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由于安全性考虑对多发性硬化症患者进行疾病修饰疗法的降级:25 名从奥瑞珠单抗转换为富马酸二甲酯的患者在 1 年的结局特征。

De-escalation of Disease-Modifying Therapy for People with Multiple Sclerosis Due to Safety Considerations: Characterizing 1-Year Outcomes in 25 People Who Switched from Ocrelizumab to Diroximel Fumarate.

机构信息

NYU Langone South Shore Neurologic Associates, PC, 77 Medford Ave, Patchogue, NY, 11772, USA.

Department of Clinical Neurosciences, University of Calgary, Hotchkiss Brain Institute, Calgary, AB, Canada.

出版信息

Adv Ther. 2024 Aug;41(8):3059-3075. doi: 10.1007/s12325-024-02902-0. Epub 2024 Jun 11.

Abstract

INTRODUCTION

Switching disease-modifying therapy (DMT) may be considered for relapsing-remitting multiple sclerosis (RRMS) if a patient's current therapy is no longer optimal. This was particularly important during the recent COVID-19 pandemic because of considerations around immune deficiency and impaired vaccine response associated with B cell-depleting DMTs. This real-world, single-center study aimed to evaluate change or decline in functional ability and overall disease stability in people with RRMS who were switched from B cell-depleting ocrelizumab (OCRE) to diroximel fumarate (DRF) because of safety concern related to the COVID-19 pandemic.

METHODS

Adults with RRMS were included if they had been clinically stable for ≥ 1 year on OCRE. Data collected at baseline and 1 year post switch included relapse rate, magnetic resonance imaging (MRI), blood work for assessment of peripheral immune parameters, the Cognitive Assessment Battery (CAB), optical coherence tomography (OCT), and patient-reported outcomes (PROs).

RESULTS

Participants (N = 25) had a mean (SD) age of 52 (9) years, and a mean (SD) duration of 26 (8) months' treatment with OCRE before the switch to DRF. Median washout duration since the last OCRE infusion was 7 months (range 4-18 months). No participants relapsed on DRF during follow-up, and all remained persistent on DRF after 1 year. There were no significant changes in peripheral immune parameters, other than an increase in the percentage of CD19 cells 1 year after switching (p < 0.05). Similarly, there were no significant changes in CAB, OCT, and PROs.

CONCLUSION

These preliminary findings suggest that transition to DRF from OCRE may be an effective treatment option for people with RRMS who are clinically stable but may need to switch for reasons unrelated to effectiveness. Longer follow-up times on larger samples are needed to confirm these observations.

摘要

介绍

如果患者目前的治疗不再是最佳选择,可能会考虑对复发缓解型多发性硬化症(RRMS)进行疾病修正治疗(DMT)的转换。在最近的 COVID-19 大流行期间,由于与 B 细胞耗竭型 DMT 相关的免疫缺陷和疫苗反应受损的考虑,这一点尤为重要。这项真实世界、单中心研究旨在评估因 COVID-19 大流行而对安全性产生担忧而从 B 细胞耗竭型奥瑞珠单抗(OCRE)转换为二羟甲基富马酸酯(DRF)的 RRMS 患者的功能能力变化或下降,以及整体疾病稳定性。

方法

如果患者在接受 OCRE 治疗 ≥1 年时临床稳定,则将其纳入 RRMS 成人患者。在转换后 1 年时收集的数据包括复发率、磁共振成像(MRI)、外周免疫参数评估的血液检查、认知评估电池(CAB)、光学相干断层扫描(OCT)和患者报告的结果(PRO)。

结果

参与者(N=25)的平均(SD)年龄为 52(9)岁,在转换为 DRF 之前接受 OCRE 治疗的平均(SD)时间为 26(8)个月。最后一次 OCRE 输注后中位洗脱期为 7 个月(范围 4-18 个月)。在随访期间,没有参与者在 DRF 上复发,所有参与者在 1 年后仍持续使用 DRF。除了在转换后 1 年时 CD19 细胞百分比增加(p<0.05)外,外周免疫参数没有显著变化。同样,CAB、OCT 和 PRO 也没有显著变化。

结论

这些初步发现表明,对于临床稳定但因与疗效无关的原因需要转换的 RRMS 患者,从 OCRE 转换为 DRF 可能是一种有效的治疗选择。需要更长的随访时间和更大的样本量来证实这些观察结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f76f/11263251/e59e4bc7f44a/12325_2024_2902_Fig1_HTML.jpg

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