Progressive Multiple Cranial Neuropathies as a Manifestation of CAR-T Neurotoxicity.

IF 0.6 Q4 CLINICAL NEUROLOGY
Zachary T Lazzari, Avi Singh Gandh, Bhagya Sannananja, Samir R Belagaje, Spencer K Hutto
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Abstract

Objective: To describe a case of delayed onset multiple cranial neuropathies as a manifestation of neurotoxicity after chimeric antigen receptor T-cell (CAR-T) therapy for multiple myeloma. While ICANS following CAR-T is a well-reported complication, it classically presents with encephalopathy, seizures, dysphasia, tremors, headache, and cerebral edema. Isolated unilateral facial neuropathies secondary to CAR-T neurotoxicity have been described, but progressive multiple cranial neuropathies have not. Herein, a 75-year-old male presented with left facial nerve palsy 19 days after initiating CAR-T therapy for multiple myeloma. Contrasted brain MRI showed contralateral right facial nerve enhancement, and his left facial palsy was treated with steroids and valacyclovir for 7 days. The facial palsy persisted and progressed to involve bilateral facial nerves and left cranial nerve VI by 31 days post-CAR-T. Specifically, his exam showed impaired abduction of left eye and nearly absent facial movement. Repeat contrasted MRI brain showed mild enhancement of bilateral facial nerves. Extensive serum and CSF testing was unremarkable. Initial treatment with oral steroids for 7 days was ineffective. Concern regarding the impact of steroids on CAR-T efficacy influenced treatment dose and duration. Anakinra was considered but not given. Subsequent treatment with intravenous high dose steroids, followed by a prolonged prednisone taper, led to resolution of CN VI palsy at 2.5 months from onset (2 weeks after completed therapy), and moderate improvement of bilateral facial palsy 5.5 months from onset (3.5 months after completed therapy). CAR-T neurotoxicity can present with progressive multiple cranial neuropathies. The best treatment of these cases is unknown; however, this patient improved in the context of corticosteroids and facial rehabilitation over a prolonged period of follow-up.

进行性多发性颅神经病变是CAR-T神经毒性的表现。
目的:描述一例迟发性多发性颅脑神经病变作为嵌合抗原受体t细胞治疗多发性骨髓瘤后神经毒性的表现。虽然CAR-T后的ICANS是一种常见的并发症,但它通常表现为脑病、癫痫发作、吞咽困难、震颤、头痛和脑水肿。CAR-T神经毒性继发的孤立单侧面神经病变已被描述,但进展性多发性颅神经病变尚未报道。本文中,一名75岁男性在接受多发性骨髓瘤CAR-T治疗19天后出现左侧面神经麻痹。脑MRI对比显示对侧右侧面神经增强,左侧面神经麻痹给予类固醇和伐昔洛韦治疗7天。car - t后31天,面瘫持续存在并进展到累及双侧面神经和左颅神经VI。具体来说,他的检查显示左眼外展受损,几乎没有面部活动。脑部重复对比MRI显示双侧面神经轻度增强。广泛的血清和脑脊液检测无明显差异。最初口服类固醇治疗7天无效。对类固醇对CAR-T疗效影响的担忧影响了治疗剂量和持续时间。阿那金拉曾被考虑过,但没有被给予。随后静脉注射大剂量类固醇治疗,再加上延长强的松逐渐减少治疗,在发病2.5个月后(治疗完成后2周)CN VI麻痹得到缓解,在发病5.5个月后(治疗完成后3.5个月)双侧面瘫得到中度改善。CAR-T神经毒性可表现为进行性多发性颅神经病变。这些病例的最佳治疗方法尚不清楚;然而,经过长时间的随访,该患者在皮质类固醇和面部康复方面有所改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Neurohospitalist
Neurohospitalist CLINICAL NEUROLOGY-
CiteScore
1.60
自引率
0.00%
发文量
108
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