Brown Landon C, Jobson Meghan A, Payan Schober Fernanda, Chang Emily H, Falk Ronald J, Nachman Patrick H, Pendergraft William F
University of North Carolina School of Medicine, Chapel Hill, NC, USA.
Am J Nephrol. 2017;45(4):365-372. doi: 10.1159/000464475. Epub 2017 Mar 18.
Minimal-change glomerulopathy is defined histologically by the presence of normal glomeruli on light microscopy and diffuse podocyte effacement on electron microscopy. Although effective in children, corticosteroid treatment in adults is more variable and time to response can be prolonged. Data to support rituximab use in adults with corticosteroid-dependent or resistant minimal-change glomerulopathy are limited. Here, we describe the clinical course of adults with corticosteroid-dependent or -resistant minimal-change glomerulopathy who received rituximab.
Demographic and clinical data were collected and analyzed from all adult patients with native kidney, biopsy-proven, minimal-change glomerulopathy who were administered rituximab between 2009 and 2014 and cared for at the UNC Kidney Center.
Ten patients with corticosteroid-resistant (n = 5) or corticosteroid-dependent (n = 5) idiopathic minimal-change glomerulopathy were treated with rituximab between 2009 and 2014. Rituximab treatment induced remission in all 10 patients with a median time to remission of 2 months. The median time from rituximab to corticosteroid discontinuation was 3.5 months. The median remission time was 29 months and follow-up time was 39.5 months. No serious adverse events attributable to rituximab were observed.
Rituximab induced remission in all patients with corticosteroid-dependent or -resistant minimal-change glomerulopathy, and may hold great therapeutic potential with good efficacy and minimal toxicity. Mounting evidence implies that a well-conducted randomized controlled clinical trial using rituximab in adults with minimal-change glomerulopathy in both corticosteroid-resistant and corticosteroid-dependent patients is warranted.
微小病变性肾小球病在组织学上的定义为,光镜下肾小球正常,电镜下足细胞弥漫性足突消失。虽然皮质类固醇治疗对儿童有效,但在成人中疗效更具变异性,且起效时间可能延长。支持利妥昔单抗用于皮质类固醇依赖或抵抗的成人微小病变性肾小球病的数据有限。在此,我们描述接受利妥昔单抗治疗的皮质类固醇依赖或抵抗的成人微小病变性肾小球病的临床过程。
收集并分析2009年至2014年间在北卡罗来纳大学肾脏中心接受利妥昔单抗治疗的所有经活检证实为原发性微小病变性肾小球病的成年患者的人口统计学和临床数据。
2009年至2014年间,10例皮质类固醇抵抗(n = 5)或皮质类固醇依赖(n = 5)的特发性微小病变性肾小球病患者接受了利妥昔单抗治疗。利妥昔单抗治疗使所有10例患者均获得缓解,缓解的中位时间为2个月。从利妥昔单抗治疗至停用皮质类固醇的中位时间为3.5个月。中位缓解时间为29个月,随访时间为39.5个月。未观察到与利妥昔单抗相关的严重不良事件。
利妥昔单抗可使所有皮质类固醇依赖或抵抗的微小病变性肾小球病患者获得缓解,且可能具有巨大的治疗潜力,疗效良好且毒性极小。越来越多的证据表明,有必要针对皮质类固醇抵抗和皮质类固醇依赖的成人微小病变性肾小球病患者开展一项使用利妥昔单抗的精心设计的随机对照临床试验。