PT  - JOURNAL ARTICLE
AU  - Silber, Eli
AU  - Kappos, L
AU  - Radue, EW
AU  - Connor, P
AU  - Amato, M
AU  - Zhang-Auberson, L
AU  - Haering, D
AU  - Francis, G
TI  - SWITCHING THERAPY TO FINGOLIMOD IMPROVES CLINICAL AND MRI OUTCOMES
AID  - 10.1136/jnnp-2014-309236.147
DP  - 2014 Oct 01
TA  - Journal of Neurology, Neurosurgery & Psychiatry
PG  - e4--e4
VI  - 85
IP  - 10
4099  - http://jnnp.bmj.com/content/85/10/e4.54.short
4100  - http://jnnp.bmj.com/content/85/10/e4.54.full
SO  - J Neurol Neurosurg Psychiatry2014 Oct 01; 85
AB  - Objectives To evaluate the long-term efficacy outcomes in patients with high-disease-activity switching from placebo to fingolimod, from the FREEDOMS extension study.Methods Patients either continued on the fingolimod dose assigned in the core phase (continuous-group ‘c-group’) or were re-randomised from placebo to fingolimod (switch-group ‘s-group’). Clinical and MRI outcomes (Month 0–24, core/ Month 24–48, extension) for fingolimod 0.5mg are presented for the following high-disease-activity subgroups: Group-1 (n=110), interferon-beta (IFN) therapy in previous year and ≥ relapse in year-1 vs. year-2;; Group-2 (n=106), IFN therapy in previous year+≥1 relapse in year-1 with either ≥1 Gd+ T1 lesion or ≥9 T2 lesions at baseline; Group-3 (n=90), treatment-naïve rapidly evolving severe RRMS patients (≥2 relapses in year-1 and ≥1 baseline Gd+-lesion).Results Annualized relapse rates were sustained from the core into extension phase for ‘c-group’ (Core/extension: Group-1: 0.16/0.20; Group-2: 0.23/0.25; Group-3: 0.26/0.20) and reduced in ‘s-group’ (Group-1: 0.62/0.29; Group-2: 0.56/0.28; Group-3: 0.62/0.18). Greater proportions of switch patients were free from new/enlarging T2-lesions (Group-1: 16.7%/16.7%; Group-2: 14.3%/28.6%; Group-3: 16.7%/66.7%) and Gd+-lesions; (Group-1: 14.3%/85.7%; Group-2: 12.5%/87.5%; Group-3: 16.7%/83.3%).Conclusion Highly active patients switched to fingolimod showed significant improvement in clinical and MRI outcomes. Continuous fingolimod treatment was associated with sustained low clinical disease activity.