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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1093/ibd/izz192</dc:identifier><dc:language>eng</dc:language><dc:creator>Casanova, M.J.</dc:creator><dc:creator>Chaparro, M.</dc:creator><dc:creator>Mínguez, M.</dc:creator><dc:creator>Ricart, E.</dc:creator><dc:creator>Taxonera, C.</dc:creator><dc:creator>García-López, S.</dc:creator><dc:creator>Guardiola, J.</dc:creator><dc:creator>López-San Román, A.</dc:creator><dc:creator>Iglesias, E.</dc:creator><dc:creator>Beltrán, B.</dc:creator><dc:creator>Sicilia, B.</dc:creator><dc:creator>Vera, M.I.</dc:creator><dc:creator>Hinojosa, J.</dc:creator><dc:creator>Riestra, S.</dc:creator><dc:creator>Domènech, E.</dc:creator><dc:creator>Calvet, X.</dc:creator><dc:creator>Pérez-Calle, J.L.</dc:creator><dc:creator>Martín-Arranz, M.D.</dc:creator><dc:creator>Aldeguer, X.</dc:creator><dc:creator>Rivero, M.</dc:creator><dc:creator>Monfort, D.</dc:creator><dc:creator>Barrio, J.</dc:creator><dc:creator>Esteve, M.</dc:creator><dc:creator>Márquez, L.</dc:creator><dc:creator>Lorente, R.</dc:creator><dc:creator>García-Planella, E.</dc:creator><dc:creator>De Castro, L.</dc:creator><dc:creator>Bermejo, F.</dc:creator><dc:creator>Merino, O.</dc:creator><dc:creator>Rodríguez-Pérez, A.</dc:creator><dc:creator>Martínez-Montiel, P.</dc:creator><dc:creator>Van Domselaar, M.</dc:creator><dc:creator>Alcaín, G.</dc:creator><dc:creator>Domínguez-Cajal, M.</dc:creator><dc:creator>Muñoz, C.</dc:creator><dc:creator>Gomollón, F.</dc:creator><dc:creator>Fernández-Salazar, L.</dc:creator><dc:creator>García-Sepulcre, M.F.</dc:creator><dc:creator>Rodríguez-Lago, I.</dc:creator><dc:creator>Gutiérrez, A.</dc:creator><dc:creator>Argüelles-Arias, F.</dc:creator><dc:creator>Rodriguez, C.</dc:creator><dc:creator>Rodríguez, G.E.</dc:creator><dc:creator>Bujanda, L.</dc:creator><dc:creator>Llaó, J.</dc:creator><dc:creator>Varela, P.</dc:creator><dc:creator>Ramos, L.</dc:creator><dc:creator>Huguet, J.M.</dc:creator><dc:creator>Almela, P.</dc:creator><dc:creator>Romero, P.</dc:creator><dc:creator>Navarro-Llavat, M.</dc:creator><dc:creator>Abad, Á.</dc:creator><dc:creator>Ramírez-De La Piscina, P.</dc:creator><dc:creator>Lucendo, A.J.</dc:creator><dc:creator>Sesé, E.</dc:creator><dc:creator>Madrigal, R.E.</dc:creator><dc:creator>Charro, M.</dc:creator><dc:creator>García-Herola, A.</dc:creator><dc:creator>Pajares, R.</dc:creator><dc:creator>Khorrami, S.</dc:creator><dc:creator>Gisbert, J.P.</dc:creator><dc:title>Effectiveness and Safety of the Sequential Use of a Second and Third Anti-TNF Agent in Patients with Inflammatory Bowel Disease: Results from the Eneida Registry</dc:title><dc:identifier>ART-2020-117227</dc:identifier><dc:description>Background: The effectiveness of the switch to another anti-tumor necrosis factor (anti-TNF) agent is not known. The aim of this study was to analyze the effectiveness and safety of treatment with a second and third anti-TNF drug after intolerance to or failure of a previous anti-TNF agent in inflammatory bowel disease (IBD) patients. Methods: We included patients diagnosed with IBD from the ENEIDA registry who received another anti-TNF after intolerance to or failure of a prior anti-TNF agent. Results: A total of 1122 patients were included. In the short term, remission was achieved in 55% of the patients with the second anti-TNF. The incidence of loss of response was 19% per patient-year with the second anti-TNF. Combination therapy (hazard ratio [HR], 2.4; 95% confidence interval [CI], 1.8-3; P &lt; 0.0001) and ulcerative colitis vs Crohn''s disease (HR, 1.6; 95% CI, 1.1-2.1; P = 0.005) were associated with a higher probability of loss of response. Fifteen percent of the patients had adverse events, and 10% had to discontinue the second anti-TNF. Of the 71 patients who received a third anti-TNF, 55% achieved remission. The incidence of loss of response was 22% per patient-year with a third anti-TNF. Adverse events occurred in 7 patients (11%), but only 1 stopped the drug. Conclusions: Approximately half of the patients who received a second anti-TNF achieved remission; nevertheless, a significant proportion of them subsequently lost response. Combination therapy and type of IBD were associated with loss of response. Remission was achieved in almost 50% of patients who received a third anti-TNF; nevertheless, a significant proportion of them subsequently lost response.</dc:description><dc:date>2020</dc:date><dc:source>http://zaguan.unizar.es/record/95040</dc:source><dc:doi>10.1093/ibd/izz192</dc:doi><dc:identifier>http://zaguan.unizar.es/record/95040</dc:identifier><dc:identifier>oai:zaguan.unizar.es:95040</dc:identifier><dc:identifier.citation>INFLAMMATORY BOWEL DISEASES 26, 4 (2020), 606-616</dc:identifier.citation><dc:rights>All rights reserved</dc:rights><dc:rights>http://www.europeana.eu/rights/rr-f/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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