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首页> 外文期刊>Hepatitis Monthly >Real World Experience with All-Oral Interferon Free Regimen for the Treatment of Lebanese Patients with Hepatitis C Virus (HCV) Infection
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Real World Experience with All-Oral Interferon Free Regimen for the Treatment of Lebanese Patients with Hepatitis C Virus (HCV) Infection

机译:全口服无干扰素疗法治疗黎巴嫩丙型肝炎病毒(HCV)感染患者的真实经验

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Objectives: The treatment of hepatitis C has dramatically improved since the introduction of new direct-acting antivirals (DAAs). The aim of this study was to assess the efficacy and safety of all oral DAAs, with or without ribavirin, in the treatment of naive and treatment experienced hepatitis C virus (HCV) Lebanese patients. Methods: This study reviewed all cases approved for hepatitis C treatment with DAAs, according to Lebanese guidelines for treatment of HCV at the Ministry of Public Health from October 2015 to December 2016. Available data on age, gender, genotype (GT) and subtype, fibrosis stage, previous treatment (if present), new DAAs treatment, and sustained virological response at week 12 (SVR12) were collected. Results: During a period of 15 months, a total of 186 patients were treated with DAAs. In total, 57% were male. The mean age of the patients was 54.3 years. Genotype 1 was the most prevalent (45%), followed by genotype four (34%) and genotype three (12%). More than 72% of patients had advanced fibrosis (F3 - F4) before starting DAAs and 42% of patients were treatment experienced. Regarding the different DAAs protocols used, SVR12 was achieved in 93% of cases, while 4% did not achieve SVR. Furthermore, 3% of cases were either lost to follow up or had major adverse events. Sustained virological response at week 12 was 93%, 96%, and 94% in GT1, GT3, and GT4, respectively. In cirrhotic patients, SVR12 was 90%. There was no difference in SVR12 between treatment naive and treatment-experienced patients. Hepatocellular carcinoma developed in five patients during the period of the study. Conclusions: This is the first real world Lebanese data concerning hepatitis C treatment with DAAs. It showed a satisfactory response rate irrespective of previous treatments or the stage of fibrosis.
机译:目标:自从引入新的直接作用抗病毒药(DAA)以来,丙型肝炎的治疗有了显着改善。这项研究的目的是评估所有口服DAA(无论是否使用利巴韦林)在治疗天真的和经验丰富的丙型肝炎病毒(黎巴嫩)患者中的疗效和安全性。方法:根据2015年10月至2016年12月,根据公共卫生部黎巴嫩关于HCV的黎巴嫩治疗指南,本研究回顾了所有经DAA丙型肝炎治疗批准的病例。有关年龄,性别,基因型(GT)和亚型的可用数据,收集纤维化阶段,先前的治疗(如果有),新的DAA治疗以及第12周(SVR12)的持续病毒学应答。结果:在15个月的时间内,共186例患者接受了DAA治疗。总计57%为男性。患者的平均年龄为54.3岁。基因型1最普遍(45%),其次是基因型4(34%)和基因型3(12%)。超过72%的患者在开始DAA之前患有晚期纤维化(F3-F4),并且42%的患者具有治疗经验。关于使用的不同DAA协议,在93%的情况下实现了SVR12,而4%的情况未实现SVR。此外,有3%的病例失访或发生重大不良事件。在第12周,GT1,GT3和GT4的持续病毒学应答分别为93%,96%和94%。在肝硬化患者中,SVR12为90%。初治患者和有治疗经验的患者之间的SVR12没有差异。在研究期间,五名患者发生了肝细胞癌。结论:这是黎巴嫩关于DAA治疗丙型肝炎的真实世界的第一份数据。无论以前的治疗或纤维化的阶段如何,它均显示令人满意的缓解率。

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