El Kassas Mohamed, Omran Dalia, Elsaeed Kadry, Alboraie Mohamed, Elakel Wafaa, El Tahan Adel, Abd El Latif Yasmeen, Nabeel Mohamed Mahmoud, Korany Mohamed, Ezzat Sameera, El-Serafy Magdy, ElShazly Yehia, Doss Wahid, Esmat Gamal
1 Endemic Medicine Department, Faculty of Medicine, Helwan University , Cairo, Egypt .
2 Endemic Medicine and Hepato-Gastroenterology Department, Faculty of Medicine, Cairo University , Cairo, Egypt .
J Interferon Cytokine Res. 2018 Feb;38(2):81-85. doi: 10.1089/jir.2017.0121. Epub 2018 Jan 22.
The aim of this study was to retrospectively analyze the outcome of an unscheduled change in national Egyptian policies for the treatment of hepatitis C virus (HCV), which was transpired as a result of a reduction in interferon supplies, and to manage patients who already started interferon-based therapy. After completing a priming 4-weeks course of sofosbuvir/pegylated interferon/ribavirin (SOF/PEG IFN/RBV), a 12-weeks course of sofosbuvir/daclatasvir (SOF/DCV) combination was initiated. We evaluated the sustained virologic response at 12 weeks posttreatment (SVR12) for 2 groups of patients; Group 1, which included patients who had the previous regimen with IFN priming, and group 2, which included the first consecutive group of patients who received SOF/DCV for 12 weeks from the start without IFN priming. All group 1 patients (1,214 patients) achieved SVR12 (100%) and this was statistically significant when compared with the overall SVR12 in group 2 [8,869 patients with sustained virologic response [SVR] of 98.9%] (P value <0.001). No serious adverse events were reported in both groups. In this real-life treatment experience, interferon-based directly acting antiviral treatment with SOF/PEG IFN/RBV as a priming for 4 weeks, followed by SOF/DCV combination for 12 weeks, led to HCV viral suppression in all treated patients.
本研究的目的是回顾性分析埃及全国丙型肝炎病毒(HCV)治疗政策意外变更的结果,该变更是由于干扰素供应减少所致,并对已开始基于干扰素治疗的患者进行管理。在完成4周的索磷布韦/聚乙二醇干扰素/利巴韦林(SOF/PEG IFN/RBV)初始疗程后,开始12周的索磷布韦/达卡他韦(SOF/DCV)联合治疗。我们评估了两组患者治疗后12周的持续病毒学应答(SVR12);第1组包括接受过IFN初始治疗方案的患者,第2组包括从开始就连续接受12周SOF/DCV治疗且未进行IFN初始治疗的第一组患者。所有第1组患者(1214例)均实现了SVR12(100%),与第2组的总体SVR12[8869例患者的持续病毒学应答(SVR)为98.9%]相比,这具有统计学意义(P值<0.001)。两组均未报告严重不良事件。在这种实际治疗经验中,以SOF/PEG IFN/RBV为初始治疗4周,随后使用SOF/DCV联合治疗12周的基于干扰素的直接抗病毒治疗,使所有接受治疗的患者实现了HCV病毒抑制。