Predictive factors for early super response to bimekizumab in 341 patients with psoriasis-a 24-week short-term multicenter real-life experience

dc.contributor.authorCetinarslan, Tubanur
dc.contributor.authorMergen, Muhammed Ali
dc.contributor.authorTurel Ermertcan, Aylin
dc.contributor.authorBülbül Başkan, Emel
dc.contributor.authorYazici, Serkan
dc.contributor.authorAn, Isa
dc.contributor.authorGurel, Gulhan
dc.date.accessioned2025-11-16T19:33:58Z
dc.date.issued2025
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractPurpose/Aim of the study: The efficacy of bimekizumab was shown in moderate to severe plaque psoriasis. The aim of this study was to investigate the early super responder (ESR) profile (at week 4) to bimekizumab. Materials and Methods: We performed a multicenter retrospective study in 20 Dermatology outpatient clinics in Turkey. Adult patients with moderate-to-severe psoriasis who were under bimekizumab for at least 12 weeks were enrolled.Results:A total of 341 adult patients were included. 136 had nail psoriasis (39.9%), 148 had psoriatic arthritis (PsA) (43.4%), 223 (65.4%) had at least one difficult-to-treat area involvement, 155 (45.5%) were bio-naive, 110 (32.5%) had >= 2 biologics history. At week 4, PASI75 was achieved in 144 patients (49.8%), PASI90 was achieved in 88 patients (30.4%), PASI100 was achieved in 51 patients (17.6%). Family history (p = 0.041), palmoplantar involvement (p = 0.008), PsA (p = 0.097), and bio-experienced status (p = 0.060) were associated with lower odds of being an ESR, whereas each 1-point increase in baseline PASI was associated with significantly lower odds of ESR (p < 0.001). Gender, age, disease duration, history of conventional systemic treatment, and presence of any comorbidity were not significantly associated with the likelihood of being an ESR (all p > 0.05). Conclusion: Bimekizumab is the effective treatment in both bio-naive and bio-experienced patients; however, it may have a more rapid onset of action in bionaive patients. Further studies are needed on the long-term efficacy and safety data of bimekizumab.
dc.identifier.doi10.1080/09546634.2025.2563657
dc.identifier.issn0954-6634
dc.identifier.issn1471-1753
dc.identifier.issue1
dc.identifier.pmid41031572
dc.identifier.urihttps://doi.org/10.1080/09546634.2025.2563657
dc.identifier.urihttps://hdl.handle.net/20.500.14730/15207
dc.identifier.volume36
dc.identifier.wosWOS:001586585200001
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherTaylor & Francis Ltd
dc.relation.ispartofJournal of Dermatological Treatment
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WOS_20250302
dc.subjectPsoriasis
dc.subjectbimekizumab
dc.subjectsuper responder
dc.subjectbiologics
dc.subjectcandidiasis
dc.titlePredictive factors for early super response to bimekizumab in 341 patients with psoriasis-a 24-week short-term multicenter real-life experience
dc.typeArticle

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