Miuma Satoshi, Miyaaki Hisamitsu, Soyama Akihiko, Hidaka Masaaki, Takatsuki Mitsuhisa, Shibata Hidetaka, Taura Naota, Eguchi Susumu, Nakao Kazuhiko
Department of Gastroenterology and Hepatology, Nagasaki University of Graduate School of Biomedical Sciences, Nagasaki, Japan.
Department of Surgery, Nagasaki University of Graduate School of Biomedical Sciences, Nagasaki, Japan.
Hepatol Res. 2018 Nov;48(12):1045-1054. doi: 10.1111/hepr.13204. Epub 2018 Jul 19.
Recently, elbasvir/grazoprevir combination therapy (EBR/GZR) was reported to have excellent antiviral effects for chronic genotype 1 hepatitis C virus (HCV) infection. However, it has not been recommended for patients with post-liver transplant (LT) HCV re-infections because of a lack of evidence for effectiveness and drug-drug interactions.
We report the usage of EBR/GZR in five post-LT HCV re-infected patients with the kinetics of renal function and tacrolimus trough levels during and after therapy. Furthermore, to evaluate the antiviral effects, we examined the HCV kinetics during and after therapy and compared this with other interferon-free therapy in post-LT patients (n = 19).
All patients treated with EBR/GZR therapy obtained rapid virologic response and sustained at 12 weeks post-treatment. There was no evidence of worsening estimated glomerular filtration rates. Three patients were given tacrolimus as immunosuppressive therapy and its trough levels were controllable with dosage adjustments. One patient developed grade 1 diarrhea 3 days after therapy induction. To evaluate the antiviral effects of EBR/GZR therapy for these patients, we compared them to the effects of daclatasvir/asunaprevir combination therapy (n = 8) and sofosbuvir/ledipasvir combination therapy (n = 11). The EBR/GZR combination was not inferior to other therapies in its early phase and late-phase antiviral effects.
Although further studies with a larger number of patients are required, we suggest that EBR/GZR therapy is an alternative therapy for patients with post-LT genotype 1 HCV re-infection.
最近,有报道称艾尔巴韦/格拉瑞韦联合疗法(EBR/GZR)对慢性1型丙型肝炎病毒(HCV)感染具有出色的抗病毒效果。然而,由于缺乏有效性证据和药物相互作用的相关研究,尚未推荐将其用于肝移植(LT)后HCV再感染的患者。
我们报告了EBR/GZR在5例LT后HCV再感染患者中的使用情况,以及治疗期间和治疗后肾功能和他克莫司谷浓度的变化情况。此外,为评估抗病毒效果,我们检测了治疗期间和治疗后的HCV变化情况,并将其与其他LT后患者(n = 19)的无干扰素疗法进行比较。
所有接受EBR/GZR治疗的患者均获得了快速病毒学应答,并在治疗后12周持续保持。没有证据表明估计肾小球滤过率恶化。3例患者接受他克莫司作为免疫抑制治疗,其谷浓度可通过调整剂量进行控制。1例患者在诱导治疗3天后出现1级腹泻。为评估EBR/GZR治疗对这些患者的抗病毒效果,我们将其与达卡他韦/阿舒瑞韦联合疗法(n = 8)和索磷布韦/维帕他韦联合疗法(n = 11)的效果进行了比较。EBR/GZR联合疗法在早期和晚期抗病毒效果方面并不逊色于其他疗法。
尽管需要对更多患者进行进一步研究,但我们建议EBR/GZR疗法可作为LT后1型HCV再感染患者的替代疗法。