Teegen Eva Maria, Globke Brigitta, Schott Eckart, Pratschke Johann, Eurich Dennis
From the Department of Surgery, Charité-Universitätsmedizin Berlin, Germany.
Exp Clin Transplant. 2018 Feb;16(1):61-67. doi: 10.6002/ect.2016.0296. Epub 2017 Nov 15.
Historically, hepatitis C virus genotype 3 infection has not been as hard to treat as genotype 1 using interferon-based therapy. Now, genotype 3 infection can be treated using interferon-free regimes such as the combination of sofosbuvir and daclatasvir, which is a highly successful and reliable therapeutic option before liver transplant. However, real world data are rather limited regarding the use of antivirals (sofosbuvir/daclatasvir) for hepatitis C virus genotype 3 recurrence after liver transplant. Here, we present the results of antiviral treatment with sofosbuvir and daclatasvir in patients with genotype 3 recurrence after liver transplant and also viewed published data, to finally close the chapter on genotype 3 elimination.
We analyzed 11 patients who received liver transplants due to hepatitis C virus genotype 3-associated cirrhosis at our center. Two patients were nadve for any antiviral therapy. All patients received antiviral treatment with sofosbuvir/daclatasvir for 12 weeks after liver transplant, with 1 patient also having ribavirin. The endpoint was hepatitis C virus RNA-free survival after 12 weeks of therapy. Secondary endpoints were preservation of renal and liver function and incidence of adverse events.
All patients were free of hepatitis C virus RNA by at least 8 weeks after therapy initiation. Elevated transaminases and gamma-glutamyltransferase at the beginning of therapy normalized quickly during treatment. Synthesis and excretion were stable at all dates. Patients displayed no severe adverse effects, especially regarding renal function and blood counts. Sustained virologic response rates at week 12 were achieved in all 11 patients.
Hepatitis C virus could be eliminated in all patients after liver transplant with 12-week sofosbuvir/daclatasvir therapy. Sofosbuvir combined with daclatasvir is safe and reliable for recurrent hepatitis C virus genotype 3 infection. Our results have closed the chapter on genotype 3 recurrence after liver transplant in our outpatient clinic.
从历史上看,丙型肝炎病毒3型感染使用基于干扰素的疗法不像1型感染那样难以治疗。现在,3型感染可以使用无干扰素方案进行治疗,例如索磷布韦和达卡他韦联合使用,这是肝移植前一种非常成功且可靠的治疗选择。然而,关于肝移植后丙型肝炎病毒3型复发使用抗病毒药物(索磷布韦/达卡他韦)的真实世界数据相当有限。在此,我们展示了肝移植后3型复发患者使用索磷布韦和达卡他韦进行抗病毒治疗的结果,并查阅了已发表的数据,以最终完成3型消除的篇章。
我们分析了在我们中心因丙型肝炎病毒3型相关肝硬化接受肝移植的11例患者。2例患者未接受过任何抗病毒治疗。所有患者在肝移植后接受索磷布韦/达卡他韦抗病毒治疗12周,其中1例患者还使用了利巴韦林。终点是治疗12周后的丙型肝炎病毒RNA清除生存情况。次要终点是肾功能和肝功能的维持以及不良事件的发生率。
所有患者在治疗开始后至少8周时丙型肝炎病毒RNA均检测不到。治疗开始时升高的转氨酶和γ-谷氨酰转移酶在治疗期间迅速恢复正常。所有时间点的合成和排泄均稳定。患者未出现严重不良反应,尤其是在肾功能和血细胞计数方面。11例患者在第12周均实现了持续病毒学应答率。
肝移植后的所有患者接受12周的索磷布韦/达卡他韦治疗后均可清除丙型肝炎病毒。索磷布韦联合达卡他韦对复发性丙型肝炎病毒3型感染安全可靠。我们的结果为我们门诊肝移植后3型复发画上了句号。