Department of Neurosurgery, Sina Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Multiple Sclerosis Research Center, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran.
Mult Scler Relat Disord. 2023 Mar;71:104564. doi: 10.1016/j.msard.2023.104564. Epub 2023 Feb 12.
Natalizumab and fingolimod are well-established, sequestrating disease-modifying treatments (DMTs), widely used as a second-line treatment in patients with relapse remitting multiple sclerosis (RRMS). However, there is no standard strategy for managing treatment failure on these agents. The present study aimed to evaluate the effectiveness of rituximab after natalizumab and fingolimod withdrawal.
A retrospective cohort was accomplished on RRMS patients treated with natalizumab and fingolimod who were switched to rituximab.
100 patients (50 cases in each group) were analyzed. After six months of follow-up, a substantial decline in clinical relapse and disability progression was observed in both groups. However, no significant change was demonstrated in the pattern of MRI activity (P = 1.000) in natalizumab pretreated patients. After adjusting for the baseline characteristics, a head-to-head comparison found a non-significant trend of lower EDSS in the pretreated fingolimod group compared to those previously treated with natalizumab(P = 0.057). However, in terms of clinical relapse and MRI activity, the clinical outcomes were comparable in both groups ((P = 0.194), (P = 0.957). Moreover, rituximab was well-tolerated, and no serious adverse events were reported.
The present study revealed the effectiveness of rituximab as an appropriate alternative option for escalation therapy after fingolimod and natalizumab discontinuation.
那他珠单抗和芬戈利莫德是两种成熟的隔离疾病修饰疗法(DMT)药物,广泛用于复发缓解型多发性硬化症(RRMS)患者的二线治疗。然而,对于这些药物的治疗失败,目前尚无标准的管理策略。本研究旨在评估利妥昔单抗在那他珠单抗和芬戈利莫德停药后的疗效。
对接受那他珠单抗和芬戈利莫德治疗后转换为利妥昔单抗的 RRMS 患者进行回顾性队列研究。
共分析了 100 例患者(每组 50 例)。在 6 个月的随访后,两组的临床复发和残疾进展均显著下降。然而,在那他珠单抗预处理患者中,MRI 活动模式没有显著变化(P=1.000)。在校正基线特征后,头对头比较发现,与先前接受那他珠单抗治疗的患者相比,预先接受芬戈利莫德治疗的患者的 EDSS 较低,但无统计学意义(P=0.057)。然而,在临床复发和 MRI 活动方面,两组的临床结果相当(P=0.194),(P=0.957)。此外,利妥昔单抗具有良好的耐受性,没有严重的不良事件报告。
本研究表明,利妥昔单抗是那他珠单抗和芬戈利莫德停药后升级治疗的合适替代选择。