Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/127335
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dc.contributor.authorLópez-Sanromán, Aen_US
dc.contributor.authorVera-Mendoza, Ien_US
dc.contributor.authorDomènech, Een_US
dc.contributor.authorTaxonera, Cen_US
dc.contributor.authorRuiz, VVen_US
dc.contributor.authorMarín-Jiménez, Ien_US
dc.contributor.authorGuardiola, Jen_US
dc.contributor.authorCastro, Len_US
dc.contributor.authorEsteve, Men_US
dc.contributor.authorIglesias, Een_US
dc.contributor.authorCeballos Santos, Daniel Sebastiánen_US
dc.contributor.authorMartínez-Montiel, Pen_US
dc.contributor.authorGisbert, JPen_US
dc.contributor.authorMínguez, Men_US
dc.contributor.authorEcharri, Aen_US
dc.contributor.authorCalvet, Xen_US
dc.contributor.authorBarrio, Jen_US
dc.contributor.authorHinojosa, Jen_US
dc.contributor.authorMartín-Arranz, MDen_US
dc.contributor.authorMárquez-Mosquera, Len_US
dc.contributor.authorBermejo, Fen_US
dc.contributor.authorRimola, Jen_US
dc.contributor.authorPons, Ven_US
dc.contributor.authorNos, Pen_US
dc.date.accessioned2023-10-20T13:10:51Z-
dc.date.available2023-10-20T13:10:51Z-
dc.date.issued2017en_US
dc.identifier.issn1873-9946en_US
dc.identifier.urihttp://hdl.handle.net/10553/127335-
dc.description.abstractBackground and Aims: Postoperative recurrence of Crohn's disease [POR-CD] is almost certain if no prophylaxis is administered. Evidence for optimal treatment is lacking. Our aim was to compare the efficacy of adalimumab [ADA] and azathioprine [AZA] in this setting. Methods: We performed a phase 3, 52-week, multicentre, randomised, superiority study [APPRECIA], in which patients with ileocolonic resection were randomised either to ADA 160-80-40 mg subcutaneously [SC] or AZA 2.5 mg/kg/day, both associated with metronidazole. The primary endpoint was endoscopic recurrence at 1 year [Rutgeerts i2b, i3, i4], as evaluated by a blinded central reader. Results: We recruited 91 patients [median age 35.0 years, disease duration 6.0 years, 23.8% smokers, 7.1% previous resections]. The study drugs were administered to 84 patients. Treatment was discontinued owing to adverse events in 11 patients [13.1%]. Discontinuation was significantly less frequent in the ADA [4.4%] than in the AZA group [23.2%] (dif.: 18.6% [95% CI 4.1-33.2], p = 0.011). According to the intention-to-treat analysis, therapy failed in 23/39 patients in the AZA group [59%] and 19/45 patients in the ADA group [42.2%] [p = 0.12]. In the per-protocol analysis [61 patients with centrally evaluable images], recurrence was recorded in 8/24 [33.3%] patients in the AZA and 11/37 [29.7%] in the ADA group [p = 0.76]. No statistically significant differences between the groups were found for recurrence in magnetic resonance images, biological markers of activity, surgical procedures, or hospital admissions. Conclusions: ADA has not demonstrated a better efficacy than AZA [both associated with metronidazole] for prophylaxis of POR-CD in an unselected population, although tolerance to ADA is significantly better.en_US
dc.languageengen_US
dc.relation.ispartofJournal of Crohn's and Colitisen_US
dc.sourceJournal of Crohn's and Colitis [1873-9946], v. 11(11), pp. 1293-1301 (Octubre 2017)en_US
dc.subject32 Ciencias médicasen_US
dc.subject3205 Medicina internaen_US
dc.subject3208 Farmacodinámicaen_US
dc.subject.otherCrohn's diseaseen_US
dc.subject.otherAzathioprineen_US
dc.subject.otherAdalimumaben_US
dc.titleAdalimumab vs Azathioprine in the Prevention of Postoperative Crohn's Disease Recurrence. A GETECCU Randomised Trialen_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1093/ecco-jcc/jjx051en_US
dc.identifier.pmid28402454-
dc.identifier.scopus2-s2.0-85033383027-
dc.identifier.isiWOS:000416121200002-
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dc.description.lastpage1301en_US
dc.identifier.issue11-
dc.description.firstpage1293en_US
dc.relation.volume11en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.description.numberofpages9en_US
dc.utils.revisionen_US
dc.date.coverdateOctubre 2017en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.sjr2,728
dc.description.jcr6,637
dc.description.sjrqQ1
dc.description.jcrqQ1
dc.description.scieSCIE
item.fulltextSin texto completo-
item.grantfulltextnone-
crisitem.author.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.orcid0000-0003-2384-4524-
crisitem.author.fullNameCeballos Santos, Daniel Sebastián-
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