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Use of follow-on fingolimod for multiple sclerosis: Analysis of effectiveness and patient reported outcomes in a real-world clinical setting

dc.contributor.authorAltunan, Bengü
dc.contributor.authorUnal, Aysun
dc.contributor.authorEfendi, Hüsnü
dc.contributor.authorKoseoğlu, Mesrure
dc.contributor.authorTerzi, Murat
dc.contributor.authorKotan, Dilcan
dc.contributor.authorTamam, Yusuf
dc.contributor.authorBoz, Cavit
dc.contributor.authorGüler, Sibel
dc.contributor.authorTuran, Ömer Faruk
dc.contributor.authorAltunrende, Burcu
dc.contributor.authorBalci, Fatma Belgin
dc.contributor.authorTurgut, Nilda
dc.contributor.authorAkcalı, Aylin
dc.contributor.authorYildirim, Kadriye Agan
dc.contributor.authorGünal, Dilek Ince
dc.contributor.authorSunter, Gülin
dc.contributor.authorBingöl, Ayhan
dc.contributor.buuauthorTURAN, ÖMER FARUK
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentNöroloji Ana Bilim Dalı
dc.contributor.researcheridJHM-3244-2023
dc.date.accessioned2024-11-20T11:31:54Z
dc.date.available2024-11-20T11:31:54Z
dc.date.issued2023-07-15
dc.description.abstractBackground: Follow-on disease modifying therapies (FO-DMTs) do not always require Phase III studies. There are concerns that cheaper FO-DMTs are only used to reduce healthcare costs. However, the well-being of people with MS (pwMS) should be a priority. We aimed to evaluate the efficacy, safety and treatment satisfaction of one of the FO-Fingolimod (FTY) used in Turkey with the approval of Turkish Ministry of Health.Methods: PwMS under FTY were recruited from 13 centers and real-world data and answers of satisfaction and adherence statements of pwMS on FTY treatment were analyzed.Results: Data of 239 pwMS were obtained. The duration of FTY treatment was 2.5 & PLUSMN; 0.8 (1-4) years in pwMS who were included in the study and whose treatment continued for at least one year. Significant decreases in annual relapse rate (p < 0.001), Expanded Disability Status Scale (p < 0.001) and neuroimaging findings (p < 0.001) were observed. While 64% of the patients were satisfied and 71.5% were found to adherent with this FO-FTY.Conclusion: This multicenter retrospective study found that the efficacy, safety and treatment adherence of a prescribed FO-FTY were consistent with the results of real-world studies. Studies including real-world data may provide guidance to address issues related to FO-FTY use.
dc.identifier.doi10.1016/j.msard.2023.104880
dc.identifier.issn2211-0348
dc.identifier.scopus2-s2.0-85165251046
dc.identifier.urihttps://doi.org/10.1016/j.msard.2023.104880
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S2211034823003814?via%3Dihub
dc.identifier.urihttps://hdl.handle.net/11452/48217
dc.identifier.volume77
dc.identifier.wos001039758400001
dc.indexed.wosWOS.SCI
dc.language.isoen
dc.publisherElsevier Sci Ltd
dc.relation.journalMultiple Sclerosis and Related Disorders
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectOral fingolimod
dc.subjectMulticenter
dc.subjectEfficacy
dc.subjectQuality
dc.subjectSafety
dc.subjectFollow-on drug
dc.subjectGeneric fingolimod
dc.subjectReal-world data
dc.subjectEfficacy
dc.subjectSafety
dc.subjectSatisfaction
dc.subjectAdherence
dc.subjectNeurosciences & neurology
dc.titleUse of follow-on fingolimod for multiple sclerosis: Analysis of effectiveness and patient reported outcomes in a real-world clinical setting
dc.typeArticle
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Nöroloji Ana Bilim Dalı
local.indexed.atWOS
local.indexed.atScopus
relation.isAuthorOfPublication75b4302d-5005-4298-900e-7a9e16afa9e2
relation.isAuthorOfPublication.latestForDiscovery75b4302d-5005-4298-900e-7a9e16afa9e2

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