Ublituximab-xiiy as a treatment option for relapsing multiple sclerosis

被引:1
|
作者
Jakimovski, Dejan [1 ]
Weinstock-Guttman, Bianca [2 ]
Zivadinov, Robert [1 ,3 ,4 ]
机构
[1] Univ Buffalo, Buffalo Neuroimaging Anal Ctr, Jacobs Sch Med & Biomed Sci, Dept Neurol, Buffalo, NY USA
[2] Univ Buffalo, State Univ New York, Jacobs Comprehens MS Treatment & Res Ctr, Jacobs Sch Med & Biomed Sci, Buffalo, NY USA
[3] Univ Buffalo, State Univ New York, Ctr Biomed Imaging Clin Translat Sci Inst, Buffalo, NY USA
[4] Univ Buffalo, Ctr Biomed Imaging Clin Translat Sci Inst, Buffalo Neuroimaging Anal Ctr, Dept Neurol,Jacobs Sch Med & Biomed Sci, 77 Goodell St, Buffalo, NY 14203 USA
关键词
Ublituximab; multiple sclerosis; anti-CD20; monoclonal antibodies; relapsing MS; CHRONIC LYMPHOCYTIC-LEUKEMIA; ANTI-CD20; MONOCLONAL-ANTIBODY; NON-HODGKIN-LYMPHOMA; TERIFLUNOMIDE; IBRUTINIB; MULTICENTER; OFATUMUMAB; RITUXIMAB; PHASE-3; TRIAL;
D O I
10.1080/14737175.2023.2268842
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction:B cell depletion has been established as an efficacious anti-inflammatory therapy in people with relapsing forms of multiple sclerosis (MS). Ublituximab (ublituximab-xiiy) is the latest approved chimeric glycoengineered anti-CD20 monoclonal antibody (mAb) for the treatment of relapsing forms of MS.Areas covered:In this narrative review, the authors explore the safety and effectiveness of data derived from the Phase 2 and Phase 3 ublituximab trials and from their respective post-hoc analyses. Moreover, they consider the similarities and differences between the currently available anti-CD20 antibodies for treatment of relapsing MS. Lastly, the authors discuss the role and place of ublituximab in the current disease modifying therapy landscape.Expert opinion:Ublituximab is a rapid-acting and effective anti-inflammatory option as a treatment in people with relapsing MS that significantly reduced the annualized relapse rate and MRI-based disease activity. When compared to the Phase III trials of the other two anti-CD20 mAbs (ocrelizumab and ofatumumab), ublituximab did not result with reduction of 3 or 6-month confirmed disability progression. These differences may be attributed to the overall low rate of progression in both the ublituximab and the active comparator teriflunomide arm. Future data from open-label extensions are warranted. There was no significant reduction of ublituximab on whole-brain atrophy compared to teriflunomide.
引用
收藏
页码:1053 / 1061
页数:9
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