Real‐world retention rates and effectiveness of secukinumab in psoriasis: Results from a multicenter cohort study (RAILWAY)

Author:

Tada Yayoi1,Morita Akimichi2ORCID,Yamanaka Keiichi3ORCID,Kono Michihiro4ORCID,Imafuku Shinichi5ORCID,Okubo Yukari6ORCID,Yamazaki Fumikazu7,Kawamura Taisuke8,Itakura Asako8,Ohtsuki Mamitaro9

Affiliation:

1. Department of Dermatology Teikyo University School of Medicine Tokyo Japan

2. Department of Geriatric and Environmental Dermatology Nagoya City University Graduate School of Medical Sciences Nagoya Japan

3. Department of Dermatology Mie University Graduate School of Medicine Tsu Japan

4. Department of Dermatology and Plastic Surgery Akita University Graduate School of Medicine Akita Japan

5. Department of Dermatology Fukuoka University Faculty of Medicine Fukuoka Japan

6. Department of Dermatology Tokyo Medical University Tokyo Japan

7. Department of Dermatology Tokai University School of Medicine Isehara Japan

8. Immunology, Hepatology & Dermatology Medical Franchise Department, Medical Division Novartis Pharma K.K. Tokyo Japan

9. Department of Dermatology Jichi Medical University Shimotsuke Japan

Abstract

AbstractPsoriasis is a chronic, immune‐mediated inflammatory skin disease with a high negative impact on patient's quality of life. Secukinumab, the first interleukin 17A inhibitor, has been used for the systemic treatment of psoriasis, but its long‐term, real‐world retention rates in Japan have not been fully investigated. In this multicenter, noninterventional, retrospective chart review study, the retention rate of secukinumab and its effectiveness among patients with psoriasis in Japan was evaluated up to 5 years. Data of patients who received secukinumab after December 26, 2014, were collected from medical charts obtained from seven sites, all certified for biologics use by the Japanese Dermatological Association. Patient characteristics, secukinumab retention, factors affecting secukinumab retention, reason for drug discontinuation, and effectiveness data were collected. The primary end point was secukinumab retention rate at week 52. A total of 123 patients were included in the analysis. Of these, 27 patients discontinued secukinumab by week 52, yielding a 78.0% (95% confidence interval, 69.6–84.4) retention rate at week 52. For patients whose Psoriasis Area and Severity Index (PASI) score was available, mean ± standard deviation PASI at baseline and at week 52 were 9.21 ± 7.37 and 1.4 ± 2.6, respectively. During the entire study period, “insufficient response” was the most common reason for discontinuation, and “history of biologics use” was a factor significantly associated with secukinumab discontinuation (hazard ratio, 1.72; p = 0.018). This study demonstrates the real‐world retention rate and effectiveness of secukinumab in patients with psoriasis in Japan for up to 5 years and provides clinical insights into psoriasis treatment strategies.

Publisher

Wiley

Subject

Dermatology,General Medicine

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