MS Center Amsterdam, Neurology, Vrije Universiteit Amsterdam, Amsterdam Neuroscience, Amsterdam UMC location VUmc, Amsterdam, Netherlands.
MS Center Amsterdam, Neurology, Vrije Universiteit Amsterdam, Amsterdam Neuroscience, Amsterdam UMC location VUmc, Amsterdam, Netherlands.
Mult Scler Relat Disord. 2024 Nov;91:105900. doi: 10.1016/j.msard.2024.105900. Epub 2024 Sep 28.
Ocrelizumab (OCR) is a highly effective treatment of multiple sclerosis (MS), and B cell repopulation profiles suggest that it might be used as an immune reconstitution therapy. However, data on disease recurrence after stopping treatment with OCR are scarce. Our objective was to evaluate the recurrence of disease activity after OCR discontinuation.
In this multicenter retrospective cohort study, we included MS patients who discontinued OCR, without switching to another treatment, for twelve months or more, after having received at least one full dosage of 600 mg. We defined focal inflammation as the occurrence of a clinical relapse or significant MRI activity (≥3 new T2 lesions or ≥2 contrast-enhancing lesions).
We included 53 MS patients; 41 relapsing remitting (RRMS), 5 secondary progressive (SPMS) and 7 primary progressive (PPMS) patients. Median follow-up period after OCR discontinuation was 16 months. We only observed focal inflammation after discontinuation in RRMS patients; 2.4 % (1/41) patients presented with significant MRI activity and matching clinical symptoms, and 7.3 % (3/41) patients presented with a suspected clinical relapse without radiological activity: a total of 9.8 % (4/41) at a median time of 17 months after the last infusion.
We found focal inflammation after discontinuation of OCR in 4 (9.8 %) of the RRMS patients, of which 1 was radiologically confirmed. Our observations highlight that recurrence of focal inflammation seems low but discontinuation may not be appropriate for everyone. Further larger studies are important to determine the immune reconstitution therapy potential of OCR.
奥瑞珠单抗(OCR)是一种治疗多发性硬化症(MS)的高效药物,B 细胞再群体分布特征表明其可用作免疫重建治疗。然而,关于停止使用 OCR 后疾病复发的数据却很少。我们的目的是评估停止使用 OCR 后疾病活动的复发情况。
在这项多中心回顾性队列研究中,我们纳入了至少接受过一次完整剂量 600mg 的 OCR 治疗且停药时间超过 12 个月的 MS 患者。我们将局灶性炎症定义为临床复发或显著 MRI 活动(≥3 个新 T2 病变或≥2 个增强病变)的发生。
我们纳入了 53 名 MS 患者;41 名复发缓解型(RRMS),5 名继发进展型(SPMS)和 7 名原发进展型(PPMS)患者。停止使用 OCR 后的中位随访时间为 16 个月。我们仅在 RRMS 患者中观察到停药后的局灶性炎症;2.4%(1/41)的患者出现了显著的 MRI 活动和匹配的临床症状,7.3%(3/41)的患者出现了可疑的临床复发但无放射学活动:共有 9.8%(4/41)在末次输注后 17 个月的中位时间出现。
我们发现 41 名 RRMS 患者中有 4 名(9.8%)在停止使用 OCR 后出现局灶性炎症,其中 1 例有放射学证实。我们的观察结果表明,局灶性炎症的复发似乎较低,但并非所有人都适合停药。进一步的大型研究对于确定 OCR 的免疫重建治疗潜力非常重要。