dc.contributor.author | Spelman, Tim | |
dc.contributor.author | Kalincik, Tomas | |
dc.contributor.author | Jokubaitis, Vilija | |
dc.contributor.author | Zhang, Annie | |
dc.contributor.author | Pellegrini, Fabio | |
dc.contributor.author | Wiendl, Heinz | |
dc.contributor.author | Lechner-Scott, Jeannette | |
dc.date.accessioned | 2020-06-21T13:33:34Z | |
dc.date.available | 2020-06-21T13:33:34Z | |
dc.date.issued | 2016 | |
dc.identifier.issn | 2163-0402 | |
dc.identifier.issn | 2163-0933 | |
dc.identifier.uri | https://doi.org/10.1212/CPJ.0000000000000227 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12712/13384 | |
dc.description | Jokubaitis, 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/0000-0001-7606-7330 | en_US |
dc.description | WOS: 000392602400009 | en_US |
dc.description.abstract | Background: 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.sponsorship | NHMRCNational 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.sponsorship | Supported 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.iso | eng | en_US |
dc.publisher | Lippincott Williams & Wilkins | en_US |
dc.relation.isversionof | 10.1212/CPJ.0000000000000227 | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.title | Comparative efficacy of first-line natalizumab vs IFN-beta or glatiramer acetate in relapsing MS | en_US |
dc.type | article | en_US |
dc.contributor.department | OMÜ | en_US |
dc.identifier.volume | 6 | en_US |
dc.identifier.issue | 2 | en_US |
dc.identifier.startpage | 102 | en_US |
dc.identifier.endpage | 115 | en_US |
dc.relation.journal | Neurology-Clinical Practice | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |