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: 0938

Comparative Effectiveness and Treatment Survival of Different TNF Inhibitors for Axial Spondyloarthritis in Real-World Clinical Practice

Javier Marrugo1, Maude Bonin1, Gilles Boire1, Louis Bessette2 and Ariel Masetto1, 1Universite de Sherbrooke, Sherbrooke, QC, Canada, 2Centre de l'Ostoporose et de Rhumatologie de Qubec, Québec City, QC, Canada

Meeting: ACR Convergence 2021

Keywords: Ankylosing spondylitis (AS), Anti-TNF Drugs, comparative effectiveness, spondyloarthritis

  • 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: Sunday, November 7, 2021

Title: Spondyloarthritis Including PsA – Treatment Poster I: Axial Spondyloarthritis (0908–0939)

Session Type: Poster Session B

Session Time: 8:30AM-10:30AM

Background/Purpose: Tumor necrosis factor (TNF) inhibitors are the mainstay treatment for NSAID refractory axial spondyloarthritis (axSpA). However, few data exist on their use during routine clinical practice. The primary aim of this study was to evaluate the effectiveness and treatment survival of different TNF blocking agents within a cohort of patients with axSpA.

Methods: We obtained data from patients who fulfilled the ASAS 2011 classification criteria for axSpA, who were treated with a TNF inhibitor and had clinical follow-up from 2003 to 2019. Effectiveness was evaluated based on the BASDAI50 response at 6 months of therapy. Multivariable linear regression models were used to estimate the predictors of improvement in BASDAI. Treatment persistence was analyzed using Kaplan-Meier survival analysis and Cox proportional hazards model.

Results: The study comprised 171 patients. The median age was 45 years and 57% were males. Mean baseline BASDAI and BASFI were 6.1 and 5.5 respectively. At 6 months, 50.9% reached a BASDAI50 response and no differences were observed within the different TNF inhibitors (Table 1). In the adjusted analysis, smokers were less likely to achieve a BASDAI50 response compared with nonsmokers HR 0.15 (95% CI 0.059 – 0.375) p < 0.0001. In contrast, patients with a higher baseline BASDAI score were more likely to reach a BASDAI50 at 6 months HR 1.29 (95% CI 1.072 - 1.564) p = 0.007. No other variables demonstrated an association with BASDAI50. The median survival for the first TNF inhibitor therapy was 5.9 years (95% CI 4.5-7.4) without significant difference in treatment survival between TNF inhibitors. There was a trend for a better survival with infliximab, but this was not statistically significant (Figure 1). In the non-radiographic (nr-axSpA) group (n=51), 57% reached a BASDAI50 response, compared to 48% in the ankylosing spondylitis (AS) group (n=119) (p=0.28) during the first TNF inhibitor treatment. The median survival, for the first TNF blocking therapy, was 5.3 years (95% CI 1.58-9.15) in the nr-axSpA group and 6,3 years in the AS group (95% CI 4.58-8.01).

After a first TNF inhibitor failure, the BASDAI50 response for subsequent second and third TNF inhibitor therapies, was 48.7% and 38.5% respectively, with no significant difference in treatment survival (Figure 2). The reasons for discontinuation of the first TNF inhibitor were primary failure 14.7%, secondary failure 61.1%, adverse events 14.7%, and others 9.5%.

Conclusion: Most patients who received TNF blocking agents for axSpA during routine clinical care showed improvement in disease activity. TNF inhibitor effectiveness and drug survival were comparable to published data. There were no significant differences in effectiveness or treatment survival among the different TNF inhibitors. Effectiveness and drug survival was not different between nr-axSpA and AS. Failure to a first TNF inhibitor did not diminish effectiveness or drug survival of subsequent TNF inhibitor treatments. The main reason for treatment discontinuation was secondary failure.


Disclosures: J. Marrugo, None; M. Bonin, None; G. Boire, Abbvie, 1, 6, 7, BMS, 6, 7, Janssen, 1, 5, 6, Eli Lilly, 1, 7, Amgen, 7, Novartis, 6, 7, Pfizer, 7, Sandoz, 6, 7, Viatris, 1, 6, Samsung Bioepis, 1; L. Bessette, Amgen, 2, 5, 6, Bristol-Myers Squibb, 2, 5, 6, Janssen, 2, 5, 6, Roche, 2, 5, 6, UCB, 2, 5, 6, AbbVie, 2, 5, 6, Pfizer, 2, 5, 6, Merck & Co, 2, 5, Celgene, 2, 5, 6, Sanofi, 2, 5, 6, Eli Lilly, 2, 5, 6, Novartis, 2, 5, 6, Gilead, 2, 5, 6, Sandoz, 2, 5, 6, Teva, 2, 6; A. Masetto, AbbVie, 2, 5, 6, BMS, 2, 5, 6, Novartis, 2, 5, 6, Pfizer, 2, 5, 6, Sanofi, 2, 5, 6, UCB, 2, 5, 6, Eli Lilly, 2, 5, 6, Janssen, 2, 5, 6, Amgen, 5, Merck, 5, Teva, 5.

To cite this abstract in AMA style:

Marrugo J, Bonin M, Boire G, Bessette L, Masetto A. Comparative Effectiveness and Treatment Survival of Different TNF Inhibitors for Axial Spondyloarthritis in Real-World Clinical Practice [abstract]. Arthritis Rheumatol. 2021; 73 (suppl 9). https://acrabstracts.org/abstract/comparative-effectiveness-and-treatment-survival-of-different-tnf-inhibitors-for-axial-spondyloarthritis-in-real-world-clinical-practice/. 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 2021

ACR Meeting Abstracts - https://acrabstracts.org/abstract/comparative-effectiveness-and-treatment-survival-of-different-tnf-inhibitors-for-axial-spondyloarthritis-in-real-world-clinical-practice/

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