干扰素治疗慢性丙型肝炎的进展

Hepatitis research and treatment Pub Date : 2010-01-01 Epub Date: 2010-10-10 DOI:10.1155/2010/140953
Chun-Hao Chen, Ming-Lung Yu
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引用次数: 19

摘要

自1986年以来,干扰素-α (IFN-α)单药治疗已被用于慢性丙型肝炎(CHC)患者。然而,持续响应率只有8%到9%。随后引入利巴韦林联合干扰素-α是治疗CHC的重大突破。持续病毒学应答率(SVRs)在丙型肝炎病毒基因型1 (HCV-1)患者中约为30%,在HCV-2或-3患者中约为65%。2000年以后,聚乙二醇干扰素(PegIFN)大大提高了SVR的发生率。目前,PegIFN-α-利巴韦林联合治疗已成为当前HCV感染患者的标准治疗方案。在HCV-1患者中,48周的治疗是最佳的,但在HCV-2或-3感染患者中,24周的治疗是足够的。临床因素已被确定为干扰素为基础的治疗效果的预测因素。最能预测SVR的基线因素是HCV-2或-3感染的存在。快速病毒学反应(RVR)是pegifn -利巴韦林治疗SVR的单一最佳预测因子。如果患者不能达到完全早期病毒学应答(RVR),但达到完全早期病毒学应答(cEVR),采用目前的标准护理治疗可提供90%以上的SVR率。未达到EVR的HCV-1患者应停止治疗。蛋白酶抑制剂的最新研究进展可能有助于开发一种新的三联疗法。
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Evolution of interferon-based therapy for chronic hepatitis C.

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.

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