Hepato-Biliary Center, AP-HP Paul Brousse Hospital, University of Paris-Sud, INSERM U935, Villejuif, France.
Transplant Center, Institute for Clinical and Experimental Medicine (IKEM), Prague, Czech Republic.
Transplantation. 2019 Sep;103(9):1844-1862. doi: 10.1097/TP.0000000000002700.
We compared, through the European Liver Transplant Registry, long-term liver transplantation outcomes with prolonged-release tacrolimus (PR-T) versus immediate-release tacrolimus (IR-T)-based immunosuppression. This retrospective analysis comprises up to 8-year data collected between 2008 and 2016, in an extension of our previously published study.
Patients with <1 month follow-up were excluded; patients were propensity score matched for baseline characteristics. Efficacy measures included: univariate/multivariate analyses of risk factors influencing graft/patient survival up to 8 years posttransplantation, and graft/patient survival up to 4 years with PR-T versus IR-T. Overall, 13 088 patients were included from 44 European centers; propensity score-matched analyses comprised 3006 patients (PR-T: n = 1002; IR-T: n = 2004).
In multivariate analyses, IR-T-based immunosuppression was associated with reduced graft survival (risk ratio, 1.49; P = 0.0038) and patient survival (risk ratio, 1.40; P = 0.0215). There was improvement with PR-T versus IR-T in graft survival (83% versus 77% at 4 y, respectively; P = 0.005) and patient survival (85% versus 80%; P = 0.017). Patients converted from IR-T to PR-T after 1 month had a higher graft survival rate than patients receiving IR-T at last follow-up (P < 0.001), or started and maintained on PR-T (P = 0.019). One graft loss in 4 years was avoided for every 14.3 patients treated with PR-T versus IR-T.
PR-T-based immunosuppression might improve long-term outcomes in liver transplant recipients than IR-T-based immunosuppression.
我们通过欧洲肝移植注册处比较了长期肝移植结果,比较了延长释放型他克莫司(PR-T)与即时释放型他克莫司(IR-T)的免疫抑制作用。这项回顾性分析包括 2008 年至 2016 年期间收集的长达 8 年的数据,是我们之前发表的研究的扩展。
排除随访时间<1 个月的患者;根据基线特征对患者进行倾向评分匹配。疗效评估包括:单变量/多变量分析影响移植后 8 年内移植物/患者存活率的风险因素,以及 PR-T 与 IR-T 相比 4 年内移植物/患者存活率。总共纳入了来自 44 个欧洲中心的 13088 名患者;在倾向评分匹配分析中纳入了 3006 名患者(PR-T:n=1002;IR-T:n=2004)。
在多变量分析中,IR-T 免疫抑制与移植物存活率降低相关(风险比,1.49;P=0.0038)和患者存活率降低相关(风险比,1.40;P=0.0215)。与 IR-T 相比,PR-T 改善了移植物存活率(分别为 4 年时的 83%和 77%;P=0.005)和患者存活率(85%和 80%;P=0.017)。在第 1 个月从 IR-T 转换为 PR-T 的患者的移植物存活率高于最后一次随访时接受 IR-T 的患者(P<0.001),或开始并维持 PR-T 的患者(P=0.019)。与 IR-T 相比,每治疗 14.3 名患者即可避免 1 例 4 年内的移植物丢失。
与 IR-T 免疫抑制相比,PR-T 免疫抑制可能改善肝移植受者的长期结局。