Disease-Modifying Treatments and Time to Loss of Ambulatory Function in Patients with Primary Progressive Multiple Sclerosis

  • Emilio Portaccio
  • , Mattia Fonderico
  • , Pietro Iaffaldano
  • , Luisa Pastò
  • , Lorenzo Razzolini
  • , Angelo Bellinvia
  • , Giovanna De Luca
  • , Paolo Ragonese
  • , Francesco Patti
  • , Vincenzo Brescia Morra
  • , Eleonora Cocco
  • , Patrizia Sola
  • , Matilde Inglese
  • , Giacomo Lus
  • , Carlo Pozzilli
  • , Davide Maimone
  • , Alessandra Lugaresi
  • , Paola Gazzola
  • , Giancarlo Comi
  • , Ilaria Pesci
  • Daniele Spitaleri, Marta Rezzonico, Marika Vianello, Carlo Avolio, Francesco O. Logullo, Franco Granella, Marco Salvetti, Mauro Zaffaroni, Giuseppe Lucisano, Massimo Filippi, Maria Trojano, Maria Pia Amato

Risultato della ricerca: Contributo su rivistaArticolo in rivistapeer review

Abstract

Importance: Except for ocrelizumab, treatment options in primary progressive multiple sclerosis (PPMS) are lacking. Objective: To investigate the effectiveness of DMTs on the risk of becoming wheelchair dependent in a real-world population of patients with PPMS. Design, Setting, and Participants: This was a multicenter, observational, retrospective, comparative effectiveness research study. Data were extracted on November 28, 2018, from the Italian multiple sclerosis register and analyzed from June to December 2021. Mean study follow-up was 11 years. Included in the study cohort were patients with a diagnosis of PPMS and at least 3 years of Expanded Disability Status Scale (EDSS) evaluations and 3 years of follow-up. Main Outcomes and Measures: The risk of reaching an EDSS score of 7.0 was assessed through multivariable Cox regression models. Exposures: Patients who received DMT before the outcome were considered treated. DMT was assessed as a time-dependent variable and by class of DMT (moderately and highly effective). Results: From a total of 3298 patients with PPMS, 2633 were excluded because they did not meet the entry criteria for the phase 3, multicenter, randomized, parallel-group, double-blind, placebo-controlled study to evaluate the efficacy and safety of ocrelizumab in adults with PPMS (ORATORIO) trial. Among the remaining 665 patients (mean [SD] age, 43.0 [10.7] years; 366 female patients [55.0%]), 409 were further selected for propensity score matching (288 treated and 121 untreated patients). In the matched cohort, during the study follow-up, 37% of patients (152 of 409) reached an EDSS score of 7.0 after a mean (SD) follow-up of 10.6 (5.6) years. A higher EDSS score at baseline (adjusted hazard ratio [aHR], 1.32; 95% CI, 1.13-1.55; P <.001), superimposed relapses (aHR, 2.37; 95% CI, 1.24-4.54; P =.009), and DMT exposure (aHR, 1.75; 95% CI, 1.04-2.94; P =.03) were associated with a higher risk of an EDSS score of 7.0, whereas the interaction term between DMT and superimposed relapses was associated with a reduced risk of EDSS score of 7.0 (aHR, 0.33; 95% CI, 0.16-0.71; P =.004). Similar findings were obtained when treatment according to DMT class was considered and when DMT was included as a time-dependent covariate. These results were confirmed in the subgroup of patients with available magnetic resonance imaging data. Conclusions and Relevance: Results of this comparative effectiveness research study suggest that inflammation also occurs in patients with PPMS, may contribute to long-term disability, and may be associated with a reduced risk of becoming wheelchair dependent by current licensed DMTs..

Lingua originaleInglese
pagine (da-a)869-878
Numero di pagine10
RivistaJAMA Neurology
Volume79
Numero di pubblicazione9
DOI
Stato di pubblicazionePubblicato - set 2022
Pubblicato esternamente

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