# Drug Survival, Safety, and Effectiveness of Secukinumab for up to 5 Years in Patients with Psoriasis and Psoriatic Arthritis: A Long-Term Real-Life Experience

**Authors:** Luca Mastorino, Paolo Dapavo, Caterina Cariti, Sara Susca, Niccolò Siliquini, Michela Ortoncelli, Elena Stroppiana, Anna Verrone, Isotta Giunipero di Corteranzo, Francesco Leo, Pietro Quaglino, Simone Ribero

PMC · DOI: 10.3390/jpm14070718 · Journal of Personalized Medicine · 2024-07-03

## TL;DR

This study shows that secukinumab is effective and well-tolerated for up to 5 years in treating psoriasis and psoriatic arthritis, with obesity affecting treatment response.

## Contribution

The study provides long-term real-life data on secukinumab's drug survival and effectiveness in psoriasis patients over 5 years.

## Key findings

- Secukinumab achieved PASI100 in 41.7% of patients at week 16 and 70.6% at week 260.
- Obesity was associated with slower response and higher risk of discontinuation.
- Drug survival was 84.3% at 12 months and 48% at 60 months.

## Abstract

Introduction: the selective IL-17 inhibitor secukinumab has demonstrated efficacy and safety in the treatment of moderate–severe psoriasis in recent years. Objective: evaluate effectiveness and drug survival (DS) of secukinumab in patients with psoriasis for up to 5 years. Methods: This is a retrospective study on a monocentric cohort of patients with psoriasis on secukinumab evaluating the achievement of PASI100, PASI90, and PASI ≤ 3 and DS analysis up to 260 weeks. DS multivariate analysis was carried out considering sex, age, age of onset of the disease, obesity, cardiovascular comorbidities, diabetes, involvement of difficult-to-treat sites, psoriatic arthritis, treatment-naïve status, and mean baseline PASI. Results: At baseline, we evaluated 255 patients on secukinumab. PASI100 was reached by 41.7% and 70.6% of patients at weeks 16 and 260, respectively. PASI90 showed a similar trend with 46.5% of patients achieving it at week 16 and 88.2% at week 260. Non-obese patients showed a faster response than patients with obesity in achieving PASI100, PASI90, and PASI ≤ 3, with significant differences at 28 weeks [55% vs. 40% (p = 0.033), 64% vs. 49% (p = 0.038), and 76% vs. 62% (p = 0.036), respectively]. The estimated DS for secukinumab was 84.3% at 12 and 48% at 60 months. Obesity and smoking habits were associated with a higher risk of discontinuation in multivariate models (HR 1.6 CI 1.05–2.45, p = 0.028; HR 1.48 CI 1.01–2.17, p = 0.043, respectively). Conclusions: Secukinumab showed effectiveness for up to 5 years of treatment, with a high DS and achievement of PASI100, PASI90, and PASI < 3 at these time points. Only obesity reduced the response and maintenance of DS.

## Linked entities

- **Proteins:** IL17A (interleukin 17A)
- **Diseases:** psoriasis (MONDO:0005083), psoriatic arthritis (MONDO:0011849), obesity (MONDO:0011122), diabetes (MONDO:0005015)

## Full-text entities

- **Genes:** IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}
- **Diseases:** Psoriasis (MESH:D011565), diabetes (MESH:D003920), Psoriatic Arthritis (MESH:D015535), smoking (MESH:D015208), Obesity (MESH:D009765)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11277693/full.md

## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC11277693/full.md

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Source: https://tomesphere.com/paper/PMC11277693