首页> 外文OA文献 >Once-daily prolonged-release tacrolimus (ADVAGRAF) versus twice-daily tacrolimus (PROGRAF) in liver transplantation.
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Once-daily prolonged-release tacrolimus (ADVAGRAF) versus twice-daily tacrolimus (PROGRAF) in liver transplantation.

机译:在肝脏移植中,每天一次的他克莫司(ADVAGRAF)与每天两次的他克莫司(PROGRAF)。

摘要

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.
机译:在多中心,1:1随机分配,两个随机对照试验中比较了每天两次他克莫司(BID; Prograf)和每天一次他克莫司(QD; Advagraf)联合使用类固醇但无抗体诱导的双重治疗方案的有效性和安全性475名原发性肝移植受者的双臂平行研究。双盲,双假24周,然后开放到移植后12个月。他克莫司BID的主要终点是活检证实的急性排斥反应(BPAR)在24周时的发生率为33.7%,而他克莫司QD为36.3%(按协议确定; p = 0.512;治疗差异2.6%,95%置信区间-7.3%,12.4%),不超过预定义的15%的自卑率。在12个月时,他克莫司的BID和QD需要治疗的BPAR发作相似(分别为28.1%和24.7%)。他克莫司BID的十二个月患者和移植物存活率分别为90.8%和85.6%,他克莫司QD的为89.2%和85.3%。他克莫司BID和QD的不良事件(AE)资料相似,而AE和严重AE的发生率相当。他克莫司QD具有良好的耐受性,其功效和安全性与他克莫司BID相似。

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