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dc.contributor.authorGenovese, M. C.
dc.contributor.authorvan der Heijde, D.
dc.contributor.authorLin, Y.
dc.contributor.authorSt John, G.
dc.contributor.authorWang, S.
dc.contributor.authorvan Hoogstraten, H.
dc.contributor.authorGómez-Reino Carnota, Juan Jesús 
dc.contributor.authorKivitz, A.
dc.contributor.authorMaldonado-Cocco, J. A.
dc.contributor.authorSeriolo, B.
dc.contributor.authorStanislav, M.
dc.contributor.authorBurmester, G. R.
dc.date.accessioned2021-10-07T08:56:28Z
dc.date.available2021-10-07T08:56:28Z
dc.date.issued2019
dc.identifier.issn2056-5933
dc.identifier.otherhttps://www.ncbi.nlm.nih.gov/pubmed/31452928es
dc.identifier.urihttp://hdl.handle.net/20.500.11940/15467
dc.description.abstractObjective: In MOBILITY (NCT01061736), sarilumab significantly reduced disease activity, improved physical function and inhibited radiographic progression at week 52 versus placebo in patients with rheumatoid arthritis (RA) and an inadequate response to methotrexate. We report 5-year safety, efficacy and radiographic outcomes of sarilumab from NCT01061736 and the open-label extension (EXTEND; NCT01146652), in which patients received sarilumab 200 mg every 2 weeks (q2w) + methotrexate. Methods: Patients (n=1197) with moderately to severely active RA were initially randomised to placebo, sarilumab 150 mg or sarilumab 200 mg subcutaneously q2w plus weekly methotrexate for 52 weeks. Completers were eligible to enrol in the open-label extension and receive sarilumab 200 mg q2w + methotrexate. Results: Overall, 901 patients entered the open-label extension. The safety profile remained stable over 5-year follow-up and consistent with interleukin-6 receptor blockade. Absolute neutrophil count <1000 cells/mm(3) was observed but not associated with increased infection rate. Initial treatment with sarilumab 200 mg + methotrexate was associated with reduced radiographic progression over 5 years versus sarilumab 150 mg + methotrexate or placebo + methotrexate (mean+/-SE change from baseline in van der Heijde-modified Total Sharp Score: 1.46+/-0.27, 2.35+/-0.28 and 3.68+/-0.27, respectively (p<0.001 for each sarilumab dose versus placebo)). Clinical efficacy was sustained through 5 years according to Disease Activity Score (28-joint count) using C reactive protein, Clinical Disease Activity Index (CDAI) and Health Assessment Questionnaire-Disability Index. The number of patients achieving CDAI </=2.8 at 5 years was similar among initial randomisation groups (placebo, 76/398 (19%); sarilumab 150 mg, 68/400 (17%); sarilumab 200 mg, 84/399 (21%)). Conclusion: Clinical efficacy, including inhibition of radiographic progression, reduction in disease activity and improvement in physical function, was sustained with sarilumab + methotrexate over 5 years. Safety appeared stable over the 5-year period.en
dc.language.isoeng
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.meshArthritis, Rheumatoid
dc.subject.meshAntirheumatic Agents
dc.subject.meshAntibodies, Monoclonal, Humanized
dc.titleLong-term safety and efficacy of sarilumab plus methotrexate on disease activity, physical function and radiographic progression: 5 years of sarilumab plus methotrexate treatmentes
dc.typeArtigoes
dc.authorsophosGenovese, M. C.
dc.authorsophosvan der Heijde, D.
dc.authorsophosLin, Y.
dc.authorsophosSt John, G.
dc.authorsophosWang, S.
dc.authorsophosvan Hoogstraten, H.
dc.authorsophosGómez-Reino, J. J.
dc.authorsophosKivitz, A.
dc.authorsophosMaldonado-Cocco, J. A.
dc.authorsophosSeriolo, B.
dc.authorsophosStanislav, M.
dc.authorsophosBurmester, G. R.
dc.identifier.doi10.1136/rmdopen-2018-000887
dc.identifier.pmid31452928
dc.identifier.sophos30770
dc.issue.number2es
dc.journal.titleRMD Openes
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago de Compostela - Complexo Hospitalario Universitario de Santiago de Compostela::Reumatoloxía
dc.page.initiale000887es
dc.relation.publisherversionhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6691511/pdf/rmdopen-2018-000887.pdf
dc.rights.accessRightsopenAccess
dc.subject.keywordCHUS
dc.typefidesArtículo Científico (incluye Original, Original breve, Revisión Sistemática y Meta-análisis)
dc.typesophosArtículo Original
dc.volume.number5es


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