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: 499

Efficacy and Safety Of Infliximab Or Adalimumab Vs Abatacept In Patients With Rheumatoid Arthritis and An Inadequate Response To Methotrexate: Attest-Ample Network Randomized Trial

Robin Christensen1, Simon Tarp1, Daniel Furst2, Lars E. Kristensen3 and Henning Bliddal4, 1Musculoskeletal Statistics Unit, The Parker Institute, Department of Rheumatology, Copenhagen University Hospital, Bispebjerg and Frederiksberg, Denmark, 2David Geffen School of Medicine, University of California, Los Angeles, CA, 3Rheumatology, Department of Clinical Sciences, Lund, Section of Rheumatology, Lund University, Lund, Sweden, 4Department of Rheumatology, The Parker Institute, Department of Rheumatology, Copenhagen University Hospital, Bispebjerg and Frederiksberg, Denmark

Meeting: 2013 ACR/ARHP Annual Meeting

Keywords: Abatacept, Adalimumab, infliximab, meta-analysis and rheumatoid arthritis (RA)

  • Tweet
  • Email
  • Print
Session Information

Title: Rheumatoid Arthritis Treatment - Small Molecules, Biologics and Gene Therapy I

Session Type: Abstract Submissions (ACR)

Background/Purpose:

Using combined data from the ATTEST [1] and AMPLE [2] study comparing infliximab and adalimumab with abatacept in patients with rheumatoid arthritis (RA), we sought to assess the relative effectiveness of infliximab, adalimumab, and abatacept in patients with RA and an inadequate response to methotrexate.

 

Methods:

The meta-dataset included results from the ATTEST (NCT00095147) and AMPLE (NCT00929864) studies. Both trials included patients who met the American College of Rheumatology (ACR) criteria for RA, were at least 18 years of age, and had an inadequate response to MTX. Major outcomes concerned the benefits and harm after 1 year on therapy, American College of Rheumatology 50% (ACR50) criterion extracted from the papers and the number of withdrawals related to adverse events (AEs), respectively. All analyses were performed using the modified intention to treat population: all patients who were randomized and received at least one dose of study drug. Patients who discontinued the study prematurely were considered non-responders subsequent to the time of discontinuation. Statistical analyses were based on mixed-effects logistic regression using an arm-based, random-effects model respecting randomization within each study [3].

 

Results:

Compared with infliximab (IV), abatacept (IV/SC) and adalimumab SC were associated with a statistical significantly higher likelihood of achieving an ACR50 response (abatacept: OR 1.49, 95% CI: 1.03 to 2.15; P = .032; Adalimumab: OR 1.49, 95% CI: 1.02 to 2.19; P = .041). In contrast,the ACR50 responses for abatacept and adalimumab were comparable  (OR 1.00, 95% CI: 0.75 to 1.32; P = .99). Abatacept was less likely than infliximab to result in discontinuation due to adverse events (OR 0.45, 95% CI: 0.21 to 0.96; P = .040) while infliximab and adalimumab were similar in this respect (OR 0.83, 95% CI: 0.39 to 1.74; P = .62)

 

Conclusion:

The network analysis allowed indirect comparisons across all three groups. We conclude that infliximab, at the recommended dose, is less efficacious than either adalimumab or abatacept and that adalimumab and abatacept are approximately equivalent both in terms of benefit and short-term harm (up to 1 year).

References:

[1] Schiff M, Ann Rheum Dis. 2008;67(8):1096-103.

[2] Weinblatt ME, Arthritis Rheum. 2013;65(1):28-38.

[3] Singh JA, CMAJ. 2009;181(11):787-96.

 


Disclosure:

R. Christensen,

Abbott, Axellus A/S, Bristol-Myers Squibb, Cambridge Weight Plan, Norpharma, Pfizer, and Roche,

5,

Axellus A/S, Cambridge Weight Plan, Mundipharma, and Roche,

2,

Abbott, Axellus, Bayer HealthCare Pharmaceuticals, Biogen Idec, Bristol-Myers Squibb, Cambridge Weight Plan, Ipsen, Laboratoires Expanscience, MSD, Mundipharma, Norpharma, Pfizer, Roche, and Wyeth,

8;

S. Tarp,
None;

D. Furst,

AbbVie, Actelion, Amgen, BMS, Gilead, GSK, NIH, Novartis, Pfizer, Roche/Genentech, UCB,

2,

AbbVie, Actelion, Amgen, BMS, Janssen, Gilead, GSK, NIH, Novartis, Pfizer, Roche/Genentech, UCB,

5,

AbbVie, Actelion, UCB ,

8;

L. E. Kristensen,
None;

H. Bliddal,
None.

  • Tweet
  • Email
  • Print

« Back to 2013 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/efficacy-and-safety-of-infliximab-or-adalimumab-vs-abatacept-in-patients-with-rheumatoid-arthritis-and-an-inadequate-response-to-methotrexate-attest-ample-network-randomized-trial/

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