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肝移植中每日 1 次延长释放他克莫司(ADVAGRAF)与每日 2 次他克莫司(PROGRAF)的比较。

Once-daily prolonged-release tacrolimus (ADVAGRAF) versus twice-daily tacrolimus (PROGRAF) in liver transplantation.

机构信息

Department of Hepatogastroenterology, IKEM, Prague, Czech Republic.

出版信息

Am J Transplant. 2010 Oct;10(10):2313-23. doi: 10.1111/j.1600-6143.2010.03255.x. Epub 2010 Sep 14.

Abstract

The efficacy and safety of dual-therapy regimens of twice-daily tacrolimus (BID; Prograf) and once-daily tacrolimus (QD; Advagraf) administered with steroids, without antibody induction, were compared in a multicenter, 1:1-randomized, two-arm, parallel-group study in 475 primary liver transplant recipients. A double-blind, double-dummy 24-week period was followed by an open extension to 12 months posttransplant. The primary endpoint, event rate of biopsy-proven acute rejection (BPAR) at 24 weeks, was 33.7% for tacrolimus BID versus 36.3% for tacrolimus QD (Per-protocol set; p = 0.512; treatment difference 2.6%, 95% confidence interval -7.3%, 12.4%), falling within the predefined 15% noninferiority margin. At 12 months, BPAR episodes requiring treatment were similar for tacrolimus BID and QD (28.1% and 24.7%). Twelve-month patient and graft survival was 90.8% and 85.6% for tacrolimus BID and 89.2% and 85.3% for tacrolimus QD. Adverse event (AE) profiles were similar for both tacrolimus BID and QD with comparable incidences of AEs and serious AEs. Tacrolimus QD was well tolerated with similar efficacy and safety profiles to tacrolimus BID.

摘要

在一项多中心、1:1 随机、双盲、双臂平行组研究中,比较了每日两次他克莫司(BID;Prograf)和每日一次他克莫司(QD;Advagraf)与类固醇联合、不使用抗体诱导的双重治疗方案在 475 例原发性肝移植受者中的疗效和安全性。在 24 周时,主要终点为活检证实的急性排斥反应(BPAR)的发生率,他克莫司 BID 组为 33.7%,他克莫司 QD 组为 36.3%(方案设定集;p=0.512;治疗差异 2.6%,95%置信区间-7.3%,12.4%),在预设的 15%非劣效性边界内。在 12 个月时,需要治疗的 BPAR 发作在他克莫司 BID 和 QD 组中相似(28.1%和 24.7%)。12 个月时,他克莫司 BID 和 QD 的患者和移植物存活率分别为 90.8%和 85.6%,89.2%和 85.3%。他克莫司 BID 和 QD 的不良事件(AE)谱相似,AE 和严重 AE 的发生率相当。他克莫司 QD 具有良好的耐受性,与他克莫司 BID 的疗效和安全性谱相似。

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