Medizinische Klinik 1, Universitätsklinikum Frankfurt, Frankfurt am Main, Germany.
Hepatology Section, Division of Gastroenterology, Department of Medicine, New York University School of Medicine and NYU Langone Health, New York, USA.
J Hepatol. 2018 Nov;69(5):1178-1187. doi: 10.1016/j.jhep.2018.07.002. Epub 2018 Jul 11.
Treatment of chronic hepatitis C virus infection has been revolutionised by the development of direct-acting antivirals (DAAs). All-oral, once-daily, 8- to 12-week treatment regimens are now standard of care, with viral eradication possible in >95% of patients across different populations. Despite these advances, several unresolved issues remain, including treatment of patients with hepatitis C virus genotype 3, chronic kidney disease, and those in whom DAA therapy has previously failed. Glecaprevir/pibrentasvir and sofosbuvir/velpatasvir/voxilaprevir are the most recently approved DAA regimens. Given the overwhelming success of modern DAA-based therapies, glecaprevir/pibrentasvir and sofosbuvir/velpatasvir/voxilaprevir are also likely to represent the last DAAs to be approved. Both are pangenotypic, once-daily, all-oral DAA combinations that have the potential to close the gaps in the current DAA treatment portfolio. Herein, we review the challenges associated with current DAAs and how these two regimens may be implemented in existing treatment algorithms.
直接作用抗病毒药物(DAAs)的发展彻底改变了慢性丙型肝炎病毒感染的治疗方法。现在,所有口服、每日一次、8-12 周的治疗方案已成为标准治疗方法,不同人群中超过 95%的患者都能实现病毒清除。尽管取得了这些进展,但仍有几个未解决的问题,包括治疗丙型肝炎病毒基因型 3、慢性肾脏病患者,以及之前 DAA 治疗失败的患者。格卡瑞韦/哌仑他韦和索磷布韦/维帕他韦/伏西瑞韦是最近批准的 DAA 方案。鉴于现代基于 DAA 的治疗方法取得了压倒性的成功,格卡瑞韦/哌仑他韦和索磷布韦/维帕他韦/伏西瑞韦也可能成为最后批准的 DAA。两者均为泛基因型、每日一次、全口服 DAA 联合用药,有可能填补当前 DAA 治疗方案中的空白。本文综述了当前 DAA 相关的挑战以及这两种方案如何在现有治疗算法中实施。