| dc.contributor | Hospital General de Granollers |
| dc.contributor.author | Rivera-Díaz, R |
| dc.contributor.author | Pozo, T |
| dc.contributor.author | Alfageme, F |
| dc.contributor.author | Díaz Ley, B |
| dc.contributor.author | Osorio G.F |
| dc.contributor.author | Chico, R |
| dc.contributor.author | Romaní, Jorge |
| dc.date.accessioned | 2024-03-12T09:15:35Z |
| dc.date.available | 2024-03-12T09:15:35Z |
| dc.date.issued | 2023-10 |
| dc.identifier.citation | Rivera-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.uri | https://hdl.handle.net/11351/11181 |
| dc.description | Biologics; Hidradenitis suppurativa; Guselkumab |
| dc.description.abstract | Background: 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.iso | eng |
| dc.publisher | Elsevier España |
| dc.relation.ispartofseries | Actas Dermo-Sifiliográficas;114(9) |
| dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 International |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ |
| dc.source | Scientia |
| dc.subject | Pell - Malalties |
| dc.subject | Medicaments - Eficàcia |
| dc.subject | Medicaments dermatològics |
| dc.subject.mesh | Hidradenitis Suppurativa |
| dc.subject.mesh | Biological Products |
| dc.subject.mesh | Retrospective Studies |
| dc.title | The Effectiveness of Guselkumab in Patients With Hidradenitis Suppurativa Under Clinical Practice Conditions: A Spanish Multicentre Retrospective Study |
| dc.title.alternative | Efectividad de guselkumab en pacientes con hidradenitis supurativa en condiciones de práctica clínica: estudio retrospectivo y multicéntrico en España |
| dc.type | info:eu-repo/semantics/article |
| dc.identifier.doi | 10.1016/j.ad.2023.06.013 |
| dc.subject.decs | hidradenitis supurada |
| dc.subject.decs | productos biológicos |
| dc.subject.decs | estudios retrospectivos |
| dc.relation.publishversion | https://doi.org/10.1016/j.ad.2023.06.013 |
| dc.type.version | info:eu-repo/semantics/publishedVersion |
| dc.audience | Professionals |
| 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.pmid | 37331620 |
| dc.rights.accessrights | info:eu-repo/semantics/openAccess |