首页> 外文期刊>Hepatology international >Extended treatment with lamivudine and adefovir dipivoxil in chronic hepatitis B patients with lamivudine resistance
【24h】

Extended treatment with lamivudine and adefovir dipivoxil in chronic hepatitis B patients with lamivudine resistance

机译:拉米夫定联合阿德福韦酯对慢性乙型肝炎拉米夫定耐药的长期治疗

获取原文
           

摘要

PurposeWe and others have reported that adding adefovir dipivoxil (adefovir) to lamivudine results in virological and biochemical improvement in cases of lamivudine resistance. The current study assessed the efficacy and safety of combined therapy after 104?weeks of combined treatment and analyzed the frequency of persistent lamivudine resistant HBV.MethodsA total of 78 patients with compensated CHB (Group A) were maintained on either adefovir 10?mg daily (n?=?38) or placebo (n?=?40) while continuing lamivudine. An additional 38 patients with decompensated cirrhosis or post liver transplantation (Group B) received lamivudine plus adefovir. The primary endpoint was HBV DNA response at year 2.ResultsAt week 104 of therapy, a significantly greater proportion of patients in Group A on combination therapy (76%) had a decline in serum HBV DNA to ≤105 copies or >2 log10 reduction from baseline compared to those receiving lamivudine alone (13%; p?
机译:目的我们和其他人已经报告说,在拉米夫定耐药的情况下,将阿德福韦酯(阿德福韦)添加到拉米夫定中可改善病毒学和生化指标。目前的研究评估了联合治疗104周后联合治疗的有效性和安全性,并分析了持续的拉米夫定耐药性HBV的发生频率。方法总共78例患有CHB补偿的患者(A组)每天服用10 mg阿德福韦( n?=?38)或安慰剂(n?=?40),同时继续使用拉米夫定。另外38例失代偿性肝硬化或肝移植后的患者(B组)接受拉米夫定加阿德福韦治疗。主要终点是第2年时的HBV DNA反应。结果在治疗的第104周,联合治疗的A组患者中有较大比例的患者(76%)的血清HBV DNA下降至≤105份或从≥2log10下降与仅接受拉米夫定的患者相比(13%; p <0.001)。接受联合治疗的A组患者中有52%继续患有M204V / I HBV突变,而单独接受拉米夫定的患者中这一比例为92%(p?=?0.0013)。表达持续性拉米夫定耐药性HBV的患者发生病毒学应答的频率降低。在B组中,第104周有87%的患者出现HBV DNA反应(中位数从基线改变为5.84 log10拷贝/ mL)。结论拉米夫定和阿德福韦的联合治疗2年通常被证明对拉米夫定耐药的患者有效,但是是代偿性患者中拉米夫定耐药突变体的持续高检出率和病毒学应答受损。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号