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多灶性播散性坏死性白质脑病作为纳武单抗治疗霍奇金淋巴瘤所致的严重中枢神经系统毒性:一例报告

Multifocal disseminated necrotizing leukoencephalopathy as severe central nervous system toxicity from nivolumab therapy for Hodgkin lymphoma: a case report.

作者信息

Algahtani Hussein, Shirah Bader, Alameen Mohamed Najm Aldeen, Saeed Abdulrahman Bin, Alqahtani Alwaleed Abdulhadi

机构信息

Neurology Section, Department of Medicine, Aseer Central Hospital, Abha, Saudi Arabia.

Department of Neuroscience, King Faisal Specialist Hospital & Research Centre, Jeddah, Saudi Arabia.

出版信息

Encephalitis. 2025 Jan;5(1):21-26. doi: 10.47936/encephalitis.2024.00101. Epub 2024 Nov 1.

DOI:10.47936/encephalitis.2024.00101
PMID:39481545
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11732269/
Abstract

Nivolumab, a monoclonal antibody approved in 2014 as an immune checkpoint inhibitor, offers benefits in cancer treatment but can cause serious neurological complications, including multifocal disseminated necrotizing leukoencephalopathy. We report a case of severe central nervous system toxicity in a 13-year-old boy with Hodgkin lymphoma who was treated with nivolumab following an inadequate response to multiple lines of chemotherapy. After six cycles of nivolumab, the patient developed multifocal disseminated necrotizing leukoencephalopathy, presenting with altered mental status, seizures, and neurological deficits with magnetic resonance imaging (MRI) findings of extensive white matter involvement, rendering him completely disabled. This case highlights the potential for disabling neurological complications associated with immune checkpoint inhibitors, emphasizing the importance of early detection through regular neurological assessment and MRI surveillance. The case also underscores the need for careful patient selection and monitoring when using nivolumab to mitigate the risk of severe central nervous system toxicity.

摘要

纳武单抗是一种于2014年获批的单克隆抗体,作为一种免疫检查点抑制剂,在癌症治疗中具有一定益处,但可能会引发严重的神经系统并发症,包括多灶性播散性坏死性白质脑病。我们报告了一例13岁患有霍奇金淋巴瘤的男孩出现严重中枢神经系统毒性的病例,该男孩在多线化疗反应不佳后接受了纳武单抗治疗。在接受六个周期的纳武单抗治疗后,患者出现了多灶性播散性坏死性白质脑病,表现为精神状态改变、癫痫发作和神经功能缺损,磁共振成像(MRI)显示广泛的白质受累,导致他完全残疾。该病例突出了免疫检查点抑制剂相关的致残性神经系统并发症的可能性,强调了通过定期神经学评估和MRI监测进行早期检测的重要性。该病例还强调了在使用纳武单抗时仔细选择患者并进行监测以降低严重中枢神经系统毒性风险的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fbf/11732269/10cdafebd219/encephalitis-2024-00101f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fbf/11732269/8929259e5748/encephalitis-2024-00101f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fbf/11732269/f024ee8ddc2b/encephalitis-2024-00101f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fbf/11732269/10cdafebd219/encephalitis-2024-00101f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fbf/11732269/8929259e5748/encephalitis-2024-00101f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fbf/11732269/f024ee8ddc2b/encephalitis-2024-00101f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fbf/11732269/10cdafebd219/encephalitis-2024-00101f3.jpg

相似文献

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本文引用的文献

1
Review of the Immune Checkpoint Inhibitors in the Context of Cancer Treatment.癌症治疗背景下免疫检查点抑制剂综述。
J Clin Med. 2023 Jun 27;12(13):4301. doi: 10.3390/jcm12134301.
2
Neurological Immune Related Adverse Events Associated with Nivolumab, Ipilimumab, and Pembrolizumab Therapy-Review of the Literature and Future Outlook.与纳武单抗、伊匹单抗和帕博利珠单抗治疗相关的神经免疫相关不良事件——文献综述与未来展望
J Clin Med. 2019 Oct 24;8(11):1777. doi: 10.3390/jcm8111777.
3
Neurological complications of immune checkpoint inhibitors: what happens when you 'take the brakes off' the immune system.
免疫检查点抑制剂的神经系统并发症:当你“松开免疫系统的刹车”时会发生什么。
Ther Adv Neurol Disord. 2018 Sep 14;11:1756286418799864. doi: 10.1177/1756286418799864. eCollection 2018.
4
Fatal Necrotizing Encephalopathy after Treatment with Nivolumab for Squamous Non-Small Cell Lung Cancer: Case Report and Review of the Literature.纳武利尤单抗治疗鳞状非小细胞肺癌后致死性坏死性脑病:病例报告及文献复习。
Front Immunol. 2018 Jan 30;9:108. doi: 10.3389/fimmu.2018.00108. eCollection 2018.
5
Neurologic Serious Adverse Events Associated with Nivolumab Plus Ipilimumab or Nivolumab Alone in Advanced Melanoma, Including a Case Series of Encephalitis.纳武单抗联合伊匹单抗或单独使用纳武单抗治疗晚期黑色素瘤相关的神经系统严重不良事件,包括一组脑炎病例
Oncologist. 2017 Jun;22(6):709-718. doi: 10.1634/theoncologist.2016-0487. Epub 2017 May 11.