Everolimus in kidney transplantation

IF 0.1 Q4 TRANSPLANTATION
J. Cooper, U. Christians, A. Wiseman
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引用次数: 4

Abstract

Correspondence: Alexander wiseman Transplant Center, University of Colorado Denver Health Sciences Center, Mail Stop F749, AOP 7089,1635 North Aurora Court, Aurora, CO 80045, USA Tel +1 720 848 0860 Fax +1 720 848 2238 email alexander.wiseman@ucdenver.edu Abstract: Everolimus is a novel target of rapamycin (mTOR)-I analog that has recently been approved in combination with cyclosporine A and steroids for use in the prevention of organ rejection in kidney transplant recipients. Compared with rapamycin, everolimus is characterized by a shorter half-life and improved bioavailability. Prior to US Food and Drug Administration approval, a number of Phase II and III clinical trials were undertaken to evaluate the effectiveness of everolimus in combination with calcineurin inhibitors for preventing acute rejection and promoting allograft survival in kidney transplant recipients. In this report, we review the pharmacokinetic properties of everolimus, the clinical efficacy studies that led to its approval for use in kidney transplantation, as well as reported data on patient safety and tolerability associated with its use.
依维莫司在肾移植中的应用
通讯:Alexander wiseman移植中心,科罗拉多大学丹佛健康科学中心,Mail Stop F749, AOP 7089,1635 North Aurora Court, Aurora, CO 80045, USA Tel +1 720 848 0860 Fax +1 720 848 2238 email alexander.wiseman@ucdenver.edu摘要:依维莫斯是雷帕霉素(mTOR)- 1类似物的新靶点,最近已被批准与环孢素a和类固醇联合用于预防肾移植受者的器官排斥反应。与雷帕霉素相比,依维莫司具有半衰期短、生物利用度高的特点。在美国食品和药物管理局批准之前,进行了许多II期和III期临床试验,以评估依维莫司与钙调磷酸酶抑制剂联合用于预防肾移植受者急性排斥反应和促进同种异体移植物存活的有效性。在本报告中,我们回顾了依维莫司的药代动力学特性,导致其被批准用于肾移植的临床疗效研究,以及与使用相关的患者安全性和耐受性的报告数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.70
自引率
0.00%
发文量
6
审稿时长
16 weeks
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