Use of follow-on fingolimod for multiple sclerosis: Analysis of effectiveness and patient reported outcomes in a real-world clinical setting
dc.authorid | Koseoglu, Mesrure/0000-0003-0469-0064 | |
dc.authorid | UNAL, Aysun/0000-0002-7702-8437 | |
dc.authorid | KOTAN, DILCAN/0000-0002-3101-4742 | |
dc.contributor.author | Altunan, Bengu | |
dc.contributor.author | Unal, Aysun | |
dc.contributor.author | Efendi, Husnu | |
dc.contributor.author | Koseoglu, Mesrure | |
dc.contributor.author | Terzi, Murat | |
dc.contributor.author | Kotan, Dilcan | |
dc.contributor.author | Tamam, Yusuf | |
dc.date.accessioned | 2024-10-29T17:58:28Z | |
dc.date.available | 2024-10-29T17:58:28Z | |
dc.date.issued | 2023 | |
dc.department | Tekirdağ Namık Kemal Üniversitesi | en_US |
dc.description.abstract | Background: 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. | en_US |
dc.identifier.doi | 10.1016/j.msard.2023.104880 | |
dc.identifier.issn | 2211-0348 | |
dc.identifier.issn | 2211-0356 | |
dc.identifier.pmid | 37459716 | en_US |
dc.identifier.scopus | 2-s2.0-85165251046 | en_US |
dc.identifier.uri | https://doi.org/10.1016/j.msard.2023.104880 | |
dc.identifier.uri | https://hdl.handle.net/20.500.11776/14335 | |
dc.identifier.volume | 77 | en_US |
dc.identifier.wos | WOS:001039758400001 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.publisher | Elsevier Sci Ltd | en_US |
dc.relation.ispartof | Multiple Sclerosis and Related Disorders | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Follow-on drug | en_US |
dc.subject | Generic fingolimod | en_US |
dc.subject | Real-world data | en_US |
dc.subject | Efficacy | en_US |
dc.subject | Safety | en_US |
dc.subject | Satisfaction | en_US |
dc.subject | Adherence | en_US |
dc.title | Use of follow-on fingolimod for multiple sclerosis: Analysis of effectiveness and patient reported outcomes in a real-world clinical setting | en_US |
dc.type | Article | en_US |