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早期识别对24周聚乙二醇干扰素α-2a(40kd)/利巴韦林治疗有反应的丙型肝炎病毒1型患者。

Early identification of HCV genotype 1 patients responding to 24 weeks peginterferon alpha-2a (40 kd)/ribavirin therapy.

作者信息

Jensen Donald M, Morgan Timothy R, Marcellin Patrick, Pockros Paul J, Reddy K Rajender, Hadziyannis Stephanos J, Ferenci Peter, Ackrill Andrew M, Willems Bernard

机构信息

Center for Liver Diseasees, University of Chicago Hospitals, 60637, USA.

出版信息

Hepatology. 2006 May;43(5):954-60. doi: 10.1002/hep.21159.

Abstract

Approximately one third of hepatitis C virus (HCV) genotype 1 patients achieved a sustained virological response (SVR) after 24 weeks of treatment with peginterferon alpha-2a (40 kd) plus ribavirin in a randomized, multinational trial. We aimed to identify factors associated with a rapid virological response (RVR) at week 4 (HCV RNA <50 IU/mL) and a SVR (HCV RNA <50 IU/mL at the end of follow-up) in these patients. Stepwise multiple logistic regression analysis was used to explore the prognostic factors for a RVR and SVR in genotype 1 patients treated for 24 weeks. Fifty-one of 216 (24%) genotype 1 patients in the 24-week treatment groups had a RVR. SVR rates were considerably higher in patients with than without [corrected] a RVR (89% vs. 19%, respectively). Patients with a baseline HCV RNA of less than 200,000 IU/mL (OR 9.7, 95% CI 4.2-22.5; P < .0001) or 200,000-600,000 IU/mL (OR 5.6, 95% CI 1.5-9.1; P = .0057) were more likely to achieve a RVR than those with HCV RNA greater than 600,000 IU/mL. HCV subtype (1b vs. 1a) was also independently associated with RVR (OR 1.8, 95% CI 0.9-3.7; P = .0954). RVR (OR 23.7 vs. no RVR, 95% CI 9.1-61.7) and baseline HCV RNA less than 200,000 IU/mL (OR 2.7 vs. > 600,000 IU/mL, 95% CI 1.1-6.3; P < .026) were significant and independent predictors of SVR in patients treated for 24 weeks. In conclusion, patients infected with HCV genotype 1 and treated with peginterferon alpha-2a/ribavirin sustained a RVR 24% of the time. This portends an 89% probability of a SVR after 24 weeks of treatment.

摘要

在一项随机、多国试验中,约三分之一的丙型肝炎病毒(HCV)基因1型患者在接受聚乙二醇化干扰素α-2a(40kd)加利巴韦林治疗24周后实现了持续病毒学应答(SVR)。我们旨在确定这些患者在第4周时快速病毒学应答(RVR,HCV RNA<50IU/mL)和SVR(随访结束时HCV RNA<50IU/mL)相关的因素。采用逐步多因素逻辑回归分析来探讨接受24周治疗的基因1型患者RVR和SVR的预后因素。24周治疗组的216例基因1型患者中有51例(24%)出现RVR。有RVR的患者SVR率显著高于无RVR的患者(分别为89%和19%)。基线HCV RNA低于200,000IU/mL(OR 9.7,95%CI 4.2 - 22.5;P<.0001)或200,000 - 600,000IU/mL(OR 5.6,95%CI 1.5 - 9.1;P =.0057)的患者比HCV RNA大于600,000IU/mL的患者更有可能实现RVR。HCV亚型(1b与1a)也与RVR独立相关(OR 1.8,95%CI 0.9 - 3.7;P =.0954)。RVR(OR 23.7对比无RVR,95%CI 9.1 - 61.7)和基线HCV RNA低于200,000IU/mL(OR 2.7对比>600,000IU/mL,95%CI 1.1 - 6.3;P<.026)是接受24周治疗患者SVR的显著且独立预测因素。总之,感染HCV基因1型并接受聚乙二醇化干扰素α-2a/利巴韦林治疗的患者有24%的时间会出现RVR。这预示着治疗24周后SVR的概率为89%。

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