Berkovich Regina, Calkwood Jonathan, Crayton Heidi, Erwin April, Faissner Simon, Gold Ralf, Katz Joshua, Leekoff Mark
Berkovich MS Center and Research Institute, West Hollywood, CA, United States.
Department of Neurology, Minnesota Center for Multiple Sclerosis, Plymouth, MN, United States.
Front Immunol. 2025 Apr 4;16:1527102. doi: 10.3389/fimmu.2025.1527102. eCollection 2025.
Anti-CD20 monoclonal antibody (mAb) therapies used to treat multiple sclerosis (MS) differ in their molecular structures, epitope recognition, and mechanisms of CD20-positive (CD20+) cell lysis, which may impact clinical efficacy and tolerability and support within-class switching for patients with suboptimal response to a prior anti-CD20 mAb.
This is a retrospective case series of 7 individuals with MS treated in private practice or at an MS clinic who switched to ublituximab from a different anti-CD20 mAb therapy due to efficacy or tolerability concerns.
Details of each case, including clinical and/or radiological outcomes on initial anti-CD20 mAb therapy, reasons for switching, and outcomes after starting ublituximab therapy are provided.
These cases highlight suboptimal B-cell depletion, inadequate MS disease control, and/or tolerability concerns in people with MS who had clinical improvements or stabilization of disease following a switch from ocrelizumab or rituximab to ublituximab.
Within-class switching from a prior anti-CD20 mAb therapy to ublituximab is feasible and may improve outcomes in some people with MS.
用于治疗多发性硬化症(MS)的抗CD20单克隆抗体(mAb)疗法在分子结构、表位识别以及CD20阳性(CD20+)细胞裂解机制方面存在差异,这可能会影响临床疗效和耐受性,并支持对先前抗CD20 mAb反应欠佳的患者进行同类药物转换。
这是一项回顾性病例系列研究,纳入了7例在私人诊所或MS诊所接受治疗的MS患者,他们因疗效或耐受性问题从不同的抗CD20 mAb疗法转换为ublituximab治疗。
提供了每个病例的详细信息,包括初始抗CD20 mAb治疗的临床和/或放射学结果、转换原因以及开始ublituximab治疗后的结果。
这些病例突出了在从奥瑞珠单抗或利妥昔单抗转换为ublituximab后病情有临床改善或稳定的MS患者中,存在B细胞耗竭欠佳、MS疾病控制不足和/或耐受性问题。
从先前的抗CD20 mAb疗法转换为ublituximab进行同类药物转换是可行的,并且可能会改善一些MS患者的治疗结果。