Tolerability of subcutaneous ofatumumab with long-term exposure in relapsing multiple sclerosis.

IF 2.5 Q2 CLINICAL NEUROLOGY Multiple Sclerosis Journal - Experimental, Translational and Clinical Pub Date : 2023-10-10 eCollection Date: 2023-10-01 DOI:10.1177/20552173231203816
John Kramer, Ralf Linker, David Paling, Adam Czaplinski, Olaf Hoffmann, V Wee Yong, Noreen Barker, Amy Perrin Ross, Elisabeth Lucassen, Mohammad Gufran, Xixi Hu, Ronald Zielman, Gustavo Seifer, Patrick Vermersch
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引用次数: 0

Abstract

Background: Ofatumumab is approved for treating relapsing multiple sclerosis (RMS). Examining tolerability will enable understanding of its risk-benefit profile.

Objective: Report the tolerability profile of ofatumumab in RMS during treatment of up to 4 years and the effect of pre-medication.

Methods: Cumulative data from the overall safety population included patients taking continuous ofatumumab or being newly switched from teriflunomide. Injection-related reactions (IRRs) by incidence and severity, and post-marketing surveillance data, with an exposure of 18,530 patient-years, were analyzed.

Results: Systemic IRRs affected 24.7% of patients (487/1969) in the overall safety population; most (99.2% [483/487]) were mild (333/487) to moderate (150/487) in Common Terminology Criteria for Adverse Events severity; most systemic IRRs occurred after first injection. Local-site IRRs affected 11.8% (233/1969) and most (99.6% [232/233]) were mild/moderate. Incidence and severity of systemic and localized IRRs were similar between continuous and newly switched patients across repeated injections. Systemic IRR incidence and severity were not substantially affected by steroidal or non-steroidal pre-medication. Post-marketing surveillance identified no new tolerability issues.

Conclusion: Ofatumumab is well tolerated, displays a consistent safety profile during continuous use or after switching from teriflunomide and does not require pre-medication. This enables home management of RMS with a high-efficacy treatment.

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复发性多发性硬化症患者长期皮下注射奥曲单抗的耐受性。
背景:Ofatumumab被批准用于治疗复发性多发性硬化症(RMS)。检查耐受性将有助于了解其风险收益状况。目的:报告奥法单抗在RMS中长达4年的治疗期间的耐受性概况以及用药前的效果。方法:来自总体安全人群的累积数据包括连续服用奥法单抗或新停用特立氟胺的患者。分析了18530患者年的注射相关反应(IRRs)的发生率和严重程度,以及上市后监测数据。结果:系统性IRRs影响了总安全人群中24.7%的患者(487/1969);在不良事件严重程度的通用术语标准中,大多数(99.2%[483/487])为轻度(333/487)至中度(150/487);大多数全身性IRR发生在第一次注射后。局部站点IRRs影响11.8%(233/1969),大多数(99.6%[232/233])为轻度/中度。在重复注射的连续和新转换患者之间,全身和局部IRRs的发生率和严重程度相似。系统性IRR的发生率和严重程度没有受到类固醇或非类固醇药物治疗前的显著影响。上市后监测未发现新的耐受性问题。结论:奥法图单抗耐受性良好,在连续使用或从特立氟胺转为特立氟米特后显示出一致的安全性,不需要用药前。这使得RMS的家庭管理具有高效的治疗效果。
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来源期刊
CiteScore
4.70
自引率
0.00%
发文量
54
审稿时长
15 weeks
期刊最新文献
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