TY - JOUR
T1 - Disease-Modifying Treatments and Time to Loss of Ambulatory Function in Patients with Primary Progressive Multiple Sclerosis
AU - Portaccio, Emilio
AU - Fonderico, Mattia
AU - Iaffaldano, Pietro
AU - Pastò, Luisa
AU - Razzolini, Lorenzo
AU - Bellinvia, Angelo
AU - De Luca, Giovanna
AU - Ragonese, Paolo
AU - Patti, Francesco
AU - Brescia Morra, Vincenzo
AU - Cocco, Eleonora
AU - Sola, Patrizia
AU - Inglese, Matilde
AU - Lus, Giacomo
AU - Pozzilli, Carlo
AU - Maimone, Davide
AU - Lugaresi, Alessandra
AU - Gazzola, Paola
AU - Comi, Giancarlo
AU - Pesci, Ilaria
AU - Spitaleri, Daniele
AU - Rezzonico, Marta
AU - Vianello, Marika
AU - Avolio, Carlo
AU - Logullo, Francesco O.
AU - Granella, Franco
AU - Salvetti, Marco
AU - Zaffaroni, Mauro
AU - Lucisano, Giuseppe
AU - Filippi, Massimo
AU - Trojano, Maria
AU - Amato, Maria Pia
N1 - Funding Information:
reported receiving travel grants for participation in advisory board and/or speaking activities from Biogen, Merck, Sanofi Genzyme, Novartis, Roche, Celgene, and Teva and serving on the editorial board of Frontiers in Neurology and Brain Sciences. Dr Ragonese reported receiving speaker honoraria or grants from Biogen, Sanofi Genzyme, Novartis, Teva, Merck, Almirall, and Roche. Dr Patti reported receiving personal fees from Almirall, Bayer, Bristol Myers Squibb, and Novartis and grants from Biogen, Merck, Roche, and Sanofi. Dr Brescia Morra reported receiving personal fees from Biogen, Teva, Genzyme, Bristol Myers Squibb, Novartis, Merck, and Almirall. Dr Cocco reported receiving grants from Biogen, Merck, and Roche and personal fees from Novartis and Sanofi. Dr Inglese reported receiving consultation fees from Biogen, Merck, Novartis, and Roche; speaker fees from Novartis and Roche; and being coeditor of Multiple Sclerosis Journal. Dr Inglese reported receiving research grants from the National Institutes of Health, National Multiple Sclerosis Society, MS Canada, and Federazione Italiana Sclerosi Multipla. Dr Pozzilli reported receiving grants from Roche, Almirall, and Biogen and personal fees from Janssen, Alexion, Merck, Bristol Myers Squibb, and Novartis. Dr Maimone reported receiving personal fees from Biogen, Bayer, Merck, Novartis, Roche, and Sanofi Genzyme. Dr Lugaresi reported receiving personal fees from Biogen, Merck Serono, Novartis, Sanofi Genzyme, Bristol Myers Squibb, Roche, and Teva and grants from Novartis and Sanofi Genzyme. Dr Comi reported receiving personal fees from Sanofi, Janssen, Bristol Myers Squibb, Novartis, and Rewind. Dr Granella reported receiving grants from Roche, Biogen, Novartis, Sanofi, Merck Serono, and Roche. Dr Salvetti reported receiving grants from Biogen and Sanofi and personal fees from Merck and Novartis. Dr Filippi reported receiving consulting services and/or speaking activity fees from Almirall, Alexion, Bayer, Biogen, Celgene, Eli Lilly, Genzyme, Merck-Serono, Novartis, Roche, Sanofi, Takeda, Teva Pharmaceutical Industries; grants from Biogen, Merck-Serono, Novartis, Roche, and Teva Pharmaceutical Industries; and serving as editor-in-chief of the Journal of Neurology and associate editor of Human Brain Mapping, Radiology, and Neurological Sciences. Dr Trojano
Funding Information:
received financial support in the form of annual research grants from the Italian University and Research Ministry and from Merck Serono, Novartis, and Biogen.
Funding Information:
reported receiving grants from Biogen, Novartis, and Merck and personal fees from Novartis, Biogen, Merck, Roche, Genzyme, and Bristol Myers Squibb. Dr Amato reported receiving grants from Merck Serono, Biogen, Roche, and Mylan and personal fees from Merck Serono, Biogen, Sanofi Genzyme, Novartis, Roche, Mylan, and Bristol Myers Squibb Celgene. No other disclosures were reported.
Publisher Copyright:
© 2022 American Medical Association. All rights reserved.
PY - 2022/9
Y1 - 2022/9
N2 - 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..
AB - 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..
UR - http://www.scopus.com/inward/record.url?scp=85134987879&partnerID=8YFLogxK
U2 - 10.1001/jamaneurol.2022.1929
DO - 10.1001/jamaneurol.2022.1929
M3 - Article
AN - SCOPUS:85134987879
SN - 2168-6149
VL - 79
SP - 869
EP - 878
JO - JAMA Neurology
JF - JAMA Neurology
IS - 9
ER -