Tainá Veras de Sandes-Freitas, Flávio Bezerra de Araújo, Raoni de Oliveira Domingues-da-Silva, Maria Luíza de Mattos Brito Oliveira Sales, Ronaldo de Matos Esmeraldo
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引用次数: 0
Abstract
Introduction: Chronic corticosteroid use, even at low doses, is associated with well-known adverse effects. However, steroid-free regimens after kidney transplantation (KT) have been linked to a higher incidence of acute rejection (AR), limiting their implementation to a few centers worldwide. In this study, we describe the pioneering experience of a Brazilian center that adopted a steroid-free immunosuppressive regimen in 2005 for patients at low to moderate immunological risk.
Methods: This single-center retrospective cohort study includes KT recipients who were submitted to steroid-free regimens between 2012 and 2019. The cohort was followed for three years in a real-world setting.
Results: A total of 562 patients were included, 71.4% male, with a median age of 48.1 years (IQR 35.5-58.6). Most (95.2%) received deceased donor allografts. All patients underwent induction therapy with antithymocyte globulin, and 82.2% received tacrolimus in combination with sirolimus or everolimus as maintenance therapy. After three years, 10.2% experienced treated AR episodes, with biopsy confirmation in 3.2%. Age (HR 0.946, 95% CI 0.923-0.969, p < 0.001) and HLA mismatches (HR 1.312, 95% CI 1.021-1.687, p = 0.034) were risk factors for rejection. Twenty-eight patients (5%) lost their grafts, and 5.7% died. Seventy-one patients (12.6%) required corticosteroid introduction over the years, with a median of 125.5 days (IQR 31.7-409) post-KT. The main reasons were perceived immunosuppressive regimen inefficacy (56.3%) and composition in a low-efficacy immunosuppressive regimen (18.6%).
Conclusion: Steroid-free immunosuppression was effective in low to moderate immunological risk KT recipients over a three-year follow-up period.
长期使用皮质类固醇,即使是低剂量,也会产生众所周知的不良反应。然而,肾移植(KT)后无类固醇方案与较高的急性排斥反应(AR)发生率有关,限制了其在全球少数中心的实施。在这项研究中,我们描述了巴西一家中心的开创性经验,该中心于2005年对低至中度免疫风险的患者采用无类固醇免疫抑制方案。方法:这项单中心回顾性队列研究包括2012年至2019年期间接受无类固醇方案治疗的KT受体。这群人在现实世界中被跟踪了三年。结果:共纳入562例患者,男性71.4%,中位年龄48.1岁(IQR 35.5-58.6)。大多数(95.2%)接受了已故供体同种异体移植。所有患者均接受抗胸腺细胞球蛋白诱导治疗,82.2%的患者接受他克莫司联合西罗莫司或依维莫司作为维持治疗。三年后,10.2%的人经历了治疗后的AR发作,3.2%的人有活检证实。年龄(HR 0.946, 95% CI 0.923-0.969, p < 0.001)和HLA不匹配(HR 1.312, 95% CI 1.021-1.687, p = 0.034)是排斥反应的危险因素。28例患者(5%)失去移植物,5.7%死亡。71例(12.6%)患者在kt后的中位时间为125.5天(IQR 31.7-409)。主要原因是认为免疫抑制方案无效(56.3%)和组成免疫抑制方案无效(18.6%)。结论:经过三年的随访,无类固醇免疫抑制对低至中度免疫风险的KT受体是有效的。