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肾移植后早期转换为贝拉西普治疗。

Early conversion to belatacept after renal transplantation.

作者信息

Nair Vinay, Liriano-Ward Luz, Kent Rebecca, Huprikar Shirish, Rana Mena, Florman Sander S, Delaney Veronica B, Menon Madhav C, Sehgal Vinita, Miko Leandra, Khaim Rafael, Benvenisty Alan, Lerner Susan, Arvelakis Antonios, Wadhera Vikram, Ames Scott, Shapiro Ron

机构信息

Department of Medicine, Hofstra Northwell School of Medicine, Great Neck, NY, USA.

Department of Medicine, Robert Wood Johnson University Hospital, New Brunswick, NJ, USA.

出版信息

Clin Transplant. 2017 May;31(5). doi: 10.1111/ctr.12951. Epub 2017 Apr 19.

Abstract

Belatacept is a non-nephrotoxic immunosuppressive agent, which may make it the ideal agent for patients with delayed or slow graft function on calcineurin inhibitors. There are limited data on conversion of patients to belatacept within 6 months of transplantation. Between January 2012 and December 2015, 16 patients were converted to belatacept for delayed or poor graft function (eGFR<30 mL/min/1.73 m , MDRD); three were HIV positive. Conversion protocols were analyzed in patients ≤4 months and 4-6 months post-transplantation. Mean serum creatinine levels after belatacept conversion were compared with preconversion levels. Patient survival was 100%, and graft survival was 88%. The mean creatinine fell from 3.9±1.82 mg/dL prebelatacept conversion to 2.1±1.1 mg/dL at 6 months and 1.9±0.47 mg/dL (median 1.8 mg/dL) at 12 months postconversion. There was no significant increased risk of rejection, infection, or malignancy. HIV parameters remained largely stable. Early conversion to belatacept in patients with DGF or slow graft function is safe and efficacious, in a single-center nonrandomized retrospective analysis.

摘要

贝拉西普是一种无肾毒性的免疫抑制剂,这可能使其成为使用钙调神经磷酸酶抑制剂后移植肾功能延迟或缓慢的患者的理想药物。关于移植后6个月内患者转换为贝拉西普治疗的数据有限。在2012年1月至2015年12月期间,16例因移植肾功能延迟或不佳(估算肾小球滤过率<30 ml/min/1.73 m²,采用肾脏病饮食改良研究公式计算)而转换为贝拉西普治疗的患者中,3例为HIV阳性。对移植后≤4个月和4 - 6个月的患者的转换方案进行了分析。将转换为贝拉西普治疗后的平均血清肌酐水平与转换前的水平进行比较。患者生存率为100%,移植肾生存率为88%。转换后6个月时,平均肌酐水平从转换前的3.9±1.82 mg/dL降至2.1±1.1 mg/dL,转换后12个月时降至1.9±0.47 mg/dL(中位数为1.8 mg/dL)。排斥反应、感染或恶性肿瘤的风险没有显著增加。HIV相关指标基本保持稳定。在一项单中心非随机回顾性分析中,移植肾功能延迟或缓慢的患者早期转换为贝拉西普治疗是安全有效的。

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