TY - JOUR
T1 - Natalizumab Versus Fingolimod in Patients with Relapsing-Remitting Multiple Sclerosis
T2 - A Subgroup Analysis From Three International Cohorts
AU - Sharmin, Sifat
AU - Lefort, Mathilde
AU - Andersen, Johanna Balslev
AU - Leray, Emmanuelle
AU - Horakova, Dana
AU - Havrdova, Eva Kubala
AU - Alroughani, Raed
AU - Izquierdo, Guillermo
AU - Ozakbas, Serkan
AU - Patti, Francesco
AU - Onofrj, Marco
AU - Lugaresi, Alessandra
AU - Terzi, Murat
AU - Grammond, Pierre
AU - Grand’Maison, Francois
AU - Yamout, Bassem
AU - Prat, Alexandre
AU - Girard, Marc
AU - Duquette, Pierre
AU - Boz, Cavit
AU - Trojano, Maria
AU - McCombe, Pamela
AU - Slee, Mark
AU - Lechner-Scott, Jeannette
AU - Turkoglu, Recai
AU - Sola, Patrizia
AU - Ferraro, Diana
AU - Granella, Franco
AU - Prevost, Julie
AU - Maimone, Davide
AU - Skibina, Olga
AU - Buzzard, Katherine
AU - Van der Walt, Anneke
AU - Van Wijmeersch, Bart
AU - Csepany, Tunde
AU - Spitaleri, Daniele
AU - Vucic, Steve
AU - Casey, Romain
AU - Debouverie, Marc
AU - Edan, Gilles
AU - Ciron, Jonathan
AU - Ruet, Aurélie
AU - Sellebjerg, Finn Thorup
AU - Soerensen, Per Soelberg
AU - Jensen, Michael Broksgaard
AU - Frederiksen, Jette Lautrup
AU - Bramow, Stephan
AU - Mathiesen, Henrik Kahr
AU - Schreiber, Karen Ingrid
AU - Magyari, Melinda
AU - Danish Multiple Sclerosis Registry, OFSEP and the MSBase investigators
N1 - Publisher Copyright: © 2021, The Author(s), under exclusive licence to Springer Nature Switzerland AG.
PY - 2021/11
Y1 - 2021/11
N2 - Introduction: Natalizumab has proved to be more effective than fingolimod in reducing disease activity in relapsing-remitting multiple sclerosis (RRMS). Whether this association is universal for all patient groups remains to be determined. Objective: The aim of this study was to compare the relative effectiveness of natalizumab and fingolimod in RRMS subgroups defined by the baseline demographic and clinical characteristics of interest. Methods: Patients with RRMS who were given natalizumab or fingolimod were identified in a merged cohort from three international registries. Efficacy outcomes were compared across subgroups based on patients’ sex, age, disease duration, Expanded Disability Status Scale (EDSS) score, and disease and magnetic resonance imaging (MRI) activity 12 months prior to treatment initiation. Study endpoints were number of relapses (analyzed with weighted negative binomial generalized linear model) and 6-month confirmed disability worsening and improvement events (weighted Cox proportional hazards model), recorded during study therapy. Each patient was weighted using inverse probability of treatment weighting based on propensity score. Results: A total of 5148 patients (natalizumab 1989; fingolimod 3159) were included, with a mean ± standard deviation age at baseline of 38 ± 10 years, and the majority (72%) were women. The median on-treatment follow-up was 25 (quartiles 15–41) months. Natalizumab was associated with fewer relapses than fingolimod (incidence rate ratio [IRR]; 95% confidence interval [CI]) in women (0.76; 0.65–0.88); in those aged ≤ 38 years (0.64; 0.54–0.76); in those with disease duration ≤ 7 years (0.63; 0.53–0.76); in those with EDSS score 38 years (1.34; 1.04–1.73); those with disease duration > 7 years (1.33; 1.01–1.74); those with EDSS score
AB - Introduction: Natalizumab has proved to be more effective than fingolimod in reducing disease activity in relapsing-remitting multiple sclerosis (RRMS). Whether this association is universal for all patient groups remains to be determined. Objective: The aim of this study was to compare the relative effectiveness of natalizumab and fingolimod in RRMS subgroups defined by the baseline demographic and clinical characteristics of interest. Methods: Patients with RRMS who were given natalizumab or fingolimod were identified in a merged cohort from three international registries. Efficacy outcomes were compared across subgroups based on patients’ sex, age, disease duration, Expanded Disability Status Scale (EDSS) score, and disease and magnetic resonance imaging (MRI) activity 12 months prior to treatment initiation. Study endpoints were number of relapses (analyzed with weighted negative binomial generalized linear model) and 6-month confirmed disability worsening and improvement events (weighted Cox proportional hazards model), recorded during study therapy. Each patient was weighted using inverse probability of treatment weighting based on propensity score. Results: A total of 5148 patients (natalizumab 1989; fingolimod 3159) were included, with a mean ± standard deviation age at baseline of 38 ± 10 years, and the majority (72%) were women. The median on-treatment follow-up was 25 (quartiles 15–41) months. Natalizumab was associated with fewer relapses than fingolimod (incidence rate ratio [IRR]; 95% confidence interval [CI]) in women (0.76; 0.65–0.88); in those aged ≤ 38 years (0.64; 0.54–0.76); in those with disease duration ≤ 7 years (0.63; 0.53–0.76); in those with EDSS score 38 years (1.34; 1.04–1.73); those with disease duration > 7 years (1.33; 1.01–1.74); those with EDSS score
UR - http://www.scopus.com/inward/record.url?scp=85115657202&partnerID=8YFLogxK
U2 - 10.1007/s40263-021-00860-7
DO - 10.1007/s40263-021-00860-7
M3 - Journal article
SN - 1172-7047
VL - 35
SP - 1217
EP - 1232
JO - CNS Drugs
JF - CNS Drugs
IS - 11
ER -