Chen Chun-Hao, Yu Ming-Lung
Digestive Division, Department of Internal Medicine, Kaohsiung Municipal United Hospital, Kaohsiung 804, Taiwan.
Hepat Res Treat. 2010;2010:140953. doi: 10.1155/2010/140953. Epub 2010 Oct 10.
Since 1986, interferon-alfa (IFN-α) monotherapy has been administered for patients with chronic hepatitis C (CHC). However, sustained response rate is only about 8% to 9%. Subsequent introduction of ribavirin in combination with IFN-α was a major breakthrough in the treatment of CHC. Sustained virological responses (SVRs) rate is about 30% in hepatitis C virus genotype 1 (HCV-1) patients, and is about 65% in HCV-2 or -3 patients. After 2000, pegylated interferon (PegIFN) much improved the rates of SVR. Presently, PegIFN-α-ribavirin combination therapy has been current standard of care for patients infected with HCV. In patients with HCV-1, treatment for 48 weeks is optimal, but 24 weeks of treatment is sufficient in HCV-2 or -3 infected patients. Clinical factors have been identified as predictors for the efficacy of the IFN-based therapy. The baseline factor most strongly predictive of an SVR is the presence of HCV-2 or -3 infections. Rapid virological response (RVR) is the single best predictor of an SVR to PegIFN-ribavirin therapy. If patients can't achieve a RVR but achieve a complete early virological response (cEVR), treatment with current standard of care can provide more than 90% SVR rate. HCV-1 patients who do not achieve an EVR should discontinue the therapy. Recent advances of protease inhibitor may contribute the development of a novel triple combination therapy.
自1986年以来,干扰素-α(IFN-α)单药疗法一直用于慢性丙型肝炎(CHC)患者。然而,持续应答率仅约为8%至9%。随后引入的利巴韦林与IFN-α联合使用是CHC治疗的一项重大突破。丙型肝炎病毒1型(HCV-1)患者的持续病毒学应答(SVR)率约为30%,而HCV-2或-3型患者的SVR率约为65%。2000年后,聚乙二醇化干扰素(PegIFN)显著提高了SVR率。目前,PegIFN-α-利巴韦林联合疗法已成为HCV感染患者的当前标准治疗方案。对于HCV-1型患者,48周的治疗是最佳的,但对于HCV-2或-3型感染患者,24周的治疗就足够了。临床因素已被确定为基于IFN治疗疗效的预测指标。最能强烈预测SVR的基线因素是存在HCV-2或-3感染。快速病毒学应答(RVR)是PegIFN-利巴韦林疗法SVR的最佳单一预测指标。如果患者不能实现RVR但实现了完全早期病毒学应答(cEVR),采用当前标准治疗方案可提供超过90%的SVR率。未实现EVR的HCV-1型患者应停止治疗。蛋白酶抑制剂的最新进展可能有助于新型三联联合疗法的开发。