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首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >Lamivudine for the treatment of hepatitis B virus-related liver disease after renal transplantation: meta-analysis of clinical trials.
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Lamivudine for the treatment of hepatitis B virus-related liver disease after renal transplantation: meta-analysis of clinical trials.

机译:拉米夫定治疗肾移植后与乙型肝炎病毒相关的肝病:临床试验的荟萃分析。

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摘要

BACKGROUND: Numerous reports have appeared on lamivudine use for the treatment of hepatitis B virus (HBV) infection after renal transplantation (RT). However, the efficacy and safety of lamivudine after RT remain unclear. METHODS: The authors evaluated the efficacy and safety of initial lamivudine monotherapy in RT recipients with hepatitis B by performing a systematic review of the literature with a meta-analysis of clinical trials. The primary outcomes were hepatitis B (HB) e antigen (Ag) and HBV-DNA clearance (as measures of efficacy); the secondary outcomes were biochemical response (as measures of efficacy), dropout rate, and lamivudine resistance (as measures of tolerability). The authors used the random effects model of DerSimonian and Laird, and outcomes were analyzed on an intent-to-treat basis. RESULTS: The authors identified 14 clinical trials (184 patients); all of these were prospective cohort studies. The mean overall estimate for HBV-DNA and HBeAg clearance, alanine aminotransferase normalization, and lamivudine resistance was 91% (95% confidence interval [CI], 86%-96%), 27% (95% CI, 16%-39%), 81% (95% CI, 70%-92%), and 18% (95% CI, 10%-37%), respectively. HBeAg seroconversion rate was assessed in four (28%) trials and ranged between 0% and 46%. The P value was greater than 0.05 for our test of study homogeneity. There was no association between rate of patients who were male patients or had cirrhosis, race, age, lamivudine dose, and HBV-DNA or HBeAg clearance. Increased duration of lamivudine therapy was positively associated with frequency of HBeAg loss (r =0.51, P =0.039) and lamivudine resistance (r =0.620, P =0.019). Only 2 (14%) of 14 studies reported a dropout rate greater than 0%. CONCLUSIONS: Our meta-analysis showed that the majority of RT recipients with hepatitis B had high virologic and biochemical response with lamivudine. Tolerance to lamivudine was good. However, lamivudine resistance was frequent with prolonged therapy, potentially limiting its long-term efficacy after RT.
机译:背景:关于拉米夫定用于肾移植(RT)后治疗乙型肝炎病毒(HBV)感染的报道很多。然而,RT后拉米夫定的疗效和安全性尚不清楚。方法:作者通过对文献进行系统评价并进行临床试验的荟萃分析,评估了最初的拉米夫定单一疗法对乙型肝炎逆转录病毒受体的疗效和安全性。主要结局为乙型肝炎(HB)e抗原(Ag)和HBV-DNA清除率(作为疗效指标)。次要结果是生化反应(作为疗效的度量),辍学率和拉米夫定耐药性(作为耐受性的度量)。作者使用了DerSimonian和Laird的随机效应模型,并在意向性治疗的基础上对结果进行了分析。结果:作者确定了14项临床试验(184例患者);其中有184例患者接受了研究。所有这些都是前瞻性队列研究。 HBV-DNA和HBeAg清除率,丙氨酸转氨酶正常化和拉米夫定耐药性的总体平均估计值为91%(95%置信区间[CI],86%-96%),27%(95%CI,16%-39%) ),81%(95%CI,70%-92%)和18%(95%CI,10%-37%)。在四项(28%)试验中评估了HBeAg血清转化率,范围在0%至46%之间。对于我们的研究均一性测试,P值大于0.05。男性或肝硬化患者的比率,种族,年龄,拉米夫定剂量与HBV-DNA或HBeAg清除率之间没有关联。拉米夫定治疗时间的延长与HBeAg丢失频率(r = 0.51,P = 0.039)和拉米夫定耐药性(r = 0.620,P = 0.019)呈正相关。 14个研究中只有2个(14%)报告辍学率大于0%。结论:我们的荟萃分析显示,大多数接受乙型肝炎的放疗接受者对拉米夫定有较高的病毒学和生化反应。拉米夫定的耐受性良好。但是,拉米夫定的耐药性在长期治疗中经常发生,可能会限制其在RT后的长期疗效。

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