TY - JOUR
T1 - Highly active immunomodulatory therapy ameliorates accumulation of disability in moderately advanced and advanced multiple sclerosis
AU - Lizak, Nathaniel
AU - Lugaresi, Alessandra
AU - Alroughani, Raed A
AU - Lechner-Scott, Jeannette
AU - Slee, Mark
AU - Havrdova, Eva
AU - Horakova, Dana
AU - Trojano, Maria
AU - Izquierdo, Guillermo
AU - Duquette, Pierre Pascal
AU - Girard, Marc
AU - Prat, Alexandre
AU - Grammond, Pierre
AU - Hupperts, Raymond
AU - Grand'Maison, Francois
AU - Sola, Patrizia
AU - Pucci, Eugenio
AU - Bergamaschi, Roberto
AU - Oreja-Guevara, Celia
AU - Van Pesch, Vincent
AU - Ramo, Cristina
AU - Spitaleri, Daniele La
AU - Iuliano, Gerardo
AU - Boz, Cavit
AU - Granella, Franco
AU - Olascoaga, Javier
AU - Verheul, Freek
AU - Rozsa, Csilla
AU - Cristiano, Edgardo
AU - Flechter, Shlomo
AU - Hodgkinson, Suzanne J
AU - Amato, Maria Pia
AU - Deri, Norma H
AU - Jokubaitis, Vilija G
AU - Spelman, Tim
AU - Butzkueven, Helmut
AU - Kalincik, Tomas
AU - the MSBase Study Group
PY - 2017/3/1
Y1 - 2017/3/1
N2 - Objective: To evaluate variability and predictability of disability trajectories in moderately advanced and advanced multiple sclerosis (MS), and their modifiability with immunomodulatory therapy. Methods The epochs between Expanded Disability Status Scale (EDSS) steps 3.6, 4.6 and 6.6.5 were analysed. Patients with relapse-onset MS and having reached 6-month confirmed baseline EDSS step (3/4/6) were identified in MSBase, a global observational MS cohort study. We used multivariable survival models to examine the impact of disease-modifying therapy, clinical and demographic factors on progression to the outcome EDSS step (6/6.5). Sensitivity analyses with varying outcome definitions and inclusion criteria were conducted. Results: For the EDSS 3.6, 4.6 and 6.6.5 epochs, 1560, 1504 and 1231 patients were identified, respectively. Disability trajectories showed large coefficients of variance prebaseline (0.92.1.11) and postbaseline (2.15.2.50), with no significant correlations. The probability of reaching the outcome step was not associated with prebaseline variables, but was increased by higher relapse rates during each epoch (HRs 1.58.3.07; p<0.001). A greater proportion of each epoch treated with higher efficacy therapies was associated with lower risk of reaching the outcome disability step (HRs 0.72.0.91 per 25%; p≤0.02). 3 sensitivity analyses confirmed these results. Conclusions: Disease progression during moderately advanced and advanced MS is highly variable and amnesic to prior disease activity. Lower relapse rates and greater time on higher efficacy immunomodulatory therapy after reaching EDSS steps 3, 4 and 6 are associated with a decreased risk of accumulating further disability. Highly effective immunomodulatory therapy ameliorates accumulation of disability in moderately advanced and advanced relapse-onset MS.
AB - Objective: To evaluate variability and predictability of disability trajectories in moderately advanced and advanced multiple sclerosis (MS), and their modifiability with immunomodulatory therapy. Methods The epochs between Expanded Disability Status Scale (EDSS) steps 3.6, 4.6 and 6.6.5 were analysed. Patients with relapse-onset MS and having reached 6-month confirmed baseline EDSS step (3/4/6) were identified in MSBase, a global observational MS cohort study. We used multivariable survival models to examine the impact of disease-modifying therapy, clinical and demographic factors on progression to the outcome EDSS step (6/6.5). Sensitivity analyses with varying outcome definitions and inclusion criteria were conducted. Results: For the EDSS 3.6, 4.6 and 6.6.5 epochs, 1560, 1504 and 1231 patients were identified, respectively. Disability trajectories showed large coefficients of variance prebaseline (0.92.1.11) and postbaseline (2.15.2.50), with no significant correlations. The probability of reaching the outcome step was not associated with prebaseline variables, but was increased by higher relapse rates during each epoch (HRs 1.58.3.07; p<0.001). A greater proportion of each epoch treated with higher efficacy therapies was associated with lower risk of reaching the outcome disability step (HRs 0.72.0.91 per 25%; p≤0.02). 3 sensitivity analyses confirmed these results. Conclusions: Disease progression during moderately advanced and advanced MS is highly variable and amnesic to prior disease activity. Lower relapse rates and greater time on higher efficacy immunomodulatory therapy after reaching EDSS steps 3, 4 and 6 are associated with a decreased risk of accumulating further disability. Highly effective immunomodulatory therapy ameliorates accumulation of disability in moderately advanced and advanced relapse-onset MS.
UR - http://www.scopus.com/inward/record.url?scp=85011277273&partnerID=8YFLogxK
U2 - 10.1136/jnnp-2016-313976
DO - 10.1136/jnnp-2016-313976
M3 - Article
C2 - 27683916
AN - SCOPUS:85011277273
SN - 0022-3050
VL - 88
SP - 196
EP - 203
JO - Journal of Neurology, Neurosurgery and Psychiatry
JF - Journal of Neurology, Neurosurgery and Psychiatry
IS - 3
ER -