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Sofosbuvir and Ribavirin With or Without Pegylated Interferon for Hepatitis C Genotype 3: A Real World Experience

机译:索非布韦和利巴韦林联合或不联合聚乙二醇干扰素治疗丙型肝炎基因型3:真实世界的体验

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Background: Documentation of the effectiveness of sofosbuvir and ribavirin with or without pegylated interferon alfa for hepatitis C virus Genotype 3 (HCV GT3) is limited in a real world setting. Objectives: The present study aimed at examining the outcome of the above therapy in a real world setting. Methods: Dual therapy of sofosbuvir and ribavirin was given for 24 weeks and triple therapy with additional pegylated interferon for 12 weeks. Patients received dual therapy when there was unwillingness to take interferon or interferon ineligibility. Results: In this analysis, 241 patients were included, of whom 175 were treated with dual and 66 with triple therapy. The mean age of the patients was 46.6 years, ranging from 20 to 72, and 136 (56.4%) were male. Clinical cirrhosis was present in 151 (62.7%) patients, and 98 (40.7%) had treatment experience. HCV RNA became negative in 225 (93.3%) patients at week 4 of the treatment. End of treatment virologic response was observed in 221 (91.7%) patients, and 199 (82.6%) had sustained virologic response 12 weeks post treatment (SVR12). Undetectable HCV RNA at week 4 was an independent parameter predicting SVR12 (P = 0.001). SVR12 was achieved in 143 (81.7%) patients treated with dual therapy and 56 (84.8%) with triple therapy (P = 0.567). Prior HCV treatment status and presence or absence of cirrhosis did not significantly affect the outcome between the 2 treatment groups. Conclusions: Treatment of HCV GT3 infection with the sofosbuvir and ribavirin with or without PEG-IFNα achieved durable responses in a significant number of cases in a real world setting.
机译:背景:在现实环境中,索非布韦和利巴韦林联合或不联合聚乙二醇干扰素α对丙型肝炎病毒基因型3(HCV GT3)的有效性的文献有限。目的:本研究旨在在现实世界中检查上述疗法的结果。方法:索非布韦和利巴韦林双重疗法为24周,三联疗法与另外的聚乙二醇化干扰素为12周。当患者不愿接受干扰素或不符合干扰素治疗条件时,接受双重治疗。结果:该分析纳入了241例患者,其中175例接受了双重治疗,66例接受了三重治疗。患者的平均年龄为46.6岁,从20到72岁不等,男性为136(56.4%)。 151名(62.7%)患者存在临床肝硬化,其中98名(40.7%)有治疗经验。在治疗的第4周,HCV RNA在225名(93.3%)患者中呈阴性。在治疗后12周(SVR12),有221例(91.7%)的患者终止了病毒学应答,其中199例(82.6%)的病毒学应答持续。第4周未检测到的HCV RNA是预测SVR12的独立参数(P = 0.001)。接受双重疗法的143名患者(81.7%)和接受双重疗法的56名(84.8%)患者达到SVR12(P = 0.567)。先前的HCV治疗状态以及是否存在肝硬化对2个治疗组之间的结局均无明显影响。结论:在现实世界中,在许多情况下,使用索非布韦和利巴韦林联合或不联合PEG-IFNα治疗HCV GT3感染均获得了持久的反应。

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