Ofatumumab用于多发性硬化症伴残疾积累。

IF 3.6 3区 医学 Q1 CLINICAL NEUROLOGY
Journal of the Neurological Sciences Pub Date : 2025-01-15 Epub Date: 2024-12-16 DOI:10.1016/j.jns.2024.123356
Masahiro Mimori, Atsuko Katsumoto, Tomoko Okamoto, Wakiro Sato, Youwei Lin, Takashi Yamamura, Yuji Takahashi
{"title":"Ofatumumab用于多发性硬化症伴残疾积累。","authors":"Masahiro Mimori, Atsuko Katsumoto, Tomoko Okamoto, Wakiro Sato, Youwei Lin, Takashi Yamamura, Yuji Takahashi","doi":"10.1016/j.jns.2024.123356","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>The ASCLEPIOS/APLIOS/APOLITOS/ALITHIOS trials highlighted the benefits of ofatumumab in reducing relapse rates and disability progression in multiple sclerosis (MS). However, its effects on patients with severe disability status remains uncertain. This study aimed to clarify the outcomes of ofatumumab in MS patients with high Expanded Disability Status Scale (EDSS) scores and prolonged disease durations.</p><p><strong>Methods: </strong>This is a retrospective cohort study of MS patients treated with ofatumumab at an MS center in Japan. At 12 months of treatment, patients with MS starting ofatumumab were classified into the treatment-responsive or treatment-resistant groups based on ofatumumab continuity, incidence of relapses with EDSS worsening, progression independent of relapse activity (PIRA). We used logistic regression analysis to identify factors associated with ofatumumab response.</p><p><strong>Results: </strong>Seventy patients were included in the analysis; 39 (56 %) patients were relapsing-remitting (RR), and 31 (44 %) patients were secondary progressive (SP) MS. Mean age at ofatumumab initiation, age at onset, and disease duration were 48.0, 33.9, and 14.1 years, respectively. The median EDSS was 4.5 (3.0-6.5); 38(56 %) patients were classified as resistant. The resistant rates by disease type were 33 % (13/39) and 81 % (26/31) for RR and SP MS, respectively. On multivariate analysis, EDSS and No evidence of disease activity (NEDA) 3 were independent factors for ofatumumab responsiveness (OR, 1.74, 0.04; 95 % CI, 1.17-2.73, 0.00-0.47; p = 0.01, 0.04).</p><p><strong>Conclusion: </strong>Ofatumumab may yield more favorable effects when initiated in patients with MS with lower EDSS scores.</p>","PeriodicalId":17417,"journal":{"name":"Journal of the Neurological Sciences","volume":"468 ","pages":"123356"},"PeriodicalIF":3.6000,"publicationDate":"2025-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Ofatumumab for multiple sclerosis with disability accumulation.\",\"authors\":\"Masahiro Mimori, Atsuko Katsumoto, Tomoko Okamoto, Wakiro Sato, Youwei Lin, Takashi Yamamura, Yuji Takahashi\",\"doi\":\"10.1016/j.jns.2024.123356\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>The ASCLEPIOS/APLIOS/APOLITOS/ALITHIOS trials highlighted the benefits of ofatumumab in reducing relapse rates and disability progression in multiple sclerosis (MS). However, its effects on patients with severe disability status remains uncertain. This study aimed to clarify the outcomes of ofatumumab in MS patients with high Expanded Disability Status Scale (EDSS) scores and prolonged disease durations.</p><p><strong>Methods: </strong>This is a retrospective cohort study of MS patients treated with ofatumumab at an MS center in Japan. At 12 months of treatment, patients with MS starting ofatumumab were classified into the treatment-responsive or treatment-resistant groups based on ofatumumab continuity, incidence of relapses with EDSS worsening, progression independent of relapse activity (PIRA). We used logistic regression analysis to identify factors associated with ofatumumab response.</p><p><strong>Results: </strong>Seventy patients were included in the analysis; 39 (56 %) patients were relapsing-remitting (RR), and 31 (44 %) patients were secondary progressive (SP) MS. Mean age at ofatumumab initiation, age at onset, and disease duration were 48.0, 33.9, and 14.1 years, respectively. The median EDSS was 4.5 (3.0-6.5); 38(56 %) patients were classified as resistant. The resistant rates by disease type were 33 % (13/39) and 81 % (26/31) for RR and SP MS, respectively. On multivariate analysis, EDSS and No evidence of disease activity (NEDA) 3 were independent factors for ofatumumab responsiveness (OR, 1.74, 0.04; 95 % CI, 1.17-2.73, 0.00-0.47; p = 0.01, 0.04).</p><p><strong>Conclusion: </strong>Ofatumumab may yield more favorable effects when initiated in patients with MS with lower EDSS scores.</p>\",\"PeriodicalId\":17417,\"journal\":{\"name\":\"Journal of the Neurological Sciences\",\"volume\":\"468 \",\"pages\":\"123356\"},\"PeriodicalIF\":3.6000,\"publicationDate\":\"2025-01-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of the Neurological Sciences\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1016/j.jns.2024.123356\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/12/16 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the Neurological Sciences","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.jns.2024.123356","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/12/16 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

