63449 Combined Skin Clearance and Quality of Life Response in Patients With Moderate-to-Severe Atopic Dermatitis With and Without Prior Systemic Exposure in the JADE Clinical Program
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Atopic dermatitis (AD) is characterized by eczematous skin lesions and impaired quality of life (QoL). This post hoc analysis included adults with moderate-to-severe AD who received abrocitinib (200/100 mg) or placebo as monotherapy (JADE MONO-1 NCT03349060]; MONO-2 NCT03575871]; 12 weeks), and abrocitinib or dupilumab 300 mg with concomitant topical therapy (DARE NCT04345367, 26 weeks]; COMPARE NCT03720470; 16 weeks]). Patients were stratified by baseline disease severity per Investigator's Global Assessment (moderate; severe) and treatment history (systemic-exposed; systemic-naive). Combined response of >=4-point improvement in Dermatology Life Quality Index and >=50% improvement in Eczema Area and Severity Index (DLQI>=4+EASI-50) was assessed. Week 12 DLQI>=4+EASI-50 response rates were greater with abrocitinib monotherapy versus placebo in systemic-exposed patients (moderate AD: 200 mg, 71.9% 23/32]; 100 mg, 45.9% 17/37] vs placebo, 4.8% 1/21]; severe AD: 73.3% 22/30]; 48.6% 18/37] vs 16.7% 2/12]) and systemic-naive patients (moderate AD: 200 mg, 69.6% 94/135]; 100 mg, 58.5% 72/123]; placebo, 17.9% 10/56]; severe AD: 58.2% 32/55]; 59.2% 29/49]; 12.9% 4/31]). In JADE DARE, comparable proportions achieved Week 16 DLQI>=4+EASI-50 response with abrocitinib and dupilumab across most severity strata and prior treatment exposure subgroups (systemic-exposed: moderate AD, abrocitinib, 75.3% 73/97] and dupilumab 72.3% 68/74]; severe AD, 77.3% 58/75] and 77.8% 63/81]; systemic-naive: moderate AD, 73.9% 85/115] and 73.4% 91/124]); response rates were higher with abrocitinib versus dupilumab for systemic-naive patients with severe AD (81.7% 58/71] vs 71.4% 45/63]). Results were similar at Week 16 in JADE COMPARE. Abrocitinib improved skin clearance and QoL, regardless of baseline disease severity or treatment history.Copyright © 2025
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Journal of the American Academy of Dermatology
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93
Issue
3
