• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

与那他珠单抗延长给药方案相关的进行性多灶性白质脑病。

Progressive multifocal leukoencephalopathy associated to natalizumab extended dosing regimen.

作者信息

Hervás José Vicente, Presas-Rodríguez Silvia, Crespo-Cuevas Ane Miren, Canento Tamara, Lozano-Sánchez Manuel, Massuet-Vilamajó Anna, Ramo-Tello Cristina

机构信息

Department of Neurosciences, Multiple Sclerosis Unit, Germans Trias i Pujol Hospital. C/Canyet s/n 08916, Badalona, Spain.

出版信息

Neurodegener Dis Manag. 2015 Oct;5(5):399-402. doi: 10.2217/nmt.15.42. Epub 2015 Oct 30.

DOI:10.2217/nmt.15.42
PMID:26517599
Abstract

A risk for developing progressive multifocal leukoencephalopathy is a major barrier to natalizumab use. Extended dosing intervals have been proposed as a way to maintain therapeutic efficacy and reduce progressive multifocal leukoencephalopathy incidence. This is the first reported case of progressive multifocal leukoencephalopathy in a patient using an extended dosing regimen (300 mg/6 weeks). A close clinical and imaging monitoring allowed early detection, which is a major prognostic factor. A favorable outcome was seen with a therapy comprising plasma exchange therapy, mirtazapine, mefloquine and cidofovir. Further studies will be needed to assess the potential role of extended dosing intervals to improve prognosis in patients receiving natalizumab and also to measure its impact clinically and/or radiologically.

摘要

发生进行性多灶性白质脑病的风险是使用那他珠单抗的主要障碍。延长给药间隔已被提议作为维持治疗效果和降低进行性多灶性白质脑病发病率的一种方法。这是首例报道的使用延长给药方案(300mg/6周)的患者发生进行性多灶性白质脑病的病例。密切的临床和影像学监测实现了早期检测,这是一个主要的预后因素。采用包括血浆置换疗法、米氮平、甲氟喹和西多福韦的治疗方案取得了良好的效果。需要进一步研究以评估延长给药间隔对接受那他珠单抗治疗的患者改善预后的潜在作用,并衡量其在临床和/或影像学方面的影响。

相似文献

1
Progressive multifocal leukoencephalopathy associated to natalizumab extended dosing regimen.与那他珠单抗延长给药方案相关的进行性多灶性白质脑病。
Neurodegener Dis Manag. 2015 Oct;5(5):399-402. doi: 10.2217/nmt.15.42. Epub 2015 Oct 30.
2
Asymptomatic progressive multifocal leukoencephalopathy during natalizumab therapy with treatment.那他珠单抗治疗期间出现无症状性进行性多灶性白质脑病并接受治疗。
J Clin Neurosci. 2016 Mar;25:145-7. doi: 10.1016/j.jocn.2015.08.027. Epub 2015 Nov 2.
3
Natalizumab-associated progressive multifocal leukoencephalopathy is not preceded by elevated drug concentrations.纳他珠单抗相关性进行性多灶性白质脑病与药物浓度升高无关。
Mult Scler. 2017 Jun;23(7):995-999. doi: 10.1177/1352458516684023. Epub 2016 Dec 13.
4
Natalizumab-associated progressive multifocal leukoencephalopathy: successful treatment without plasma exchange and its associated risks.那他珠单抗相关的进行性多灶性白质脑病:无需血浆置换及其相关风险的成功治疗
J Neurol. 2017 Feb;264(2):401-403. doi: 10.1007/s00415-016-8372-0. Epub 2016 Dec 30.
5
Progressive multifocal leukoencephalopathy and granule cell neuronopathy with novel mutation flanking VP1 C-terminus in natalizumab-extended interval dosing.进行性多灶性白质脑病和颗粒细胞神经元病,在那他珠单抗延长给药间隔时伴有位于VP1 C末端侧翼的新突变。
Neurol Neuroimmunol Neuroinflamm. 2020 Mar 20;7(3). doi: 10.1212/NXI.0000000000000709. Print 2020 May 4.
6
Fingolimod treatment after natalizumab-related progressive multifocal leukoencephalopathy: three new cases.那他珠单抗相关的进行性多灶性白质脑病后使用芬戈莫德治疗:三例新病例
Mult Scler. 2015 Apr;21(5):671-2. doi: 10.1177/1352458514549823. Epub 2014 Oct 10.
7
Assessing understanding of individual risk and symptoms of progressive multifocal leukoencephalopathy in patients prescribed natalizumab for multiple sclerosis.评估接受那他珠单抗治疗多发性硬化症的患者对进行性多灶性白质脑病个体风险和症状的理解。
Intern Med J. 2017 Feb;47(2):194-199. doi: 10.1111/imj.13318.
8
Long-term safety evaluation of natalizumab for the treatment of multiple sclerosis.那他珠单抗治疗多发性硬化症的长期安全性评估。
Expert Opin Drug Saf. 2017 Aug;16(8):963-972. doi: 10.1080/14740338.2017.1346082. Epub 2017 Jul 5.
9
Quantitative electroencephalography supports diagnosis of natalizumab-associated progressive multifocal leukoencephalopathy.定量脑电图有助于诊断那他珠单抗相关性进行性多灶性白质脑病。
J Neurovirol. 2019 Feb;25(1):133-136. doi: 10.1007/s13365-018-0689-2. Epub 2018 Nov 9.
10
Application of serum natalizumab levels during plasma exchange in MS patients with progressive multifocal leukoencephalopathy.在患有进行性多灶性白质脑病的多发性硬化症患者血浆置换过程中血清那他珠单抗水平的应用。
Mult Scler. 2015 Apr;21(4):481-4. doi: 10.1177/1352458514541507. Epub 2014 Jul 30.

