Division of Gastroenterology and Hepatology, Hospital de Clínicas de Porto Alegre, Porto Alegre, RS, Brazil.
World Gastroenterology Organisation Porto Alegre Hepatology Training Center, Porto Alegre, RS, Brazil.
Ann Hepatol. 2019 May-Jun;18(3):450-455. doi: 10.1016/j.aohep.2018.09.004. Epub 2019 Apr 15.
Recurrent HCV infection after liver transplant (LT) has a negative impact on graft and patient survival. The aim of this study is to describe the efficacy and safety of sofosbuvir (SOF-based) regimens in the treatment of recurrent HCV after liver transplant (LT).
This retrospective study included 68 adults with recurrent HCV infection after LT, treated with different SOF-based regimens between March 2015 and December 2016. The choice of regimens, their duration and use of ribavirin (RBV) was made by the treating physician. The efficacy of antiviral treatment was assessed based on the sustained viral response obtained 12 weeks after the end of treatment (SVR12), according to an intention-to-treat analysis.
The most frequent HCV genotypes were 1 and 3 (n=35, 51.4% and n=31, 45.6%, respectively). Only 22 patients were treatment naïve (32.3%) and 7 had cirrhosis (10.2%). SOF+daclatasvir (DCV) was the most commonly used regimen (n=63, 92.6%). Most patients used RBV (n=56, 82.3%) and were treated for 12 weeks (n=66, 97%). Overall SVR12 was 95.5% (65/68 patients). Three patients had virologic failure. Three patients had serious adverse events, however, no one discontinued treatment prematurely. RBV-related anaemia was the most frequent adverse event (n=34, 50%). Four patients had severe cellular graft rejection after HCV elimination, while immunosuppression remained stable.
SOF-based therapy is highly effective and safe to treat HCV recurrence after LT. Cellular graft rejection following the successful treatment of HCV needs further investigation.
肝移植(LT)后丙型肝炎病毒(HCV)的复发对移植物和患者的生存有负面影响。本研究的目的是描述索非布韦(SOF)为基础的方案在治疗肝移植后 HCV 复发的疗效和安全性。
这项回顾性研究纳入了 68 例 LT 后 HCV 复发的成年人,他们在 2015 年 3 月至 2016 年 12 月期间接受了不同的 SOF 为基础的方案治疗。方案的选择、其持续时间和利巴韦林(RBV)的使用由治疗医生决定。根据意向治疗分析,根据治疗结束后 12 周(SVR12)获得的持续病毒应答来评估抗病毒治疗的疗效。
最常见的 HCV 基因型为 1 型和 3 型(n=35,分别为 51.4%和 n=31,45.6%)。只有 22 例患者为初治(32.3%),7 例患者有肝硬化(10.2%)。SOF+达卡他韦(DCV)是最常用的方案(n=63,92.6%)。大多数患者使用 RBV(n=56,82.3%),治疗时间为 12 周(n=66,97%)。总的 SVR12 为 95.5%(65/68 例患者)。3 例患者发生病毒学失败。3 例患者出现严重不良事件,但无人提前停药。RBV 相关贫血是最常见的不良事件(n=34,50%)。4 例患者在 HCV 清除后出现严重的细胞移植物排斥反应,而免疫抑制仍保持稳定。
SOF 为基础的治疗方案治疗 LT 后 HCV 复发的疗效高且安全。成功治疗 HCV 后出现的细胞移植物排斥反应需要进一步研究。