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恩替卡韦与拉米夫定治疗慢性乙型肝炎的系统评价

Entecavir versus lamivudine for the treatment of chronic hepatitis B: a systematic review.

作者信息

Liang Jian, Tang Yan-Fang, Wu Fa-Sheng, Deng Xin

机构信息

Ruikang Hospital of Guangxi Traditional Chinese Medical University, Nanning, China.

出版信息

Pharmazie. 2012 Nov;67(11):883-90.

Abstract

The aim of this study was to systematically review the efficacy and safety of entecavir versus lamivudine for the treatment of chronic hepatitis B (CHB). A computerized search of The Cochrane Library (CENTRAL, Issue 5, 2011), MEDLINE (PubMed, 1978-June 2011), EMbase (1974-June 2011) and CNKI (1978-June 2011) databases was conducted. In addition, a manual search was made of the references of the included studies and relevant articles. The searches were restricted to studies published in Chinese or English from the time the database was created to June 2011. Studies were selected according to prespecified inclusion and exclusion criteria and then subjected for quality assessment and data extraction. Meta-analysis was performed using the statistical software (RevMan 5.1.1) provided by the Cochrane Collaboration. A total of 8 studies, all of which were randomized clinical trials (RCTs), involving 2178 patients with CHB were included. Subgroup analyses by treatment duration were conducted. The quality of the evidence was classified as moderate by the GRADED approach for all the included RCTs. Meta-analysis showed the following. Entecavir was associated with significantly improved liver histology, compared with lamivudine (RR 1.16, 95, CI [1.07, 1.26], P=0.0004). Patients were significantly more likely to experience HBV-DNA loss and have normalized ALT levels when treated with entecavir versus lamivudine for either 48 or 96 weeks (RR 1.65, 95, CI [1.37, 1.98], P<0.00001; RR 1.15, 95, CI [1.11, 1.20], P<0.00001, respectively). There were no statistically significant differences in the proportion of patients who achieved HBeAg loss or HBeAg seroconversion, or who developed adverse events between entecavir and lamivudine treatments (RR 1.03, 95, CI [0.83, 1.26], P=0.81; RR 0.92, 95, CI [0.75, 1.12], P=0.39; RR 1.09, 95, CI [0.92, 1.30], P=0.31, respectively). Current clinical evidence suggests that despite of short- or long-term use, entecavir appears to be more effective than lamivudine in reducing serum HBV-DNA load, improving liver histology, and normalizing ALT in patients with CHB. However, the probability for patients to experience HBeAg loss or HBeAg seroconversion, or the risk for adverse events seems to be similar between entecavir and lamivudine regimens.

摘要

本研究旨在系统评价恩替卡韦与拉米夫定治疗慢性乙型肝炎(CHB)的疗效和安全性。通过计算机检索了Cochrane图书馆(CENTRAL,2011年第5期)、MEDLINE(PubMed,1978年 - 2011年6月)、EMbase(1974年 - 2011年6月)和CNKI(1978年 - 2011年6月)数据库。此外,还对纳入研究的参考文献及相关文章进行了手工检索。检索限于从数据库创建至2011年6月发表的中文或英文研究。根据预先设定的纳入和排除标准选择研究,然后进行质量评估和数据提取。使用Cochrane协作网提供的统计软件(RevMan 5.1.1)进行荟萃分析。共纳入8项研究,均为随机临床试验(RCT),涉及2178例CHB患者。按治疗疗程进行亚组分析。所有纳入的RCT证据质量经GRADED方法分类为中等。荟萃分析结果如下。与拉米夫定相比,恩替卡韦可使肝脏组织学显著改善(RR 1.16,95%CI [1.07,1.26],P = 0.0004)。恩替卡韦治疗48周或96周时,患者出现HBV - DNA转阴和ALT水平正常化的可能性显著高于拉米夫定(RR 1.65,95%CI [1.37,1.98],P < 0.00001;RR 1.15,95%CI [1.11,1.2],P < 0.00001)。恩替卡韦与拉米夫定治疗在实现HBeAg转阴或HBeAg血清学转换的患者比例,或不良事件发生方面无统计学显著差异(RR 1.03,95%CI [0.83,1.26],P = 0.81;RR 0.92,95%CI [0.75,1.12],P = 0.39;RR 1.09,95%CI [0.92, 1.30],P = 0.31)。目前的临床证据表明,无论短期或长期使用,恩替卡韦在降低CHB患者血清HBV - DNA载量、改善肝脏组织学和使ALT正常化方面似乎比拉米夫定更有效。然而,恩替卡韦和拉米夫定治疗方案在患者出现HBeAg转阴或HBeAg血清学转换的概率,或不良事件风险方面似乎相似。

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