Toscano Simona, Spelman Tim, Ozakbas Serkan, Alroughani Raed, Chisari Clara G, Lo Fermo Salvatore, Prat Alexandre, Girard Marc, Duquette Pierre, Izquierdo Guillermo, Eichau Sara, Grammond Pierre, Boz Cavit, Kalincik Tomas, Blanco Yolanda, Buzzard Katherine, Skibina Olga, Sa Maria Jose, van der Walt Anneke, Butzkueven Helmut, Terzi Murat, Gerlach Oliver, Grand'Maison Francois, Foschi Matteo, Surcinelli Andrea, Barnett Michael, Lugaresi Alessandra, Onofrj Marco, Yamout Bassem, Khoury Samia J, Prevost Julie, Lechner-Scott Jeannette, Maimone Davide, Amato Maria Pia, Spitaleri Daniele, Van Pesch Vincent, Macdonell Richard, Cartechini Elisabetta, de Gans Koen, Slee Mark, Castillo-Triviño Tamara, Soysal Aysun, Sanchez-Menoyo Jose Luis, Laureys Guy, Van Hijfte Liesbeth, McCombe Pamela, Altintas Ayse, Weinstock-Guttman Bianca, Aguera-Morales Eduardo, Etemadifar Masoud, Ramo-Tello Cristina, John Nevin, Turkoglu Recai, Hodgkinson Suzanne, Besora Sarah, Van Wijmeersch Bart, Fernandez-Bolaños Ricardo, Patti Francesco
Department of Biomedical and Biotechnological Sciences, University of Catania, Via Santa Sofia 78, 95123 Catania, Italy; Multiple Sclerosis Unit, University-Hospital G. Rodolico - San Marco, Catania, Italy.
MSBase Foundation, VIC, Melbourne, Australia; Department of Clinical Neuroscience, Karolinska Institute, Stockholm, Sweden.
Neurotherapeutics. 2025 Mar;22(2):e00552. doi: 10.1016/j.neurot.2025.e00552. Epub 2025 Feb 17.
Predicting long-term prognosis and choosing the appropriate therapeutic approach in patients with Multiple Sclerosis (MS) at the time of diagnosis is crucial in view of a personalized medicine. We investigated the impact of early therapeutic response on the 5-year prognosis of patients with relapsing-remitting MS (RRMS). We recruited patients from MSBase Registry covering the period between 1996 and 2022. All patients were diagnosed with RRMS and actively followed-up for at least 5 years to explore the following outcomes: clinical relapses, confirmed disability worsening (CDW) and improvement (CDI), EDSS 3.0, EDSS 6.0, conversion to secondary progressive MS (SPMS), new MRI lesions, Progression Independent of Relapse Activity (PIRA). Predictors included demographic, clinical and radiological data, and sub-optimal response (SR) within the first year of treatment. Female sex (HR 1.27; 95 % CI 1.16-1.40) and EDSS at baseline (HR 1.19; 95 % CI 1.15-1.24) were independent risk factors for the occurrence of relapses during the first 5 years after diagnosis, while high-efficacy treatment (HR 0.78; 95 % CI 0.67-0.91) and age at diagnosis (HR 0.83; 95 % CI 0.79-0.86) significantly reduced the risk. SR predicted clinical relapses (HR = 3.84; 95 % CI 3.51-4.19), CDW (HR = 1.74; 95 % CI 1.56-1.93), EDSS 3.0 (HR = 3.01; 95 % CI 2.58-3.51), EDSS 6.0 (HR = 1.77; 95 % CI 1.43-2.20) and new brain (HR = 2.33; 95 % CI 2.04-2.66) and spinal (HR 1.65; 95 % CI 1.29-2.09) MRI lesions. This study highlights the importance of selecting the appropriate DMT for each patient soon after MS diagnosis, also providing clinicians with a practical tool able to calculate personalized risk estimates for different outcomes.
鉴于个性化医疗,在多发性硬化症(MS)患者诊断时预测其长期预后并选择合适的治疗方法至关重要。我们研究了早期治疗反应对复发缓解型多发性硬化症(RRMS)患者5年预后的影响。我们从MSBase注册中心招募了1996年至2022年期间的患者。所有患者均被诊断为RRMS,并积极随访至少5年,以探究以下结果:临床复发、确认的残疾恶化(CDW)和改善(CDI)、扩展残疾状态量表(EDSS)达到3.0、EDSS达到6.0、转化为继发进展型多发性硬化症(SPMS)、新的MRI病灶、与复发活动无关的进展(PIRA)。预测因素包括人口统计学、临床和放射学数据,以及治疗第一年的次优反应(SR)。女性(风险比[HR] 1.27;95%置信区间[CI] 1.16 - 1.40)和基线时的EDSS(HR 1.19;95% CI 1.15 - 1.24)是诊断后前5年复发的独立危险因素,而高效治疗(HR 0.78;95% CI 0.67 - 0.91)和诊断时的年龄(HR 0.83;95% CI 0.79 - 0.86)可显著降低风险。SR可预测临床复发(HR = 3.84;95% CI 3.51 - 4.19)、CDW(HR = 1.74;95% CI 1.56 - 1.93)、EDSS 3.0(HR = 3.01;95% CI 2.58 - 3.51)、EDSS 6.0(HR = 1.77;95% CI 1.43 - 2.20)以及新的脑(HR = 2.33;95% CI 2.04 - 2.66)和脊髓(HR 1.65;95% CI 1.29 - 2.09)MRI病灶。本研究强调了在MS诊断后不久为每位患者选择合适的疾病修正治疗(DMT)的重要性,同时也为临床医生提供了一种实用工具,能够计算不同结果的个性化风险估计值。