Service d'Hépatologie, Hôpital Saint-Antoine, APHP, UPMC Paris 6, Paris, France.
Liver Int. 2015 Jan;35 Suppl 1:18-20. doi: 10.1111/liv.12722.
Second wave direct acting antivirals such as sofosbuvir, simeprevir and daclatasvir can be combined with pegylated interferon alpha and ribavirin (PEG-IFN/RBV) as triple therapy in patients with hepatitis C virus (HCV) infection. In patients with HCV genotype 1 (HCV-1), a PEG-IFN/RBV-based regimen with sofosbuvir is highly effective but the presence of cirrhosis and the non-CC IFNL3 genotype have been associated with a poorer response. A PEG-IFN/RBV-based regimen with simeprevir or daclatasvir is based on response-guided therapy and its efficacy depends on predictors of response to IFN. HCV-1 subtype is also a major predictor of response. In HCV-1a infected patients, the K80Q mutation in NS3 or the presence of NS5A variants at baseline are associated with poor response with simeprevir- or daclatasvir-containing regimens respectively. Thus, these regimens should be only used in HCV-1b patients with good predictors of response to IFN.
第二代直接作用抗病毒药物如索非布韦、西美瑞韦和达卡他韦可与聚乙二醇干扰素α和利巴韦林(PEG-IFN/RBV)联合用于丙型肝炎病毒(HCV)感染患者的三联治疗。在 HCV-1 型(HCV-1)患者中,基于 PEG-IFN/RBV 的索非布韦方案具有很高的疗效,但肝硬化的存在和非 CC IFNL3 基因型与较差的反应相关。基于西美瑞韦或达卡他韦的 PEG-IFN/RBV 方案基于应答指导治疗,其疗效取决于对 IFN 反应的预测因素。HCV-1 亚型也是反应的主要预测因素。在 HCV-1a 感染患者中,NS3 中的 K80Q 突变或基线时 NS5A 变异的存在分别与西美瑞韦或达卡他韦方案的不良反应相关。因此,这些方案仅应在对 IFN 反应有良好预测因素的 HCV-1b 患者中使用。