Department of Nephrology, Royal Melbourne Hospital, Parkville, Vic., Australia.
Victorian Transplantation and Immunogenetics Service, Australian Red Cross Life Blood, Melbourne, Vic., Australia.
Transpl Int. 2021 Nov;34(11):2353-2362. doi: 10.1111/tri.13998. Epub 2021 Sep 21.
The optimum approach towards immunosuppression withdrawal following kidney transplant failure is unclear. Prolonged weaning may be associated with reduced sensitization, less graft nephrectomy and greater likelihood of retransplantation, but conversely increased risk of infection, malignancy and death. We conducted a single-centre retrospective analysis of patients experiencing graft failure between 2007 and 2017, comparing rates of sensitization, retransplantation, nephrectomy, infection, malignancy and death between patients who had immunosuppression weaned over <90 vs. 90-180 vs. >180 days. Patient survival after immunosuppression withdrawal over <90 vs. 90-180 vs. >180 days was 73.3%, 72.1% and 80.4%, respectively (P = 0.35), with no differences in cPRA (80.06 vs. 81.21 vs. 85.42, P = 0.66) or retransplantation rate [24/31 (77.4%) vs. 21/35 (60.0%) vs. 22/36 (61.1%), P = 0.13]. There was significantly less nephrectomy after late immunosuppression cessation [10/42 (23.8%) vs. 7/42 (16.7%) vs. 3/43 (7.0%), P = 0.01] but no differences in infections or malignancy. On competing risk regression (death as competing risk) controlling for cofactors including age, nephrectomy and rejection, prolonged immunosuppression did not predict likelihood of retransplantation (SHR 1.000, P = 0.88). Prolonged immunosuppression withdrawal does not reduce sensitization or improve retransplantation rates but is associated with less nephrectomy. Immunosuppression withdrawal should be tailored to individual circumstances after graft failure.
肾移植失败后免疫抑制停药的最佳方法尚不清楚。长时间逐渐停药可能与降低致敏、减少移植物切除和增加再移植的可能性有关,但相反也会增加感染、恶性肿瘤和死亡的风险。我们对 2007 年至 2017 年间经历移植物失败的患者进行了单中心回顾性分析,比较了免疫抑制药物在<90、90-180 和>180 天内逐渐停药的患者之间的致敏、再移植、切除、感染、恶性肿瘤和死亡的发生率。免疫抑制停药后<90、90-180 和>180 天的患者生存率分别为 73.3%、72.1%和 80.4%(P=0.35),cPRA 无差异(80.06%比 81.21%比 85.42%,P=0.66)或再移植率[24/31(77.4%)比 21/35(60.0%)比 22/36(61.1%),P=0.13]。晚期免疫抑制停止后,切除明显减少[10/42(23.8%)比 7/42(16.7%)比 3/43(7.0%),P=0.01],但感染或恶性肿瘤无差异。在竞争风险回归(死亡为竞争风险)中,控制年龄、切除和排斥等因素后,延长免疫抑制时间并不能预测再移植的可能性(SHR 1.000,P=0.88)。延长免疫抑制停药不会降低致敏率或提高再移植率,但与减少切除有关。免疫抑制停药应根据移植失败后的个体情况进行调整。