Werner C R, Egetemeyr D P, Nadalin S, Königsrainer A, Malek N P, Lauer U M, Berg C P
University Hospital Tübingen, Medical Clinic, Department of Gastroenterology, Hepatology, and Infectiology, Tübingen, Germany.
University Hospital Tübingen, Department of General, Visceral and Transplant Surgery, Tübingen, Germany.
Z Gastroenterol. 2014 Jan;52(1):27-34. doi: 10.1055/s-0033-1356345. Epub 2014 Jan 13.
Recurrent HCV infection post-liver transplantation (post-LT) is still a major challenge in the treatment of hepatitis C virus (HCV) infection. In this retrospective analysis we gathered data about treatment response and safety of all 14 post-LT patients who were treated between 2011 and 2013 at our centre with a telaprevir (TVR)-based triple therapy. Seven out of 14 patients completed the full treatment course of 48 weeks. Five patients achieved a SVR 24, while 3 additional HCV RNA-negative patients are still in follow-up (end of treatment, SVR 12 and 22). Four patients discontinued treatment prematurely due to side effects. A virological non-response at TW 4 was seen in 1 patient. Virological breakthrough was observed in 2 patients at TW 16 and 28, respectively; 1 patient displayed a virological relapse after the end of treatment (EOT). Patients with a complicated course post-LT accumulated most of the severe side effects, largely infections. One patient with cholestatic hepatitis died 11 weeks after discontinuation of treatment due to progressive graft failure. In conclusion, TVR-based triple therapy in post-LT patients reveals an acceptable antiviral efficacy. Unfortunately, severe side effects are frequent and often require therapeutic interventions. Therefore, with the approval of less straining DAA like sofosbuvir in sight, TVR-based triple therapy in post-LT patients should be, if possible avoided.
肝移植后复发性丙型肝炎病毒(HCV)感染仍是丙型肝炎病毒(HCV)感染治疗中的一项重大挑战。在这项回顾性分析中,我们收集了2011年至2013年期间在我们中心接受基于特拉匹韦(TVR)的三联疗法治疗的所有14例肝移植后患者的治疗反应和安全性数据。14例患者中有7例完成了48周的完整疗程。5例患者实现了治疗结束后24周持续病毒学应答(SVR 24),另有3例HCV RNA阴性患者仍在随访中(治疗结束时,SVR 12和22)。4例患者因副作用提前停药。1例患者在治疗第4周时出现病毒学无应答。分别在治疗第16周和28周时观察到2例患者出现病毒学突破;1例患者在治疗结束后出现病毒学复发。肝移植后病程复杂的患者出现了大部分严重副作用,主要是感染。1例胆汁淤积性肝炎患者在停药11周后因移植肝功能进行性衰竭死亡。总之,肝移植后患者基于TVR的三联疗法显示出可接受的抗病毒疗效。不幸的是,严重副作用很常见,且常常需要进行治疗干预。因此,鉴于索磷布韦等负担较小的直接抗病毒药物(DAA)已获批,肝移植后患者应尽可能避免使用基于TVR的三联疗法。