Newton Laura E, D'Angelo Thomas W, Chobanian Michael C, Daily Michael F, Zimmerman Asha M
Department of General Surgery, Dartmouth Health, Lebanon, New Hampshire, USA.
Department of Surgery, Veterans Affairs Medical Center, White River Junction, Vermont, USA.
Clin Transplant. 2025 Apr;39(4):e70154. doi: 10.1111/ctr.70154.
Belatacept shows promise as an alternative immunosuppressant without the nephrotoxicity of calcineurin inhibitors. Avoiding nephrotoxicity is important with the expanding use of organs at risk of marginal graft function. To date, no large studies have compared belatacept directly with tacrolimus after T-cell depleting induction in renal transplantation.
The Standard Transplant Analysis and Research file was used to compare adult kidney transplant recipients induced with T-cell depleting agents treated with belatacept to propensity score-matched recipients treated with tacrolimus between August 10, 2011 and June 29, 2023. Kaplan-Meier survival analysis was used to compare death censored graft survival, patient survival, and time to acute rejection.
During the study period, 4391 adult kidney transplant recipients were treated with belatacept. Estimated GFR improved for belatacept-treated patients through year 9, whereas it decreased for the control group through year 10. Belatacept-treated patients had a higher rejection rate at 5 years (21% vs. 15%, p < 0.001). Death-censored graft survival did not differ between groups (p = 0.383). Among patients who had rejection, death-censored graft survival was superior in belatacept-treated patients at 5 years (70% vs. 60%, p = 0.026). Overall, patient survival did not differ between groups (p = 0.120).
This is the largest longitudinal study to compare outcomes of belatacept versus tacrolimus-based therapy following T-cell depleting induction. Belatacept was associated with improved graft function despite an increased acute rejection rate. There was no difference in overall graft or patient survival compared to tacrolimus. This study suggests that belatacept-based therapy is not inferior to tacrolimus-based therapy following T-cell depletion.
贝拉西普作为一种替代免疫抑制剂显示出前景,它没有钙调神经磷酸酶抑制剂的肾毒性。随着具有边缘性移植物功能风险的器官使用的增加,避免肾毒性很重要。迄今为止,尚无大型研究在肾移植中T细胞清除诱导后直接比较贝拉西普与他克莫司。
使用标准移植分析和研究文件,比较2011年8月10日至2023年6月29日期间接受T细胞清除剂诱导并用贝拉西普治疗的成年肾移植受者与倾向评分匹配的接受他克莫司治疗的受者。采用Kaplan-Meier生存分析比较死亡删失后的移植物存活、患者存活及急性排斥反应时间。
在研究期间,4391例成年肾移植受者接受了贝拉西普治疗。接受贝拉西普治疗的患者估计肾小球滤过率在第9年之前有所改善,而对照组在第10年之前则下降。接受贝拉西普治疗的患者5年时排斥反应发生率更高(21%对15%,p<0.001)。两组间死亡删失后的移植物存活无差异(p = 0.383)。在发生排斥反应的患者中,接受贝拉西普治疗的患者5年时死亡删失后的移植物存活情况更好(70%对60%,p = 0.026)。总体而言,两组间患者存活无差异(p = 0.120)。
这是比较T细胞清除诱导后贝拉西普与基于他克莫司治疗结局的最大规模纵向研究。尽管急性排斥反应率增加,但贝拉西普与改善的移植物功能相关。与他克莫司相比,总体移植物或患者存活无差异。这项研究表明,T细胞清除后基于贝拉西普的治疗并不劣于基于他克莫司的治疗。