Barten Markus J, Hirt Stephan W, Garbade Jens, Bara Christoph, Doesch Andreas O, Knosalla Christoph, Grinninger Carola, Stypmann Jörg, Sieder Christian, Lehmkuhl Han B, Porstner Martina, Schulz Uwe
Department of Cardiovascular Surgery, University Heart Center Hamburg, Martinistrasse 52, 20246, Hamburg, Germany.
Department of Cardiothoracic Surgery, University Hospital Regensburg, Franz-Josef-Strauß-Allee 11, 93053, Regensburg, Germany.
Am J Transplant. 2019 Mar 18. doi: 10.1111/ajt.15361.
In the 12-month, open-label MANDELA study, patients were randomized at month 6 after heart transplantation to (i) convert to calcineurin inhibitor (CNI)-free immunosuppression with everolimus (EVR), mycophenolic acid and steroids (CNI-free, n=71), or to (ii) continue reduced-exposure CNI, with EVR and steroids (EVR/redCNI, n=74). Tacrolimus was administered in 48.8% of EVR/redCNI patients and 52.6% of CNI-free patients at radomization. Both strategies improved and stabilized renal function based on the primary endpoint (estimated GFR at month 18 post-transplant post-randomization) with superiority of the CNI-free group versus EVR/redCNI : mean 64.1mL/min/1.73m versus 52.9mL/min/1.73m ; difference +11.3mL/min/1.73m (p<0.001). By month 18, estimated GFR had increased by ≥10mL/min/1.73 in 31.8% and 55.2% of EVR/redCNI and CNI-free patients, respectively, and by ≥25 mL/min/1.73m in 4.5% and 20.9%. Rates of biopsy-proven acute rejection (BPAR) were 6.8% and 21.1%; all cases were without hemodynamic compromise. BPAR was less frequent with EVR/redCNI versus the CNI-free regimen (p=0.015); 6/15 episodes in CNI-free patients occurred with EVR concentration <5ng/mL. Rates of adverse events and associated discontinuations were comparable EVR/redCNI from month 6 achieved stable renal function with infrequent BPAR. One-year renal function can be improved by early conversion to EVR-based CNI-free therapy but requires close EVR monitoring. This article is protected by copyright. All rights reserved.
在为期12个月的开放标签曼德拉研究中,心脏移植术后6个月的患者被随机分为:(i) 转换为使用依维莫司(EVR)、霉酚酸和类固醇的无钙调神经磷酸酶抑制剂(CNI)免疫抑制方案(无CNI组,n = 71),或 (ii) 继续使用低剂量CNI,并联合EVR和类固醇(EVR/低剂量CNI组,n = 74)。随机分组时,48.8%的EVR/低剂量CNI组患者和52.6%的无CNI组患者使用他克莫司。基于主要终点指标(随机分组后移植后18个月的估计肾小球滤过率),两种策略均改善并稳定了肾功能,无CNI组优于EVR/低剂量CNI组:平均为64.1mL/min/1.73m² 对比 52.9mL/min/1.73m²;差值为 +11.3mL/min/1.73m²(p < 0.001)。到18个月时,EVR/低剂量CNI组和无CNI组中分别有31.8%和55.2%的患者估计肾小球滤过率增加≥10mL/min/1.73m²,4.5%和20.9%的患者增加≥25mL/min/1.73m²。活检证实的急性排斥反应(BPAR)发生率分别为6.8%和21.1%;所有病例均无血流动力学损害。与无CNI方案相比,EVR/低剂量CNI组的BPAR发生率更低(p = 0.015);无CNI组的15次发作中有6次发生在EVR浓度<5ng/mL时。不良事件发生率及相关停药率在EVR/低剂量CNI组和无CNI组相当,EVR/低剂量CNI组从第6个月起肾功能稳定,BPAR发生率低。早期转换为基于EVR的无CNI治疗可改善1年的肾功能,但需要密切监测EVR。本文受版权保护。保留所有权利。