Disability improvement as a clinically relevant outcome in clinical trials of relapsing forms of multiple sclerosis

Disease-modifying therapies (DMTs) can reduce the risk of disability worsening in patients with relapsing forms of multiple sclerosis (RMS). High-efficacy DMTs can lead to confirmed or sustained disability improvement (CDI and SDI). Post hoc analyses of data from the TRANSFORMS, FREEDOMS, and FREEDO...

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Vydáno v:Multiple sclerosis Ročník 27; číslo 14; s. 2219
Hlavní autoři: Cree, Bruce Ac, Cohen, Jeffrey A, Reder, Anthony T, Tomic, Davorka, Silva, Diego, Piani Meier, Daniela, Laflamme, Annik K, Ritter, Shannon, Leppert, David, Kappos, Ludwig
Médium: Journal Article
Jazyk:angličtina
Vydáno: England 01.12.2021
Témata:
Fingolimod Hydrochloride - therapeutic use
Humans
Immunosuppressive Agents - therapeutic use
Interferon-beta - therapeutic use
Multiple Sclerosis
Multiple Sclerosis, Relapsing-Remitting - drug therapy
confirmed disability improvement
Disease-modifying therapies
fingolimod
multiple sclerosis
outcome measurement
relapsing/remitting
ISSN:1477-0970, 1477-0970
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Shrnutí:Disease-modifying therapies (DMTs) can reduce the risk of disability worsening in patients with relapsing forms of multiple sclerosis (RMS). High-efficacy DMTs can lead to confirmed or sustained disability improvement (CDI and SDI). Post hoc analyses of data from the TRANSFORMS, FREEDOMS, and FREEDOMS II trials and their extensions assessed the effects of fingolimod (0.5-1.25 mg/day) on stabilizing or improving disability over ⩽8 years in participants with RMS. CDI and SDI rates were compared between participants initially randomized to fingolimod, interferon (IFNβ-1a), or placebo. At 8 years' follow-up in TRANSFORMS, 35.1% (95% confidence interval [CI], 28.2%-43.1%) of assessed participants in the IFNβ-1a-fingolimod switch group and 41.9% (36.6%-47.6%) on continuous fingolimod experienced CDI; disability did not worsen in approximately 70%. Similar results were seen in the combined FREEDOMS population. Proportionally fewer TRANSFORMS participants achieved SDI in the IFNβ-1a-fingolimod switch group than on continuous fingolimod (5.4% [3.0%-9.5%] vs 14.2% [10.8%-18.4%],  = 0.01). CDI and SDI are outcomes of interest for clinical trials and for long-term follow-up of participants with RMS. Monitoring CDI and SDI in addition to disability worsening may facilitate understanding of the therapeutic benefit of RMS treatments.
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ISSN:1477-0970
1477-0970
DOI:10.1177/13524585211000280