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Relapse Frequency in Transitioning from Natalizumab to Dimethyl Fumarate: Assessment of Risk Factors

Overview
Journal J Neurol
Specialty Neurology
Date 2016 May 20
PMID 27193310
Citations 3
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Abstract

Risk of relapse after natalizumab (NAT) cessation and switch to dimethyl fumarate (DMF) is unknown. The objective of this paper is to identify the risk and associated risk factors for relapse after switching from NAT to DMF in relapsing-remitting multiple sclerosis. Patients (n = 30) were treated with NAT for ≥12 months and then switched to DMF in a mean of 50 days. Patient age, annualized relapse rates (ARR), Expanded Disability Status Scale scores (EDSS), and lymphocyte counts were assessed. Overall, eight patients (27 %) had relapses after switching to DMF. Five patients (17 %) suffered severe relapses with multifocal clinical and radiological findings. New lesions by MRI (T2 hyperintense or enhancing) were observed in 35 % of patients. Relapses occurred at a mean of 3.5 months after NAT cessation. Patient age and elevated ARR prior to NAT use were significantly associated with risk of relapse after switch to DMF. Once on DMF for 4 months prior to relapse, lymphocyte count decreased more significantly in patients without relapses than those with relapses. Switching from NAT to DMF correlated with increased relapses. Young patient age, high ARR and stability of lymphocyte counts were risk factors for relapse after transition from NAT to DMF.

Citing Articles

Real-World Effectiveness of Natalizumab in Korean Patients With Multiple Sclerosis.

Kim K, Kim S, Park N, Hyun J, Kim H Front Neurol. 2021; 12:714941.

PMID: 34305808 PMC: 8299833. DOI: 10.3389/fneur.2021.714941.


Effect of switching from natalizumab to moderate- vs high-efficacy DMT in clinical practice.

Hersh C, Harris H, Conway D, Hua L Neurol Clin Pract. 2021; 10(6):e53-e65.

PMID: 33510948 PMC: 7837445. DOI: 10.1212/CPJ.0000000000000809.


Effectiveness and Safety of Dimethyl Fumarate Treatment in Relapsing Multiple Sclerosis Patients: Real-World Evidence.

Alroughani R, Farouk Ahmed S, Behbehani R, Al-Hashel J Neurol Ther. 2017; 6(2):189-196.

PMID: 28780745 PMC: 5700902. DOI: 10.1007/s40120-017-0080-x.

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