引用本文的文献

1
Safety and efficacy of extended versus standard interval dosing of natalizumab in multiple sclerosis patients: a systematic review and meta-analysis.扩展与标准间隔给药纳武利尤单抗治疗多发性硬化症患者的安全性和有效性:系统评价和荟萃分析。
Acta Neurol Belg. 2024 Apr;124(2):407-417. doi: 10.1007/s13760-024-02480-6. Epub 2024 Mar 8.
2
Progressive multifocal leukoencephalopathy successfully treated with mefloquine and literature review.用甲氟喹成功治疗进行性多灶性白质脑病及文献综述
Encephalitis. 2021 Oct;1(4):111-119. doi: 10.47936/encephalitis.2021.00094. Epub 2021 Sep 28.
3
No evidence for loss of natalizumab effectiveness with every-6-week dosing: a propensity score-matched comparison with every-4-week dosing in patients enrolled in the Tysabri Observational Program (TOP).
每6周给药方案未显示那他珠单抗有效性丧失的证据:在泰萨比观察项目(TOP)入组患者中与每4周给药方案的倾向评分匹配比较。
Ther Adv Neurol Disord. 2021 Sep 27;14:17562864211042458. doi: 10.1177/17562864211042458. eCollection 2021.
4
The Use of Antimalarial Drugs against Viral Infection.抗疟药物在病毒感染治疗中的应用。
Microorganisms. 2020 Jan 8;8(1):85. doi: 10.3390/microorganisms8010085.
5
Risk of natalizumab-associated PML in patients with MS is reduced with extended interval dosing.多发性硬化症患者使用延长间隔剂量可降低纳他珠单抗相关进行性多灶性脑白质病的风险。
Neurology. 2019 Oct 8;93(15):e1452-e1462. doi: 10.1212/WNL.0000000000008243. Epub 2019 Sep 12.
6
Four cases of natalizumab-related PML: a less severe course in extended interval dosing?四起与那他珠单抗相关的进行性多灶性白质脑病:在延长间隔给药时病程更轻?
Neurol Sci. 2019 Oct;40(10):2119-2124. doi: 10.1007/s10072-019-03959-4. Epub 2019 Jun 7.
7
Progressive multifocal leukoencephalopathy with extended natalizumab dosing.使用延长剂量那他珠单抗治疗的进行性多灶性白质脑病。
Neurol Clin Pract. 2018 Jun;8(3):e12-e14. doi: 10.1212/CPJ.0000000000000457.