Chen Ting-Yi, Jain Mamta K
Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas.
AIDS Patient Care STDS. 2015 Jun;29(6):329-37. doi: 10.1089/apc.2014.0247.
Hepatitis C (HCV)-related liver disease has become one of the leading causes of death in HIV patients. With the development of new direct-acting antivirals for HCV, treatment regimens have become shorter, more effective, and easier to tolerate without interferon. However, cost may be a significant impediment to the widespread use of these newer agents in both resource-rich and resource-poor settings. In HIV patients, treatment for HCV is not always as straightforward compared with HCV monoinfected patients due to potential drug-drug interactions. In this article, we will examine by genotypes the FDA approved direct-acting antivirals, as well as those in clinical trials that will soon be FDA-approved focusing on data in HCV/HIV co-infection. Preferred agents for HCV treatment and potential drug-drug interactions with antiretroviral therapy (ART) will be highlighted.
丙型肝炎(HCV)相关肝病已成为HIV患者的主要死因之一。随着用于HCV的新型直接抗病毒药物的发展,治疗方案变得更短、更有效,且无需干扰素,耐受性更好。然而,成本可能是这些新型药物在资源丰富和资源匮乏地区广泛应用的重大障碍。在HIV患者中,由于潜在的药物相互作用,与单纯感染HCV的患者相比,HCV治疗并不总是那么简单直接。在本文中,我们将按基因型研究美国食品药品监督管理局(FDA)批准的直接抗病毒药物,以及即将获得FDA批准的处于临床试验阶段的药物,重点关注HCV/HIV合并感染的数据。将重点介绍HCV治疗的首选药物以及与抗逆转录病毒疗法(ART)潜在的药物相互作用。