Flanagan Stuart, Crawford-Jones Andrew, Orkin Chloe
Department of Infection and Immunology, Royal London Hospital, Whitechapel Road, London E1 1BB.
Expert Rev Clin Pharmacol. 2014 Nov;7(6):691-704. doi: 10.1586/17512433.2014.956091. Epub 2014 Sep 11.
Hepatitis C virus (HCV) is a major cause of chronic hepatitis in 170 million people worldwide and can progress to fibrosis, cirrhosis, liver failure and hepatocellular carcinoma, a disease process accelerated in HIV co-infection. Approximately 25% of HIV infected people are co-infected with HCV (worldwide prevalence 4-5 million) and up to 16.7% of deaths in this population are attributable to HCV co-infection. Previous treatment options for HCV were limited to pegylated interferon and ribavirin (PEG-IFN/RBV), a combination that demonstrated lower successful cure rates in genotype 1 HCV mono-infection and HIV/HCV co-infection, and is also associated with a considerable adverse side-effect profile. The development of directly acting antivirals (DAAs) offers the first class of drug to achieve good viral suppression in previously hard-to-treat patient groups. We review the benefits, tolerability and drug interactions with concomitant drugs of the DAA simeprevir for patients who have HCV mono-infection and hep C/HIV co-infection.
丙型肝炎病毒(HCV)是全球1.7亿人慢性肝炎的主要病因,可进展为纤维化、肝硬化、肝衰竭和肝细胞癌,在合并感染HIV时这一疾病进程会加速。约25%的HIV感染者合并感染HCV(全球患病率为400万至500万),该人群中高达16.7%的死亡归因于HCV合并感染。先前针对HCV的治疗选择仅限于聚乙二醇干扰素和利巴韦林(PEG-IFN/RBV),这种联合用药在1型HCV单感染和HIV/HCV合并感染中显示出较低的成功治愈率,并且还伴有相当多的不良副作用。直接作用抗病毒药物(DAAs)的出现为一类能够在既往难以治疗的患者群体中实现良好病毒抑制效果的药物。我们综述了DAA药物西米普明对HCV单感染和HCV/HIV合并感染患者的益处、耐受性以及与伴随药物的药物相互作用。