Department of Neurology, AP-HP, Henri Mondor University Hospital, Créteil, France.
Center for Interdisciplinary Research in Biology, Collège de France, CNRS UMR 7241, INSERM U1050, Labex Memolife, PSL Research University, Paris, France.
Eur J Neurol. 2024 Jul;31(7):e16285. doi: 10.1111/ene.16285. Epub 2024 Mar 21.
Peripheral neuropathy is a frequent complication of brentuximab vedotin (BV), used in CD30+ lymphoma treatment. Classic BV-induced neuropathy (BV-CN) is a mild distal sensory axonal polyneuropathy. Severe BV-induced inflammatory neuropathies (BV-IN) have been described. BV-IN contribute to lymphoma-associated morbidity but might be immunotherapy-responsive. Our primary objective was to evaluate the rate of BV-IN. Our secondary objectives were to determine risk factors and warning signs.
We conducted a retrospective cohort study on all patients treated with BV at our center between April 2014 and September 2021. Clinical, biological, and electrophysiological data were collected. BV-induced neuropathy was defined as the occurrence of neuropathy up to 3 months after BV discontinuation. BV-IN was defined with criteria adapted from European Academy of Neurology/Peripheral Nerve Society 2021 electrodiagnostic criteria for chronic inflammatory demyelinating polyradiculoneuropathy. Other neuropathies were classified as BV-CN.
Among 83 patients, 41 (49%) developed neuropathy: 35 BV-CN and 6 BV-IN. Thus, the rate of BV-IN was 7.2%. Compared to patients with BV-CN, no predisposing factor was identified. However, patients with BV-IN more frequently presented muscle weakness (67% vs. 5.7%, p < 0.05), gait disorders (83% vs. 20%, p < 0.05), or acute or subacute onset (67% vs. 14%, p < 0.05). BV-IN was frequently more severe (Common Terminology Criteria for Adverse Events grade ≥3; 50% vs. 0%, p < 0.05). Four patients were treated with immunotherapy.
Brentuximab vedotin-induced neuropathy is an overlooked complication. Based on four easily identifiable "red flags", we provide an algorithm to help non-neurologist physicians that care for BV-treated patients to detect BV-IN. The aim of the algorithm is to decrease the diagnostic and management delay of this disabling neuropathy.
Brentuximab vedotin(BV)是一种用于治疗 CD30+淋巴瘤的药物,外周神经病变是其常见的并发症。经典的 BV 诱导性神经病(BV-CN)是一种轻度的远端感觉性轴索性多发性神经病。严重的 BV 诱导性炎症性神经病(BV-IN)也曾被描述过。BV-IN 会导致淋巴瘤相关的发病率增加,但可能对免疫治疗有反应。我们的主要目的是评估 BV-IN 的发生率。我们的次要目标是确定危险因素和预警信号。
我们对 2014 年 4 月至 2021 年 9 月在我们中心接受 BV 治疗的所有患者进行了回顾性队列研究。收集了临床、生物学和电生理学数据。BV 诱导性神经病的定义是在 BV 停药后 3 个月内发生的神经病。BV-IN 的定义采用了欧洲神经病学会/周围神经学会 2021 年慢性炎症性脱髓鞘性多发性神经病电诊断标准改编的标准。其他神经病被归类为 BV-CN。
在 83 名患者中,有 41 名(49%)出现了神经病:35 名 BV-CN 和 6 名 BV-IN。因此,BV-IN 的发生率为 7.2%。与 BV-CN 患者相比,没有发现任何易患因素。然而,BV-IN 患者更常出现肌无力(67% vs. 5.7%,p<0.05)、步态障碍(83% vs. 20%,p<0.05)或急性或亚急性发作(67% vs. 14%,p<0.05)。BV-IN 更常伴有严重程度(不良事件常用术语标准≥3 级;50% vs. 0%,p<0.05)。4 名患者接受了免疫治疗。
Brentuximab vedotin 诱导性神经病是一种被忽视的并发症。根据四个容易识别的“红旗”,我们提供了一个算法,帮助治疗接受 BV 治疗的患者的非神经科医生识别 BV-IN。该算法的目的是减少这种致残性神经病的诊断和治疗延误。