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通用的 ledipasvir-sofosbuvir 治疗慢性丙型肝炎患者:一项真实世界的观察性研究。

Generic ledipasvir-sofosbuvir for patients with chronic hepatitis C: A real-life observational study.

机构信息

Department of Infectious Diseases and Hepatology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan Province, China.

Department of Infectious Diseases, The Affiliated Hospital of Yan'an University, Yan'an, Shaanxi Province, China.

出版信息

J Hepatol. 2017 Jun;66(6):1123-1129. doi: 10.1016/j.jhep.2017.01.025. Epub 2017 Feb 9.

Abstract

BACKGROUND & AIMS: Few patients from developing countries can afford brand name direct-acting antiviral agents for treating hepatitis C virus (HCV) infection, and controversy regarding the bioequivalence of generics exists. This study aimed to observe the safety and efficacy of 8 or 12weeks of generic ledipasvir-sofosbuvir with or without ribavirin for Chinese genotype 1b HCV-infected patients.

METHODS

In this open-labelled observational study, 63 cirrhotic (group 1) and 65 non-cirrhotic (group 2) patients were administered generic ledipasvir-sofosbuvir plus 1000-1200mg of ribavirin daily for 12 and 8weeks, respectively; and 64 non-cirrhotic patients (group 3) received ledipasvir-sofosbuvir for 8weeks. The primary efficacy endpoint was undetectable HCV RNA at week 12 (SVR12) after cessation of therapy. Safety and pharmacokinetic data were collected.

RESULTS

One hundred and eighty-seven patients completed treatment, and the latest undetectable HCV RNA was observed in three patients with cirrhosis at week 5 during treatment. Intention-to-treat analysis revealed 96.8% (61/63), 96.9% (63/65), and 96.9% (62/64) of SVR12 rates in groups 1, 2, and 3, respectively. One patient in group 3 relapsed at post-treatment week 4. The regimens were generally well-tolerated. The most common adverse events were fatigue (17.8%), diarrhea (10.9%), and headache (9.9%). Four patients discontinued therapy due to diarrhea and vomiting. One patient from group 2 discontinued treatment on day 29 because of drug-unaffordability; fortunately, she achieved SVR12.

CONCLUSION

This study demonstrated that 8 or 12weeks of generic ledipasvir-sofosbuvir with or without ribavirin are safe and effective for patients with genotype 1b HCV infection.

LAY SUMMARY

The price of Harvoni® has led to restrictions and access limitations in many developing and even developed countries with limited healthcare budgets. Gilead approved generic ledipasvir-sofosbuvir costs far less than Harvoni® and presents a similar cure rate for patients with chronic hepatitis C.

摘要

背景与目的

很少有来自发展中国家的患者能够负担得起治疗丙型肝炎病毒(HCV)感染的品牌名直接作用抗病毒药物,而且关于仿制药的生物等效性存在争议。本研究旨在观察替诺福韦艾拉酚胺-索磷布韦的仿制药 8 或 12 周疗程联合或不联合利巴韦林治疗中国 1b 型 HCV 感染患者的安全性和疗效。

方法

在这项开放标签观察性研究中,63 例肝硬化(第 1 组)和 65 例非肝硬化患者(第 2 组)分别接受每日 1000-1200mg 利巴韦林联合替诺福韦艾拉酚胺-索磷布韦 12 周和 8 周的治疗;64 例非肝硬化患者(第 3 组)接受替诺福韦艾拉酚胺-索磷布韦 8 周的治疗。主要疗效终点是治疗停止后第 12 周(SVR12)时 HCV RNA 不可检测。收集安全性和药代动力学数据。

结果

187 例患者完成了治疗,3 例肝硬化患者在治疗期间第 5 周时出现了最新的 HCV RNA 不可检测。意向治疗分析显示第 1、2 和 3 组的 SVR12 率分别为 96.8%(61/63)、96.9%(63/65)和 96.9%(62/64)。第 3 组的 1 例患者在治疗后第 4 周复发。这些方案总体上耐受性良好。最常见的不良事件是疲劳(17.8%)、腹泻(10.9%)和头痛(9.9%)。4 例患者因腹泻和呕吐而停止治疗。第 2 组的 1 例患者因药物负担不起而在第 29 天停止治疗;幸运的是,她实现了 SVR12。

结论

本研究表明,替诺福韦艾拉酚胺-索磷布韦的仿制药 8 或 12 周疗程联合或不联合利巴韦林治疗 1b 型 HCV 感染患者是安全有效的。

概要

哈瓦尼的价格导致许多发展中国家甚至医疗保健预算有限的发达国家对其的限制和获取限制。吉利德公司批准的替诺福韦艾拉酚胺-索磷布韦仿制药的价格要低得多,而且对慢性丙型肝炎患者的治愈率相似。

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