摘要

背景:ASCLEPIOS/ applios /APOLITOS/ALITHIOS试验强调了ofatumumab在降低多发性硬化症(MS)复发率和残疾进展方面的益处。然而,其对重度残疾患者的影响仍不确定。本研究旨在阐明ofatumumab在具有高扩展残疾状态量表(EDSS)评分和延长疾病持续时间的MS患者中的结果。方法:这是一项在日本多发性硬化症中心接受ofatumumab治疗的多发性硬化症患者的回顾性队列研究。在治疗12个月时,开始使用ofatumumab的MS患者根据ofatumumab的连续性、EDSS恶化的复发发生率、独立于复发活动的进展(PIRA)被分为治疗反应组或治疗抵抗组。我们使用逻辑回归分析来确定与ofatumumab反应相关的因素。结果:70例患者纳入分析;39例(56%)患者为复发缓解型(RR), 31例(44%)患者为继发性进展型(SP) ms, ofatumumab起始的平均年龄、发病年龄和病程分别为48.0年、33.9年和14.1年。中位EDSS为4.5 (3.0-6.5);38例(56%)患者被分类为耐药。按疾病类型划分,RR和SP MS的耐药率分别为33%(13/39)和81%(26/31)。在多变量分析中,EDSS和无疾病活动性证据(NEDA) 3是影响ofatumumab反应性的独立因素(OR, 1.74, 0.04;95% ci, 1.17-2.73, 0.00-0.47;P = 0.01, 0.04)。结论:对于EDSS评分较低的MS患者,Ofatumumab可能会产生更有利的效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ofatumumab for multiple sclerosis with disability accumulation.

Background: The ASCLEPIOS/APLIOS/APOLITOS/ALITHIOS trials highlighted the benefits of ofatumumab in reducing relapse rates and disability progression in multiple sclerosis (MS). However, its effects on patients with severe disability status remains uncertain. This study aimed to clarify the outcomes of ofatumumab in MS patients with high Expanded Disability Status Scale (EDSS) scores and prolonged disease durations.

Methods: This is a retrospective cohort study of MS patients treated with ofatumumab at an MS center in Japan. At 12 months of treatment, patients with MS starting ofatumumab were classified into the treatment-responsive or treatment-resistant groups based on ofatumumab continuity, incidence of relapses with EDSS worsening, progression independent of relapse activity (PIRA). We used logistic regression analysis to identify factors associated with ofatumumab response.

Results: Seventy patients were included in the analysis; 39 (56 %) patients were relapsing-remitting (RR), and 31 (44 %) patients were secondary progressive (SP) MS. Mean age at ofatumumab initiation, age at onset, and disease duration were 48.0, 33.9, and 14.1 years, respectively. The median EDSS was 4.5 (3.0-6.5); 38(56 %) patients were classified as resistant. The resistant rates by disease type were 33 % (13/39) and 81 % (26/31) for RR and SP MS, respectively. On multivariate analysis, EDSS and No evidence of disease activity (NEDA) 3 were independent factors for ofatumumab responsiveness (OR, 1.74, 0.04; 95 % CI, 1.17-2.73, 0.00-0.47; p = 0.01, 0.04).

Conclusion: Ofatumumab may yield more favorable effects when initiated in patients with MS with lower EDSS scores.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of the Neurological Sciences
Journal of the Neurological Sciences 医学-临床神经学
CiteScore
7.60
自引率
2.30%
发文量
313
审稿时长
22 days
期刊介绍: The Journal of the Neurological Sciences provides a medium for the prompt publication of original articles in neurology and neuroscience from around the world. JNS places special emphasis on articles that: 1) provide guidance to clinicians around the world (Best Practices, Global Neurology); 2) report cutting-edge science related to neurology (Basic and Translational Sciences); 3) educate readers about relevant and practical clinical outcomes in neurology (Outcomes Research); and 4) summarize or editorialize the current state of the literature (Reviews, Commentaries, and Editorials). JNS accepts most types of manuscripts for consideration including original research papers, short communications, reviews, book reviews, letters to the Editor, opinions and editorials. Topics considered will be from neurology-related fields that are of interest to practicing physicians around the world. Examples include neuromuscular diseases, demyelination, atrophies, dementia, neoplasms, infections, epilepsies, disturbances of consciousness, stroke and cerebral circulation, growth and development, plasticity and intermediary metabolism.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信