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依维莫司在减少肾移植受者巨细胞病毒事件方面对类固醇避免策略的影响:一项随机临床试验的 3 年随访结果。

The impact of everolimus in reducing cytomegalovirus events in kidney transplant recipients on steroid-avoidance strategy: 3-year follow-up of a randomized clinical trial.

机构信息

Transplant Division, Hospital Geral de Fortaleza, Fortaleza, Ceará, Brazil.

Department of Clinical Medicine, Federal University of Ceará, Fortaleza, Ceará, Brazil.

出版信息

Transpl Int. 2018 Dec;31(12):1345-1356. doi: 10.1111/tri.13313. Epub 2018 Jul 31.

Abstract

There is no evidence of whether everolimus (EVR) reduces cytomegalovirus (CMV) events in patients receiving steroid-free regimens. Besides, studies evaluating a tacrolimus (TAC) and EVR regimen are limited to 1-year follow-up. In this single-center prospective randomized trial, the incidence of CMV and 3-year efficacy and safety outcomes of EVR were compared to those of mycophenolate sodium (MPS) in a steroid-free regimen based on low-exposure TAC. Both groups received rabbit anti-thymocyte globulin (r-ATG) induction (6 mg/kg) and the steroids were withdrawn at day 7. Maintenance immunosuppression consisted of TAC (4-7 ng/ml until month 3 and 2-4 ng/ml thereafter) plus EVR (3-8 ng/ml) in the EVR group (n = 59); and TAC (4-7 ng/ml during all follow-up) plus MPS (1440 mg) in the MPS group (n = 56). The EVR group presented with a lower incidence of CMV events (18.6% vs. 50%, P = 0.001). No differences were observed in biopsy-proven acute rejection (6.8% vs. 3.6%, P = 0.680),graft loss (0.0% vs. 1.8%, P = 0.487),death (6.8% vs. 1.8%, P = 0.365), or estimated glomerular filtration rate at 36 months (61.1 ± 25.4 vs. 66.3 ± 24 ml/min/1.73 m , P = 0.369). A higher proportion of patients discontinued MPS treatment (8.5% vs. 26.8%, P = 0.013) for safety issues. In conclusion, EVR was associated with lower rates of CMV events in patients induced with standard dose r-ATG and a maintenance steroid-free regimen based on TAC. This regimen effectively prevented acute rejection and demonstrated a more favorable safety profile. (ClinicalTrials.gov:NCT02084446).

摘要

目前尚无证据表明依维莫司(EVR)可降低接受无类固醇方案治疗的患者的巨细胞病毒(CMV)事件发生率。此外,评估他克莫司(TAC)和 EVR 方案的研究仅限于为期 1 年的随访。在这项单中心前瞻性随机试验中,与霉酚酸酯钠(MPS)相比,EVR 在基于低暴露 TAC 的无类固醇方案中的疗效和安全性结果(CMV 发生率和 3 年)进行了比较。两组均接受兔抗胸腺细胞球蛋白(r-ATG)诱导(6mg/kg),第 7 天停用类固醇。维持性免疫抑制包括 EVR 组中的 TAC(4-7ng/ml,直至第 3 个月,此后为 2-4ng/ml)加 EVR(3-8ng/ml)(n=59);和 MPS 组中的 TAC(4-7ng/ml 随访期间)加 MPS(1440mg)(n=56)。EVR 组 CMV 事件发生率较低(18.6%比 50%,P=0.001)。在活检证实的急性排斥反应(6.8%比 3.6%,P=0.680)、移植物丢失(0.0%比 1.8%,P=0.487)、死亡(6.8%比 1.8%,P=0.365)或 36 个月时的估计肾小球滤过率(61.1±25.4 比 66.3±24ml/min/1.73m,P=0.369)方面无差异。由于安全性问题,更多的患者停止使用 MPS 治疗(8.5%比 26.8%,P=0.013)。总之,在接受标准剂量 r-ATG 诱导和基于 TAC 的无类固醇维持方案治疗的患者中,EVR 与较低的 CMV 事件发生率相关。该方案有效预防了急性排斥反应,并表现出更有利的安全性。(ClinicalTrials.gov:NCT02084446)。

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