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Campath, calcineurin inhibitor reduction and chronic allograft nephropathy (3C) study: background, rationale, and study protocol

机译:Campath,钙调神经磷酸酶抑制剂减少和慢性同种异体肾病(3C)研究:背景,基本原理和研究方案

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Background Kidney transplantation is the best treatment for patients with end-stage renal failure, but uncertainty remains about the best immunosuppression strategy. Long-term graft survival has not improved substantially, and one possible explanation is calcineurin inhibitor (CNI) nephrotoxicity. CNI exposure could be minimized by using more potent induction therapy or alternative maintenance therapy to remove CNIs completely. However, the safety and efficacy of such strategies are unknown. Methods/Design The Campath, Calcineurin inhibitor reduction and Chronic allograft nephropathy (3C) Study is a multicentre, open-label, randomized controlled trial with 852 participants which is addressing two important questions in kidney transplantation. The first question is whether a Campath (alemtuzumab)-based induction therapy strategy is superior to basiliximab-based therapy, and the second is whether, from 6 months after transplantation, a sirolimus-based maintenance therapy strategy is superior to tacrolimus-based therapy. Recruitment is complete, and follow-up will continue for around 5 years post-transplant. The primary endpoint for the induction therapy comparison is biopsy-proven acute rejection by 6 months, and the primary endpoint for the maintenance therapy comparison is change in estimated glomerular filtration rate from baseline to 2 years after transplantation. The study is sponsored by the University of Oxford and endorsed by the British Transplantation Society, and 18 centers for adult kidney transplant are participating. Discussion Late graft failure is a major issue for kidney-transplant recipients. If our hypothesis that minimizing CNI exposure with Campath-based induction therapy and/or an elective conversion to sirolimus-based maintenance therapy can improve long-term graft function and survival is correct, then patients should experience better graft function for longer. A positive outcome could change clinical practice in kidney transplantation. Trial registration ClinicalTrials.gov, NCT01120028 and ISRCTN88894088
机译:背景肾脏移植是终末期肾衰竭患者的最佳治疗方法,但最佳免疫抑制策略仍存在不确定性。长期移植物的存活率没有实质性改善,一种可能的解释是钙调神经磷酸酶抑制剂(CNI)的肾毒性。通过使用更有效的诱导疗法或替代性维持疗法完全去除CNI,可以使CNI暴露程度降至最低。但是,这种策略的安全性和有效性尚不清楚。方法/设计Campath,钙调神经磷酸酶抑制剂减少和慢性同种异体移植肾病(3C)研究是一项多中心,开放标签,随机对照试验,有852名参与者,该研究解决了肾脏移植中的两个重要问题。第一个问题是基于Campath(alemtuzumab)的诱导治疗策略是否优于基于basiliximab的治疗,第二个问题是从移植后6个月起,基于西罗莫司的维持治疗策略是否优于基于他克莫司的治疗。招聘已经完成,后续工作将在移植后的5年内继续进行。诱导疗法比较的主要终点是活检证实的6个月急性排斥反应,而维持疗法比较的主要终点是从基线到移植后2年的估计肾小球滤过率变化。该研究由牛津大学赞助,并得到英国移植学会的认可,有18个成人肾脏移植中心参加。讨论对于肾移植接受者,晚期移植失败是一个主要问题。如果我们的假设以基于Campath的诱导疗法和/或选择性转换为基于Sirolimus的维持疗法来最大程度地减少CNI暴露可以改善长期移植物功能和存活率的假设是正确的,那么患者应长期接受更好的移植物功能。积极的结果可能会改变肾脏移植的临床实践。试用注册ClinicalTrials.gov,NCT01120028和ISRCTN88894088

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