Donaghy Ryan, Singer Lauren, Dixit Karan
Department of Neurology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Department of Neurology, University of Chicago, Chicago, Illinois, USA.
Neurooncol Pract. 2024 Jun 12;11(5):665-669. doi: 10.1093/nop/npae051. eCollection 2024 Oct.
Methotrexate (MTX) is administered for the treatment of central nervous system (CNS) hematologic cancers, prophylaxis of CNS dissemination of certain hematological cancers, and in solid tumor leptomeningeal disease. MTX treatment can be limited by CNS toxicity. Dextromethorphan is used to treat MTX neurotoxicity, with most data derived from pediatric case series. In this report, we profile 4 adult patients who developed intrathecal (IT) MTX neurotoxicity to better characterize their response to dextromethorphan treatment.
A case series of 4 patients who developed neurologic symptoms attributed to IT MTX neurotoxicity subsequently treated with dextromethorphan was devised. Demographic data, clinical characteristics, electroencephalography results, magnetic resonance imaging, cerebrospinal fluid (CSF) characteristics, and dextromethorphan treatment outcomes were described.
Of the 4 patients developing MTX neurotoxicity, neurologic symptoms developed over a timeframe of 2 to 14 days from the precedent MTX exposure. Radiologic phenotypes included subcortical white matter diffusion-restricting lesions, bi-hemispheric subcortical white matter T2-FLAIR hyperintensities, as well as other findings described in the report. Time elapsed from initiation of dextromethorphan to neurologic symptom resolution ranged from 1 to 2 days.
The profiles of 4 adult patients developing suspected IT MTX neurotoxicity syndromes with subsequent response to Dextromethorphan add further data to guide the management of such patients.
甲氨蝶呤(MTX)用于治疗中枢神经系统(CNS)血液系统癌症、预防某些血液系统癌症的CNS播散以及实体瘤软脑膜疾病。MTX治疗可能会受到CNS毒性的限制。右美沙芬用于治疗MTX神经毒性,大多数数据来自儿科病例系列。在本报告中,我们对4例发生鞘内注射(IT)MTX神经毒性的成年患者进行了分析,以更好地描述他们对右美沙芬治疗的反应。
设计了一个病例系列,包括4例出现归因于IT MTX神经毒性的神经症状并随后接受右美沙芬治疗的患者。描述了人口统计学数据、临床特征、脑电图结果、磁共振成像、脑脊液(CSF)特征以及右美沙芬治疗结果。
在4例发生MTX神经毒性的患者中,神经症状在先前MTX暴露后的2至14天内出现。放射学表型包括皮质下白质扩散受限病变、双侧皮质下白质T2-FLAIR高信号,以及报告中描述的其他表现。从开始使用右美沙芬到神经症状缓解的时间为1至2天。
4例疑似发生IT MTX神经毒性综合征并随后对右美沙芬有反应的成年患者的资料,为指导此类患者的管理提供了更多数据。