT01185860。)