多发性硬化症患者的ocrelizumab诱导的中性质减退:单中心研究
Arianna Sartori1, Anna Favero1, Lucrezia Rossi1
1Clinical Unit of Neurology, Department of Medicine, Surgery and Health Sciences, Cattinara University Hospital ASUGI, University of Trieste, Strada Di Fiume, 447 34149, Trieste, Italy.
Multiple sclerosis and related disorders
|August 22, 2025
概括
治疗多发性硬化症的ocrelizumab (OCR) 可能会导致超过20%的患者中性. 基线中性粒细胞计数可以帮助预测哪些患者有这种疾病的风险.
科学领域:
- 神经学
- 免疫学
- 药理学
背景情况:
- 包括ocrelizumab (OCR) 在内的CD20消耗剂用于多发性硬化症 (MS).
- 这些疗法的已知并发症是中性肥胖症,但其患病率尚未确立.
- 了解中性质减退的频率对于治疗OCR的多发性硬化症患者至关重要.
研究的目的:
- 通过使用ocrelizumab (OCR) 治疗的多发性硬化症 (pwMS) 患者中中性衰竭的发生频率.
- 在OCR治疗期间识别发生中性质衰竭的危险因素.
主要方法:
- 有望招收74个接受OCR的 pwMS.
- 收集临床和实验室数据,重点是白细胞和绝对中性细胞数量 (ANC) 在基线和随访时.
- 中性衰减的定义为ANC<2 × 10^3/μL.
主要成果:
- 中性症发生在21. 9%的pwMS患者中 (16/ 73),其中7例为2-4级中性症.
- 在第二次OCR循环后,中性衰竭最常见.
- 基线ANC和WBC数量可以预测中性衰竭的发生.
- 在中性衰竭期间没有观察到细菌感染.
结论:
- 与ocrelizumab相关的中性质减退影响超过20%的患者.
- 大多数病例无症状且没有感染.
- 基线WBC和ANC是确定患有中性衰竭风险的关键指标.
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