Cagol Alessandro, Schaedelin Sabine, Ocampo-Pineda Mario, Benkert Pascal, Melie-Garcia Lester, Luchetti Ludovico, Yaldizli Özgür, Oechtering Johanna, D'Souza Marcus, Fischer-Barnicol Bettina, Müller Stefanie, Finkener Sebastian, Vehoff Jochen, Disanto Giulio, Chan Andrew, Pot Caroline, Zecca Chiara, Derfuss Tobias, Lieb Johanna M, Diepers Michael, Wagner Franca, Du Pasquier Renaud, Lalive Patrice H, Pravatà Emanuele, Kim Olaf Chan-Hi, Hoepner Robert, Roth Patrick, Gobbi Claudio, Leppert David, Battaglini Marco, Kappos Ludwig, Sormani Maria Pia, Kuhle Jens, Granziera Cristina
Translational Imaging in Neurology (ThINk) Basel, Department of Biomedical Engineering, Faculty of Medicine, University Hospital Basel and University of Basel, Hegenheimermattweg 167b, 4123, Allschwil, Basel, Switzerland.
Multiple Sclerosis Centre, Departments of Neurology, Clinical Research and Biomedicine, University Hospital Basel and University of Basel, Basel, Switzerland.
J Neurol. 2025 Jul 2;272(8):491. doi: 10.1007/s00415-025-13221-x.
This study aimed to compare the effects of teriflunomide and ocrelizumab on clinical and MRI endpoints related to smoldering activity in relapsing-remitting multiple sclerosis (RRMS).
In this observational, longitudinal, multicenter study, we included 128 people with RRMS (pwRRMS) treated with teriflunomide and 495 treated with ocrelizumab. Outcomes included time to progression independent of relapse activity (PIRA). In a subset, we also assessed brain volume loss (BVL), longitudinal changes in diffusion tensor imaging (DTI) metrics, and the burden of paramagnetic rim lesions (PRLs). Propensity score matching was used for between-group comparisons.
Over a median follow-up of 3.1 years in the ocrelizumab group and 1.9 years in the teriflunomide group, there were no significant differences in the risk of PIRA (HR for teriflunomide vs. ocrelizumab: 0.80 [95%-CI:0.40-1.60]; p = 0.53). PwRRMS treated with teriflunomide exhibited lower annualized rates of BVL (-0.80 [95%-CI: -0.91; -0.69] vs. -1.06 [95%-CI: -1.25; -0.86]; p = 0.025) and gray matter volume loss (-0.92 [95%-CI: -1.05; -0.79] vs. -1.20 [95%-CI: -1.43; -0.97]; p = 0.035). No differences were observed in DTI metrics or PRL count.
This real-world study suggests that teriflunomide shows similar efficacy to ocrelizumab on smoldering activity, with a potentially greater effect in reducing BVL. Further research is needed to confirm these findings and understand their long-term implications.
本研究旨在比较特立氟胺和奥瑞珠单抗对复发缓解型多发性硬化症(RRMS)中与隐匿性活动相关的临床和MRI终点的影响。
在这项观察性、纵向、多中心研究中,我们纳入了128例接受特立氟胺治疗的RRMS患者(pwRRMS)和495例接受奥瑞珠单抗治疗的患者。结局包括与复发活动无关的疾病进展时间(PIRA)。在一个亚组中,我们还评估了脑容量损失(BVL)、扩散张量成像(DTI)指标的纵向变化以及顺磁性边缘病变(PRL)的负担。采用倾向得分匹配进行组间比较。
在奥瑞珠单抗组中位随访3.1年、特立氟胺组中位随访1.9年期间,PIRA风险无显著差异(特立氟胺与奥瑞珠单抗的HR:0.80 [95%CI:0.40 - 1.60];p = 0.53)。接受特立氟胺治疗的pwRRMS患者的年化BVL率较低(-0.80 [95%CI:-0.91;-0.69] 对比 -1.06 [95%CI:-1.25;-0.86];p = 0.025),灰质体积损失也较低(-0.92 [95%CI:-1.05;-0.79] 对比 -1.20 [95%CI:-1.43;-0.97];p = 0.035)。在DTI指标或PRL计数方面未观察到差异。
这项真实世界研究表明,特立氟胺在隐匿性活动方面显示出与奥瑞珠单抗相似的疗效,在减少BVL方面可能有更大的效果。需要进一步研究来证实这些发现并了解其长期影响。