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dc.contributorHospital General de Granollers
dc.contributor.authorRivera-Díaz, R
dc.contributor.authorPozo, T
dc.contributor.authorAlfageme, F
dc.contributor.authorDíaz Ley, B
dc.contributor.authorOsorio G.F
dc.contributor.authorChico, R
dc.contributor.authorRomaní, Jorge
dc.date.accessioned2024-03-12T09:15:35Z
dc.date.available2024-03-12T09:15:35Z
dc.date.issued2023-10
dc.identifier.citationRivera-Díaz R, Pozo T, Alfageme F, Díaz Ley B, Osorio GF, Chico R, et al. The Effectiveness of Guselkumab in Patients With Hidradenitis Suppurativa Under Clinical Practice Conditions: A Spanish Multicentre Retrospective Study. Actas Dermosifiliogr. 2023 Oct;114(9):755-762.
dc.identifier.urihttps://hdl.handle.net/11351/11181
dc.descriptionBiologics; Hidradenitis suppurativa; Guselkumab
dc.description.abstractBackground: Hidradenitis suppurativa (HS) is a chronic skin condition causing lesions in which high levels of interleukin (IL)-23 and T-helper 17 cells are found. Adalimumab remains the only approved treatment. Guselkumab, an antibody targeting the p19 protein subunit of extracellular IL-23, is approved for the treatment of moderate-severe psoriasis, but evidence on its efficacy in treating HS is limited. Objectives: To assess the effectiveness and safety of guselkumab in treating moderate-severe HS under clinical practice conditions. Methods: A multicentre retrospective observational study was carried out in 13 Spanish Hospitals including adult HS patients treated with guselkumab within a compassionate use programme (March 2020-March 2022). Data referred to patient demographic and clinical characteristics at treatment initiation (baseline), patient-reported outcomes (Numerical Pain Rating Scale [NPRS] and Dermatology Life Quality Index [DLQI]), physician scores (International Hidradenitis Suppurativa Severity Score System [IHS4], HS Physical Global Score [HS-PGA] and Hidradenitis Suppurativa Clinical Response [HiSCR]) were recorded at baseline and at 16, 24, and 48 weeks of treatment. Results: A total of 69 patients were included. Most (84.10%) had severe HS (Hurley III) and had been diagnosed for over ten years (58.80%). The patients had been subjected to multiple non-biological (mean 3.56) or biological (mean 1.78) therapies, and almost 90% of those treated with biologics had received adalimumab. A significant decrease in IHS4, HS-PGA, NPRS, and DLQI scores was observed from baseline to 48 weeks of guselkumab treatment (all p<0.01). HiSCR was achieved in 58.33% and 56.52% of the patients at 16 and 24 weeks, respectively. Overall, 16 patients discontinued treatment, mostly due to inefficacy (n=7) or loss of efficacy (n=3). No serious adverse events were observed. Conclusions: Our results indicate that guselkumab may be a safe and effective therapeutic alternative for patients with severe HS that fail to respond to other biologics.
dc.language.isoeng
dc.publisherElsevier España
dc.relation.ispartofseriesActas Dermo-Sifiliográficas;114(9)
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScientia
dc.subjectPell - Malalties
dc.subjectMedicaments - Eficàcia
dc.subjectMedicaments dermatològics
dc.subject.meshHidradenitis Suppurativa
dc.subject.meshBiological Products
dc.subject.meshRetrospective Studies
dc.titleThe Effectiveness of Guselkumab in Patients With Hidradenitis Suppurativa Under Clinical Practice Conditions: A Spanish Multicentre Retrospective Study
dc.title.alternativeEfectividad de guselkumab en pacientes con hidradenitis supurativa en condiciones de práctica clínica: estudio retrospectivo y multicéntrico en España
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/j.ad.2023.06.013
dc.subject.decshidradenitis supurada
dc.subject.decsproductos biológicos
dc.subject.decsestudios retrospectivos
dc.relation.publishversionhttps://doi.org/10.1016/j.ad.2023.06.013
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.authoraffiliation[Rivera-Díaz R] Department of Dermatology, Hospital Universitario 12 de Octubre, Universidad Complutense, Madrid, Spain. [ Pozo T] Department of Dermatology, Hospital Rio Hortega, Valladolid, Spain. [Alfageme F] Department of Dermatology, Hospital Universitario Puerta de Hierro Majadahonda, Madrid,Spain. [Díaz Ley B] Department of Dermatology, Hospital Universitario del Sureste, Arganda, Madrid, Spain. [Osorio GF] Department of Dermatology, Hospital Universitario Virgen del Rocío, Universidad de Sevilla, Sevilla, Spain. [Chico R] Department of Dermatology, Hospital Infanta Sofía, Alcobendas, Madrid, Spain. [Romaní J] Department of Dermatology, Hospital General de Granollers, Granollers, Spain
dc.identifier.pmid37331620
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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