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利妥昔单抗对比安慰剂治疗慢性炎性脱髓鞘性多发性神经根神经病:一项随机试验。

Rituximab versus placebo for chronic inflammatory demyelinating polyradiculoneuropathy: a randomized trial.

作者信息

Nobile-Orazio Eduardo, Cocito Dario, Manganelli Fiore, Fazio Raffaella, Lauria Pinter Giuseppe, Benedetti Luana, Mazzeo Anna, Peci Erdita, Spina Emanuele, Falzone Yuri, Dalla Bella Eleonora, Germano Francesco, Gentile Luca, Liberatore Giuseppe, Gallia Francesca, Collet-Vidiella Roger, Bianchi Elisa, Doneddu Pietro Emiliano

机构信息

Neuromuscular and Neuroimmunology Unit, IRCCS Humanitas Research Hospital, Milan, Rozzano 20089, Italy.

Department of Medical Biotechnology and Translational Medicine, Milan University, Milano 20133, Italy.

出版信息

Brain. 2025 Apr 3;148(4):1112-1121. doi: 10.1093/brain/awae400.

Abstract

Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) often requires prolonged ongoing treatment to prevent worsening. The efficacy of rituximab in preventing worsening after the discontinuation of immunoglobulin therapy in patients with CIDP was assessed. In this randomized, double-blind, placebo-controlled study, conducted at seven Italian hospitals, CIDP patients under immunoglobulin therapy were assigned to receive either rituximab (1 g on Days 1, 15 and 180 ± 7) or placebo. Both groups continued their regular immunoglobulin doses for 6 months post-intervention. The primary end point was the proportion of patients who worsened in any of the following three measures at Month 12, within 6 months after immunoglobulin discontinuation: a decrease of at least one point on the adjusted INCAT score, two points on the MRC sum score, or four points on the RODS centile score. Secondary end points included the proportion of patients deteriorating at Month 18 (within 12 months after immunoglobulin discontinuation), treatment cessation due to adverse events or voluntary reasons, and the time until deterioration after immunoglobulin discontinuation. This study was registered with ClinicalTrials.gov (NCT06325943) and EUDRACT (number 2017-005034-36), and is now complete. From April 2019 to March 2022, 39 patients were recruited; two withdrew consent. The remaining 37 patients were assigned to rituximab (n = 19) or placebo (n = 18). Median age was 53 (interquartile range 45-64), with 11 (30%) females. A similar proportion of patients in both the rituximab (12/19, 63.2%) and placebo (12/18, 66.6%) groups worsened at Month 12 [odds ratio (OR) 0.86; 95% confidence interval (CI) 0.22-3.32]. No significant differences were noted at Month 18 (OR 0.62; 95% CI 0.14-2.70), or in the mean scores of each scale at Months 6, 12 and 18. The median time to worsening was 5 months for rituximab and 2 months for placebo (Log-rank P = 0.4372). Treatment was suspended due to adverse events in one rituximab patient. In this study, rituximab was not more effective than placebo in preventing clinical deterioration following the discontinuation of immunoglobulin therapy in CIDP. Further studies might evaluate the efficacy of more frequent or earlier administration of rituximab.

摘要

慢性炎症性脱髓鞘性多发性神经根神经病(CIDP)通常需要长期持续治疗以防止病情恶化。本研究评估了利妥昔单抗在CIDP患者免疫球蛋白治疗中断后预防病情恶化的疗效。在这项在七家意大利医院进行的随机、双盲、安慰剂对照研究中,接受免疫球蛋白治疗的CIDP患者被分配接受利妥昔单抗(第1、15和180±7天各1g)或安慰剂治疗。两组在干预后6个月内继续使用常规免疫球蛋白剂量。主要终点是在免疫球蛋白停药后6个月内的第12个月,在以下三项指标中任何一项出现恶化的患者比例:调整后的INCAT评分降低至少1分、MRC总分降低2分或RODS百分位数评分降低4分。次要终点包括在第18个月(免疫球蛋白停药后12个月内)病情恶化的患者比例、因不良事件或自愿原因停止治疗的情况,以及免疫球蛋白停药后至病情恶化的时间。本研究已在ClinicalTrials.gov(NCT06325943)和欧盟临床试验数据库(编号2017 - 005034 - 36)注册,现已完成。2019年4月至2022年3月,共招募了39例患者;2例撤回同意书。其余37例患者被分配接受利妥昔单抗(n = 19)或安慰剂(n = 18)治疗。中位年龄为53岁(四分位间距45 - 64岁),女性11例(30%)。利妥昔单抗组(12/19,63.2%)和安慰剂组(12/18,66.6%)在第12个月病情恶化的患者比例相似[优势比(OR)0.86;95%置信区间(CI)0.22 - 3.32]。在第18个月未观察到显著差异(OR 0.62;95% CI 0.14 - 2.70),在第6、12和18个月各量表的平均评分也无显著差异。利妥昔单抗组病情恶化的中位时间为5个月,安慰剂组为2个月(对数秩检验P = 0.4372)。1例接受利妥昔单抗治疗的患者因不良事件暂停治疗。在本研究中,在CIDP患者免疫球蛋白治疗中断后,利妥昔单抗在预防临床病情恶化方面并不比安慰剂更有效。进一步的研究可能会评估更频繁或更早使用利妥昔单抗的疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e694/11967823/631025b11b3d/awae400f1.jpg

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