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首页> 外文期刊>Value in health: the journal of the International Society for Pharmacoeconomics and Outcomes Research >Mixed treatment comparison meta-analysis evaluating the relative efficacy of nucleos(t)ides for treatment of nucleos(t)ide-naive patients with chronic hepatitis B.
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Mixed treatment comparison meta-analysis evaluating the relative efficacy of nucleos(t)ides for treatment of nucleos(t)ide-naive patients with chronic hepatitis B.

机译:混合治疗比较荟萃分析评估了核苷酸(t)的治疗相对于未接受核苷酸(t)的慢性乙型肝炎患者的相对疗效。

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摘要

BACKGROUND/AIMS: Five nucleosideucleotide treatments are now available for chronic hepatitis B (CHB). This meta-analysis aimed to assess the relative efficacy of adefovir, entecavir, lamivudine, telbivudine, tenofovir disoproxil fumarate (TDF), and nucleos(t)ide combinations in the treatment of CHB. METHODS: A systematic review of MEDLINE and the Cochrane library was conducted to identify all studies evaluating these nucleos(t)ides in adults with CHB. Randomized controlled trials were included in the meta-analysis if they reported the proportion of patients with undetectable hepatitis B virus (HBV) DNA or hepatitis B e antigen (HBeAg) loss/seroconversion at 1 year. Bayesian mixed treatment comparison meta-analyses were conducted in WinBUGS to assess relative efficacy. RESULTS: A random-effects meta-analysis of trials on treatment-naive patients with HBeAg-positive CHB demonstrated that 94% of patients will achieve HBV DNA < 300 copies/ml after 1 year with TDF, compared with 73% for entecavir, 50% for adefovir, and 38% for lamivudine. There was a 97.7% probability that TDF enabled a greater proportion of patients to achieve HBV DNA < 300 copies/ml at 1 year than all other treatments considered in the analysis. TDF was significantly superior to all nucleos(t)ides for this outcome at the 0.05 level. There were no statistically significant differences between nucleos(t)ides in HBeAg seroconversion at 1 year, based on a fixed-effects meta-analysis in the same population. More trials on HBeAg-negative and drug-resistant patients are required to facilitate meta-analyses for these subgroups. CONCLUSIONS: In nucleos(t)ide-naive patients with HBeAg-positive CHB, TDF is associated with the highest probability of achieving undetectable HBV DNA at 1 year of all nucleos(t)ides considered.
机译:背景/目的:现在有五种核苷/核苷酸治疗可用于慢性乙型肝炎(CHB)。这项荟萃分析旨在评估阿德福韦,恩替卡韦,拉米夫定,替比夫定,替诺福韦富马酸替诺福韦酯(TDF)和核苷酸(t)联合治疗CHB的相对疗效。方法:对MEDLINE和Cochrane文库进行了系统综述,以鉴定所有评估成人CHB患者中这些核苷酸的研究。如果荟萃分析报告了在1年时检测不到乙型肝炎病毒(HBV)DNA或乙型肝炎e抗原(HBeAg)丢失/血清转换的患者比例,则该荟萃分析中包括了随机对照试验。在WinBUGS中进行贝叶斯混合治疗比较荟萃分析,以评估相对疗效。结果:对未接受过治疗的HBeAg阳性CHB患者进行的一项试验的随机效应荟萃分析表明,使用TDF 1年后,有94%的患者将达到HBV DNA <300拷贝/毫升,而恩替卡韦为73%,50阿德福韦为%,拉米夫定为38%。与分析中考虑的所有其他治疗方法相比,TDF在1年内使更多比例的患者实现HBV DNA <300拷贝/ ml的可能性为97.7%。 TDF在0.05水平上显着优于所有核苷酸(t)。基于对同一人群的固定效应荟萃分析,在1年时HBeAg血清转化中的核苷之间没有统计学上的显着差异。需要对HBeAg阴性和耐药患者进行更多试验,以促进对这些亚组的荟萃分析。结论:在未接受HBeAg阳性CHB的核苷酸患者中,TDF与所有考虑的核苷酸1年内获得不可检测的HBV DNA的可能性最高相关。

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