期刊
HEPATOLOGY
卷 54, 期 5, 页码 1591-1599出版社
WILEY
DOI: 10.1002/hep.24555
关键词
-
资金
- F. Hoffmann-La Roche, Basel, Switzerland
As there is currently a lack of consensus on the most appropriate dose and duration of peginterferon alfa-2a (PEG-IFN alpha-2a) therapy in hepatitis B e antigen (HBeAg)-positive patients, the efficacy and safety of either 24 or 48 weeks' duration and 90 mu g/week or 180 mu g/week doses were compared. HBeAg-positive patients (n = 544; 34% genotype B, 51% genotype C) were randomized to receive PEG-IFN alpha-2a (2 x 2 factorial design) for 24 or 48 weeks and at 90 mu g/week or 180 mu g/week and included in the per-protocol population. The primary efficacy endpoint of the noninferiority study was HBeAg seroconversion 6 months posttreatment. The prespecified odds ratio (OR) noninferiority margin was 1.88 with a one-sided significance level of 0.025. The highest rates of HBeAg seroconversion 6 months posttreatment were in the 180/48 arm (36.2% versus 14.1%-25.8% in the other arms). When the dose and duration arms were pooled, the OR for noninferiority of 24 weeks versus 48 weeks was 2.17 (95% confidence interval [CI] 1.43, 3.31; P = 0.749) and for 90 mu g versus 180 mu g was 1.79 (95% CI 1.18, 2.72; P = 0.410). As the upper limit of the 95% CI of the ORs were >1.88, 24 weeks were inferior to 48 weeks and 90 mu g/week was inferior to 180 mu g/week. The highest rates of response in the 180/48 arm were achieved by patients with HBsAg <1,500 IU/mL at Week 12 (58%) or Week 24 (57%), whereas patients with HBsAg >20,000 IU/mL did not respond. Adverse events were typical of those associated with PEG-IFN alpha-2a. Conclusion: Compared with lower doses and shorter durations, the licensed PEG-IFN alpha-2a treatment regimen (180 mu g/48 weeks) was the most efficacious and beneficial for HBeAg-positive patients predominantly infected with hepatitis B virus genotypes B or C. (HEPATOLOGY 2011;54:1591-1599)
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据