Institute of Liver, Gastroenterology, & Pancreatico-Biliary Sciences, Sir Ganga Ram Hospital, New Delhi, India.
Indian J Med Res. 2017 Jul;146(1):23-33. doi: 10.4103/ijmr.IJMR_679_15.
Approximately three per cent of the world's population (170-200 million people) is chronically infected with hepatitis C virus (HCV) and almost 500,000 people die each year (mostly in lower middle-income countries) from complications secondary to HCV infection. In India, HCV infection imposes a considerable burden of mortality, morbidity and healthcare costs. In the last two decades, the treatment of HCV has evolved from interferon (IFN)-based therapies with or without ribavirin (RBV) to pegylated-IFN (PEG-IFN) and RBV-based therapies that were better tolerated by patients. However, the introduction of oral drugs, which specifically target virus-specific proteins, has now revolutionized the treatment of chronic HCV. These agents are known as direct-acting antivirals (DAAs). These drugs have resulted in very high HCV cure rates even with reduced treatment duration and an excellent tolerability by the patients compared to PEG-IFN- and RBV-based therapies. In India, sofosbuvir (SOF), one of the most effective DAAs, has been made available at a compassionate price; thus only those DAA-based management strategies, which contain SOF are adopted in India. Here, we review different DAAs and their possible roles in different genotypes and stages of liver disease, stressing upon the role of SOF. An attempt has also been made to devise strategies using SOF for the most prevalent genotypes in our country (genotypes 3 and 1) and cirrhosis.
全球约有 3%的人口(1.7 亿至 2 亿人)慢性感染丙型肝炎病毒(HCV),每年约有 50 万人(主要在中低收入国家)死于 HCV 感染的并发症。在印度,HCV 感染给死亡率、发病率和医疗保健成本带来了相当大的负担。在过去的二十年中,HCV 的治疗已经从干扰素(IFN)为基础的治疗方法(联合或不联合利巴韦林(RBV))发展为聚乙二醇化 IFN(PEG-IFN)和 RBV 为基础的治疗方法,这些方法更能被患者耐受。然而,专门针对病毒特异性蛋白的口服药物的出现,现在已经彻底改变了慢性 HCV 的治疗方法。这些药物被称为直接作用抗病毒药物(DAAs)。与基于 PEG-IFN 和 RBV 的治疗方法相比,这些药物即使治疗时间缩短,且患者的耐受性极好,也能使 HCV 的治愈率非常高。在印度,索菲布韦(SOF)是最有效的 DAA 之一,以同情价格提供,因此印度只采用包含 SOF 的 DAA 管理策略。在这里,我们回顾了不同的 DAA 及其在不同基因型和肝病阶段的可能作用,重点介绍了 SOF 的作用。还尝试制定了使用 SOF 治疗我国(基因型 3 和 1)和肝硬化最常见基因型的策略。