Fingolimod Treatment in Relapsing-Remitting Multiple Sclerosis Patients: A Prospective Observational Multicenter Postmarketing Study
Objective. The aim of this prospective observational multicenter postmarketing study was to evaluate fingolimod efficacy in a real world clinical setting. Methods. One hundred forty-two subjects with relapsing-remitting multiple sclerosis (RRMS) were enrolled in three multiple sclerosis centers thro...
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Series: | Multiple Sclerosis International |
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doaj-57086192fddf479590313c0d9ece63b82020-11-24T22:23:18ZengHindawi LimitedMultiple Sclerosis International2090-26542090-26622015-01-01201510.1155/2015/763418763418Fingolimod Treatment in Relapsing-Remitting Multiple Sclerosis Patients: A Prospective Observational Multicenter Postmarketing StudyRocco Totaro0Caterina Di Carmine1Gianfranco Costantino2Roberta Fantozzi3Paolo Bellantonio4Aurora Fuiani5Ciro Mundi6Stefano Ruggieri7Carmine Marini8Antonio Carolei9Department of Neurology, University of L’Aquila, L’Aquila, ItalyDepartment of Neurology, University of L’Aquila, L’Aquila, ItalyDepartment of Neurology, Ospedali Riuniti, Foggia, ItalyDepartment of Neurology, IRCCS MEUROMED, Pozzilli, ItalyDepartment of Neurology, IRCCS MEUROMED, Pozzilli, ItalyDepartment of Neurology, Ospedali Riuniti, Foggia, ItalyDepartment of Neurology, Ospedali Riuniti, Foggia, ItalyDepartment of Neurology, IRCCS MEUROMED, Pozzilli, ItalyDepartment of Neurology, University of L’Aquila, L’Aquila, ItalyDepartment of Neurology, University of L’Aquila, L’Aquila, ItalyObjective. The aim of this prospective observational multicenter postmarketing study was to evaluate fingolimod efficacy in a real world clinical setting. Methods. One hundred forty-two subjects with relapsing-remitting multiple sclerosis (RRMS) were enrolled in three multiple sclerosis centers throughout Central and Southern Italy between January 2011 and September 2013. After enrollment, regular visits and EDSS assessment were scheduled every 3 months, and MRI scan was obtained every 12 months. Patients were followed up from 1 to 33 months (mean 14.95 ± 9.15 months). The main efficacy endpoints included the proportion of patients free from clinical relapses, from disability progression, from magnetic resonance imaging activity, and from any disease activity. Results. Out of 142 patients enrolled in the study, 88.1% were free from clinical relapse and 69.0% were free from disability progression; 68.5% of patients remained free from new or newly enlarging T2 lesions and 81.7% of patients were free from gadolinium enhancing lesions. Overall the proportion of patients free from any disease activity was 41.9%. Conclusions. Our data in a real world cohort are consistent with previous findings that yield convincing evidence for the efficacy of fingolimod in patients with RRMS.http://dx.doi.org/10.1155/2015/763418 |
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DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Rocco Totaro Caterina Di Carmine Gianfranco Costantino Roberta Fantozzi Paolo Bellantonio Aurora Fuiani Ciro Mundi Stefano Ruggieri Carmine Marini Antonio Carolei |
spellingShingle |
Rocco Totaro Caterina Di Carmine Gianfranco Costantino Roberta Fantozzi Paolo Bellantonio Aurora Fuiani Ciro Mundi Stefano Ruggieri Carmine Marini Antonio Carolei Fingolimod Treatment in Relapsing-Remitting Multiple Sclerosis Patients: A Prospective Observational Multicenter Postmarketing Study Multiple Sclerosis International |
author_facet |
Rocco Totaro Caterina Di Carmine Gianfranco Costantino Roberta Fantozzi Paolo Bellantonio Aurora Fuiani Ciro Mundi Stefano Ruggieri Carmine Marini Antonio Carolei |
author_sort |
Rocco Totaro |
title |
Fingolimod Treatment in Relapsing-Remitting Multiple Sclerosis Patients: A Prospective Observational Multicenter Postmarketing Study |
title_short |
Fingolimod Treatment in Relapsing-Remitting Multiple Sclerosis Patients: A Prospective Observational Multicenter Postmarketing Study |
title_full |
Fingolimod Treatment in Relapsing-Remitting Multiple Sclerosis Patients: A Prospective Observational Multicenter Postmarketing Study |
title_fullStr |
Fingolimod Treatment in Relapsing-Remitting Multiple Sclerosis Patients: A Prospective Observational Multicenter Postmarketing Study |
title_full_unstemmed |
Fingolimod Treatment in Relapsing-Remitting Multiple Sclerosis Patients: A Prospective Observational Multicenter Postmarketing Study |
title_sort |
fingolimod treatment in relapsing-remitting multiple sclerosis patients: a prospective observational multicenter postmarketing study |
publisher |
Hindawi Limited |
series |
Multiple Sclerosis International |
issn |
2090-2654 2090-2662 |
publishDate |
2015-01-01 |
description |
Objective. The aim of this prospective observational multicenter postmarketing study was to evaluate fingolimod efficacy in a real world clinical setting. Methods. One hundred forty-two subjects with relapsing-remitting multiple sclerosis (RRMS) were enrolled in three multiple sclerosis centers throughout Central and Southern Italy between January 2011 and September 2013. After enrollment, regular visits and EDSS assessment were scheduled every 3 months, and MRI scan was obtained every 12 months. Patients were followed up from 1 to 33 months (mean 14.95 ± 9.15 months). The main efficacy endpoints included the proportion of patients free from clinical relapses, from disability progression, from magnetic resonance imaging activity, and from any disease activity. Results. Out of 142 patients enrolled in the study, 88.1% were free from clinical relapse and 69.0% were free from disability progression; 68.5% of patients remained free from new or newly enlarging T2 lesions and 81.7% of patients were free from gadolinium enhancing lesions. Overall the proportion of patients free from any disease activity was 41.9%. Conclusions. Our data in a real world cohort are consistent with previous findings that yield convincing evidence for the efficacy of fingolimod in patients with RRMS. |
url |
http://dx.doi.org/10.1155/2015/763418 |
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