The efficacy of DMDs is typically established via short clinical trials with a follow-up of 2-3 years, in highly select and motivated groups of MS patients. In clinical practice, DMDs are used for many years in a much more diverse patient population. Relatively little is known about the use of DMDs for MS in the population-based universal healthcare setting. The current study from Canada described the characteristics of a cohort of 10,418 MS patients exposed to their first DMD in the real-world setting; 74% were women [1].
At study entry, 17% of patients had some comorbidity (Charlson Comorbidity Index score ≥1). Mean age at first DMD was 39.6 years. Nearly 20% was aged ≥50 years when filling their first DMD and 3% was ≥60 years old. The mean age at first DMD prescription ranged from 35.9 years for alemtuzumab (n=37) to 43.6 years for teriflunomide (n=338).
Pattern of treatment changed over time, reflecting increased availability of DMDs. From 1996-2012, the most common first DMD prescriptions filled were for beta-interferon (72%) or glatiramer acetate (27%). From 2013-2018, the most common first DMD prescriptions filled were for glatiramer acetate (33%), dimethyl fumarate (27%), or beta-interferon (22%).
- Ng HS, et al. Characteristics of a population-based MS cohort treated with disease-modifying drugs. ECF 28th Annual Meeting. Abstract 06.
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Table of Contents: ECF 2020
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