Department of Gastroenterology and Metabology, Ehime University Graduate School of Medicine, Toon, Ehime, Japan.
Center for Liver-Biliary-Pancreatic Diseases, Matsuyama Red Cross Hospital, Matsuyama, Ehime, Japan.
J Med Virol. 2017 Sep;89(9):1567-1573. doi: 10.1002/jmv.24776. Epub 2017 May 23.
The tolerability and efficacy of sofosbuvir and ribavirin in patients infected with hepatitis C virus (HCV) genotype 2 were investigated under actual clinical conditions. A total of 208 patients with chronic HCV genotype 2 infection were treated with sofosbuvir 400 mg and ribavirin (weight-based dosing) for 12 weeks. Treatment discontinuation and sustained virological response 12 (SVR12) were evaluated. Moreover, factors associated with SVR12, hemoglobin decreasing to less than 10 g/dL during treatment, and alanine aminotransferase (ALT) non-normalization after treatment were evaluated. In all patients, SVR12 responses were 96.1% (200/208). About 6 of 8 patients (3.8%) who did not achieve SVR12 were re-treatment patients, and eight patients who did not achieve SVR all had liver cirrhosis. Multivariate analysis also identified body mass index (OR = 0.79; P < 0.001), platelet count (OR = 0.88; P = 0.003), and estimated glomerular filtration rate (eGFR) (OR = 0.96; P = 0.007) as independent contributing factors associated with hemoglobin decreasing to less than 10 g/dL during treatment, and only Mac-2 Binding Protein Glycosylation isomer (M2BpGi) (OR = 2.46; P = 0.017) as an independent contributing factor associated with ALT non-normalization after treatment. Cirrhotic patients may have a relatively high rate of treatment failure. In patients whose M2BpGi levels are elevated, their ALT tended to not normalize after treatment completion. These patients who did not achieve normalization of ALT after sofosbuvir plus RBV treatment need more careful observation for emergence of hepatocellular carcinoma even after achievement of SVR.
在实际临床情况下,研究了索非布韦和利巴韦林在感染丙型肝炎病毒(HCV)基因型 2 的患者中的耐受性和疗效。208 例慢性 HCV 基因型 2 感染患者接受索非布韦 400mg 和利巴韦林(基于体重的剂量)治疗 12 周。评估了治疗停药和 12 周持续病毒学应答(SVR12)。此外,还评估了与 SVR12 相关的因素、治疗期间血红蛋白降至 10g/dL 以下以及治疗后丙氨酸氨基转移酶(ALT)未正常化的因素。在所有患者中,SVR12 反应率为 96.1%(200/208)。约 6 例(3.8%)未达到 SVR12 的患者为再治疗患者,而所有未达到 SVR 的 8 例患者均患有肝硬化。多变量分析还确定了体重指数(OR=0.79;P<0.001)、血小板计数(OR=0.88;P=0.003)和估计肾小球滤过率(eGFR)(OR=0.96;P=0.007)是与治疗期间血红蛋白降至 10g/dL 以下相关的独立因素,而只有 Mac-2 结合蛋白糖基化异构体(M2BpGi)(OR=2.46;P=0.017)是与治疗后 ALT 未正常化相关的独立因素。肝硬化患者可能有较高的治疗失败率。在 M2BpGi 水平升高的患者中,他们的 ALT 在治疗完成后往往不会正常化。在索非布韦联合 RBV 治疗后未能使 ALT 正常化的这些患者,即使在达到 SVR 后,也需要更仔细地观察肝细胞癌的发生。