Recurrent late-onset neutropenia after ofatumumab treatment in a case of multiple sclerosis.

IF 3.2 Q2 Medicine Neurological research and practice Pub Date : 2025-03-24 DOI:10.1186/s42466-025-00377-0
Jessy Chen, Thomas Burmeister, Lou Frankenstein, Inga Laumeier, Volker Siffrin
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Abstract

Objective: Immunomodulatory treatment options for multiple sclerosis show an inverse risk‒benefit ratio of side effects and treatment efficacy. Although rare, anti-B-cell therapies can cause acute or late-onset neutropenia.

Methods: We report a case of severe recurrent fluctuating neutropenia after ofatumumab treatment.

Results: We observed four recurrences even after pausing with ofatumumab and repeated granulocyte stimulating factor (G-CSF) treatment. In total, neutropenia occurred five times and was associated with recurrent pulmonary, urinary tract, and skin infections. Bone marrow investigation revealed no signs of lymphoma or leukemia. Interestingly, routine molecular testing revealed two gene variants of unknown significance for BCORL1 and ASXL1, both of which play a role in hematopoiesis. The neutrophil count recovered spontaneously six months after the cessation of treatment with ofatumumab.

Discussion: This case highlights the necessity of identifying patients at risk and monitoring white blood cell counts regularly for up to 6 months after initial neutropenia.

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多发性硬化治疗后复发性迟发性中性粒细胞减少1例。
目的:多发性硬化症的免疫调节治疗方案显示副作用和治疗效果的风险-收益比成反比。尽管罕见,抗b细胞疗法可引起急性或迟发性中性粒细胞减少症。方法:我们报告一例阿图单抗治疗后严重复发性波动中性粒细胞减少症。结果:我们观察到4例复发,甚至在暂停使用欧妥珠单抗和重复粒细胞刺激因子(G-CSF)治疗后。总的来说,中性粒细胞减少症发生了5次,并与复发性肺、尿路和皮肤感染有关。骨髓检查未发现淋巴瘤或白血病的迹象。有趣的是,常规分子检测揭示了BCORL1和ASXL1的两个未知意义的基因变异,它们都在造血中发挥作用。中性粒细胞计数在停止使用欧图单抗治疗6个月后自然恢复。讨论:该病例强调了在初始中性粒细胞减少后6个月内识别高危患者和定期监测白细胞计数的必要性。
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CiteScore
7.40
自引率
0.00%
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审稿时长
14 weeks
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