Relative Efficacy of Immunomodulatory Monotherapies for Psoriasis of the Scalp: A Network Meta‐Analysis Study

We are the first to provide comparative evidence on the efficacy of newly investigated agents such as deucravacitinib, tildrakizumab, roflumilast and icotrokinra. In general, the IL-17 inhibitors (bimekizumab, ixekizumab, secukinumab, brodalumab) and IL-23 inhibitors (icotrokinra, guselkumab, tildrakizumab) were effective depending upon the outcome and time-point being considered. At 16 weeks, for PSSI-100, ixekizumab 150 mg at weeks 0, 2, 4, 8, and 12 ranked highest; at 16 weeks, for Sc-PGA 0/1 bimekizumab 320 mg every 4 weeks ranked highest; at 8 weeks, for PSSI-100 ixekizumab 80 mg every 2 weeks ranked highest; at 8 weeks, for Sc-PGA 0/1 secukinumab 300 mg at weeks 1, 2, 3 and then every 4 weeks ranked highest. Small-molecule therapies (apremilast, deucravacitinib, roflumilast) improved scalp psoriasis modestly. Our work would guide the design of future studies and clinical decision-making.

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Publication Details

Journal
Journal of Cosmetic Dermatology
Published
2026-01-01
DOI
https://doi.org/10.1111/jocd.70662
Primary Topic
Psoriasis: Treatment and Pathogenesis
Type
article
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article

Relative Efficacy of Immunomodulatory Monotherapies for Psoriasis of the Scalp: A Network Meta‐Analysis Study

Vincent Piguet, Mary A. Bamimore, Mesbah Talukder, Tong Wang et al.
Journal of Cosmetic Dermatology
Psoriasis: Treatment and Pathogenesis
article

Relative Efficacy of Immunomodulatory Monotherapies for Psoriasis of the Scalp: A Network Meta‐Analysis Study

Vincent Piguet, Mary A. Bamimore, Mesbah Talukder, Tong Wang, Aditya Gupta
article en

Abstract

We are the first to provide comparative evidence on the efficacy of newly investigated agents such as deucravacitinib, tildrakizumab, roflumilast and icotrokinra. In general, the IL-17 inhibitors (bimekizumab, ixekizumab, secukinumab, brodalumab) and IL-23 inhibitors (icotrokinra, guselkumab, tildrakizumab) were effective depending upon the outcome and time-point being considered. At 16 weeks, for PSSI-100, ixekizumab 150 mg at weeks 0, 2, 4, 8, and 12 ranked highest; at 16 weeks, for Sc-PGA 0/1 bimekizumab 320 mg every 4 weeks ranked highest; at 8 weeks, for PSSI-100 ixekizumab 80 mg every 2 weeks ranked highest; at 8 weeks, for Sc-PGA 0/1 secukinumab 300 mg at weeks 1, 2, 3 and then every 4 weeks ranked highest. Small-molecule therapies (apremilast, deucravacitinib, roflumilast) improved scalp psoriasis modestly. Our work would guide the design of future studies and clinical decision-making.

Journal of Cosmetic DermatologyVol. 25(1)
University of Toronto (CA), Women's College Hospital (CA), Mediprobe Research (Canada) (CA), BRAC University (BD)
Openalex Percentile: Top 96%
Psoriasis: Treatment and Pathogenesis
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