Stevens R Brian, Foster Kirk W, Miles Clifford D, Kalil Andre C, Florescu Diana F, Sandoz John P, Rigley Theodore H, Malik Tamer, Wrenshall Lucile E
Department of Surgery, Wright State University Boonshoft School of Medicine, Dayton, Ohio, United States of America.
Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, Nebraska, United States of America.
PLoS One. 2015 Oct 14;10(10):e0139247. doi: 10.1371/journal.pone.0139247. eCollection 2015.
The two most significant impediments to renal allograft survival are rejection and the direct nephrotoxicity of the immunosuppressant drugs required to prevent it. Calcineurin inhibitors (CNI), a mainstay of most immunosuppression regimens, are particularly nephrotoxic. Until less toxic antirejection agents become available, the only option is to optimize our use of those at hand.
To determine whether intensive rabbit anti-thymocyte globulin (rATG) induction followed by CNI withdrawal would individually or combined improve graft function and reduce graft chronic histopathology-surrogates for graft and, therefore, patient survival. As previously reported, a single large rATG dose over 24 hours was well-tolerated and associated with better renal function, fewer infections, and improved patient survival. Here we report testing whether complete CNI discontinuation would improve renal function and decrease graft pathology.
Between April 20, 2004 and 4-14-2009 we conducted a prospective, randomized, non-blinded renal transplantation trial of two rATG dosing protocols (single dose, 6 mg/kg vs. divided doses, 1.5 mg/kg every other day x 4; target enrollment = 180). Subsequent maintenance immunosuppression consisted of tacrolimus, a CNI, and sirolimus, a mammalian target of rapamycin inhibitor. We report here the outcome of converting patients after six months either to minimized tacrolimus/sirolimus or mycophenolate mofetil/sirolimus. Primary endpoints were graft function and chronic histopathology from protocol kidney biopsies at 12 and 24 months.
CNI withdrawal (on-treatment analysis) associated with better graft function (p <0.001) and lower chronic histopathology composite scores in protocol biopsies at 12 (p = 0.003) and 24 (p = 0.013) months, without affecting patient (p = 0.81) or graft (p = 0.93) survival, or rejection rate (p = 0.17).
CNI (tacrolimus) withdrawal at six months may provide a strategy for decreased nephrotoxicity and improved long-term function in steroid-free low immunological risk renal transplant patients.
ClinicalTrials.gov NCT00556933.
肾移植存活的两个最主要障碍是排斥反应以及预防排斥反应所需免疫抑制药物的直接肾毒性。钙调神经磷酸酶抑制剂(CNI)是大多数免疫抑制方案的主要药物,具有特别强的肾毒性。在出现毒性更低的抗排斥药物之前,唯一的选择是优化现有药物的使用。
确定强化兔抗胸腺细胞球蛋白(rATG)诱导后停用CNI,单独使用或联合使用是否能改善移植肾功能,并减少移植肾慢性组织病理学改变,从而提高移植肾以及患者的存活率。如先前报道,24小时内单次大剂量使用rATG耐受性良好,且与更好的肾功能、更少的感染及更高的患者存活率相关。在此,我们报告关于完全停用CNI是否能改善肾功能及减少移植肾病理改变的试验情况。
在2004年4月20日至2009年4月14日期间,我们进行了一项前瞻性、随机、非盲法的肾移植试验,比较两种rATG给药方案(单次剂量6mg/kg与分剂量给药,每隔一天1.5mg/kg,共4次;目标入组人数=180)。后续维持免疫抑制治疗包括使用他克莫司(一种CNI)和西罗莫司(一种雷帕霉素哺乳动物靶点抑制剂)。我们在此报告6个月后将患者转换为最小剂量他克莫司/西罗莫司或霉酚酸酯/西罗莫司后的结果。主要终点为12个月和24个月时方案肾活检的移植肾功能和慢性组织病理学结果。
停用CNI(治疗中分析)与更好的移植肾功能相关(p<0.001),且在12个月(p=0.003)和24个月(p=0.013)时方案活检的慢性组织病理学综合评分更低,同时不影响患者(p=0.81)或移植肾(p=0.93)的存活率,也不影响排斥反应发生率(p=0.17)。
对于无类固醇、低免疫风险的肾移植患者,6个月时停用CNI(他克莫司)可能是一种降低肾毒性并改善长期功能的策略。
ClinicalTrials.gov NCT00556933。