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Long-term (up to 4.5 years) treatment with fingolimod in multiple sclerosis: results from the extension of the randomised TRANSFORMS study
by
Tomic, Davorka
, Montalban, Xavier
, Khatri, Bhupendra
, von Rosenstiel, Philipp
, Hartung, Hans-Peter
, Pelletier, Jean
, Barkhof, Frederik
, Stites, Tracy
, Cohen, Jeffrey A
, Comi, Giancarlo
, Ritter, Shannon
, Kappos, Ludwig
in
Adult
/ Bioengineering
/ Disability Evaluation
/ Double-Blind Method
/ Female
/ Fingolimod Hydrochloride - therapeutic use
/ Humans
/ Immunosuppressive Agents - therapeutic use
/ Interferon beta-1a - therapeutic use
/ Life Sciences
/ Magnetic Resonance Imaging
/ Male
/ Multiple Sclerosis
/ Multiple Sclerosis, Relapsing-Remitting - drug therapy
/ Multiple Sclerosis, Relapsing-Remitting - pathology
/ Neuroimaging
/ Patients
/ Recurrence
/ Treatment Outcome
/ Young Adult
2016
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Long-term (up to 4.5 years) treatment with fingolimod in multiple sclerosis: results from the extension of the randomised TRANSFORMS study
by
Tomic, Davorka
, Montalban, Xavier
, Khatri, Bhupendra
, von Rosenstiel, Philipp
, Hartung, Hans-Peter
, Pelletier, Jean
, Barkhof, Frederik
, Stites, Tracy
, Cohen, Jeffrey A
, Comi, Giancarlo
, Ritter, Shannon
, Kappos, Ludwig
in
Adult
/ Bioengineering
/ Disability Evaluation
/ Double-Blind Method
/ Female
/ Fingolimod Hydrochloride - therapeutic use
/ Humans
/ Immunosuppressive Agents - therapeutic use
/ Interferon beta-1a - therapeutic use
/ Life Sciences
/ Magnetic Resonance Imaging
/ Male
/ Multiple Sclerosis
/ Multiple Sclerosis, Relapsing-Remitting - drug therapy
/ Multiple Sclerosis, Relapsing-Remitting - pathology
/ Neuroimaging
/ Patients
/ Recurrence
/ Treatment Outcome
/ Young Adult
2016
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Long-term (up to 4.5 years) treatment with fingolimod in multiple sclerosis: results from the extension of the randomised TRANSFORMS study
by
Tomic, Davorka
, Montalban, Xavier
, Khatri, Bhupendra
, von Rosenstiel, Philipp
, Hartung, Hans-Peter
, Pelletier, Jean
, Barkhof, Frederik
, Stites, Tracy
, Cohen, Jeffrey A
, Comi, Giancarlo
, Ritter, Shannon
, Kappos, Ludwig
in
Adult
/ Bioengineering
/ Disability Evaluation
/ Double-Blind Method
/ Female
/ Fingolimod Hydrochloride - therapeutic use
/ Humans
/ Immunosuppressive Agents - therapeutic use
/ Interferon beta-1a - therapeutic use
/ Life Sciences
/ Magnetic Resonance Imaging
/ Male
/ Multiple Sclerosis
/ Multiple Sclerosis, Relapsing-Remitting - drug therapy
/ Multiple Sclerosis, Relapsing-Remitting - pathology
/ Neuroimaging
/ Patients
/ Recurrence
/ Treatment Outcome
/ Young Adult
2016
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Long-term (up to 4.5 years) treatment with fingolimod in multiple sclerosis: results from the extension of the randomised TRANSFORMS study
Journal Article
Long-term (up to 4.5 years) treatment with fingolimod in multiple sclerosis: results from the extension of the randomised TRANSFORMS study
2016
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Overview
ObjectiveThe 12-month (M), phase 3, double-blind, randomised TRANSFORMS study demonstrated significant benefits of fingolimod 0.5 or 1.25 mg over interferon β-1a (IFNβ-1a) in patients with relapsing–remitting multiple sclerosis. We report the results of long-term (up to 4.5 years) extension of TRANSFORMS.MethodsPatients randomised to fingolimod (0.5/1.25 mg) in the core phase continued the same dose (continuous-fingolimod) in the extension, whereas those on IFNβ-1a were re-randomised (1:1) to fingolimod (IFN-switch; IFN: 0.5/1.25 mg). Outcomes included annualised relapse rate (ARR), confirmed disability progression and MRI measures. Results are presented here for the continuous-fingolimod 0.5 mg and pooled IFN-switch groups.ResultsOf the 1027 patients who entered the extension, 772 (75.2%) completed the study. From baseline to the end of the study (EOS), ARR in patients on continuous-fingolimod 0.5 mg was significantly lower than in the IFN-switch group (M0–EOS: 0.17 vs 0.27). After switching to fingolimod (M0–12 vs M13–EOS), patients initially treated with IFN had a 50% reduction in ARR (0.40 vs 0.20), reduced MRI activity and a lower rate of brain volume loss. In a post hoc analysis, the proportion of IFN-switch patients with no evidence of disease activity increased by approximately 50% in the first year after switching to fingolimod treatment (44.3% to 66.0%). The safety profile was consistent with that observed in the core phase.ConclusionsThese results support a continued effect of long-term fingolimod therapy in maintaining a low rate of disease activity and sustained improved efficacy after switching from IFNβ-1a to fingolimod.Clinical trial registration NoNCT00340834.
Publisher
BMJ Publishing Group LTD,BMJ Publishing Group
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