TrAnsFOrM:一项评估依维莫司对肾移植术后长期预后影响的新研究

IF 1.4 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Open Access Journal of Clinical Trials Pub Date : 2014-06-10 DOI:10.2147/OAJCT.S63058
J. Pascual, T. Srinivas, S. Chadban, F. Citterio, F. Oppenheimer, H. Tedesco, M. Henry, C. Legendre, Y. Watarai, C. Sommerer, P. Lee, J. Hexham, Gaohong Dong, P. Bernhardt, F. Vincenti
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引用次数: 24

摘要

同种异体肾移植失败的两个明确的、可改变的危险因素是急性排斥反应和移植后一年内移植物功能差。美国和欧洲的监管机构和专家小组已经认识到,在评估免疫抑制方案时,应该评估急性排斥反应和一年移植功能。TRANSFORM (Clinicaltrials.gov NCT01950819)是第一批采用这种方法的试验之一,也是第一个应用一种新的联合临床有意义的终点,向改变肾移植患者免疫抑制范式迈出了第一步。依维莫司与减少暴露钙调磷酸酶抑制剂(CNI)治疗是一种策略,旨在降低慢性肾毒性和其他剂量依赖性并发症与CNI治疗相关的风险。在TRANSFORM试验中,新肾移植患者随机接受依维莫司减少CNI暴露组或霉酚酸标准CNI暴露组,同时接受诱导治疗和维持类固醇治疗。主要终点是经活检证实的急性排斥反应或移植后12个月估计的肾小球滤过率(50 mL/min/1.73 m2)的综合指标,该指标预计对急性和慢性同种异体移植排斥反应以及免疫抑制疗法的肾毒性副作用都很敏感。该端点的构造允许将连续结果(嫁接函数)与逻辑结果(拒绝)集成。该试验采用随机、多中心、开放标签、双臂设计。在完成2年的核心研究后,患者进入另一个3年的前瞻性观察研究。通过5年的随访,TRANSFORM将提供关于移植物丢失、移植物功能障碍、癌症、心血管事件和其他患者相关结局的大量数据。TRANSFORM将确定与标准CNI相比,依维莫司为基础的方案是否能获得短期的CNI减少。作为迄今为止在肾移植领域进行的最大的临床试验,TRANSFORM招募了2000多名患者,随访时间延长至5年,将提供帮助最大化长期结果所需的关键数据。
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TrAnsFOrM: a novel study design to evaluate the effect of everolimus on long-term outcomes after kidney transplantation
Two well defined, modifiable risk factors for kidney allograft failure are acute rejection and poor graft function at one year post-transplant. Regulatory bodies and expert panels in the USA and Europe have recognized that both acute rejection and one-year graft function should be assessed when evaluating immunosuppressive regimens. TRANSFORM (Clinicaltrials.gov NCT01950819) is one of the first trials to adopt this approach and the first that applies a novel combined clinically meaningful endpoint to take the first step towards changing the paradigm for immunosuppression in kidney transplant patients. Everolimus with reduced-exposure calcineurin inhibitor (CNI) therapy is a strategy designed to reduce the risk of chronic nephrotoxicity and other dose-dependent complications associated with CNI therapy. In TRANSFORM, de novo kidney transplant patients are randomized to everolimus with reduced-exposure CNI, or mycophenolic acid with standard-exposure CNI, both with induction therapy and maintenance steroids. The primary endpoint is a composite of treated biopsy-proven acute rejection or estimated glomerular filtration rate ,50 mL/min/1.73 m 2 at month 12 post-transplant, which is expected to be sensitive both to the effects of acute and chronic allograft rejection and nephrotoxic side effects of immunosuppressive therapies. The construct of this endpoint allows the integration of a continuous outcome (graft function) with a logistic outcome (rejection). The trial uses a randomized, multicenter, open-label, two-arm design. After completion of a 2-year core study, patients enter a further 3-year prospective observational study. By capturing follow-up to 5 years, TRANSFORM will provide substantial data on the incidence of graft loss, graft dysfunction, cancer, cardiovascular events, and other patient-relevant outcomes. TRANSFORM will determine whether de novo CNI reduction with an everolimus-based regimen achieves short-term outcomes compared with standard CNI. As the largest clinical trial undertaken to date in kidney transplantation, recruiting more than 2,000 patients, and with extended follow-up to 5 years, TRANSFORM will provide critical data required to help maximize long-term outcomes.
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来源期刊
Open Access Journal of Clinical Trials
Open Access Journal of Clinical Trials MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
3.90
自引率
0.00%
发文量
2
审稿时长
16 weeks
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