Please use this identifier to cite or link to this item:
http://hdl.handle.net/10553/127335
DC Field | Value | Language |
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dc.contributor.author | López-Sanromán, A | en_US |
dc.contributor.author | Vera-Mendoza, I | en_US |
dc.contributor.author | Domènech, E | en_US |
dc.contributor.author | Taxonera, C | en_US |
dc.contributor.author | Ruiz, VV | en_US |
dc.contributor.author | Marín-Jiménez, I | en_US |
dc.contributor.author | Guardiola, J | en_US |
dc.contributor.author | Castro, L | en_US |
dc.contributor.author | Esteve, M | en_US |
dc.contributor.author | Iglesias, E | en_US |
dc.contributor.author | Ceballos Santos, Daniel Sebastián | en_US |
dc.contributor.author | Martínez-Montiel, P | en_US |
dc.contributor.author | Gisbert, JP | en_US |
dc.contributor.author | Mínguez, M | en_US |
dc.contributor.author | Echarri, A | en_US |
dc.contributor.author | Calvet, X | en_US |
dc.contributor.author | Barrio, J | en_US |
dc.contributor.author | Hinojosa, J | en_US |
dc.contributor.author | Martín-Arranz, MD | en_US |
dc.contributor.author | Márquez-Mosquera, L | en_US |
dc.contributor.author | Bermejo, F | en_US |
dc.contributor.author | Rimola, J | en_US |
dc.contributor.author | Pons, V | en_US |
dc.contributor.author | Nos, P | en_US |
dc.date.accessioned | 2023-10-20T13:10:51Z | - |
dc.date.available | 2023-10-20T13:10:51Z | - |
dc.date.issued | 2017 | en_US |
dc.identifier.issn | 1873-9946 | en_US |
dc.identifier.uri | http://hdl.handle.net/10553/127335 | - |
dc.description.abstract | Background 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.language | eng | en_US |
dc.relation.ispartof | Journal of Crohn's and Colitis | en_US |
dc.source | Journal of Crohn's and Colitis [1873-9946], v. 11(11), pp. 1293-1301 (Octubre 2017) | en_US |
dc.subject | 32 Ciencias médicas | en_US |
dc.subject | 3205 Medicina interna | en_US |
dc.subject | 3208 Farmacodinámica | en_US |
dc.subject.other | Crohn's disease | en_US |
dc.subject.other | Azathioprine | en_US |
dc.subject.other | Adalimumab | en_US |
dc.title | Adalimumab vs Azathioprine in the Prevention of Postoperative Crohn's Disease Recurrence. A GETECCU Randomised Trial | en_US |
dc.type | info:eu-repo/semantics/Article | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1093/ecco-jcc/jjx051 | en_US |
dc.identifier.pmid | 28402454 | - |
dc.identifier.scopus | 2-s2.0-85033383027 | - |
dc.identifier.isi | WOS:000416121200002 | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
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dc.contributor.orcid | #NODATA# | - |
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dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.contributor.orcid | #NODATA# | - |
dc.description.lastpage | 1301 | en_US |
dc.identifier.issue | 11 | - |
dc.description.firstpage | 1293 | en_US |
dc.relation.volume | 11 | en_US |
dc.investigacion | Ciencias de la Salud | en_US |
dc.type2 | Artículo | en_US |
dc.description.numberofpages | 9 | en_US |
dc.utils.revision | Sí | en_US |
dc.date.coverdate | Octubre 2017 | en_US |
dc.identifier.ulpgc | Sí | en_US |
dc.contributor.buulpgc | BU-MED | en_US |
dc.description.sjr | 2,728 | |
dc.description.jcr | 6,637 | |
dc.description.sjrq | Q1 | |
dc.description.jcrq | Q1 | |
dc.description.scie | SCIE | |
item.grantfulltext | none | - |
item.fulltext | Sin texto completo | - |
crisitem.author.dept | Departamento de Ciencias Médicas y Quirúrgicas | - |
crisitem.author.orcid | 0000-0003-2384-4524 | - |
crisitem.author.fullName | Ceballos Santos, Daniel Sebastián | - |
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