Lorscheider Johannes, Signori Alessio, Subramaniam Suvitha, Benkert Pascal, Vukusic Sandra, Trojano Maria, Hillert Jan, Glaser Anna, Hyde Robert, Spelman Tim, Magyari Melinda, Elberling Frederik, Pontieri Luigi, Koch-Henriksen Nils, Sørensen Per Soelberg, Gerlach Oliver, Prat Alexandre, Girard Marc, Eichau Sara, Grammond Pierre, Horakova Dana, Ramo-Tello Cristina, Roos Izanne, Buzzard Katherine, Lechner Scott Jeanette, Sánchez-Menoyo José Luis, Alroughani Raed, Prévost Julie, Kuhle Jens, Gray Orla, Mathey Guillaume, Michel Laure, Ciron Jonathan, De Sèze Jérôme, Maillart Elisabeth, Ruet Aurelie, Labauge Pierre, Zephir Helene, Kwiatkowski Arnaud, van der Walt Anneke, Kalincik Tomas, Butzkueven Helmut
Department of Neurology, University Hospital Basel, Basel, Switzerland
Research Center for Clinical Neuroimmunology and Neuroscience Basel (RC2NB), University of Basel, Basel, Switzerland.
J Neurol Neurosurg Psychiatry. 2025 May 14;96(6):606-615. doi: 10.1136/jnnp-2024-334700.
Effectiveness of disease-modifying treatment (DMT) in people affected by primary progressive multiple sclerosis (PPMS) is limited. Whether specific subgroups may benefit more from DMT in a real-world setting remains unclear. Our aim was to investigate the potential effect of DMT on disability worsening among patients with PPMS stratified by different disability trajectories.
Within the framework of the Big MS Data network, we merged data from the Observatoire Français de la Sclérose en Plaques, the Swedish and Italian MS registries, and MSBase. We identified patients with PPMS that started DMT or were never treated during the observed period. Subpopulations with comparable baseline characteristics were selected by propensity score matching. Disability outcomes were analysed in time-to-recurrent event analyses, which were repeated in subclasses with different disability trajectories determined by latent class mixed models.
Of the 3243 included patients, we matched 739 treated and 1330 untreated patients with a median follow-up of 3 years after pairwise censoring. No difference in the risk of confirmed disability worsening (CDW) was observed between the groups in the fully matched dataset (HR 1.11, 95% CI 0.97 to 1.23, p=0.127). However, we found a lower risk for CDW among the class of treated patients with an aggressive disability trajectory (n=360, HR 0.68, 95% CI 0.50 to 0.92, p=0.014).
In line with previous studies, our data suggest that DMT does not ameliorate disability worsening in PPMS, in general. However, we observed a beneficial effect of DMT on disability worsening in patients with aggressive predicted disability trajectories.
疾病修饰治疗(DMT)对原发性进行性多发性硬化症(PPMS)患者的有效性有限。在现实环境中,特定亚组是否能从DMT中获益更多仍不清楚。我们的目的是研究DMT对按不同残疾轨迹分层的PPMS患者残疾恶化的潜在影响。
在大MS数据网络的框架内,我们合并了来自法国多发性硬化症观察站、瑞典和意大利MS登记处以及MSBase的数据。我们确定了在观察期内开始接受DMT治疗或从未接受治疗的PPMS患者。通过倾向得分匹配选择具有可比基线特征的亚组。在复发事件时间分析中分析残疾结局,并在由潜在类别混合模型确定的具有不同残疾轨迹的亚类中重复进行。
在纳入的3243例患者中,我们匹配了739例接受治疗和1330例未接受治疗的患者,配对删失后中位随访时间为3年。在完全匹配的数据集中,两组之间在确诊残疾恶化(CDW)风险方面未观察到差异(风险比1.11,95%置信区间0.97至1.23,p = 0.127)。然而,我们发现残疾轨迹呈侵袭性的治疗患者亚组中CDW风险较低(n = 360,风险比0.68,95%置信区间0.50至0.92,p = 0.014)。
与先前的研究一致,我们的数据表明,一般而言,DMT并不能改善PPMS患者的残疾恶化情况。然而,我们观察到DMT对预测残疾轨迹呈侵袭性的患者的残疾恶化有有益影响。