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4
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本文引用的文献

1
High-Dose Methotrexate as CNS Prophylaxis in High-Risk Aggressive B-Cell Lymphoma.大剂量甲氨蝶呤作为高危侵袭性 B 细胞淋巴瘤中枢神经系统预防的治疗方案。
J Clin Oncol. 2023 Dec 10;41(35):5376-5387. doi: 10.1200/JCO.23.00365. Epub 2023 Oct 5.
2
Prevalence and management of methotrexate-induced neurotoxicity in pediatric patients with osteosarcoma: a single-center experience.骨肉瘤患儿甲氨蝶呤诱导的神经毒性的患病率和处理:单中心经验。
Int J Clin Oncol. 2022 Aug;27(8):1372-1378. doi: 10.1007/s10147-022-02184-y. Epub 2022 May 31.
3
Methotrexate encephalopathy: Two cases in adult cancer patients, who recovered with pathophysiologically based therapy.甲氨蝶呤脑病:两例成年癌症患者病例,经基于病理生理学的治疗后康复。
SAGE Open Med Case Rep. 2017 May 4;5:2050313X17706875. doi: 10.1177/2050313X17706875. eCollection 2017.
4
Review of dextromethorphan administration in 18 patients with subacute methotrexate central nervous system toxicity.18例亚急性甲氨蝶呤中枢神经系统毒性患者右美沙芬给药情况回顾。
Pediatr Neurol. 2014 Jun;50(6):625-9. doi: 10.1016/j.pediatrneurol.2014.01.048. Epub 2014 Jan 31.
5
Persistent cognitive deficits, induced by intrathecal methotrexate, are associated with elevated CSF concentrations of excitotoxic glutamate analogs and can be reversed by an NMDA antagonist.鞘内注射甲氨蝶呤引起的持续性认知缺陷与兴奋性谷氨酸类似物的脑脊液浓度升高有关,并可被 NMDA 拮抗剂逆转。
Behav Brain Res. 2011 Dec 1;225(2):491-7. doi: 10.1016/j.bbr.2011.08.006. Epub 2011 Aug 12.
6
Intrathecal methotrexate neurotoxicity: clinical correlates and antidotal treatment.鞘内注射甲氨蝶呤的神经毒性:临床相关性和解毒治疗。
Environ Toxicol Pharmacol. 2005 May;19(3):721-5. doi: 10.1016/j.etap.2004.12.031. Epub 2005 Jan 26.
7
Dextromethorphan: a review of N-methyl-d-aspartate receptor antagonist in the management of pain.右美沙芬:N-甲基-D-天冬氨酸受体拮抗剂治疗疼痛的综述
CNS Drug Rev. 2007 Spring;13(1):96-106. doi: 10.1111/j.1527-3458.2007.00006.x.
8
Neurotoxic complications of chemotherapy in patients with cancer: clinical signs and optimal management.癌症患者化疗的神经毒性并发症:临床体征与最佳管理
Drugs. 2003;63(15):1549-63. doi: 10.2165/00003495-200363150-00003.
9
Dextromethorphan is effective in the treatment of subacute methotrexate neurotoxicity.右美沙芬对亚急性甲氨蝶呤神经毒性的治疗有效。
Pediatr Hematol Oncol. 2002 Jul-Aug;19(5):319-27. doi: 10.1080/08880010290057336.

鞘内注射甲氨蝶呤、中枢神经系统毒性及对N-甲基-D-天冬氨酸拮抗剂的反应:成人病例系列

Intrathecal methotrexate, central nervous system toxicity, and response to N-methyl-D-aspartate antagonism: An adult case series.

作者信息

Donaghy Ryan, Singer Lauren, Dixit Karan

机构信息

Department of Neurology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.

Department of Neurology, University of Chicago, Chicago, Illinois, USA.

出版信息

Neurooncol Pract. 2024 Jun 12;11(5):665-669. doi: 10.1093/nop/npae051. eCollection 2024 Oct.

DOI:10.1093/nop/npae051
PMID:39279773
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11398929/
Abstract

BACKGROUND

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

背景

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。

方法

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。

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。

结论

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。