Abstract
Background: Scalp involvement in plaque psoriasis is challenging to treat. Objective: To evaluate the efficacy and safety of deucravacitinib (DEUC) in scalp psoriasis. Methods: POETYK PSO-1 and PSO-2 were global phase 3, 52-week, double-blinded trials in adults with moderate to severe psoriasis. Patients were randomized 1:2:1 to oral placebo, DEUC 6 mg once daily, or apremilast 30 mg twice daily. This pooled secondary analysis evaluated scalp-specific Physician Global Assessment score of 0 or 1 (0/1), ≥90% improvement from baseline in Psoriasis Scalp Severity Index, and change from baseline in Psoriasis Scalp Severity Index. Adverse events were evaluated through week 16. Results: Overall, 1084 patients with moderate to severe scalp psoriasis at baseline were included. At week 16, response rates were greater with DEUC versus placebo or apremilast for scalp-specific Physician Global Assessment 0/1 (64.0% vs 17.3% vs 37.7%; P < .0001), ≥90% improvement from baseline in Psoriasis Scalp Severity Index (50.6% vs 10.5% vs 26.1%; P < .0001), and change from baseline in Psoriasis Scalp Severity Index. Responses were maintained through 52 weeks with continuous DEUC. Safety was consistent with the entire study population. Limitations: Lack of data in milder scalp psoriasis. Conclusion: DEUC was significantly more efficacious than placebo or apremilast in improving moderate to severe scalp psoriasis and was well tolerated.
Original language | English |
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Pages (from-to) | 775-782 |
Number of pages | 8 |
Journal | Journal of the American Academy of Dermatology |
Volume | 90 |
Issue number | 4 |
DOIs | |
State | Published - Apr 2024 |
Keywords
- TYK2
- apremilast
- clinical trial
- deucravacitinib
- psoriasis
- scalp psoriasis
- tyrosine kinase 2