Benazzo Alberto, Cho Ara, Nechay Anna, Schwarz Stefan, Frommlet Florian, Wekerle Thomas, Hoetzenecker Konrad, Jaksch Peter
Medizinische Universitat Wien, Vienna, Austria.
Trials. 2021 Jan 4;22(1):6. doi: 10.1186/s13063-020-04843-9.
Long-term outcomes of lung transplantation are severely affected by comorbidities and development of chronic rejection. Among the comorbidities, kidney insufficiency is one of the most frequent and it is mainly caused by the cumulative effect of calcineurin inhibitors (CNIs). Currently, the most used immunosuppression protocols worldwide include induction therapy and a triple-drug maintenance immunosuppression, with one calcineurin inhibitor, one anti-proliferative drug, and steroids. Our center has pioneered the use of alemtuzumab as induction therapy, showing promising results in terms of short- and long-term outcomes. The use of alemtuzumab followed by a low-dose double drug maintenance immunosuppression, in fact, led to better kidney function along with excellent results in terms of acute rejection, chronic lung allograft dysfunction, and survival (Benazzo et al., PLoS One 14(1):e0210443, 2019). The hypothesis driving the proposed clinical trial is that de novo introduction of low-dose everolimus early after transplantation could further improve kidney function via a further reduction of tacrolimus. Based on evidences from kidney transplantation, moreover, alemtuzumab induction therapy followed by a low-dose everolimus and low-dose tacrolimus may have a permissive action on regulatory immune cells thus stimulating allograft acceptance.
A randomized prospective clinical trial has been set up to answer the research hypothesis. One hundred ten patients will be randomized in two groups. Treatment group will receive the new maintenance immunosuppression protocol based on low-dose tacrolimus and low-dose everolimus and the control group will receive our standard immunosuppression protocol. Both groups will receive alemtuzumab induction therapy. The primary endpoint of the study is to analyze the effect of the new low-dose immunosuppression protocol on kidney function in terms of eGFR change. The study will have a duration of 24 months from the time of randomization. Immunomodulatory status of the patients will be assessed with flow cytometry and gene expression analysis.
For the first time in the field of lung transplantation, this trial proposes the combined use of significantly reduced tacrolimus and everolimus after alemtuzumab induction. The new protocol may have a twofold advantage: (1) further reduction of nephrotoxic tacrolimus and (2) permissive influence on regulatory cells development with further reduction of rejection episodes.
EUDRACT Nr 2018-001680-24. Registered on 15 May 2018.
肺移植的长期预后受到合并症和慢性排斥反应的严重影响。在合并症中,肾功能不全是最常见的之一,主要由钙调神经磷酸酶抑制剂(CNIs)的累积效应引起。目前,全球最常用的免疫抑制方案包括诱导治疗和三联药物维持免疫抑制,即一种钙调神经磷酸酶抑制剂、一种抗增殖药物和类固醇。我们中心率先将阿仑单抗用作诱导治疗,在短期和长期预后方面均显示出有前景的结果。事实上,使用阿仑单抗后进行低剂量双药维持免疫抑制,可使肾功能更好,在急性排斥反应、慢性肺移植功能障碍和生存率方面也有出色表现(贝纳佐等人,《公共科学图书馆·综合》14(1):e0210443,2019)。本临床试验的假设是,移植后早期重新引入低剂量依维莫司可通过进一步减少他克莫司来进一步改善肾功能。此外,基于肾移植的证据,阿仑单抗诱导治疗后联合低剂量依维莫司和低剂量他克莫司可能对调节性免疫细胞有允许作用,从而促进移植器官的接受。
已开展一项随机前瞻性临床试验以回答该研究假设。110名患者将被随机分为两组。治疗组将接受基于低剂量他克莫司和低剂量依维莫司的新维持免疫抑制方案,对照组将接受我们的标准免疫抑制方案。两组都将接受阿仑单抗诱导治疗。该研究的主要终点是根据估算肾小球滤过率(eGFR)变化分析新的低剂量免疫抑制方案对肾功能的影响。该研究从随机分组时起为期24个月。将通过流式细胞术和基因表达分析评估患者的免疫调节状态。
在肺移植领域,本试验首次提出在阿仑单抗诱导后联合使用显著减量的他克莫司和依维莫司。新方案可能有双重优势:(1)进一步减少具有肾毒性的他克莫司;(2)对调节性细胞发育有允许作用,进一步减少排斥反应发作次数。
欧盟临床试验注册号2018 - 001680 - 24。于2018年5月15日注册。