JEADV Clinical Practice (Sep 2023)

Long‐term secukinumab efficacy and safety in bio‐naïve patients with moderate‐to‐severe cutaneous psoriasis: A real‐world retrospective noninterventional multicentric experience (128 patients)

  • Francisco Javier Melgosa Ramos,
  • Almudena Mateu Puchades,
  • Santiago Guillén Climent,
  • Marta Galarreta Pascual,
  • Marina Saéz Belló,
  • María Angels Martínez Ferrer,
  • Fernando Toledo Alberola,
  • Jorge Magdaleno Tapial,
  • Jose Luís Sánchez Carazo,
  • Javier Matáix Díaz,
  • Luca Schneller‐Pavelescu Apetrei,
  • Laura García Fernández,
  • Iris González Villanueva,
  • Isabel Belinchón Romero,
  • Sergio Martín Jiménez,
  • Sergio Santos Alarcón

DOI
https://doi.org/10.1002/jvc2.185
Journal volume & issue
Vol. 2, no. 3
pp. 576 – 582

Abstract

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Abstract Background There is limited evidence over the real‐life secukinumab survival in psoriatic patients, especially in the long‐term bio‐naïve subjects, and to date biological treatments have been assessed in patients with a chronic and recalcitrant psoriasis. It has been hypothesised that early intensive treatment with biological therapies could decrease pathogenic tissue resident memory (TRm) cells migration and potentially modify the natural course of psoriasis and related comorbidities. Objectives To analyze long‐term secukinumab efficacy, safety and survival, and its predictive factors for psoriasis treatment determining also whether early intervention may result in better outcomes for patients. Methods Bio‐naïve psoriatic patients under treatment with secukinumab (n = 128 patients) in a daily practice setting were analyzed in a retrospective multicentric study and followed up to 8 years. Drug survival rate, efficacy, posology and safety were reported. Results The overall secukinumab survival was 81.9% for an average treatment exposure of 147.9 weeks. The approved posology was the most commonly prescribed regimen (78.7%), and 17.7% could be optimized. An absolut‐PASI ≤3 was reached by 86.6%, 82.6% and 91.7% at the weeks 48,156 and 264, respectively. The incidence of arthritis or psoriasis related comorbidities was low. The response was not influenced by weight, age (>65), gender or the presence of arthritis. No severe adverse events were reported. Conclusions In our bio‐naïve series, the high efficacy and long‐term survival rates observed and the low prevalence of arthritis and comorbidities might suggest that early intervention could contribute to modify the course of the disease, but further studies are needed.

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