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Comparative efficacy and safety of systemic therapies used in moderate-to-severe atopic dermatitis: a systematic literature review and network meta-analysis.
Silverberg, J I; Thyssen, J P; Fahrbach, K; Mickle, K; Cappelleri, J C; Romero, W; Cameron, M C; Myers, D E; Clibborn, C; DiBonaventura, M.
Afiliación
  • Silverberg JI; The George Washington University School of Medicine and Health Sciences, Washington, DC, USA.
  • Thyssen JP; Bispebjerg Hospital, University of Copenhagen, Copenhagen, Denmark.
  • Fahrbach K; Evidera Inc, Waltham, MA, USA.
  • Mickle K; Evidera Inc, Waltham, MA, USA.
  • Cappelleri JC; Pfizer Inc, Groton, CT, USA.
  • Romero W; Pfizer Ltd, Surrey, UK.
  • Cameron MC; Pfizer Inc, New York, NY, USA.
  • Myers DE; Pfizer Inc, Collegeville, PA, USA.
  • Clibborn C; Pfizer Ltd, Surrey, UK.
  • DiBonaventura M; Pfizer Inc, New York, NY, USA.
J Eur Acad Dermatol Venereol ; 35(9): 1797-1810, 2021 Sep.
Article en En | MEDLINE | ID: mdl-33991374
Given the lack of head-to-head studies of systemic therapies in moderate-to-severe atopic dermatitis (AD), network meta-analyses (NMAs) can provide comparative efficacy and safety data to inform clinical decision-making. In this NMA, eligible randomized controlled trials (RCTs) published before 24 October 2019 were identified by a systematic literature review. Short-term (12-16 weeks) efficacy (Investigator's Global Assessment [IGA] and Eczema Area and Severity Index [EASI] responses), patient-reported outcomes (PROs) and safety data from each trial were abstracted and analysed separately for monotherapy and combination therapy (systemic plus topical anti-inflammatory therapy). RCTs were analysed in fixed-effects and random-effects Bayesian NMA models. Overall, 19 phase 2 and phase 3 RCTs of abrocitinib, baricitinib, dupilumab, lebrikizumab, nemolizumab, tralokinumab and upadacitinib were included. In monotherapy RCTs, upadacitinib 30 mg once daily (QD) had the numerically highest efficacy (83.6% achieved ≥50% improvement in EASI [EASI-50 response]), followed by abrocitinib 200 mg QD (74.6%), upadacitinib 15 mg QD (70.5%), dupilumab 300 mg every 2 weeks (Q2W) (63.4%) and abrocitinib 100 mg QD (56.7%). Similar trends in EASI-75 and EASI-90 response were observed. In combination therapy RCTs, abrocitinib 200 mg QD had the highest EASI-50 (86.6%), followed by dupilumab 300 mg Q2W (82.4%) and abrocitinib 100 mg QD (79.7%). Similar findings were observed for IGA response and PROs. In monotherapy and combination therapy RCTs, the probability of treatment-emergent adverse events (TEAEs) was higher among all active treatments than with placebo (except for dupilumab 300 mg Q2W [odds ratio (OR), 0.96; 95% credible interval (CrI), 0.45-2.18] and abrocitinib 100 mg QD [OR, 0.95; 95% CrI, 0.35-2.66] in combination therapy RCTs), although active treatments did not significantly differ from one another. Abrocitinib, dupilumab and upadacitinib were consistently the most effective systemic therapies in adult and adolescent patients with AD, with no significant TEAE differences in short-term RCTs.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Dermatitis Atópica / Eccema Tipo de estudio: Clinical_trials / Prognostic_studies / Systematic_reviews Límite: Adolescent / Adult / Humans Idioma: En Revista: J Eur Acad Dermatol Venereol Asunto de la revista: DERMATOLOGIA / DOENCAS SEXUALMENTE TRANSMISSIVEIS Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Dermatitis Atópica / Eccema Tipo de estudio: Clinical_trials / Prognostic_studies / Systematic_reviews Límite: Adolescent / Adult / Humans Idioma: En Revista: J Eur Acad Dermatol Venereol Asunto de la revista: DERMATOLOGIA / DOENCAS SEXUALMENTE TRANSMISSIVEIS Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos