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首页> 外文期刊>The New England journal of medicine >Entecavir versus lamivudine for patients with HBeAg-negative chronic hepatitis B.
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Entecavir versus lamivudine for patients with HBeAg-negative chronic hepatitis B.

机译:恩替卡韦vs拉米夫定治疗HBeAg阴性慢性乙型肝炎患者。

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BACKGROUND: Entecavir is a potent and selective antiviral agent that has demonstrated efficacy in phase 2 studies in patients with hepatitis B e antigen (HBeAg)-negative chronic hepatitis B. METHODS: In this phase 3, double-blind trial, we randomly assigned 648 patients with HBeAg-negative chronic hepatitis B who had not previously been treated with a nucleoside analogue to receive 0.5 mg of entecavir or 100 mg of lamivudine once daily for a minimum of 52 weeks. The primary efficacy end point was histologic improvement (a decrease by at least two points in the Knodell necroinflammatory score, without worsening of fibrosis). RESULTS: Histologic improvement after 48 weeks of treatment occurred in 208 of 296 patients in the entecavir group who had adequate baseline liver-biopsy specimens that could be evaluated (70 percent), as compared with 174 of 287 such patients in the lamivudine group (61 percent, P=0.01). More patients in the entecavir group than in the lamivudine group had undetectable serum hepatitis B virus (HBV) DNA levels according to a polymerase-chain-reaction assay (90 percent vs. 72 percent, P<0.001) and normalization of alanine aminotransferase levels (78 percent vs. 71 percent, P=0.045). The mean reduction in serum HBV DNA levels from baseline to week 48 was greater with entecavir than with lamivudine (5.0 vs. 4.5 log [on a base-10 scale] copies per milliliter, P<0.001). There was no evidence of resistance to entecavir. Safety and adverse-event profiles were similar in the two groups. CONCLUSIONS: Among patients with HBeAg-negative chronic hepatitis B who had not previously been treated with a nucleoside analogue, the rates of histologic improvement, virologic response, and normalization of alanine aminotransferase levels were significantly higher at 48 weeks with entecavir than with lamivudine. The safety profile of the two agents was similar, and there was no evidence of viral resistance to entecavir. (ClinicalTrials.gov number, NCT00035789.).
机译:背景:恩替卡韦是一种有效的选择性抗病毒药,已在2期研究中证明对乙型肝炎e抗原(HBeAg)阴性的慢性乙型肝炎患者有效。方法:在该3期双盲试验中,我们随机分配了648先前未接受核苷类似物治疗的HBeAg阴性慢性乙型肝炎患者每天接受0.5 mg恩替卡韦或100 mg拉米夫定每日一次,至少持续52周。主要疗效终点是组织学改善(Knodell坏死性炎症评分至少降低了两个点,而纤维化没有恶化)。结果:恩替卡韦组296例患者中有208例在治疗48周后组织学改善,基线肝活检标本可评估(70%),而拉米夫定组287例此类患者中有174例(61%)百分比,P = 0.01)。根据聚合酶链反应分析(90%vs. 72%,P <0.001)和丙氨酸转氨酶水平正常化,恩替卡韦组比拉米夫定组患者的血清乙型肝炎病毒(HBV)DNA水平检测不到(90%vs. 72%,P <0.001) 78%比71%,P = 0.045)。从基线到第48周,从基线到第48周,血清HBV DNA水平的平均降低大于拉米夫定(每毫升5.0 vs. 4.5 log [以10为基数的量级]对数,P <0.001)。没有证据表明对恩替卡韦有抗药性。两组的安全性和不良事件情况相似。结论:在先前未接受核苷类似物治疗的HBeAg阴性慢性乙型肝炎患者中,恩替卡韦治疗48周时的组织学改善,病毒学应答和丙氨酸转氨酶水平正常化的比率明显高于拉米夫定。两种药物的安全性相似,没有证据表明对恩替卡韦有病毒抗药性。 (ClinicalTrials.gov编号,NCT00035789。)。

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