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Therapy-Associated Progressive Multifocal Leukoencephalopathy During Disease-Modifying Treatment of Multiple Sclerosis

机译:多发性硬化症疾病改良治疗期间与治疗相关的进行性多灶性白质脑病

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During the past 10 years, therapy-associated progressive multifocal leukoencephalopathy has gained an inglorious relevance, particularly among patients with MS who are on long-term treatment with natalizumab. More than 500 cases of this serious therapy complication have been reported worldwide until 2015, and, recently, progressive multifocal leukoencephalopathy has also been described in patients with MS who received monotherapy with dimethyl fumarate, fingolimod, and interferon β1a. (The neuroimmunologic features of this case and some of the MR images have recently been published elsewhere by the authors.) Finally, therapy-associated progressive multifocal leukoencephalopathy can also occur in patients without MS during disease-modifying immunotherapy with monoclonal antibodies other than natalizumab. As we still lack reliable predictive factors of this adverse event and although its risk factors are under intense debate, all of us must apparently learn to live with this “uninvited guest.” The objective of this article was to share and contribute some clinical experience and neuroradiologic features to further meet the diagnostic and therapeutic challenges of this potentially fatal therapy complication. Besides a review of the literature, we presented specific clinical and imaging data of 4 patients with relapsing-remitting MS who developed therapy-associated progressive multifocal leukoencephalopathy. We included results from patient-specific databases on continuous magnetization-transfer ratio monitoring before, during, and after the onset of therapy-associated progressive multifocal leukoencephalopathy and immune-reconstitution-inflammatory syndrome in 3 patients. They might be of additional benefit given the urgent need of further diagnostic tools to better assess the progressive multifocal leukoencephalopathy risk and its course in individual patients with MS during disease-modifying immunotherapy. Learning Objective: Discuss the clinical and imaging features that suggest a diagnosis of progressive multifocal leukoencephalopathy in MS-patients during long-term treatment with monoclonal antibodies.
机译:在过去的10年中,与治疗相关的进行性多灶性白质脑病的相关性已变得根深蒂固,尤其是在接受那他珠单抗长期治疗的MS患者中。截止到2015年,全球已报告了500多例这种严重的治疗并发症,最近,在接受过富马酸二甲酯,芬戈莫德和干扰素β1a单药治疗的MS患者中,也出现了进行性多灶性白质脑病。 (该病例的神经免疫学特征和一些MR图像最近已在其他地方发表。)最后,在无MS的患者中,使用那他珠单抗以外的单克隆抗体进行疾病改良免疫治疗时,与治疗相关的进行性多灶性白质脑病也可能发生。由于我们仍然缺乏关于这一不良事件的可靠预测因素,尽管其危险因素仍在激烈辩论中,所以我们所有人显然都必须学会与这位“不速之客”共处。本文的目的是分享并贡献一些临床经验和神经放射学特征,以进一步满足这种潜在致命治疗并发症的诊断和治疗挑战。除了对文献进行回顾之外,我们还介绍了4例复发性多发性MS患者,这些患者发生了与治疗相关的进行性多灶性白质脑病。我们纳入了3例患者在与治疗相关的进行性多灶性白质脑病和免疫重建-炎症综合征发作之前,期间和之后进行连续磁化转移率监测的患者特定数据库的结果。考虑到急需进一步的诊断工具,以更好地评估疾病改善免疫疗法中个别MS患者的进行性多灶性白质脑病风险及其病程,它们可能会带来更多益处。学习目标:讨论临床和影像学特征,以期在长期接受单克隆抗体治疗的MS患者中诊断出进行性多灶性白质脑病。

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