Disease-Modifying Treatments and Time to Loss of Ambulatory Function in Patients With Primary Progressive Multiple Sclerosis.
Journal
JAMA neurology
ISSN: 2168-6157
Titre abrégé: JAMA Neurol
Pays: United States
ID NLM: 101589536
Informations de publication
Date de publication:
01 09 2022
01 09 2022
Historique:
pubmed:
26
7
2022
medline:
15
9
2022
entrez:
25
7
2022
Statut:
ppublish
Résumé
Except for ocrelizumab, treatment options in primary progressive multiple sclerosis (PPMS) are lacking. To investigate the effectiveness of DMTs on the risk of becoming wheelchair dependent in a real-world population of patients with PPMS. 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. The risk of reaching an EDSS score of 7.0 was assessed through multivariable Cox regression models. 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). 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. 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.
Identifiants
pubmed: 35877104
pii: 2794292
doi: 10.1001/jamaneurol.2022.1929
pmc: PMC9315975
doi:
Types de publication
Clinical Trial, Phase III
Journal Article
Multicenter Study
Observational Study
Randomized Controlled Trial
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
869-878Investigateurs
Vincenzo Di Lazzaro
(V)
Umberto Aguglia
(U)
Tiziana Tassinari
(T)
Simonetta Venturi
(S)
Simonetta Galgani
(S)
Simone Tonietti
(S)
Sergio Parodi
(S)
Salvatore Cottone
(S)
Rocco Totaro
(R)
Roberto Bergamaschi
(R)
Roberto Balgera
(R)
Renato Mantegazza
(R)
Raffaella Clerici
(R)
Patrizia Perrone
(P)
Paola Valentino
(P)
Paola Cavalla
(P)
Paola Banfi
(P)
Nicola Renato Pizio
(NR)
Michela Bruzzone
(M)
Maurizio Leone
(M)
Maurizia Gatto
(M)
Mario Di Napoli
(M)
Mariarosa Rottoli
(M)
Maria Teresa Ferrò
(MT)
Maria Luisa Piras
(ML)
Maria Grazia Grasso
(MG)
Marco Rovaris
(M)
Marco Ronzoni
(M)
Lorenzo Capone
(L)
Leonardo Sinisi
(L)
Guido Cavaletti
(G)
Giuseppe Santuccio
(G)
Giuseppe Salemi
(G)
Gioacchino Tedeschi
(G)
Giancarlo Di Battista
(G)
Franco Valzania
(F)
Francesco D'Andrea
(F)
Francesco Corea
(F)
Francesca De Robertis
(F)
Fabio Bandini
(F)
Enrico Millefiorini
(E)
Elio Scarpini
(E)
Dott Ssa Maria Merello
(DSM)
Dott Ssa Aurora Fuiani
(DSA)
Diego Centonze
(D)
Davide Nasuelli
(D)
Cristoforo Comi
(C)
Ciro Florio
(C)
Carlo Piantadosi
(C)
Bruno Passarella
(B)
Antonio Bertolotto
(A)
Alessandra Protti
(A)
Commentaires et corrections
Type : CommentIn
Références
Mult Scler Relat Disord. 2020 Nov;46:102472
pubmed: 32890817
Mult Scler Relat Disord. 2014 Nov;3(6):705-11
pubmed: 25891549
Mult Scler. 2009 Oct;15(10):1195-205
pubmed: 19797261
Mult Scler Relat Disord. 2017 Feb;12:70-78
pubmed: 28283111
Mult Scler. 2017 Oct;23(12):1583-1592
pubmed: 29041872
Neurology. 2014 Jul 15;83(3):278-86
pubmed: 24871874
Ann Neurol. 2001 Jul;50(1):121-7
pubmed: 11456302
Eur J Neurol. 2022 Apr;29(4):1082-1090
pubmed: 33724638
JAMA Neurol. 2020 Nov 1;77(11):1398-1407
pubmed: 32716480
Neurol Sci. 2019 Jan;40(1):155-165
pubmed: 30426289
Arch Neurol. 2011 Nov;68(11):1421-7
pubmed: 22084124
CNS Drugs. 2018 Dec;32(12):1145-1157
pubmed: 30141001
Neurology. 2005 Dec 27;65(12):1919-23
pubmed: 16380613
Ann Transl Med. 2019 Jan;7(1):16
pubmed: 30788363
Nat Rev Neurol. 2019 May;15(5):287-300
pubmed: 30940920
Neurology. 2009 Nov 17;73(20):1616-23
pubmed: 19890070
Lancet Neurol. 2020 Apr;19(4):307-316
pubmed: 32199096
Brain. 2000 Mar;123 Pt 3:641-9
pubmed: 10686184
Lancet Neurol. 2018 Feb;17(2):162-173
pubmed: 29275977
JAMA Neurol. 2018 Nov 1;75(11):1407-1415
pubmed: 30083762
N Engl J Med. 2000 Nov 16;343(20):1430-8
pubmed: 11078767
Neurology. 2015 Jan 6;84(1):81-8
pubmed: 25398229
Brain. 2020 Sep 1;143(9):2742-2756
pubmed: 32947619
Brain. 1999 Oct;122 ( Pt 10):1941-50
pubmed: 10506095
Ann Neurol. 2011 Feb;69(2):292-302
pubmed: 21387374
N Engl J Med. 2017 Jan 19;376(3):209-220
pubmed: 28002688
Ann Neurol. 2021 Apr;89(4):780-789
pubmed: 33480077
Brain. 2020 Oct 1;143(10):3013-3024
pubmed: 32935843
JAMA Neurol. 2019 Mar 1;76(3):274-281
pubmed: 30615019
Mult Scler. 2014 Jan;20(1):112-5
pubmed: 23635909
Ann Neurol. 2009 Oct;66(4):460-71
pubmed: 19847908