Hilgenfeldt Eric G, Schlachterman Alex, Firpi Roberto J
Eric G Hilgenfeldt, Department of Internal Medicine, University of Florida College of Medicine, Gainesville, FL 32610, United States.
World J Hepatol. 2015 Jul 28;7(15):1953-63. doi: 10.4254/wjh.v7.i15.1953.
Over the past several years, more so recently, treatment options for hepatitis C virus (HCV) have seemed to exponentially grow. Up until recently, the regimen of pegylated interferon (peg-IFN) and ribavirin (RBV) stood as the standard of care. Direct acting antivirals, which target nonstructural proteins involved in replication and infection of HCV were first approved in 2011 as an addition to the peg-IFN and RBV regimen and with them have come increased sustained virological response rates (SVR). The previously reported 50%-70% SVR rates using the combination of peg-IFN and RBV are no longer the standard of care with direct acting antiviral (DAA) based regimens now achieving SVR of 70%-90%. Peg-IFN free as well as "all oral" regimens are also available. The current randomized controlled trials available show favorable SVRs in patients who are naive to treatment, non-cirrhotic, and not human immunodeficiency virus (HIV)-co-infected. What about patients who do not fit into these categories? In this review, we aim to discuss the currently approved and soon to be approved DAAs while focusing on their roles in patients that are treatment experienced, cirrhotic, or co-infected with HIV. In this discussion, review of the clinical trials leading to recent consensus guidelines as well as discussion of barriers to treatment will occur. A case will attempt will be made that social services, including financial support and drug/alcohol treatment, should be provided to all HCV infected patients to improve chances of cure and thus prevention of late stage sequela.
在过去几年里,尤其是最近,丙型肝炎病毒(HCV)的治疗选择似乎呈指数级增长。直到最近,聚乙二醇干扰素(peg-IFN)和利巴韦林(RBV)方案一直是标准治疗方案。直接作用抗病毒药物靶向参与HCV复制和感染的非结构蛋白,于2011年首次获批,作为peg-IFN和RBV方案的补充,随着它们的出现,持续病毒学应答率(SVR)有所提高。先前报道的使用peg-IFN和RBV联合方案的SVR率为50%-70%,现在基于直接作用抗病毒药物(DAA)的方案已不再是标准治疗方案,目前其SVR可达70%-90%。不含peg-IFN的方案以及“全口服”方案也已出现。目前现有的随机对照试验表明,对于初治、非肝硬化且未合并人类免疫缺陷病毒(HIV)感染的患者,SVR情况良好。那么不符合这些类别的患者呢?在本综述中,我们旨在讨论目前已获批和即将获批的DAA药物,同时重点关注它们在经治、肝硬化或合并HIV感染患者中的作用。在本次讨论中,将回顾导致近期共识指南的临床试验,并讨论治疗障碍。我们将尝试提出一个观点,即应向所有HCV感染患者提供包括经济支持和药物/酒精治疗在内的社会服务,以提高治愈几率,从而预防晚期后遗症。