Department of Hepatology, Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Tokyo, Japan.
Liver Research Laboratory, Toranomon Hospital, Tokyo, Japan.
J Med Virol. 2017 Jan;89(1):91-98. doi: 10.1002/jmv.24592. Epub 2016 Jun 8.
The combination of daclatasvir and asunaprevir is efficacious in the treatment of hepatitis C virus (HCV) infection, but its efficacy and predictors of efficacy in the elderly (≥70 years) remain unclear. In this study, 844 patients with chronic HCV genotype 1b infection, were treated with daclatasvir (60 mg once daily) plus asunaprevir (100 mg twice daily) for 24 weeks. Using the intention-to-treat analysis, the sustained virological response (SVR) rates were 87% and 88% for all 844 patients and 411 elderly (>70 years of age), respectively. In both groups, multivariate analysis identified NS5A-Y93H mutation (<20%), pretreatment (failure of treatment except for triple therapy with simeprevir, or treatment naive), and level of viremia (<6.0 log IU/ml) as independent predictors of SVR. Direct sequencing showed a significantly higher rate of NS3-D168 mutation at baseline in non-responders to triple therapy with simeprevir (44%) than others (2%). Alfa-fetoprotein (AFP) level and liver stiffness were significantly lower after end of treatment than at baseline, in both the SVR and non-SVR groups. In conclusion, daclatasvir-asunaprevir combination achieved high SVR in HCV genotype 1b patients, including elderly patients. Viral factors negatively influenced the response to treatment. Treatment improved AFP level and liver stiffness (surrogate markers of hepatocellular carcinoma), regardless of treatment efficacy. J. Med. Virol. 89:91-98, 2017. © 2016 Wiley Periodicals, Inc.
达卡他韦与asunaprevir 的联合治疗方案对丙型肝炎病毒(HCV)感染有效,但在老年人(≥70 岁)中的疗效及其疗效预测因素仍不清楚。在这项研究中,844 例慢性 HCV 基因型 1b 感染患者接受达卡他韦(60mg 每日 1 次)加asunaprevir(100mg 每日 2 次)治疗 24 周。采用意向治疗分析,844 例患者的持续病毒学应答(SVR)率分别为 87%和 88%,411 例年龄较大(>70 岁)患者的 SVR 率分别为 87%和 88%。在两组中,多变量分析确定 NS5A-Y93H 突变(<20%)、治疗前(除三药联合simeprevir 治疗失败或治疗初治外)和病毒载量(<6.0 log IU/ml)为 SVR 的独立预测因素。直接测序显示,simeprevir 三药联合治疗无应答者基线时 NS3-D168 突变率显著高于其他患者(44%比 2%)。在 SVR 和非 SVR 组中,治疗结束后 AFP 水平和肝硬度均显著低于基线。结论:达卡他韦- asunaprevir 联合方案在 HCV 基因型 1b 患者中,包括老年患者中,取得了较高的 SVR。病毒因素对治疗反应有负面影响。无论治疗效果如何,治疗均可改善 AFP 水平和肝硬度(肝癌的替代标志物)。J. Med. Virol. 89:91-98, 2017. © 2016 Wiley Periodicals, Inc.