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dc.rights.licenseopenen_US
dc.contributor.authorSTRIZZOLO, Rémi
hal.structure.identifierImmunology from Concept and Experiments to Translation = Immunologie Conceptuelle, Expérimentale et Translationnelle [ImmunoConcept]
dc.contributor.authorSENESCHAL, Julien
dc.contributor.authorSORIA, Angèle
dc.contributor.authorSTAUMONT-SALLÉ, Delphine
dc.contributor.authorBARBAROT, Sébastien
dc.contributor.authorVIGUIER, Manuelle
dc.contributor.authorJACHIET, Marie
dc.contributor.authorNOSBAUM, Audrey
dc.contributor.authorCLÉMENT, Aude
dc.contributor.authorTAUBER, Marie
dc.contributor.authorMALLET, Stéphanie
dc.contributor.authorDU-THANH, Aurélie
dc.date.accessioned2025-01-16T15:00:23Z
dc.date.available2025-01-16T15:00:23Z
dc.date.issued2024-07
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/204327
dc.description.abstractEnn patients with moderate to severe atopic dermatitis (AD) showing an inadequate response to dupilumab 300mg/2weeks, few real-life studies reported the response to alternative regimen maintaining dupilumab. To assess and analyze the response to an increased dose of dupilumab or its combination with cyclosporin A (CsA), methotrexate (MTX), or itraconazole (ITRA), all adult AD patients from 7 French University Hospitals were retrospectively included if they achieved an inadequate response to dupilumab 300mg/2weeks and were subsequently treated with an increased dose of dupilumab (300mg every 7 or 10 days), or a combination of dupilumab 300mg/2weeks with CsA, MTX or ITRA. The response after 3 months, along with epidemiological, clinical, and therapeutic baseline characteristics, were collected. Overall, 68.75% of the 48 included patients achieved an improved response, including 45.8% of complete response (CR). No strategy proved significantly better. Patients showing an initial no response never achieved a further CR versus 52.4% of patients with an initial partial response (p = 0.025). Digestive intolerance and tachycardia led to MTX and ITRA discontinuation in 3 patients. Increasing the dose of dupilumab or combining it with CsA, MTX, or ITRA could be alternative and safe options, to be evaluated in further medico-economic studies.
dc.language.isoENen_US
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
dc.subject.enDermatitis
dc.subject.enAtopic
dc.subject.enDupilumab
dc.subject.enCyclosporine
dc.subject.enMethotrexate
dc.subject.enItraconazole
dc.title.enReal-life management of atopic dermatitis patients with an inadequate response to on-label use of dupilumab
dc.typeArticle de revueen_US
dc.identifier.doi10.1016/j.waojou.2024.100923en_US
dc.subject.halSciences du Vivant [q-bio]/Immunologieen_US
dc.identifier.pubmed39157196en_US
bordeaux.journalWorld Allergy Organization Journalen_US
bordeaux.volume17en_US
bordeaux.hal.laboratoriesImmunoConcEpT - UMR 5164en_US
bordeaux.issue7en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exportfalse
dc.rights.ccCC BY-NC-NDen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=World%20Allergy%20Organization%20Journal&rft.date=2024-07&rft.volume=17&rft.issue=7&rft.au=STRIZZOLO,%20R%C3%A9mi&SENESCHAL,%20Julien&SORIA,%20Ang%C3%A8le&STAUMONT-SALL%C3%89,%20Delphine&BARBAROT,%20S%C3%A9bastien&rft.genre=article


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