Literature DB >> 26121423

Efficacy of fingolimod in patients with highly active relapsing-remitting multiple sclerosis.

T Derfuss1, N K Bergvall2, N Sfikas2, D L Tomic2.   

Abstract

OBJECTIVE: There is a need to identify effective switch therapies for patients with relapsing-remitting multiple sclerosis (RRMS) who experience high disease activity despite receiving disease-modifying therapy (DMT). The objective of this study was to assess the efficacy of fingolimod versus placebo in patients with RRMS who had experienced high disease activity despite previously receiving DMT, using post hoc analyses of two phase 3 trials: FREEDOMS (NCT00289978) and FREEDOMS II (NCT00355134). RESEARCH DESIGN AND METHODS: Clinical and magnetic resonance imaging outcomes over 24 months were analyzed in patients from FREEDOMS and FREEDOMS II who had received treatment in the previous year and had: (1) ≥1 relapse in the previous year and either ≥1 gadolinium (Gd) enhancing T1 lesion or ≥9 T2 lesions at baseline and/or (2) as many or more relapses in the year before baseline as in the previous year (as per fingolimod's EU label). MAIN OUTCOME MEASURES: The inclusion criteria were fulfilled by 249 and 257 patients in the fingolimod and placebo groups, respectively. Annualized relapse rates were reduced by 48% for fingolimod versus placebo (p < 0.001). Fingolimod reduced the risk of 3 month and 6 month confirmed disability progression by 34% (p = 0.031) and 45% (p = 0.016), respectively, versus placebo. Brain volume loss was reduced by 46% for fingolimod versus placebo (p < 0.001). The reduction in Gd-enhancing T1 lesion counts for fingolimod versus placebo was 65% (p < 0.001). Furthermore, fingolimod reduced the number of new or newly enlarged T2 lesions by 69% relative to placebo (p < 0.001). LIMITATION: The analyses are post hoc, but the population is specified by the European Medicines Agency in the label for fingolimod.
CONCLUSIONS: Fingolimod demonstrated efficacy across all four key RRMS disease measures analyzed in patients with high disease activity despite previous DMT.

Entities:  

Keywords:  Fingolimod; High disease activity; Highly active RRMS; Multiple sclerosis

Mesh:

Substances:

Year:  2015        PMID: 26121423     DOI: 10.1185/03007995.2015.1067191

Source DB:  PubMed          Journal:  Curr Med Res Opin        ISSN: 0300-7995            Impact factor:   2.580


  9 in total

1.  Early use of fingolimod is associated with better clinical outcomes in relapsing-remitting multiple sclerosis patients.

Authors:  Massimo Filippi; Federica Esposito; Miryam Cannizzaro; Laura Ferré; Ferdinando Clarelli; Antonino Giordano; Francesca Sangalli; Bruno Colombo; Giancarlo Comi; Lucia Moiola; Vittorio Martinelli
Journal:  J Neurol       Date:  2022-06-27       Impact factor: 6.682

2.  Early Reduction of MRI Activity During 6 Months of Treatment With Cladribine Tablets for Highly Active Relapsing Multiple Sclerosis: MAGNIFY-MS.

Authors:  Nicola de Stefano; Frederik Barkhof; Xavier Montalban; Anat Achiron; Tobias Derfuss; Andrew Chan; Suzanne Hodgkinson; Alexandre Prat; Letizia Leocani; Klaus Schmierer; Finn Sellebjerg; Patrick Vermersch; Heinz Wiendl; Birgit Keller; Sanjeev Roy
Journal:  Neurol Neuroimmunol Neuroinflamm       Date:  2022-06-14

Review 3.  Management of neurogenic bladder in patients with multiple sclerosis.

Authors:  Véronique Phé; Emmanuel Chartier-Kastler; Jalesh N Panicker
Journal:  Nat Rev Urol       Date:  2016-03-31       Impact factor: 14.432

Review 4.  Intractable and highly active relapsing multiple sclerosis - role of alemtuzumab.

Authors:  Divyanshu Dubey; Christopher A Cano; Olaf Stuve
Journal:  Neuropsychiatr Dis Treat       Date:  2015-09-18       Impact factor: 2.570

Review 5.  Fingolimod for multiple sclerosis and emerging indications: appropriate patient selection, safety precautions, and special considerations.

Authors:  Ilya Ayzenberg; Robert Hoepner; Ingo Kleiter
Journal:  Ther Clin Risk Manag       Date:  2016-02-19       Impact factor: 2.423

6.  Impact of alemtuzumab on health-related quality of life over 6 years in CARE-MS II trial extension patients with relapsing-remitting multiple sclerosis.

Authors:  Rafael Arroyo; Denise P Bury; Jennifer D Guo; David H Margolin; Maria Melanson; Nadia Daizadeh; David Cella
Journal:  Mult Scler       Date:  2019-05-30       Impact factor: 6.312

7.  Efficacy and Safety of Alemtuzumab Through 9 Years of Follow-up in Patients with Highly Active Disease: Post Hoc Analysis of CARE-MS I and II Patients in the TOPAZ Extension Study.

Authors:  Tjalf Ziemssen; Ann D Bass; Regina Berkovich; Giancarlo Comi; Sara Eichau; Jeremy Hobart; Samuel F Hunter; Christopher LaGanke; Volker Limmroth; Daniel Pelletier; Carlo Pozzilli; Sven Schippling; Livia Sousa; Anthony Traboulsee; Bernard M J Uitdehaag; Bart Van Wijmeersch; Zia Choudhry; Nadia Daizadeh; Barry A Singer
Journal:  CNS Drugs       Date:  2020-09       Impact factor: 5.749

8.  Aggressive multiple sclerosis (2): Treatment.

Authors:  Georgina Arrambide; Ellen Iacobaeus; Maria Pia Amato; Tobias Derfuss; Sandra Vukusic; Bernhard Hemmer; Lou Brundin; Mar Tintore
Journal:  Mult Scler       Date:  2020-06-12       Impact factor: 6.312

9.  The Neutrophil-to-Lymphocyte Ratio is Related to Disease Activity in Relapsing Remitting Multiple Sclerosis.

Authors:  Emanuele D'Amico; Aurora Zanghì; Alessandra Romano; Mariangela Sciandra; Giuseppe Alberto Maria Palumbo; Francesco Patti
Journal:  Cells       Date:  2019-09-20       Impact factor: 6.600

  9 in total

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