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dc.contributor.authorSpelman, Tim
dc.contributor.authorKalincik, Tomas
dc.contributor.authorJokubaitis, Vilija
dc.contributor.authorZhang, Annie
dc.contributor.authorPellegrini, Fabio
dc.contributor.authorWiendl, Heinz
dc.contributor.authorLechner-Scott, Jeannette
dc.date.accessioned2020-06-21T13:33:34Z
dc.date.available2020-06-21T13:33:34Z
dc.date.issued2016
dc.identifier.issn2163-0402
dc.identifier.issn2163-0933
dc.identifier.urihttps://doi.org/10.1212/CPJ.0000000000000227
dc.identifier.urihttps://hdl.handle.net/20.500.12712/13384
dc.descriptionJokubaitis, Vilija G./0000-0002-3942-4340; pietrolongo, erika/0000-0002-6311-5994; Horakova, Dana/0000-0003-1915-0036; Lugaresi, Alessandra/0000-0003-2902-5589; Belachew, Shibeshih/0000-0003-3976-1950; Havrdova, Eva Kubala/0000-0002-9543-4359; Trojano, Maria/0000-0002-6329-8946; Butzkueven, Helmut/0000-0003-3940-8727; Kalincik, Tomas/0000-0003-3778-1376; pucci, eugenio/0000-0001-7606-7330en_US
dc.descriptionWOS: 000392602400009en_US
dc.description.abstractBackground: We compared efficacy and treatment persistence in treatment-naive patients with relapsing-remitting multiple sclerosis (RRMS) initiating natalizumab compared with interferon-beta (IFN-beta)/glatiramer acetate (GA) therapies, using propensity score-matched cohorts from observational multiple sclerosis registries. Methods: The study population initiated IFN-beta/GA in the MSBase Registry or natalizumab in the Tysabri Observational Program, had >= 3 months of on-treatment follow-up, and had active RRMS, defined as >= 1 gadolinium-enhancing lesion on cerebral MRI at baseline or >= 1 relapse within the 12 months prior to baseline. Baseline demographics and disease characteristics were balanced between propensity-matched groups. Annualized relapse rate (ARR), time to first relapse, treatment persistence, and disability outcomes were compared between matched treatment arms in the total population (n = 366/group) and subgroups with higher baseline disease activity. Results: First-line natalizumab was associated with a 68% relative reduction in ARR from a mean (SD) of 0.63 (0.92) on IFN-beta/GA to 0.20 (0.63) (p [signed-rank] < 0.0001), a 64% reduction in the rate of first relapse (hazard ratio [HR] 0.36, 95% confidence interval [CI] 0.28-0.47; p < 0.001), and a 27% reduction in the rate of discontinuation (HR 0.73, 95% CI 0.58-0.93; p = 0.01), compared with first-line IFN-beta/GA therapy. Confirmed disability progression and area under the Expanded Disability Status Scale-time curve analyses were not significant. Similar relapse and treatment persistence results were observed in each of the higher disease activity subgroups. Conclusions: This study provides Class IV evidence that first-line natalizumab for RRMS improves relapse and treatment persistence outcomes compared to first-line IFN-beta/GA. This needs to be balanced against the risk of progressive multifocal leukoencephalopathy in natalizumab-treated patients. Classification of evidence: This study provides Class IV evidence that first-line natalizumab for RRMS improves relapse rates and treatment persistence outcomes compared to first-line IFN-beta/GA.en_US
dc.description.sponsorshipNHMRCNational Health and Medical Research Council of Australia [628856, 1071124, 1032484, 1083539]; NHMRC Center for Research ExcellenceNational Health and Medical Research Council of Australia [1001216]; MSBase Foundation; Merck SeronoMerck SeronoMerck & Company; BiogenBiogen; Novartis Pharma; Bayer-ScheringBayer AG; Sanofi-AventisSanofi-Aventis; BioCSL; Czech Ministry of EducationMinistry of Education, Youth & Sports - Czech Republic [PRVOUK-P26/LF1/4]en_US
dc.description.sponsorshipSupported by the NHMRC Career Development Award (Clinical) to H.B. (ID628856), NHMRC Early Career Fellowship (1071124), NHMRC Project Grants (1032484 and 1083539), NHMRC Center for Research Excellence (Grant ID 1001216), and the MSBase Foundation. The MSBase Foundation is a not-for-profit organization that receives support from Merck Serono, Biogen, Novartis Pharma, Bayer-Schering, Sanofi-Aventis, and BioCSL. The Tysabri Observational Program is fully funded by Biogen. E. Havrdova and D. Horakova have been supported by Research Grant of Czech Ministry of Education, PRVOUK-P26/LF1/4.en_US
dc.language.isoengen_US
dc.publisherLippincott Williams & Wilkinsen_US
dc.relation.isversionof10.1212/CPJ.0000000000000227en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleComparative efficacy of first-line natalizumab vs IFN-beta or glatiramer acetate in relapsing MSen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume6en_US
dc.identifier.issue2en_US
dc.identifier.startpage102en_US
dc.identifier.endpage115en_US
dc.relation.journalNeurology-Clinical Practiceen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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