Isakov Vasily, Zhdanov Konstantin, Kersey Kathryn, Svarovskaia Evguenia, Massetto Benedetta, Zhu Yanni, Knox Steven J, Bakulin Igor, Chulanov Vladimir
Department of Gastroenterology and Hepatology, Institute of Nutrition of Russian Academy of Medical Sciences, Moscow, Russia.
Department of Infectious Diseases, Military Medical Academy, St Petersburg, Russia.
Antivir Ther. 2016;21(8):671-678. doi: 10.3851/IMP3065. Epub 2016 Jul 4.
In this Phase IIIb study, we evaluated the efficacy and safety of the oral nucleotide analogue inhibitor sofosbuvir plus ribavirin, with special attention given to viral resistance, in Russian patients with HCV genotype-1 or -3.
Treatment-naive patients with and without compensated cirrhosis were randomized (1:1) to receive 16 or 24 weeks of once-daily sofosbuvir 400 mg plus twice-daily oral ribavirin 1,000 or 1,200 mg/day. The primary efficacy end point was the proportion of patients with sustained viral response 12 weeks after the end of treatment (SVR12). Viral resistance testing was performed by deep sequencing on all baseline samples and for patients who experienced virological failure.
SVR12 rates for patients with genotype-1 HCV were 50% and 76% for those in the 16-week and 24-week groups, respectively, and for patients with genotype-3 HCV, SVR12 rates were 87% and 90% for patients in the 16-week and 24-weeks groups, respectively. Genotype-1 patients with the L159F resistance-associated variant who received 16 weeks of treatment had lower SVR12 rates than those without, but in patients who received 24 weeks of treatment, response rates were similar in those with and without L159F (80% versus 74%). Sofosbuvir plus ribavirin was well tolerated with no deaths, adverse event-related study drug discontinuations, or grade 3 or 4 adverse events, and few grade 3 or 4 laboratory abnormalities.
Sofosbuvir plus ribavirin for 16 or 24 weeks was associated with a high SVR rate in patients with HCV genotype-3. Among HCV genotype-1b patients, the presence of the L159F variant at baseline was associated with a lower SVR rate in those treated for 16 weeks but not in those treated for 24 weeks. Sofosbuvir plus ribavirin was safe and well tolerated regardless of treatment duration. Clinicaltrials.gov number NCT01896193.
在这项IIIb期研究中,我们评估了口服核苷酸类似物抑制剂索磷布韦联合利巴韦林在俄罗斯丙型肝炎病毒(HCV)1型或3型患者中的疗效和安全性,并特别关注病毒耐药性。
未接受过治疗的有或无代偿性肝硬化的患者按1:1随机分组,接受为期16周或24周的每日一次索磷布韦400mg联合每日两次口服利巴韦林1000或1200mg/天的治疗。主要疗效终点是治疗结束后12周持续病毒学应答(SVR12)的患者比例。对所有基线样本以及出现病毒学失败的患者进行深度测序以进行病毒耐药性检测。
HCV 1型患者16周组和24周组的SVR12率分别为50%和76%,HCV 3型患者16周组和24周组的SVR12率分别为87%和90%。携带L159F耐药相关变异的1型患者接受16周治疗后的SVR12率低于未携带该变异的患者,但接受24周治疗的患者中,有或无L159F变异的患者应答率相似(80%对74%)。索磷布韦联合利巴韦林耐受性良好,无死亡病例、因不良事件导致的研究药物停用或3级或4级不良事件,3级或4级实验室异常情况也很少。
索磷布韦联合利巴韦林治疗16周或24周在HCV 3型患者中与高SVR率相关。在HCV 1b型患者中,基线时存在L159F变异与接受16周治疗患者的较低SVR率相关,但与接受24周治疗患者无关。无论治疗持续时间如何,索磷布韦联合利巴韦林均安全且耐受性良好。Clinicaltrials.gov编号:NCT01896193。