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COVID-19 大流行期间多发性硬化症患者奥瑞珠单抗的个性化 B 细胞靶向剂量调整。

Personalized B-cell tailored dosing of ocrelizumab in patients with multiple sclerosis during the COVID-19 pandemic.

机构信息

Department of Neurology, MS Center Amsterdam, Amsterdam Neuroscience, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.

Department of Neurology, MS Center Amsterdam, Amsterdam Neuroscience, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands/Department of Neurology, OLVG Hospital, Amsterdam, The Netherlands.

出版信息

Mult Scler. 2022 Jun;28(7):1121-1125. doi: 10.1177/13524585211028833. Epub 2021 Jul 9.

Abstract

In this observational study, 159 patients with multiple sclerosis received personalized dosing of ocrelizumab incentivized by the COVID-19 pandemic. Re-dosing was scheduled when CD19 B-cell count was ⩾10 cells/µL (starting 24 weeks after the previous dose, repeated 4-weekly). Median interval until re-dosing or last B-cell count was 34 [30-38] weeks. No clinical relapses were reported and a minority of patients showed Expanded Disability Status Scale (EDSS) progression. Monthly serum neurofilament light levels remained stable during extended intervals. Two (1.9%) of 107 patients with a follow-up magnetic resonance imaging (MRI) scan showed radiological disease activity. Personalized dosing of ocrelizumab could significantly extend intervals with low short-term disease activity incidence, encouraging future research on long-term safety and efficacy.

摘要

在这项观察性研究中,159 例多发性硬化症患者在 COVID-19 大流行期间接受了奥瑞珠单抗的个性化剂量治疗。当 CD19 B 细胞计数 ⩾10 个/µL 时(上一次剂量后 24 周开始,每 4 周重复一次),进行重新给药。重新给药或最后一次 B 细胞计数的中位间隔时间为 34 [30-38] 周。未报告临床复发,少数患者出现扩展残疾状况量表(EDSS)进展。在延长的间隔内,每月血清神经丝轻链水平保持稳定。在进行后续磁共振成像(MRI)扫描的 107 例患者中,有 2 例(1.9%)出现影像学疾病活动。奥瑞珠单抗的个性化剂量治疗可显著延长短期疾病活动发生率低的间隔时间,这为长期安全性和疗效的进一步研究提供了依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca04/9131403/c51367be46d3/10.1177_13524585211028833-fig1.jpg

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