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肺移植后早期依维莫司为基础的四联疗法与标准三联疗法的随机试验。

A randomized trial of everolimus-based quadruple therapy vs standard triple therapy early after lung transplantation.

机构信息

Department of Respiratory Medicine, Hannover Medical School, Hannover, Germany.

Biomedical Research in Endstage and Obstructive Lung Disease Hannover (BREATH), Member of the German Center for Lung Research (DZL), Hannover, Germany.

出版信息

Am J Transplant. 2019 Jun;19(6):1759-1769. doi: 10.1111/ajt.15251. Epub 2019 Feb 5.

DOI:10.1111/ajt.15251
PMID:30615259
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6590654/
Abstract

Calcineurin inhibitor (CNI) therapy after lung transplantation increases risk of kidney failure. Early everolimus-based quadruple low CNI immunosuppression may improve renal function without compromising efficacy or safety. A prospective, randomized, open-label, 12-month multicenter trial was conducted at 8 German sites. Patients 3-18 months after lung transplantation were randomized (1:1), stratified by baseline estimated glomerular filtration rate (eGFR). In the quadruple low CNI regimen, patients received everolimus (target trough level 3-5 ng/mL) with reduced CNI (tacrolimus 3-5 ng/mL or cyclosporine 25-75 ng/mL) and a cell cycle inhibitor plus prednisone. In the standard triple CNI regimen, patients received tacrolimus (target trough level >5 ng/mL) or cyclosporine (>100 ng/mL) and a cell cycle inhibitor plus prednisone. Of the 180 patients screened, 130 were randomized: 67 in the quadruple low CNI group and 63 in the standard triple CNI group. The primary endpoint (eGFR after 12 months) demonstrated superiority of the quadruple low CNI regimen: 64.5 mL/min vs 54.6 mL/min for the standard triple group (least squares mean, analysis of covariance; P < .001). Key efficacy parameters (biopsy-proven acute rejection, chronic lung allograft dysfunction, and death) and safety endpoints were similar between both groups. Quadruple low CNI immunosuppression early after lung transplantation was demonstrated to be efficacious and safe. Clinical trials registry: ClinicalTrials.gov NCT01404325.

摘要

钙调神经磷酸酶抑制剂(CNI)治疗肺移植后会增加肾衰竭的风险。早期使用依维莫司为基础的四联低 CNI 免疫抑制可能会改善肾功能,而不会影响疗效或安全性。在德国的 8 个地点进行了一项前瞻性、随机、开放标签、为期 12 个月的多中心试验。肺移植后 3-18 个月的患者按 1:1 随机分组(1:1),并按基线估计肾小球滤过率(eGFR)分层。在四联低 CNI 方案中,患者接受依维莫司(目标谷浓度 3-5ng/mL)联合减少 CNI(他克莫司 3-5ng/mL 或环孢素 25-75ng/mL)和细胞周期抑制剂加泼尼松。在标准三联 CNI 方案中,患者接受他克莫司(目标谷浓度>5ng/mL)或环孢素(>100ng/mL)和细胞周期抑制剂加泼尼松。在筛选的 180 名患者中,有 130 名被随机分组:四联低 CNI 组 67 名,标准三联 CNI 组 63 名。主要终点(12 个月后的 eGFR)显示四联低 CNI 方案具有优越性:64.5mL/min 比标准三联组的 54.6mL/min(最小二乘均数,协方差分析;P<0.001)。两组之间的关键疗效参数(活检证实的急性排斥反应、慢性肺移植物功能障碍和死亡)和安全性终点相似。肺移植后早期四联低 CNI 免疫抑制被证明是有效和安全的。临床试验注册:ClinicalTrials.gov NCT01404325。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5260/6590654/ed8f270035a0/AJT-19-1759-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5260/6590654/c9fdb13f6003/AJT-19-1759-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5260/6590654/f407768ac0fb/AJT-19-1759-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5260/6590654/ed8f270035a0/AJT-19-1759-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5260/6590654/c9fdb13f6003/AJT-19-1759-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5260/6590654/f407768ac0fb/AJT-19-1759-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5260/6590654/ed8f270035a0/AJT-19-1759-g003.jpg

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