Trachtman Howard, Gipson Debbie S, Somers Michael, Spino Cathie, Adler Sharon, Holzman Lawrence, Kopp Jeffrey B, Sedor John, Overfield Sandra, Elegbe Ayanbola, Maldonado Michael, Greka Anna
Division of Nephrology, Department of Pediatrics, New York University Langone Medical Center, New York, New York, USA.
Department of Pediatrics, University of Michigan, Ann Arbor, Michigan, USA.
Kidney Int Rep. 2017 Aug 31;3(1):115-121. doi: 10.1016/j.ekir.2017.08.013. eCollection 2018 Jan.
Treatment-resistant nephrotic syndrome is a rare form of glomerular disease that occurs in children and adults. No Food and Drug Administration-approved treatments consistently achieve remission of proteinuria and preservation of kidney function. CD80 (B7-1) can be expressed on injured podocytes, and administration of abatacept (modified CTLA4-Ig based on a natural ligand to CD80) has been associated with sustained normalization of urinary protein excretion and maintenance of glomerular filtration rate in experimental and clinical settings.
In this report, we describe the rationale for and design of a randomized, placebo-controlled, clinical trial of abatacept in patients with treatment-resistant nephrotic syndrome caused by focal segmental glomerulosclerosis or minimal change disease. The design is a hybrid of a parallel-group and crossover design (switchover) with the primary objectives assessed in the first period of the study and the secondary objectives assessed using data from both periods. All participants will receive the active agent in 1 of the periods. The duration of treatment will be 4 months per period.
The primary outcome will be improvement in nephrotic-range proteinuria to subnephrotic range, that is, reduction from baseline to 4 months in urine protein:creatinine ratio ≥ 50% and to a level < 3. The projected sample size is 90 patients, which has 80% power to detect a treatment difference of 28%.
This study advances efforts to validate CD80 as a therapeutic target for treatment-resistant nephrotic syndrome, and implements a precision medicine-based approach to this serious kidney condition in which the selection of a therapeutic agent is guided by the underlying disease mechanism operating in individual patients.
难治性肾病综合征是一种在儿童和成人中发生的罕见肾小球疾病形式。美国食品药品监督管理局批准的治疗方法均无法持续实现蛋白尿缓解和肾功能保留。CD80(B7-1)可在受损足细胞上表达,在实验和临床环境中,给予阿巴西普(基于CD80天然配体的改良CTLA4-Ig)与尿蛋白排泄持续正常化及肾小球滤过率维持相关。
在本报告中,我们描述了一项针对由局灶节段性肾小球硬化或微小病变疾病引起的难治性肾病综合征患者进行阿巴西普随机、安慰剂对照临床试验的基本原理和设计。该设计是平行组和交叉设计(转换)的混合体,主要目标在研究的第一阶段进行评估,次要目标使用两个阶段的数据进行评估。所有参与者将在其中一个阶段接受活性药物。每个阶段的治疗持续时间为4个月。
主要结局将是肾病范围蛋白尿改善至亚肾病范围,即尿蛋白:肌酐比值从基线降至4个月时降低≥50%且降至<3的水平。预计样本量为90名患者,检测28%治疗差异的功效为80%。
本研究推进了将CD80验证为难治性肾病综合征治疗靶点的工作,并针对这种严重肾脏疾病实施了基于精准医学的方法,其中治疗药物的选择由个体患者中起作用的潜在疾病机制指导。