Show simple item record

dc.contributor.authorCalderón-Goercke, Mónica
dc.contributor.authorLoricera García, Javier
dc.contributor.authorAldasoro, Vicente
dc.contributor.authorCastañeda, Santos
dc.contributor.authorVilla, Ignacio
dc.contributor.authorHumbría, Alicia
dc.contributor.authorMoriano, Clara
dc.contributor.authorRomero-Yuste, Susana
dc.contributor.authorNarváez, Javier
dc.contributor.authorGómez-Arango, Catalina
dc.contributor.authorPérez-Pampín, Eva
dc.contributor.authorMelero, Rafael
dc.contributor.authorPalmou Fontana, Natalia
dc.contributor.authorCalvo Río, Vanesa
dc.contributor.authorPrieto Peña, Diana
dc.contributor.authorGonzález Vela, María del Carmen 
dc.contributor.authorCorrales Martínez, Alfonso
dc.contributor.authorHernández Hernández, José Luis 
dc.contributor.authorGonzález-Gay Mantecón, Miguel Ángel 
dc.contributor.authorBlanco Alonso, Ricardo
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2019-08-01T16:26:07Z
dc.date.issued2019-08
dc.identifier.issn0049-0172
dc.identifier.issn1532-866X
dc.identifier.urihttp://hdl.handle.net/10902/16652
dc.description.abstractOBJECTIVE: Tocilizumab (TCZ) has shown efficacy in clinical trials on giant cell arteritis (GCA). Real-world data are scarce. Our objective was to assess efficacy and safety of TCZ in unselected patients with GCA in clinical practice Methods: Observational, open-label multicenter study from 40 national referral centers of GCA patients treated with TCZ due to inefficacy or adverse events of previous therapy. Outcomes variables were improvement of clinical features, acute phase reactants, glucocorticoid-sparing effect, prolonged remission and relapses. A comparative study was performed: (a) TCZ route (SC vs. IV); (b) GCA duration (?6 vs. >6 months); (c) serious infections (with or without); (d) ?15 vs. >15 mg/day at TCZ onset. RESULTS: 134 patients; mean age, 73.0 ± 8.8 years. TCZ was started after a median [IQR] time from GCA diagnosis of 13.5 [5.0-33.5] months. Ninety-eight (73.1%) patients had received immunosuppressive agents. After 1 month of TCZ 93.9% experienced clinical improvement. Reduction of CRP from 1.7 [0.4-3.2] to 0.11 [0.05-0.5] mg/dL (p < 0.0001), ESR from 33 [14.5-61] to 6 [2-12] mm/1st hour (p < 0.0001) and decrease in patients with anemia from 16.4% to 3.8% (p < 0.0001) were observed. Regardless of administration route or disease duration, clinical improvement leading to remission at 6, 12, 18, 24 months was observed in 55.5%, 70.4%, 69.2% and 90% of patients. Most relevant adverse side-effect was serious infections (10.6/100 patients-year), associated with higher doses of prednisone during the first three months of therapy. CONCLUSION: In clinical practice, TCZ yields a rapid and maintained improvement of refractory GCA. Serious infections appear to be higher than in clinical trials.es_ES
dc.format.extent10 p.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rights© 2019. This manuscript version is made available under the CC-BY-NC-ND 4.0 licensees_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.sourceSemin Arthritis Rheum. 2019 Aug;49(1):126-135es_ES
dc.subject.otherBiological Therapyes_ES
dc.subject.otherGiant Cell Arteritises_ES
dc.subject.otherLarge-Vessel Vasculitises_ES
dc.subject.otherTocilizumabes_ES
dc.titleTocilizumab in giant cell arteritis. Observational, open-label multicenter study of 134 patients in clinical practicees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1016/j.semarthrit.2019.01.003es_ES
dc.rights.accessRightsembargoedAccesses_ES
dc.identifier.DOI10.1016/j.semarthrit.2019.01.003
dc.type.versionacceptedVersiones_ES
dc.date.embargoEndDate2020-08-01


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record

© 2019. This manuscript version is made available under the CC-BY-NC-ND 4.0 licenseExcept where otherwise noted, this item's license is described as © 2019. This manuscript version is made available under the CC-BY-NC-ND 4.0 license