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首页> 外文期刊>Transplant international : >ADHERE: randomized controlled trial comparing renal function in de novo kidney transplant recipients receiving prolonged-release tacrolimus plus mycophenolate mofetil or sirolimus
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ADHERE: randomized controlled trial comparing renal function in de novo kidney transplant recipients receiving prolonged-release tacrolimus plus mycophenolate mofetil or sirolimus

机译:坚持:随机对照试验比较肾功能在De Novo肾移植受者接受延长释放的Tacrolimus加霉霉素或西罗莫司

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摘要

ADHERE was a randomized, open-label, Phase IV study comparing renal function at Week 52 postkidney transplant, in patients who received prolonged-release tacrolimus-based immunosuppressive regimens. On Days 0-27, patients received prolonged-release tacrolimus (initially 0.2 mg/kg/day), corticosteroids, and mycophenolate mofetil (MMF). Patients were randomized on Day 28 to receive either prolonged-release tacrolimus plus MMF (Arm 1) or prolonged-release tacrolimus (>= 25% dose reduction on Day 42) plus sirolimus (Arm 2). The primary endpoint was glomerular filtration rate by iohexol clearance (mGFR) at Week 52. Secondary endpoints included eGFR, creatinine clearance (CrCl), efficacy failure (patient withdrawal or graft loss), and patient/graft survival. Tolerability was analyzed. The full-analysis set comprised 569 patients (Arm 1: 287; Arm 2: 282). Week 52 mean mGFR was similar in Arm 1 versus Arm 2 (40.73 vs. 41.75 ml/min/1.73 m(2); P = 0.405), as were the secondary endpoints, except composite efficacy failure, which was higher in Arm 2 versus 1 (18.2% vs. 11.5%; P = 0.002) owing to a higher postrandomization withdrawal rate due to adverse events (AEs) (14.4% vs. 5.2%). Results from this study show comparable renal function between arms at Week 52, with fewer AEs leading to study discontinuation with prolonged-release tacrolimus plus MMF (Arm 1) versus lower dose prolonged-release tacrolimus plus sirolimus (Arm 2).
机译:粘附是一项随机的开放标签,相对于肾功能在第52周Postkidney移植的肾功能,接受延长释放的Tacrolimus的免疫抑制方案的患者。在第0-27天,患者接受延长释放的躯干(最初0.2mg / kg /天),皮质类固醇和霉酚酸酯MofeTil(MMF)。患者在第28天中随机化,以接收延长释放的Tacrolimus加mMF(ARM 1)或延长的释放Tacrolimus(> = 25%的剂量减少)加西罗莫司(ARM 2)。主要终点是在第52周的碘己酮间隙(MGFR)的肾小球过滤速率。次要终点包括EGFR,肌酐清除(CRCL),功效失败(患者戒断或移植物损失)和患者/移植物存活。分析了可耐受性。全分析组包括569名患者(ARM 1:287; ARM 2:282)。第52周的平均mgfr在臂1与臂2中相似(40.73与41.75ml / min / 1.73m(2); p = 0.405),除了复合功效失效之外的次要终点,其手臂2与abs 2更高由于不良事件(AES)(AES)增加,1(18.2%vs.11.5%; p = 0.002)(14.4%vs.5.2%)。本研究的结果显示在第52周的臂之间的相当肾功能,较少的AES导致研究停止,延长释放的Tacrolimus Plus MMF(ARM 1)与较低剂量延长释放的Tacrolimus加西罗莫司(ARM 2)。

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