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进行性多灶性白质脑病与那他珠单抗。

Progressive multifocal leukoencephalopathy and natalizumab.

机构信息

Department of Neurology, St. Josef Hospital, Ruhr University Bochum, Gudrunstrasse 56, 44791 Bochum, Germany.

出版信息

J Neurol. 2011 Nov;258(11):1920-8. doi: 10.1007/s00415-011-6116-8. Epub 2011 Jun 7.

Abstract

Natalizumab (TYSABRI(®)), a specific α4-integrin antagonist, is approved as a second-line treatment of relapsing-remitting MS (RRMS) patients who fail therapy with interferons or as first-line treatment of patients with highly active relapsing-remitting disease. Since the market introduction of natalizumab as a monotherapy in July of 2006, 111 cases of PML have been reported in natalizumab-treated MS patients as of April 2011. This review focuses on the available data regarding risk stratification for PML under long-term natalizumab therapy, and summarizes the current approach for PML management, as a natalizumab treatment complication is not necessarily associated with a fatal outcome. There is a need for development of surrogate markers that would help to better define the risk of PML in individual patients.

摘要

那他珠单抗(TYSABRI(®))是一种特异性的 α4-整合素拮抗剂,被批准用于治疗对干扰素治疗无效的复发缓解型多发性硬化症(RRMS)患者,或用于治疗活动期高复发 RRMS 患者。自 2006 年 7 月那他珠单抗作为单药疗法上市以来,截至 2011 年 4 月,在接受那他珠单抗治疗的 MS 患者中已报告了 111 例进行性多灶性白质脑病(PML)病例。这篇综述重点介绍了长期那他珠单抗治疗下 PML 的风险分层的现有数据,并总结了目前 PML 的管理方法,因为那他珠单抗治疗的并发症不一定与致命结局相关。需要开发替代标志物,以帮助更好地确定个体患者发生 PML 的风险。

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