ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstract Number: 2138

Real-world Persistence and Treatment Patterns in Psoriatic Arthritis Patients Treated with Anti-IL17 Therapy

BEATRIZ E. JOVEN1, Concepción Fito Manteca2, Enrique Rubio3, Enrique Raya Álvarez4, Alba Pérez5, Raquel Hernández6, Sara Manrique Arija7, Mercedes Núñez8, Silvia Díaz8, Luis Trancho8, Sebastian Moyano8, Alessandra Lacetera9, Noelia Alfaro-Oliver9 and Rosario Garcia-Vicuña10, 1Hospital Universitario 12 de Octubre, Madrid, Spain, 2Hospitalario de Navarra, Pamplona, Spain, 3Division of Rheumatology, Hospital Universitario Virgen del Rocío, Sevilla, Spain, 4Hospital Universitario San Cecilio, Granada, Spain, 5Hospital Puerta del Mar, Cádiz, Spain, 6Virgen de Valme University Hospital, Sevilla, Spain, 7Hospital Regional Universitario Málaga, Málaga, Spain, 8Lilly, Alcobendas, Spain, 9OXON Epidemiology, Madrid, Spain, 10Hospital Universitario de La Princesa, IIS-Princesa, Madrid, Spain

Meeting: ACR Convergence 2022

Keywords: Biologicals, Cohort Study, Disease-Modifying Antirheumatic Drugs (Dmards), Outcome measures, Psoriatic arthritis

  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print
Session Information

Date: Monday, November 14, 2022

Title: Spondyloarthritis Including PsA – Treatment Poster III: PsA

Session Type: Poster Session D

Session Time: 1:00PM-3:00PM

Background/Purpose: Interleukin-17A inhibitors (anti-IL17) have provided an additional treatment option in the management of the psoriatic arthritis (PsA). This study aims to describe the patient profile, treatment patterns and persistence in PsA patients treated with ixekizumab and secukinumab in a real-life setting.

Methods: A multicenter retrospective study was conducted at 8 Spanish hospitals. Three cohorts of adult PsA patients, newly initiating treatment with an anti-IL17 (secukinumab 150mg [SECU150], secukinumab 300mg [SECU300] or ixekizumab [IXE]), between January-2019 and March-2020 were included. Data of patients exposed to anti-IL17 drugs and with a follow-up visit available were collected until March-2021. Demographic and clinical characteristics, treatment patterns, and persistence were analyzed descriptively. Continuous data were presented as mean (Standard Deviation (SD)) and categorical variables as frequencies with percentage. Persistence rates at 3/6/12 months were calculated.

Results: A total of 221 PsA patients were analysed (SECU150: 103 [46.6%], SECU300: 38 [17.2%] and IXE: 80 [36.2%]). Patients in the SECU150 group presented higher proportion of moderate PsA and less peripheral joint counts. The highest proportion of patients with enthesitis and active skin lessions due to psoriasis in the moment of the prescription was in the SECU300 group. Patients in the IXE group showed longer time since PsA diagnosis, had more frequent comorbidities, joint damage and psoriasis diagnosed (Table 1). 77.8% of patients were previously treated with csDMARDs in monotherapy and 72.9% with bDMARDs/tsDMARDs. The lowest proportion of patients with a prior bDMARDS/tsDMARDS use was observed in the SECU150 group (58.3%), followed by SECU300 (68.4%) and the highest in the IXE group (93.8%). Mean number of previous bDMARDS/tsDMARDS for SECU150, SECU300 and IXE groups were 1.6(1.0), 1.7 (0.9) and 2.4 (1.5), respectively. Anti-IL17 persistence is shown in Figure 1. Most frequent reason for discontinuation was lack of effectiveness (13.8%).

Conclusion: Most of PsA patients treated with anti-IL17 in Spain had a moderate or high disease activity, high peripheral joint damage and skin involvement and had received at least 1 previous bDMARDS/tsDMARDS. More than 80% of patients with one year follow-up were persistent to anti-IL17 treatments, observing the highest rate with IXE, followed by SECU150 and SECU300.

Supporting image 1

Table 1- Demographic and clinical patient characteristics at baseline

Supporting image 2

Figure 1- Anti-IL17 persistence, overall and by study cohorts over one year follow-up


Disclosures: B. JOVEN, Novartis, UCB, Janssen, Amgen, AbbVie/Abbott, Eli Lilly; C. Fito Manteca, None; E. Rubio, None; E. Raya Álvarez, None; A. Pérez, None; R. Hernández, Novartis, Janssen, Pfizer, AbbVie/Abbott, Eli Lilly; S. Manrique Arija, None; M. Núñez, Eli Lilly; S. Díaz, Eli Lilly; L. Trancho, Eli Lilly; S. Moyano, Eli Lilly; A. Lacetera, None; N. Alfaro-Oliver, None; R. Garcia-Vicuña, Novartis, Sanofi, Merck/MSD, Bristol-Myers Squibb(BMS), Eli Lilly, UCB, Janssen, Sandoz, Pfizer, Biogen.

To cite this abstract in AMA style:

JOVEN B, Fito Manteca C, Rubio E, Raya Álvarez E, Pérez A, Hernández R, Manrique Arija S, Núñez M, Díaz S, Trancho L, Moyano S, Lacetera A, Alfaro-Oliver N, Garcia-Vicuña R. Real-world Persistence and Treatment Patterns in Psoriatic Arthritis Patients Treated with Anti-IL17 Therapy [abstract]. Arthritis Rheumatol. 2022; 74 (suppl 9). https://acrabstracts.org/abstract/real-world-persistence-and-treatment-patterns-in-psoriatic-arthritis-patients-treated-with-anti-il17-therapy/. Accessed .
  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print

« Back to ACR Convergence 2022

ACR Meeting Abstracts - https://acrabstracts.org/abstract/real-world-persistence-and-treatment-patterns-in-psoriatic-arthritis-patients-treated-with-anti-il17-therapy/

Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM ET on November 14, 2024. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology