Comparative effectiveness of biologics in clinical practice

Background: Clinical trials study treatment outcomes under stringent conditions, capturing incompletely the heterogeneity of patient populations and treatment complexities encountered in real-world practice. Objectives: To compare the effectiveness of anti-interleukin (IL)-17A biologics relative to...

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Detalles Bibliográficos
Autores: Pinter, Andreas|||0000-0002-1330-1502, Puig Sanz, Lluís|||0000-0001-6083-0952, Schäkel, Knut, Reich, Adam|||0000-0002-5573-1754, Zaheri, Shirin, Costanzo, Antonio|||0000-0001-9697-2557, Tsai, Tsen-Fang|||0000-0002-1498-1474, Smith, Saxon Donald, Lynde, Charles, Brnabic, Alan, Reed, Catherine L.|||0000-0002-3499-0677, Hill, Julie, Schuster, Christopher F., Riedl, Elisabeth, Paul, Carle|||0000-0003-0165-5263
Tipo de recurso: artículo
Fecha de publicación:2022
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:284476
Acceso en línea:https://ddd.uab.cat/record/284476
https://dx.doi.org/urn:doi:10.1111/jdv.18376
Access Level:acceso abierto
Palabra clave:Adult
Arthritis, Psoriatic
Biological Products
Humans
Psoriasis
Severity of Illness Index
Sulfonamides
Treatment Outcome
Descripción
Sumario:Background: Clinical trials study treatment outcomes under stringent conditions, capturing incompletely the heterogeneity of patient populations and treatment complexities encountered in real-world practice. Objectives: To compare the effectiveness of anti-interleukin (IL)-17A biologics relative to other approved biologics in patients with moderate-to-severe psoriasis. Methods: The Psoriasis Study of Health Outcomes (PSoHO) is an ongoing 3-year observational cohort study in adults with chronic moderate-to-severe plaque psoriasis initiating or switching to a new biologic. Primary study endpoint is the proportion of patients achieving 90% improvement in Psoriasis Area and Severity Index (PASI 90) and/or static Physician Global Assessment (sPGA) 0/1 at Week 12 (W12) in the anti-IL-17A cohort (ixekizumab [IXE], secukinumab) vs. all other approved biologics. Secondary outcomes include the proportion of patients who achieve PASI 75/90/100, absolute PASI scores ≤5, ≤2 and ≤1, Dermatology Life Quality Index (DLQI) score of 0/1 at W12 between the two cohorts and among the individual biologics. Comparative effectiveness analyses were conducted using Frequentist Model Averaging (FMA), a novel causal inference machine learning approach. Missing data for binary outcomes were imputed as non-response. Results: Patient profiles in the anti-IL-17A cohort and other biologics cohort were similar, with more frequent comorbid psoriatic arthritis and less frequent exposure to conventional treatments in the patients receiving anti-IL-17A biologics. At W12, 71.4% of patients who received an anti-IL-17A biologic achieved PASI 90 and/or sPGA 0/1 compared to 58.6% of patients who received other biologics (odds ratios [OR], 1.9; 95% confidence intervals [CI], [1.6, 2.4]). Similar findings were observed for secondary outcomes. Conclusions: These results reflect the high efficacy and early onset of skin clearance of IL-17A inhibitors observed in randomized clinical trials and confirm the effectiveness of anti-IL-17A biologics in the real-world setting.