Yamauchi Junji, Raghavan Divya, Jweehan Duha, Oygen Suayp, Marineci Silviana, Hall Isaac E, Molnar Miklos Z
Division of Nephrology and Hypertension, Department of Internal Medicine, Spencer Fox Eccles School of Medicine at the University of Utah, Salt Lake City, UT.
Department of Rare Diseases Research, Institute of Medical Science, St. Marianna University School of Medicine, Kawasaki, Japan.
Transplantation. 2025 Apr 1;109(4):691-700. doi: 10.1097/TP.0000000000005196. Epub 2024 Sep 4.
It is unclear whether kidney grafts from deceased donors with acute kidney injury (AKI) are more vulnerable to calcineurin inhibitor nephrotoxicity, and whether de novo use of belatacept is more beneficial than tacrolimus for recipients of these types of kidney transplants.
In this retrospective cohort study using the US Organ Procurement and Transplantation Network database, we created 1:4 matches with highly similar characteristics for recipients of AKI-donor kidneys receiving belatacept versus tacrolimus for initial maintenance immunosuppression and compared outcomes for graft function, patient and graft survival, and rejection.
The matched cohort consisted of 567 and 2268 recipients administered belatacept and tacrolimus, respectively. Posttransplant estimated glomerular filtration rate was significantly higher in the belatacept group at 6 mo (58.2 ± 24.2 versus 54.6 ± 21.6 mL/min/1.73 m 2 , P < 0.001); however, the between-group difference did not reach statistical significance at 12 mo (57.2 ± 24.3 versus 55.7 ± 22.2 mL/min/1.73 m 2 , P = 0.057). Median follow-up periods were 3.2 and 3.1 y for patient and graft survival, respectively. There were no significant differences between belatacept versus tacrolimus for mortality (hazard ratio 1.18 [95% confidence interval, 0.95-1.47], P = 0.14) or death-censored graft failure (hazard ratio 1.17 [0.85-1.61], P = 0.33). Rejection rate within 12 mo was significantly higher in the belatacept group (13% versus 7%, P < 0.001).
In this matched cohort study, initial use of belatacept for AKI-donor kidney recipients was associated with small benefits in early graft function when compared with tacrolimus. Although rejection risk was significantly higher in recipients administered belatacept, patient and graft survival were not significantly different between groups.
来自急性肾损伤(AKI)已故供体的肾移植受者的肾脏移植是否更容易受到钙调神经磷酸酶抑制剂肾毒性的影响,以及对于这类肾移植受者,从头使用贝拉西普是否比他克莫司更有益,目前尚不清楚。
在这项使用美国器官获取与移植网络数据库的回顾性队列研究中,我们为接受贝拉西普与他克莫司进行初始维持免疫抑制的AKI供体肾受者创建了1:4的特征高度相似的匹配组,并比较了移植肾功能、患者和移植肾存活以及排斥反应的结果。
匹配队列分别由567例和2268例接受贝拉西普和他克莫司治疗的受者组成。贝拉西普组移植后6个月的估计肾小球滤过率显著更高(58.2±24.2对54.6±21.6ml/min/1.73m²,P<0.001);然而,12个月时组间差异未达到统计学显著性(57.2±24.3对55.7±22.2ml/min/1.73m²,P=0.057)。患者和移植肾存活的中位随访期分别为3.2年和3.1年。贝拉西普与他克莫司在死亡率(风险比1.18[95%置信区间,0.95 - 1.47],P=0.14)或死亡审查的移植肾失败率(风险比1.17[0.85 - 1.61],P=0.33)方面无显著差异。贝拉西普组12个月内的排斥率显著更高(13%对7%,P<0.001)。
在这项匹配队列研究中,与他克莫司相比,AKI供体肾受者初始使用贝拉西普在早期移植肾功能方面有小的益处。尽管接受贝拉西普治疗的受者排斥风险显著更高,但两组间患者和移植肾存活无显著差异。