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Abstract Details

Real-world Effectiveness of Dimethyl Fumarate Versus Fingolimod on Cognitive Outcomes
Multiple Sclerosis
MS and CNS Inflammatory Disease Posters (7:00 AM-5:00 PM)
050
To compare effect of dimethyl fumarate (DMF) and fingolimod (FTY) on cognition in US patients from a heterogenous multiple sclerosis (MS) cohort.

Impact of MS therapies on cognition is important for patient management and needs further real-world assessment. Cognitive status and disease-modifying therapy choice can also be impacted by non-MS factors e.g., age/chronic comorbidities. US patients prescribed DMF are often older and more likely to have cardiovascular disease versus FTY, due to different safety profile and prescribing preferences. 

Eligible patients were on DMF/FTY at enrollment in MS Partners Advancing Technology and Health Solutions (MS PATHS) network with ≥1y follow-up. Sensitivity analysis included a sub-group who initiated DMF/FTY ≤2y before MS PATHS. Propensity score weighting (PSW) covariates included age, sex, race, education, MS duration, prior therapy, cardiovascular disease, diabetes, and time since DMF/FTY initiation (sensitivity analysis). Generalized estimating equation models assessed differences in means and 1-year change in processing speed test (PST).

702 DMF and 600 FTY patients were eligible; 632 and 541 had PST assessments, respectively. Mean time (SD) since treatment initiation was 2.3 (1.7) [DMF] and 2.7 (2.1) years [FTY]. Mean number (SD) of follow-up assessments was the same between groups (2.3 [0.9]). At first MS PATHS visit, 324 (46%) [DMF] and 236 (39%) [FTY] had cardiovascular disease (p=0.01); mean (SD) PST was 49 (13) [DMF] and 51 (12) [FTY] for overall patients (p=0.007) and 51 (13) [DMF] and 52 (12) [FTY] without cardiovascular comorbidities (p=0.10). Following PSW (DMF as reference), difference in mean PST (-0.63, p=0.4) and slope of change in PST (0.06, p=0.88) during 1-year follow-up was not significant. Sensitivity analyses, including 135 and 134 patients with mean time (SD) since DMF/FTY initiation of 11.2 (7.2) and 10.1 (6.9) months, showed similar findings.

DMF and FTY demonstrated similar effectiveness on cognitive outcomes in a heterogeneous, real-world cohort.
Authors/Disclosures
Carrie M. Hersh, DO, MSc, FAAN (Cleveland Clinic Lou Ruvo Center for Brain Health)
PRESENTER
Dr. Hersh has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Biogen. Dr. Hersh has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Novartis. Dr. Hersh has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Genentech_GN41791. Dr. Hersh has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Genzyme. Dr. Hersh has received personal compensation in the range of $500-$4,999 for serving as a Consultant for EMD Serono. Dr. Hersh has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Bristol-Myers Squibb . Dr. Hersh has received personal compensation in the range of $500-$4,999 for serving as a Consultant for TG Therapeutics. Dr. Hersh has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Alexion. Dr. Hersh has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Horizon Therapeutics. Dr. Hersh has received personal compensation in the range of $500-$4,999 for serving on a Speakers Bureau for Biogen. Dr. Hersh has received personal compensation in the range of $500-$4,999 for serving on a Speakers Bureau for Genzyme. Dr. Hersh has received personal compensation in the range of $500-$4,999 for serving as an Editor, Associate Editor, or Editorial Advisory Board Member for Elsevier. The institution of Dr. Hersh has received research support from Biogen. The institution of Dr. Hersh has received research support from Novartis. The institution of Dr. Hersh has received research support from Genentech_GN41791. The institution of Dr. Hersh has received research support from PCORI. The institution of Dr. Hersh has received research support from Bristol Myers Squibb.
No disclosure on file
Carl DeMoor Carl DeMoor has received personal compensation for serving as an employee of Biogen. Carl DeMoor has received stock or an ownership interest from Biogen. An immediate family member of Carl DeMoor has received personal compensation in the range of $100,000-$499,999 for serving as a Program Director with NIH.
James R. Williams III, PhD Dr. Williams has received personal compensation for serving as an employee of Biogen. Dr. Williams has received stock or an ownership interest from Biogen.
Catherine Miller Catherine Miller has received personal compensation for serving as an employee of Biogen. Catherine Miller has received stock or an ownership interest from Biogen.
Irene Koulinska Irene Koulinska has received personal compensation for serving as an employee of Biogen.