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dc.rights.licenseopenen_US
dc.contributor.authorDUPONT, A.
dc.contributor.authorEYRAUD, A.
dc.contributor.authorMILPIED, B.
dc.contributor.authorDE BATAILLE, S.
dc.contributor.authorCASASSA, E.
dc.contributor.authorDARRIGADE, A.-S.
dc.contributor.authorBARNETCHE, T.
dc.contributor.authorDOUTRE, M.-S.
dc.contributor.authorMATARD, B.
dc.contributor.authorBEYLOT-BARRY, M.
hal.structure.identifierImmunology from Concept and Experiments to Translation = Immunologie Conceptuelle, Expérimentale et Translationnelle [ImmunoConcept]
dc.contributor.authorSENESCHAL, Julien
dc.date.accessioned2024-09-23T14:08:26Z
dc.date.available2024-09-23T14:08:26Z
dc.date.issued2023
dc.identifier.issn0001-5555en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/201748
dc.description.abstractEnFolliculitis decalvans is a chronic inflammatory skin disease leading to scarring alopecia. Management of this disabling disease is difficult and no treatment is currently approved. Current knowledge regarding the pathogenesis of folliculitis decalvans suggests the benefit of using anti-tumour necrosis factor-α. This pilot study aimed to evaluate the clinical efficacy of anti-tumour necrosis factor-α for management of folliculi-tis decalvans. A single-centre retrospective pilot study included patients with refractory folliculitis decalvans treated by tumour necrosis factor-α inhibitors. An Investigator’s Global Assessment (IGA) score was de-signed and validated to assess the efficacy of the th-erapy. Response to treatment was considered good to excellent when an IGA ≤ 2 was obtained at month 12. Eleven patients were included, with a mean time from diagnosis of folliculitis decalvans to the introduction of infliximab (n = 9) or adalimumab (n = 2) of 8.55 ± 1.26 years. Nine patients had failed on at least 2 lines of systemic therapies before starting anti-tumour necrosis factor-α. The median IGA score at baseline was 3. At the end of follow-up, 5 patients were considered responders. Overall, the safety profile of anti-tumour necrosis factor-α was good. The results suggest that the clinical benefit of anti-tumour necrosis factor-α is obtained after at least 6 months of treatment. How-ever, further prospective studies are needed to con-firm these results.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enFolliculitis decalvans
dc.subject.enInfliximab
dc.subject.enAdalimumab; TNFα inhibitors
dc.subject.enCicatricial alopecia
dc.title.enEfficacy and Safety of Tumour Necrosis Factor-α Antagonists for Folliculitis Decalvans: A Retrospective Case-series Pilot Study
dc.typeArticle de revueen_US
dc.identifier.doi10.2340/actadv.v103.3713en_US
dc.subject.halSciences du Vivant [q-bio]/Immunologieen_US
dc.identifier.pubmed36987539en_US
bordeaux.journalActa Dermato-Venereologicaen_US
bordeaux.volume103en_US
bordeaux.hal.laboratoriesImmunoConcEpT - UMR 5164en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-04706391
hal.version1
hal.date.transferred2024-09-23T14:08:29Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exporttrue
dc.rights.ccCC BYen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Acta%20Dermato-Venereologica&rft.date=2023&rft.volume=103&rft.eissn=0001-5555&rft.issn=0001-5555&rft.au=DUPONT,%20A.&EYRAUD,%20A.&MILPIED,%20B.&DE%20BATAILLE,%20S.&CASASSA,%20E.&rft.genre=article


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