TY - JOUR
T1 - Early Intensive Versus Escalation Approach
T2 - Ten-Year Impact on Disability in Relapsing Multiple Sclerosis
AU - the Italian MS Register
AU - Iaffaldano, Pietro
AU - Lucisano, Giuseppe
AU - Guerra, Tommaso
AU - Caputo, Francesca
AU - Simone, Marta
AU - Copetti, Massimiliano
AU - Paolicelli, Damiano
AU - Portaccio, Emilio
AU - Patti, Francesco
AU - Perini, Paola
AU - Brescia Morra, Vincenzo
AU - Di Sapio, Alessia
AU - Inglese, Matilde
AU - Pozzilli, Carlo
AU - Lus, Giacomo
AU - Salemi, Giuseppe
AU - Curti, Erica
AU - De Luca, Giovanna
AU - Valentino, Paola
AU - Cocco, Eleonora
AU - Cavalla, Paola
AU - Avolio, Carlo
AU - Lugaresi, Alessandra
AU - Gallo, Antonio
AU - Annovazzi, Pietro
AU - Rocca, Maria A.
AU - Chisari, Clara Grazia
AU - Filippi, Massimo
AU - Amato, Maria Pia
AU - Trojano, Maria
AU - Biolzi, Beatrice
AU - Dell’Anna, Daniele
AU - Cesare, Daniele Di Giulio
AU - Di Lemme, Sonia
AU - Di Tillio, Chiara
AU - Fonsdituri, Teresa
AU - Maietta, Ilaria
AU - Marchese, Agata
AU - Marinetto, Silvia
AU - Martini, Federica
AU - Morano, Cristiana
AU - Perugini, Silvia
AU - Piredda, Giovanna Ramona
AU - Raimondi, Chiara
AU - Rossi, Ilaria
AU - Tallarico, Valentina
AU - Treccarichi, Stefania
N1 - Publisher Copyright:
© 2025 The Author(s). Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association.
PY - 2025/10
Y1 - 2025/10
N2 - Objective: To evaluate the long-term impact of early intensive treatment (EIT) versus escalation (ESC) strategies using high-efficacy disease-modifying therapies (HE-DMTs) on disability progression in relapsing multiple sclerosis (RMS). Methods: This observational study included 4878 RMS patients from the Italian Multiple Sclerosis Register. Eligible participants initiated their first disease-modifying therapy (DMT) within 3 years of disease onset and had ≥ 5 years of follow-up with at least three Expanded Disability Status Scale (EDSS) evaluations. Patients were categorized into the EIT group if they started with HE-DMTs and into the ESC group if HE-DMTs were initiated after ≥ 1 year of moderate-efficacy therapy. Propensity score matching was performed to balance baseline characteristics. Outcomes included disability trajectories assessed using linear mixed models for repeated measures and risks of confirmed disability accrual (CDA), progression independent of relapse activity (PIRA), and relapse-associated worsening (RAW) evaluated using Cox proportional hazards models. Results: Post-matching analysis of 908 pairs revealed significantly slower disability progression in the EIT group compared to the ESC group. At 10 years, the delta-EDSS difference between groups was −0.63 (95% CI: −0.83 to −0.43; p < 0.0001). ESC was associated with higher risks of CDA (HR 1.36, 95% CI: 1.20–1.54; p < 0.0001), PIRA (HR 1.22, 95% CI: 1.05–1.40; p = 0.0074), and RAW (HR 1.55, 95% CI: 1.17–2.05; p = 0.0021). Interpretation: EIT significantly reduces long-term disability progression in RMS compared to ESC. These findings underscore the potential of EIT to optimize long-term outcomes in RMS patients.
AB - Objective: To evaluate the long-term impact of early intensive treatment (EIT) versus escalation (ESC) strategies using high-efficacy disease-modifying therapies (HE-DMTs) on disability progression in relapsing multiple sclerosis (RMS). Methods: This observational study included 4878 RMS patients from the Italian Multiple Sclerosis Register. Eligible participants initiated their first disease-modifying therapy (DMT) within 3 years of disease onset and had ≥ 5 years of follow-up with at least three Expanded Disability Status Scale (EDSS) evaluations. Patients were categorized into the EIT group if they started with HE-DMTs and into the ESC group if HE-DMTs were initiated after ≥ 1 year of moderate-efficacy therapy. Propensity score matching was performed to balance baseline characteristics. Outcomes included disability trajectories assessed using linear mixed models for repeated measures and risks of confirmed disability accrual (CDA), progression independent of relapse activity (PIRA), and relapse-associated worsening (RAW) evaluated using Cox proportional hazards models. Results: Post-matching analysis of 908 pairs revealed significantly slower disability progression in the EIT group compared to the ESC group. At 10 years, the delta-EDSS difference between groups was −0.63 (95% CI: −0.83 to −0.43; p < 0.0001). ESC was associated with higher risks of CDA (HR 1.36, 95% CI: 1.20–1.54; p < 0.0001), PIRA (HR 1.22, 95% CI: 1.05–1.40; p = 0.0074), and RAW (HR 1.55, 95% CI: 1.17–2.05; p = 0.0021). Interpretation: EIT significantly reduces long-term disability progression in RMS compared to ESC. These findings underscore the potential of EIT to optimize long-term outcomes in RMS patients.
KW - PIRA
KW - disability trajectories
KW - multiple sclerosis
UR - https://www.scopus.com/pages/publications/105011203182
U2 - 10.1002/acn3.70131
DO - 10.1002/acn3.70131
M3 - Article
C2 - 40619726
AN - SCOPUS:105011203182
SN - 2328-9503
VL - 12
SP - 2012
EP - 2019
JO - Annals of Clinical and Translational Neurology
JF - Annals of Clinical and Translational Neurology
IS - 10
ER -