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Treatment of hepatitis C in renal transplantation candidates: a single-center experience.肾移植候选者丙型肝炎的治疗:单中心经验。
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2
Early identification of achieving a sustained virological response in chronic hepatitis C patients without a rapid virological response.慢性丙型肝炎患者无快速病毒学应答者获得持续病毒学应答的早期识别。
J Gastroenterol Hepatol. 2010 Apr;25(4):758-65. doi: 10.1111/j.1440-1746.2009.06148.x.
3
Chemical genetics strategy identifies an HCV NS5A inhibitor with a potent clinical effect.化学遗传学策略鉴定出一种具有强大临床效果的 HCV NS5A 抑制剂。
Nature. 2010 May 6;465(7294):96-100. doi: 10.1038/nature08960. Epub 2010 Apr 21.
4
Telaprevir for previously treated chronic HCV infection.替拉瑞韦治疗既往治疗的慢性 HCV 感染。
N Engl J Med. 2010 Apr 8;362(14):1292-303. doi: 10.1056/NEJMoa0908014.
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Review article: specifically targeted anti-viral therapy for hepatitis C - a new era in therapy.综述文章:针对丙型肝炎的特异性抗病毒治疗 - 治疗新时代。
Aliment Pharmacol Ther. 2010 Jul;32(1):14-28. doi: 10.1111/j.1365-2036.2010.04317.x. Epub 2010 Mar 31.
6
Pegylated interferon plus optimized weight-based ribavirin dosing negate the influence of weight and body mass index on early viral kinetics and sustained virological response in chronic hepatitis C.聚乙二醇干扰素联合优化的基于体重的利巴韦林剂量可消除体重和体重指数对慢性丙型肝炎早期病毒动力学和持续病毒学应答的影响。
J Viral Hepat. 2010 Dec;17(12):834-8. doi: 10.1111/j.1365-2893.2010.01248.x.
7
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Hepatology. 2010 Jun;51(6):1897-903. doi: 10.1002/hep.23531.
8
Peginterferon alpha-2a is associated with higher sustained virological response than peginterferon alfa-2b in chronic hepatitis C: systematic review of randomized trials.聚乙二醇干扰素 alpha-2a 与聚乙二醇干扰素 alfa-2b 相比,在慢性丙型肝炎中具有更高的持续病毒学应答率:随机试验的系统评价。
Hepatology. 2010 Apr;51(4):1176-84. doi: 10.1002/hep.23504.
9
Genetic variation in IL28B is associated with chronic hepatitis C and treatment failure: a genome-wide association study.IL28B 基因变异与慢性丙型肝炎及治疗失败相关:一项全基因组关联研究。
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10
The efficacy and safety of telaprevir - a new protease inhibitor against hepatitis C virus.替拉瑞韦 - 一种新型抗丙型肝炎病毒蛋白酶抑制剂的疗效和安全性。
Expert Opin Investig Drugs. 2010 Jan;19(1):151-9. doi: 10.1517/13543780903501505.

慢性丙型肝炎基于干扰素治疗的演变

Evolution of interferon-based therapy for chronic hepatitis C.

作者信息

Chen Chun-Hao, Yu Ming-Lung

机构信息

Digestive Division, Department of Internal Medicine, Kaohsiung Municipal United Hospital, Kaohsiung 804, Taiwan.

出版信息

Hepat Res Treat. 2010;2010:140953. doi: 10.1155/2010/140953. Epub 2010 Oct 10.

DOI:10.1155/2010/140953
PMID:21152178
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2990099/
Abstract

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.

摘要

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。