TY - JOUR
T1 - First-year treatment response predicts the following 5-year disease course in patients with relapsing-remitting multiple sclerosis
AU - the MSBase Study Group
AU - Toscano, Simona
AU - Spelman, Tim
AU - Ozakbas, Serkan
AU - Alroughani, Raed
AU - Chisari, Clara G.
AU - Lo Fermo, Salvatore
AU - Prat, Alexandre
AU - Girard, Marc
AU - Duquette, Pierre
AU - Izquierdo, Guillermo
AU - Eichau, Sara
AU - Grammond, Pierre
AU - Boz, Cavit
AU - Kalincik, Tomas
AU - Blanco, Yolanda
AU - Buzzard, Katherine
AU - Skibina, Olga
AU - Sa, Maria Jose
AU - van der Walt, Anneke
AU - Butzkueven, Helmut
AU - Terzi, Murat
AU - Gerlach, Oliver
AU - Grand'Maison, Francois
AU - Foschi, Matteo
AU - Surcinelli, Andrea
AU - Barnett, Michael
AU - Lugaresi, Alessandra
AU - Onofrj, Marco
AU - Yamout, Bassem
AU - Khoury, Samia J.
AU - Prevost, Julie
AU - Lechner-Scott, Jeannette
AU - Maimone, Davide
AU - Amato, Maria Pia
AU - Spitaleri, Daniele
AU - Van Pesch, Vincent
AU - Macdonell, Richard
AU - Cartechini, Elisabetta
AU - de Gans, Koen
AU - Slee, Mark
AU - Castillo-Triviño, Tamara
AU - Soysal, Aysun
AU - Sanchez-Menoyo, Jose Luis
AU - Laureys, Guy
AU - Van Hijfte, Liesbeth
AU - McCombe, Pamela
AU - Altintas, Ayse
AU - Weinstock-Guttman, Bianca
AU - Aguera-Morales, Eduardo
AU - Etemadifar, Masoud
N1 - Publisher Copyright:
© 2025 The Authors
PY - 2025/3
Y1 - 2025/3
N2 - 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.
AB - 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.
KW - Disease-modifying treatment
KW - High-efficacy drugs
KW - Multiple sclerosis
KW - Nomogram
KW - Prognosis
UR - https://www.scopus.com/pages/publications/85217934551
U2 - 10.1016/j.neurot.2025.e00552
DO - 10.1016/j.neurot.2025.e00552
M3 - Article
C2 - 39965993
AN - SCOPUS:85217934551
SN - 1933-7213
VL - 22
JO - Neurotherapeutics
JF - Neurotherapeutics
IS - 2
M1 - e00552
ER -