New treatments for chronic hepatitis C.

Jae Young Jang, Raymond T Chung
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Abstract

Treatments for chronic hepatitis C has evolved significantly in the past 15 years. The standard of care (SOC) is peginterferon alfa-2a/-2b with ribavirin for 48 weeks or 24 weeks in patients infected with HCV genotype 1 or 2/3, respectively. The treatment duration can be individualized based on the baseline viral load and the speed of the virologic response during treatment. However, current therapies are associated with side effects, complications, and poor patient tolerability. Therefore, there is an urgent need to identify better strategies for treating this disease. An improved sustained virologic response (SVR) can be achieved with new HCV-specific inhibitors against NS3/4A and NS5B polymerases. Recent trials have found SVR rates in patients with HCV genotype 1 infection of 61~68% and 67~75% for combining the SOC with the protease inhibitors telaprevir and boceprevir, respectively. Several new HCV-specific inhibitors such as protease inhibitors and nucleoside and non-nucleoside polymerase inhibitors as well as non-HCV-specific compounds with anti-HCV activity are currently in clinical evaluation. In this review we discuss these new treatments for chronic hepatitis C.

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慢性丙型肝炎的新疗法。
在过去的 15 年中,慢性丙型肝炎的治疗方法有了长足的发展。对于感染 HCV 基因型 1 或 2/3 的患者,标准治疗(SOC)是聚乙二醇干扰素 alfa-2a/-2b 联合利巴韦林,疗程分别为 48 周或 24 周。治疗持续时间可根据基线病毒载量和治疗期间病毒学应答的速度进行个体化。然而,目前的疗法存在副作用、并发症和患者耐受性差等问题。因此,迫切需要找到更好的治疗策略。针对 NS3/4A 和 NS5B 聚合酶的新型 HCV 特异性抑制剂可改善持续病毒学应答(SVR)。最近的试验发现,将 SOC 与蛋白酶抑制剂 telaprevir 和 boceprevir 联用,HCV 基因型 1 感染患者的 SVR 率分别为 61% 至 68% 和 67% 至 75%。目前,一些新的 HCV 特异性抑制剂(如蛋白酶抑制剂、核苷和非核苷聚合酶抑制剂)以及具有抗 HCV 活性的非 HCV 特异性化合物正在接受临床评估。在本综述中,我们将讨论这些治疗慢性丙型肝炎的新疗法。
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