Short-Term Efficacy of Lebrikizumab Versus Dupilumab in Combination with Topical Corticosteroids in Adults with Moderate-to-Severe Atopic Dermatitis: Matching-Adjusted Indirect Comparison

IntroductionA matching-adjusted indirect comparison evaluated the short-term efficacy of lebrikizumab plus topical corticosteroids (TCS) versus dupilumab plus TCS in adults with moderate-to-severe atopic dermatitis (AD).MethodsIndividual patient data from the ADhere trial (lebrikizumab 250 mg every...

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Detalhes bibliográficos
Autores: Chovatiya, R, Armstrong, A, Kircik, L, Puig, L, Kirchhof, MG, Torres, T, Binamer, Y, Duarte, G, Akmaz, B, Dossenbach, M, Gallo, G, Yang, C, Seminario-Vidal, L, Ding, YX, Silverberg, JI
Tipo de documento: artigo
Estado:Versão publicada
Data de publicação:2026
País:España
Recursos:Institut d’Investigació Biomèdica Sant Pau (IIB Sant Pau)
Repositório:r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
OAI Identifier:oai:dnet:r-iibsantpa_::9de5ebdcc3e1bcb16d26b0f6d0868c34
Acesso em linha:https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=21466
Access Level:Acceso aberto
Palavra-chave:Atopic dermatitis
Combination therapy
Eczema Area and Severity Index
Investigator Global Assessment
Dermatology Life Quality Index
Dupilumab
Lebrikizumab
Matching-adjusted indirect comparison
Pruritus Numeric Rating Scale
Topical corticosteroids
Descrição
Resumo:IntroductionA matching-adjusted indirect comparison evaluated the short-term efficacy of lebrikizumab plus topical corticosteroids (TCS) versus dupilumab plus TCS in adults with moderate-to-severe atopic dermatitis (AD).MethodsIndividual patient data from the ADhere trial (lebrikizumab 250 mg every 2 weeks [Q2W] plus TCS) and aggregate data from the CHRONOS trial (dupilumab 300 mg Q2W plus TCS) were matched using the method of moments approach to adjust baseline differences. Matching was done at the study level (primary analysis) and at the study arm level (sensitivity analysis). Efficacy endpoints up to week 16 included the proportion of patients achieving an Investigator's Global Assessment of 0 or 1 (IGA 0/1); a >= 50%, >= 75%, and >= 90% improvement from baseline in the Eczema Area and Severity Index (EASI 50/75/90); a >= 4-point improvement from baseline in the Pruritus Numerical Rating Scale score (PNRS >= 4); and a >= 4-point improvement from baseline in the Dermatology Life Quality Index score (DLQI >= 4). Placebo-adjusted efficacy outcomes were compared using odds ratios (ORs), risk ratios (RRs), and risk differences (RDs) with 95% confidence intervals (CIs).ResultsAt week 16, lebrikizumab plus TCS had comparable odds to dupilumab plus TCS of achieving EASI 75 (OR 1.14, 95% CI 0.42-3.09), IGA 0/1 (OR 1.39, 95% CI 0.42-4.59), PNRS >= 4 (OR 0.48, 95% CI 0.17-1.37), and DLQI >= 4 (OR 0.89, 95% CI 0.29-2.69). At earlier timepoints, lebrikizumab plus TCS had comparable odds to dupilumab plus TCS of achieving PNRS >= 4 at week 2 (OR 2.04, 95% CI 0.24-17.05) and week 4 (OR 3.59, 95% CI 0.90-14.36). RR and RD estimates were consistent with OR estimates of efficacy. Sensitivity analyses confirmed the findings of the primary analysis.ConclusionLebrikizumab plus TCS was comparable to dupilumab plus TCS across all efficacy endpoints at week 16.