Schmidt Stephan, Schulten Thomas
Neurologische Gemeinschaftspraxis Bonn, Gesundheitszentrum St. Johannes, Kölnstr. 54, 53111 Bonn, Germany.
Klinikum Leverkusen gGmbH, Leverkusen, Germany.
Ther Adv Neurol Disord. 2019 May 6;12:1756286419846818. doi: 10.1177/1756286419846818. eCollection 2019.
Fingolimod (FTY), an oral treatment for patients with relapsing-remitting multiple sclerosis (RRMS), has been associated with a significant rebound of disease activity after cessation of therapy.
We present the clinical and radiological findings of two patients with severe rebound after FTY withdrawal, which was further aggravated by the initiation of treatment with the B cell-depleting monoclonal antibody, ocrelizumab.
Both patients exhibited significant Expanded Disability Status Scale progression after administration of ocrelizumab despite immune reconstitution more than 3 months after FTY withdrawal.
Although the observed effect may be coincidental, ocrelizumab may complicate recovery of rebound after cessation of FTY. Further studies are warranted to better understand and predict the clinical and immunological consequences of sequential immunosuppressive and immunomodulatory treatments in patients with highly active RRMS.
芬戈莫德(FTY)是一种用于复发缓解型多发性硬化症(RRMS)患者的口服治疗药物,在停药后与疾病活动的显著反弹有关。
我们展示了两名患者在停用FTY后出现严重反弹的临床和影像学结果,在用B细胞耗竭单克隆抗体奥瑞珠单抗开始治疗后,病情进一步加重。
尽管在停用FTY超过3个月后免疫功能得到重建,但两名患者在使用奥瑞珠单抗后均出现了显著的扩展残疾状态量表进展。
尽管观察到的效果可能是巧合,但奥瑞珠单抗可能会使停用FTY后的反弹恢复复杂化。有必要进行进一步研究,以更好地理解和预测在高活性RRMS患者中序贯免疫抑制和免疫调节治疗的临床和免疫学后果。