Neuroimaging Findings of CAR T-Cell-Associated Neurotoxicity: A Review.

IF 3.2 Q3 CLINICAL NEUROLOGY
Neurology. Clinical practice Pub Date : 2025-08-01 Epub Date: 2025-07-17 DOI:10.1212/CPJ.0000000000200488
Aditi Vichare, Jimmy S Lee, Tim Q Duong
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引用次数: 0

Abstract

Chimeric antigen receptor T-cell (CAR-T) therapy has remarkable efficacy in treating refractory hematologic malignancies. However, CAR-T therapy may induce neurotoxic effects in some patients. Common symptoms of neurotoxicity range from early signs such as headache, confusion, delirium, and aphasia to severe manifestations such as seizures, motor weakness, increased intracranial pressure, cerebral edema, and coma. Magnetic resonance imaging (MRI) can offer invaluable insight into resulting abnormalities in the structure, physiology, and function of the central nervous system. This review aims to examine the current literature on brain MRI findings of CAR-T-induced neurotoxicity, elucidating its diagnostic capabilities, clinical implications, and emerging trends in advancing imaging modalities. An improved understanding of neural correlates of CAR-T neurotoxicity is important for early detection, development of neuroprotective strategies, and optimization of CAR-T regimens to maximize therapeutic efficacy while minimizing adverse neurotoxic effects.

CAR - t细胞相关神经毒性的神经影像学表现:综述
嵌合抗原受体t细胞(CAR-T)治疗难治性恶性血液病疗效显著。然而,CAR-T疗法可能会对一些患者产生神经毒性作用。神经毒性的常见症状包括从头痛、精神错乱、谵妄和失语等早期症状到癫痫发作、运动无力、颅内压升高、脑水肿和昏迷等严重症状。磁共振成像(MRI)可以为中枢神经系统的结构、生理和功能异常提供宝贵的见解。本综述旨在研究car - t诱导神经毒性的脑MRI结果,阐明其诊断能力、临床意义以及先进成像方式的新趋势。更好地了解CAR-T神经毒性的神经相关因素,对于早期发现、开发神经保护策略和优化CAR-T治疗方案,以最大限度地提高治疗效果,同时最大限度地减少不良神经毒性作用至关重要。
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来源期刊
Neurology. Clinical practice
Neurology. Clinical practice CLINICAL NEUROLOGY-
CiteScore
4.00
自引率
0.00%
发文量
77
期刊介绍: Neurology® Genetics is an online open access journal publishing peer-reviewed reports in the field of neurogenetics. The journal publishes original articles in all areas of neurogenetics including rare and common genetic variations, genotype-phenotype correlations, outlier phenotypes as a result of mutations in known disease genes, and genetic variations with a putative link to diseases. Articles include studies reporting on genetic disease risk, pharmacogenomics, and results of gene-based clinical trials (viral, ASO, etc.). Genetically engineered model systems are not a primary focus of Neurology® Genetics, but studies using model systems for treatment trials, including well-powered studies reporting negative results, are welcome.
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