Division of Gastroenterology and Hepatology, University of Alabama at Birmingham, 1808 7th Ave South, BDB 391, Birmingham, AL, 5294, USA.
Department of Internal Medicine, Tinsley Harrison Internal Medicine Residency Program, University of Alabama at Birmingham, 1720 2nd Ave South, BDB 327, Birmingham, AL, 35294, USA.
Hepatol Int. 2017 Sep;11(5):434-439. doi: 10.1007/s12072-016-9778-6. Epub 2017 Jan 12.
BACKGROUND/AIM: Recurrent hepatitis C virus infection is a challenging complication post-liver transplant. Current guidelines recommend the combination of ribavirin and ledipasvir/sofosbuvir for 12 weeks for the treatment of recurrent HCV genotype 1 post-liver transplant. Data are limited on the use of ledipasvir/sofosbuvir without ribavirin. The aim of this study was to evaluate the use of ledipasvir/sofosbuvir without ribavirin for the treatment of recurrent hepatitis C virus post-liver transplant.
This is a retrospective study of liver transplant patients who received ledipasvir/sofosbuvir without ribavirin for the treatment of recurrent hepatitis C virus in our liver center from 2014 to 2016.
A total of 60 patients were enrolled of which 70% were male, 88% Caucasian, age 60 ± 7 years, 15% cirrhotic, and 45% treatment-experienced with recurrent hepatitis C virus infection genotype 1 post-liver transplant. Treatment duration varied from 8 to 24 weeks. There were no serious adverse events and no discontinuation of treatment. A total of 71% of patients had undetectable serum hepatitis C virus at 4 weeks. However, irrespective of treatment duration, 100% of patients had undetectable serum hepatitis C virus at the end of treatment and 100% of patients achieved sustained viral response at 12 weeks.
Ledipasvir/sofosbuvir without ribavirin is an effective treatment of recurrent hepatitis C virus infection post-liver transplant. The entire group achieved sustained viral response at 12 weeks irrespective of the length of treatment. The combination of ledipasvir/sofosbuvir was well tolerated without serious adverse effects or discontinuation.
背景/目的:肝移植后复发的丙型肝炎病毒感染是一个具有挑战性的并发症。目前的指南建议对于肝移植后复发的丙型肝炎病毒基因型 1,使用利巴韦林联合 ledipasvir/索非布韦治疗 12 周。关于不使用利巴韦林的 ledipasvir/索非布韦的数据有限。本研究旨在评估不使用利巴韦林的 ledipasvir/索非布韦治疗肝移植后复发的丙型肝炎病毒。
这是一项回顾性研究,研究对象为 2014 年至 2016 年期间在我们的肝脏中心接受 ledipasvir/索非布韦治疗而不使用利巴韦林治疗肝移植后复发的丙型肝炎病毒的患者。
共纳入 60 例患者,其中 70%为男性,88%为白种人,年龄 60±7 岁,15%为肝硬化,45%为肝移植后复发的丙型肝炎病毒感染基因型 1的治疗经验患者。治疗持续时间为 8 至 24 周。4 周时,71%的患者血清丙型肝炎病毒检测不到,但无论治疗持续时间如何,治疗结束时 100%的患者血清丙型肝炎病毒检测不到,12 周时 100%的患者达到持续病毒应答。
不使用利巴韦林的 ledipasvir/索非布韦是治疗肝移植后复发丙型肝炎病毒感染的有效方法。整个治疗组在 12 周时均达到持续病毒应答,而不论治疗时间长短。ledipasvir/索非布韦联合用药耐受性良好,无严重不良事件或停药。