Effectiveness and safety of secukinumab updosing in patients with moderate to severe plaque psoriasis: data from the PURE registry.


Journal

Archives of dermatological research
ISSN: 1432-069X
Titre abrégé: Arch Dermatol Res
Pays: Germany
ID NLM: 8000462

Informations de publication

Date de publication:
08 Jun 2024
Historique:
received: 28 03 2024
accepted: 26 04 2024
revised: 28 03 2024
medline: 8 6 2024
pubmed: 8 6 2024
entrez: 8 6 2024
Statut: epublish

Résumé

Secukinumab is a fully human IgG1 antibody that selectively binds to and neutralizes the proinflammatory cytokine interleukin-17A. Secukinumab is an effective and well-tolerated treatment for plaque psoriasis. There is a limited real-word evidence for dose optimisation of secukinumab based on clinical response. PURE is a multi-national, prospective, observational study in patients with moderate to severe chronic plaque psoriasis in Canada and Latin America, assessing the real-world safety and effectiveness of secukinumab and other indicated therapies. The aim of the current snapshot analysis was to evaluate the effectiveness and safety of on-label dose and updosed secukinumab in patients with plaque psoriasis enrolled in the PURE study. At the time of analysis, 676 patients received secukinumab, of which 84.6% (n = 572) remained on the on-label dose, while 15.4% (n = 104) were updosed. With on-label secukinumab, the absolute Psoriasis Area and Severity Index (PASI) score was reduced from 13.6 at baseline to 1.2 over 36 months, with treatment persistence of 73% at 40 months. At Month 36, 73.2% of the patients receiving on-label secukinumab achieved Investigator's Global Assessment (IGA) 0/1. With updosed secukinumab (300 mg every 2 weeks, 300 mg every 3 weeks, 450 mg every 4 weeks, or 450 mg every 3 weeks), 57.9% of the patients showed improvement in the absolute PASI score at the first visit after updosing, with treatment persistence of 50% at 12 months after updosing. At Month 15, 40% of patients receiving updosed secukinumab achieved IGA 0/1. Patients with previous biologic exposure (odds ratio [OR]: 3.25; 95% confidence interval [CI]: 2.03, 5.18, p < 0.0001) were more likely to be updosed while those with a body weight < 90 kg (OR: 0.49; 95% CI [0.31, 0.77], p = 0.0019) were less likely to be updosed. Previous biologic exposure (HR [hazard ratio]: 1.47; 95% CI [1.24, 1.75], p < 0.0001) and current biologic exposure (secukinumab vs. other indicated therapies: HR 0.57; 95% CI [0.43, 0.75], p = 0.0001) were significantly associated with time to secukinumab updosing. No new or unexpected safety signals were observed with updosed secukinumab. Secukinumab updosing was efficacious and well-tolerated in patients with psoriasis who failed to respond to the approved on-label regimen, suggesting that updosing may be a useful therapeutic option for approved dose non-responders.

Identifiants

pubmed: 38850346
doi: 10.1007/s00403-024-03122-w
pii: 10.1007/s00403-024-03122-w
doi:

Substances chimiques

secukinumab DLG4EML025
Antibodies, Monoclonal, Humanized 0
Dermatologic Agents 0
Interleukin-17 0
IL17A protein, human 0

Types de publication

Journal Article Observational Study Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

362

Informations de copyright

© 2024. The Author(s).

Références

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Auteurs

Kim A Papp (KA)

Alliance Clinical Trials and Probity Medical Research, Waterloo, ON, Canada. kapapp@probitymedical.com.
The University of Toronto, Toronto, ON, Canada. kapapp@probitymedical.com.

Melinda Gooderham (M)

SKiN Center for Dermatology, Queen's University and Probity Medical Research, Peterborough, ON, Canada.

Charles Lynde (C)

Lynde Institute for Dermatology, University of Toronto and Probity Medical Research, Markham, ON, Canada.

Danielle Brassard (D)

Clinique D, Laval, QC, Canada.

Faisal Al-Mohammedi (F)

Dermcare Clinic and, University of Toronto, Mississauga, ON, Canada.

Vimal H Prajapati (VH)

Division of Community Pediatrics and Pediatric Rheumatology, Department of Pediatrics, University of Calgary, Calgary, AB, Canada.
Division of Dermatology, Department of Medicine, University of Calgary, Calgary, AB, Canada.

Isabelle Delorme (I)

Dermatology Research Institute and Probity Medical Research, Calgary, AB, Canada.
Skin Health & Wellness Centre, Calgary, AB, Canada.

Lorne Albrecht (L)

Dr. Isabelle Delorme Inc, Drummondville, QC, Canada.

Richard Haydey (R)

Enverus Medical Research, University of British Columbia and Probity Medical Research, Surrey, BC, Canada.

Maryam Shayesteh Alam (MS)

Winnipeg Clinic, Winnipeg, MB, Canada.

Jennifer Beecker (J)

Simcoderm Medical and Surgical Dermatology Centre and Probity Medical Research, Barrie, ON, Canada.
University of Ottawa, Ottawa, ON, Canada.

Sanjay Siddha (S)

Division of Dermatology, The Ottawa Hospital, Ottawa Hospital Research Institute and Probity Medical Research, Ottawa, ON, Canada.

Marie Maguin (M)

Probity Medical Research, Division of Dermatology, University Health Network Hospitals, Toronto, ON, Canada.

Mahmoud S Farag (MS)

Novartis Canada Pharmaceutical Inc, Montreal, Canada.

Antonio Vieira (A)

Novartis Canada Pharmaceutical Inc, Montreal, Canada.

Lenka Rihakova (L)

Novartis Canada Pharmaceutical Inc, Montreal, Canada.

Richard G Langley (RG)

Division of Clinical Dermatology & Cutaneous Science, Department of Medicine, Halifax, Canada.

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