Augustine Erika F, Beck Christopher A, Adams Heather R, Defendorf Sara, Vierhile Amy, Timm Derek, Weimer Jill M, Mink Jonathan W, Marshall Frederick J
Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA.
Department of Pediatrics, University of Rochester Medical Center, Rochester, NY, USA.
JIMD Rep. 2019;43:117-124. doi: 10.1007/8904_2018_113. Epub 2018 Jun 20.
Mycophenolate, an immunosuppressant, is commonly used off-label for autoimmune neurological conditions. In CLN3 disease, a neurodegenerative disorder of childhood, preclinical and clinical data suggest secondary autoimmunity and inflammation throughout the central nervous system are key components of pathogenesis. We tested the short-term tolerability of mycophenolate in individuals with CLN3 disease, in preparation for possible long-term efficacy trials of this drug. We conducted a randomized, double-blind, placebo-controlled, crossover study of mycophenolate in 19 ambulatory individuals with CLN3 disease to determine the safety and tolerability of short-term administration (NCT01399047). The study included two 8-week treatment periods with a 4-week intervening washout. Mycophenolate was well tolerated. 89.5% of participants completed the mycophenolate arm, on the assigned study dose (95% CI: 66.9-98.7%), and there were no significant differences in tolerability rates between mycophenolate and placebo arms (10.5%; 95% CI: -3.3-24.3%, p = 0.21). All reported adverse events were mild in severity; the most common adverse events on mycophenolate were vomiting (31.6%; 95% CI: 12.6-56.6%), diarrhea (15.8%; 95% CI: 3.4-39.6%), and cough (15.8%; 95% CI: 3.4-39.6%). These did not occur at a significantly increased frequency above placebo. There were no definite effects on measured autoimmunity or clinical outcomes in the setting of short-term administration. Study of long-term exposure is needed to test the impact of mycophenolate on key clinical features and CLN3 disease trajectory.
霉酚酸酯是一种免疫抑制剂,常用于自身免疫性神经疾病的非标签用药。在CLN3病(一种儿童神经退行性疾病)中,临床前和临床数据表明,继发于中枢神经系统的自身免疫和炎症是发病机制的关键组成部分。我们测试了霉酚酸酯在CLN3病患者中的短期耐受性,为该药物可能的长期疗效试验做准备。我们对19名CLN3病门诊患者进行了一项随机、双盲、安慰剂对照的霉酚酸酯交叉研究,以确定短期给药的安全性和耐受性(NCT01399047)。该研究包括两个8周的治疗期,中间有4周的洗脱期。霉酚酸酯耐受性良好。89.5%的参与者按照指定的研究剂量完成了霉酚酸酯治疗组(95%置信区间:66.9 - 98.7%),霉酚酸酯组和安慰剂组的耐受性率无显著差异(10.5%;95%置信区间:-3.3 - 24.3%,p = 0.21)。所有报告的不良事件严重程度均为轻度;霉酚酸酯组最常见的不良事件是呕吐(31.6%;95%置信区间:12.6 - 56.6%)、腹泻(15.8%;95%置信区间:3.4 - 39.6%)和咳嗽(15.8%;95%置信区间:3.4 - 39.6%)。这些不良事件的发生频率没有显著高于安慰剂组。短期给药对测量的自身免疫或临床结局没有明确影响。需要进行长期暴露研究,以测试霉酚酸酯对关键临床特征和CLN3病病程的影响。