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恩替卡韦治疗拉米夫定失效的慢性乙型肝炎患者5年的临床疗效
引用本文:李红,王志毅,张大志,石小枫,周智,任红.恩替卡韦治疗拉米夫定失效的慢性乙型肝炎患者5年的临床疗效[J].中华肝脏病杂志,2009,17(5).
作者姓名:李红  王志毅  张大志  石小枫  周智  任红
作者单位:重庆医科大学第二附属医院感染科,400010
摘    要:目的 评价恩替卡韦(ETV)对重庆地区拉米夫定治疗失效的慢性乙型肝炎(CHB)患者5年的疗效和安全性.方法 选取拉米夫定治疗失效的CHB患者32例,随机分为ETV组(剂量1.0 mg/d)28例和安慰剂组4例,完成12周的双盲治疗后,患者均接受开放的ETV(剂量1.0 mg/d)治疗,持续治疗至240周.分别检测治疗2、4、8、12、24、48、96、144、168、240周时患者的血清HBV DNA水平、HBsAg与HBeAg状态和肝功能情况.双盲阶段HBV DNA水平变化情况经Mauchly"球对称"检验后采用重复测量数据方差分析;连续性变量的统计描述用均数±标准差(x±s)表示.结果 在接受ETV治疗后,12周时ETV组患者血清HBV DNA水平平均下降4.05 log10拷贝/ml,安慰剂组平均下降0.08 log10拷贝/ml(P<0.05).治疗240周时,ETV组患者HBV DNA水平均值下降至2.58 log10拷贝/ml.HBV DNA<3 log10拷贝/ml患者的百分比在治疗前为0,从第8周开始上升(6.25%),24周时为15.6%,尤其在96周明显上升(50%),到240周末为57.14%.240周末有2例出现HBsAg血清学转换,4例出现HBeAg血清学转换.服用ETV后ALT水平下降较迅速,12周后均数达正常水平,且5年持续低于40 U/L.5年治疗期间,患者不良事件发生率为21%,有1例出现严重不良事件. 结论 ETV(1.0 mg/d)治疗拉米夫定失效的CHB患者具有显著的抗病毒和临床疗效,且安全性及耐受性良好.

关 键 词:肝炎  乙型  慢性  临床试验  拉米夫定  恩替卡韦

Five years trial of entecavir for chronic hepatitis B patients failed with lamivudine therapy in the Chongqing area
LI Hong,WANG Zhi-yi,ZHANG Da-zhi,SHI Xiao-feng,ZHOU Zhi,REN Hong.Five years trial of entecavir for chronic hepatitis B patients failed with lamivudine therapy in the Chongqing area[J].Chinese Journal of Hepatology,2009,17(5).
Authors:LI Hong  WANG Zhi-yi  ZHANG Da-zhi  SHI Xiao-feng  ZHOU Zhi  REN Hong
Abstract:Objective To evaluate the efficacy and safety of five-year trail of entecavir for chronic hepatitis B patients failed with lamivudine therapy in the Chongqing area. Methods 32 patients failed with lamivudine therapy were enrolled in this study. In the double-blind phase, patients were randomly divided into entecavir 1.0 mg/d group (n = 28) and placebo group(n = 4) for 12 weeks. In the open-lable phase, patients received ETV 1.0 mg/d for 240 weeks. HBV DNA level, fiver function, HBV serology were observed. Results The mean reduction in HBV DNA level at week 12 was 4.05 log10 copies/ml in ETV group, and 0.08 log10 copies/ml in placebo group (P<0.05). The mean of HBV DNA level after 240 weeks of ETV treatment was decreased to 2.58 log10 copies/ml. The proportion of patients with HBV DNA< 3 log10 copies/ml was 0, 6.25%, 15.6%, 50%, and 57.14% at 0, 8, 24, 96 and 240 weeks respectivfely. There were 2 patients with HBsAg seroconversion and 4 patients with HBeAg seroconversion at the end of the study. The ALT level returned to normal at week 12 and remained normal throughout the following 240 weeks. One patient had a severe adverse event during the trail. Condusion Entecavir is effective and safe for the chronic hepatitis B patients failed with lamivudine therapy.
Keywords:Hepatitis B  chronic  Clinical trials  Lamivudine  Entecavir
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