Ermis Fatih, Senocak Tasci Elif
Fatih Ermis, Department of Gastroenterology, Duzce University Faculty of Medicine, 81620 Duzce, Turkey.
World J Hepatol. 2015 Aug 18;7(17):2100-9. doi: 10.4254/wjh.v7.i17.2100.
Hepatitis C infection can lead to cirrhosis and hepatocellular carcinoma and it is an important cause of mortality and morbidity. Achieving a sustained virological response has been the major aim for decades. Interferon treatment was the primarily developed therapy against the infection. Addition of the guanosine analog ribavirin to stop viral RNA synthesis increased the response rates as well as the adverse effects of the treatment. The increasing demands for alternative regimens led to the development of direct-acting antivirals (DAAs). The approval of sofosbuvir and simeprevir signaled a new era of antiviral treatment for hepatitis C infection. Although the majority of studies have been performed with DAAs in combination with interferon and resulted in a decrease in treatment duration and increase in response rates, the response rates achieved with interferon-free regimens provided hope for patients ineligible for therapy with interferon. Most DAA studies are in phase II leading to phase III. In the near future more DAAs are expected to be approved. The main disadvantage of the therapy remains the cost of the drugs. Here, we focus on new treatment strategies for hepatitis C infection as well as agents targeting hepatitis C virus replication that are in clinical development.
丙型肝炎感染可导致肝硬化和肝细胞癌,是导致死亡和发病的重要原因。几十年来,实现持续病毒学应答一直是主要目标。干扰素治疗是最初开发的针对该感染的疗法。添加鸟苷类似物利巴韦林以阻止病毒RNA合成,提高了应答率,但也增加了治疗的不良反应。对替代治疗方案的需求不断增加,促使了直接抗病毒药物(DAAs)的开发。索非布韦和simeprevir的获批标志着丙型肝炎感染抗病毒治疗的新时代。尽管大多数研究是将DAAs与干扰素联合使用,导致治疗疗程缩短和应答率提高,但不含干扰素方案所达到的应答率为不符合干扰素治疗条件的患者带来了希望。大多数DAA研究处于II期,随后进入III期。在不久的将来,预计会有更多的DAAs获批。该疗法的主要缺点仍然是药物成本。在此,我们重点关注丙型肝炎感染的新治疗策略以及正在临床开发中的针对丙型肝炎病毒复制的药物。