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首页> 外文期刊>Journal of Medical Virology >Comparison of the Efficacies of Entecavir 0.5 and 1.0mg Combined With Adefovir in Patients With Chronic Hepatitis B Who Had Failed on Prior Nucleos(t)ide Analogue Treatments
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Comparison of the Efficacies of Entecavir 0.5 and 1.0mg Combined With Adefovir in Patients With Chronic Hepatitis B Who Had Failed on Prior Nucleos(t)ide Analogue Treatments

机译:恩替卡韦0.5和1.0mg联合阿德福韦对先前接受核苷类似物治疗失败的慢性乙型肝炎患者的疗效比较

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Entecavir (ETV) plus adefovir (ADV) combination therapy is one of the useful treatment option for the patients with chronic hepatitis B (CHB) who had failed on prior nucleos(t) ide analogue (NA) treatments. This study compared the efficacies of the combinations of ETV 0.5mg plus ADV and ETV 1.0mg plus ADV in patients who had failed on prior multiple NA treatments. This retrospective analysis included 148 consecutive patients with CHB infection in Korea (n=37 with ETV 0.5mg plus ADV and n=111 with ETV 1.0mg plus ADV). The virological and biochemical responses were compared between the two groups. The cumulative probability of viral suppression of ETV 0.5mg plus ADV was not inferior to that of ETV 1.0mg plus ADV (hazard ratio [HR], 0.64; 95% confidence interval [CI], 0.38-1.08; P=0.094). The changes in serum HBV DNA level in the ETV 0.5mg plus ADV group were not different between the two groups over 12 months. Moreover, no significant difference was observed in acquiring ETV-resistant variants between the two groups during the treatment (HR, 0.95; P=0.953). This study suggests the proof-of-concept that the lower dose of NA in combination with other NA might be the theoretical option for rescue combination therapy in patients with CHB who had failed on prior multiple NA treatments in order to reduce systemic exposure and possible side effects of NA. J. Med. Virol. 87:999-1007, 2015. (c) 2015 Wiley Periodicals, Inc.
机译:恩替卡韦(ETV)联合阿德福韦(ADV)联合疗法是对先前的核苷酸(t)类似物治疗失败的慢性乙型肝炎(CHB)患者的一种有用的治疗选择。这项研究比较了ETV 0.5mg加ADV和ETV 1.0mg加ADV联合治疗对先前多次NA治疗无效的患者的疗效。这项回顾性分析包括了韩国的148例连续的CHB感染患者(n = 37 ETV 0.5mg加ADV,n = 111 eTV 1.0mg加ADV)。比较了两组的病毒学和生化反应。 ETV 0.5mg + ADV的病毒抑制累积概率不低于ETV 1.0mg + ADV的累积病毒抑制率(危险比[HR]为0.64; 95%置信区间[CI]为0.38-1.08; P = 0.094)。两组在12个月内,ETV 0.5mg加ADV组的血清HBV DNA水平变化无差异。此外,在治疗期间两组之间在获得抗ETV的变异体中没有观察到显着差异(HR,0.95; P = 0.953)。这项研究提出了概念证明,即在先前多次NA治疗失败的CHB患者中,将较低剂量的NA与其他NA联合使用可能是抢救组合治疗的理论选择,以减少全身暴露和可能的副作用NA的影响。 J. Med。病毒。 87:999-1007,2015.(c)2015威利期刊公司

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