Background: For patients with MS, medication switches increase the risk of disease reactivation.
Objective: Compare discontinuation rates due to treatment failure or side effects between teriflunomide and dimethyl fumarate, and investigate clinical variables affecting discontinuation rates.
Methods: All patients who received teriflunomide or dimethyl fumarate at Haukeland University Hospital from 2013 until 2018 were identified. Clinical and demographic variables were extracted from the Norwegian MS Registry. Cause-specific Cox regression models estimated the rate of discontinuation due to treatment failure or side effects.
Results: We included 354 patients treated with either dimethyl fumarate ( = 185) or teriflunomide ( = 169). We found 38% lower risk of discontinuation because of treatment failure for patients using dimethyl fumarate compared to teriflunomide ( < 0.05). In a treatment-naive subgroup ( = 183), we found a 38% reduced risk of discontinuation for any reason among patients using dimethyl fumarate ( < 0.05). There was no significant difference between treatment groups in discontinuation rate due to side effects, although more patients reported side effects when treated with dimethyl fumarate.
Conclusion: Our findings suggests that dimethyl fumarate has a lower risk of discontinuation because of treatment failure among both treatment-experienced and treatment-naive patients.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8209840 | PMC |
http://dx.doi.org/10.1177/20552173211022027 | DOI Listing |
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