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: 2419

Efficacy of Biologic Medications in Active Rheumatoid Arthritis: A Systematic Review

Lynden Roberts1,2, Kathleen Tymms3, Julien de Jager4, Geoffrey Littlejohn5, Hedley Griffiths6, David Nicholls7, Paul Bird8, Jennifer Young9 and Jane Zochling10, 1JCU Clinical School, Townsville, QLD, Australia, 2Monash Medical Centre, Clayton, VIC, Australia, 3Canberra Rheumatology, Canberra, ACT, Australia, 4Olser House, Southport, QLD, Australia, 5Rheumatology, Monash Medical Centre and Monash University, Clayton, VIC, Australia, 6Barwon Rheumatology Service, Geelong, VIC, Australia, 7Coast Joint Care, Maroochydore, QLD, Australia, 8Combined Rheumatology Practice, Sydney, NSW, Australia, 94-10 Inman Road, Roche Products Pty Limited, Sydney, NSW, Australia, 10Department of Rheumatology, Menzies Research Institute Tasmania, Hobart, TAS, Australia

Meeting: 2014 ACR/ARHP Annual Meeting

Keywords: biologic drugs and rheumatoid arthritis (RA), DMARDs

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

Title: Rheumatoid Arthritis - Clinical Aspects (ACR): Impact of Various Interventions and Therapeutic Approaches

Session Type: Abstract Submissions (ACR)

Background/Purpose: In the last decade, biologic medications have transformed the management of RA. The effectiveness of these medications has been reported in numerous randomized controlled trials and cohort studies. A summary of the effect size for biologic medications would be useful to inform expectations of rheumatologists and patients when considering and commencing these medications. Further, with an increased interest in real-life effectiveness data from clinical registries, comparisons between controlled trial and registry effectiveness outcomes would be of interest.

Methods: Using PRISMA methodology, a pre-specified search and review strategy was devised to answer the question “what are the EULAR response rates for biologic medications in adults with active RA?” MEDLINE and EMBASE were searched for Rheumatoid Arthritis (Both Mesh term and free text) in Title/Abstract AND Name of biologic drug (free text) in Title/Abstract OR Biologic Therapy (Mesh term) OR ‘Biologic’ (free text) in Title/Abstract AND EULAR response (free text) in Entire Document AND Adult (free text) Entire Document. All articles were reviewed independently by 2 experts; duplicates and non-primary research articles were removed along with those using medication doses outside of the approved Australian indications, and only patients with ≥ moderate DAS or tender/swollen joint count ≥ 4 were included. Whether the patients were naïve to biologic DMARD and whether the response assessment was at 3 (2.0 – 4.5) months or 6 (4.5 – 7.0) months was recorded. The percentage of patients achieving a moderate, good, or either EULAR response was calculated overall and for subgroups.

Results: Overall, 27,280 patients were included representing 62 studies. Mean baseline DAS28 was 6.0 (SD=0.6). Good (G) and moderate (M) EULAR responses were achieved in 25.8% and 47.3% respectively, with 28.1% failing to achieve a Good or Moderate EULAR response when all patients were pooled. Response rates were similar for patients who were naïve to biologics (G-24.0% & M-47.5%), those who had failed to respond to at least 1 biologic (G-28.1% & M-47.1%) and at both 3 months (G-27.1% & M-50.4%) and 6 months (G-25.2% & M- 46.3). Sufficient data was present for separate analyses of adalimumab (ADA), etanercept (ETN) and tocilizumab (TCZ) and EULAR response rates were similar, however tocilizumab had a higher rate of good EULAR response [37.4% (TCZ), 28.2% (ADA), 27.6% (ETN)].

Conclusion: A systematic review of studies reporting EULAR response rates for biologic medications in active RA showed that only 28.1% of patients fail to achieve at least a moderate EULAR response. Response rates were similar for patients who were naïve or had previous exposure to biologics, for 3 and 6 months assessment time points, and for different biologic medications. Comparison of these controlled trial data with real life response rates reported in clinical registries will be of interest.


Disclosure:

L. Roberts,
None;

K. Tymms,
None;

J. de Jager,
None;

G. Littlejohn,
None;

H. Griffiths,
None;

D. Nicholls,
None;

P. Bird,
None;

J. Young,

An employee of Roche Products, Pty. Limited,

3;

J. Zochling,
None.

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

« Back to 2014 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/efficacy-of-biologic-medications-in-active-rheumatoid-arthritis-a-systematic-review/

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