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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:ADHERE:一项随机对照试验,比较接受长期释放他克莫司和霉酚酸酯或西罗莫司治疗的新肾移植受者的肾功能

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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:ADHERE是一项随机,开放标签,IV期研究,比较了接受基于他克莫司延长释放的免疫抑制方案的患者,在肾脏移植后第52周时的肾功能。在第0-27天,患者接受他克莫司的缓释(最初为0.2 mg / kg /天),皮质类固醇和霉酚酸酯(MMF)。患者在第28天随机接受延长释放他克莫司加MMF(Arm 1)或延长释放他克莫司(第42天剂量减少≥25%)加西罗莫司(Arm 2)。主要终点为第52周时通过碘海醇清除率(mGFR)得出的肾小球滤过率。次要终点包括eGFR,肌酐清除率(CrCl),疗效衰竭(患者停药或移植物丢失)以及患者/移植物存活。公差进行了分析。全套分析包括569例患者(手臂1:287;手臂2:282)。第52周,第1组与第2组的平均mGFR相似(40.73对41.75 ml / min / 1.73 m(2); P = 0.405),次要终点也是如此,除了复合功效失败外,第2组的平均mGFR高于第二组1(18.2%比11.5%; P = 0.002),这是由于不良事件(AE)导致的随机后撤回率更高(14.4%比5.2%)。这项研究的结果表明,在第52周时,两臂之间的肾功能相当,而较少的AEs导致研究中止使用长效他克莫司加MMF(Arm 1)与较低剂量的长效他克莫司加西罗莫司(Arm 2)。

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