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首页> 外文期刊>African Journal of Biotechnology >Comparison of the efficacy of entecavir and lamivudine in the treatment of chronic hepatitis B: A meta-analysis
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Comparison of the efficacy of entecavir and lamivudine in the treatment of chronic hepatitis B: A meta-analysis

机译:恩替卡韦和拉米夫定治疗慢性乙型肝炎疗效比较:一项荟萃分析

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Some researches demonstrate that entecavir increases the incidence of virological and biochemical responses compared?to lamivudine, although,?they have shown inconsistent response rates.?A meta-analysis was conducted to compare the efficacy of entecavir and lamivudine for chronic hepatitis B treatment. Two independent researchers identified pertinent clinical controlled trials.?Our analysis includes nine case-control studies, which had?1251 entecavir groups and 1188 lamivudine groups. Analyses were performed with STATA version 9.0. Rates of virology and biochemical responses and HBeAg clearance and seroconversion were used as primary efficacy measures. Greater virological and biochemical responses rates were observed with entecavir to lamivudine after treatment of 48 weeks (odds ratio (OR) = 3.422, 95% confidence intervals (CI) = 2.349 - 4.985, P = 0.000; OR = 2.173, 95% CI = 1.462 - 3.230, P = 0.000, respectively), but?no statistically significant differences were observed between cases and controls forclearance and seroconversion of HBeAg?(P > 0.05). Safety and adverse-event profiles were similar in the two groups. In conclusion, this meta-analysis suggestedthat entecavir increases the incidence of virological and biochemical responses compared with lamivudine after treatment for 48 weeks.
机译:一些研究表明,恩替卡韦与拉米夫定相比增加了病毒学和生化反应的发生率,尽管它们显示出不一致的反应率。荟萃分析比较了恩替卡韦和拉米夫定在慢性乙型肝炎治疗中的疗效。两名独立研究人员确定了相关的临床对照试验。我们的分析包括9个病例对照研究,其中包括1251个恩替卡韦组和1188个拉米夫定组。使用STATA 9.0版进行分析。病毒学和生化反应率以及HBeAg清除率和血清转化率被用作主要疗效指标。用恩替卡韦治疗拉米夫定48周后观察到更高的病毒学和生化反应率(优势比(OR)= 3.422,95%置信区间(CI)= 2.349-4.985,P = 0.000; OR = 2.173,95%CI =分别为1.462-3.230,P = 0.000),但是在病例与对照组之间,对于HBeAg的清除和血清转化没有统计学上的显着差异(P> 0.05)。两组的安全性和不良事件情况相似。总之,这项荟萃分析表明,与拉米夫定治疗48周相比,恩替卡韦增加了病毒学和生化反应的发生率。

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