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: 2155

The Annualized Progression of Radiologic Damage in Placebo Arms of Rheumatoid Arthritis Trials Is Much Lower Than the Mean Annual Progression Since Disease Onset

Jean-Marie Berthelot and Celine Cozic, Rheumatology Unit, Nantes University Hospital, Nantes, France

Meeting: 2012 ACR/ARHP Annual Meeting

Keywords: biologic response modifiers, DMARDs, glucocorticoids, joint destruction and radiography

  • 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 Treatment - Small Molecules, Biologics and Gene Therapy

Session Type: Abstract Submissions (ACR)

Background/Purpose : A previous meta-analysis by Graudal and Jürgens (Arthritis Rheum. 2010;62:2852–63) challenged the belief that biologics better protect rheumatoid arthritis (RA) from joint destruction than DMARDs or glucocorticoids. Destruction rates had been expressed as percentages of the maximal scores and annualized. We aimed to re-analyse this work and: 1-seek for differences in baseline radiologic scores, and mean progression of destruction rates since the onset of RA, according to the subset of drug tested (DMARD, combination of DMARDS, glucocorticoids, biologics); 2-compare destruction rates since RA onset and during the period of the trial, both in the verum arms and placebo arms.

Methods: All studies from groups II to V of this meta-analysis were retrieved and re-analysed by two independent readers. Destruction rates could be calculated both since RA onset and per-trials in 41/55 studies (41 verum arms, and 43 control arms).

 

Results: Baseline scores were higher in patients from biologic trials, but duration of RA was also longer. Consequently, destruction rates before baseline were even lower in biologic trials. In absolute values, difference between verum and controls were not superior in trials of biologics, but when expressed as % of reduction as compared to per-trial destruction rates in the control arms, biologics seemed more efficient (71% +/ 19, median: 78%), than DMARDs (52% +/- 41, median: 64%) and glucocorticoids (52% +/- 22, median: 48%). The per-trial mean destruction rates were (much) lower than the mean destruction rates since RA onset in the four groups, even in the placebo arms, especially in biologic trials. Only placebo arms appear in the figure below. Boxplots represent median, lower and upper quartile, and 95th percentiles.

Conclusion: 1-The difference of per-trial radiographic progression might have biased the results of the previous meta-analysis. When expressed as ratio of destruction rates between verum and control arms, biologics performed better, although DMARDS and glucocorticoids were also clearly effective; 2-‘expected worsening’ as a substitute for placebo arms is inappropriate, and should be banned.

 

 

 

 

 

 

 

 

 


Disclosure:

J. M. Berthelot,
None;

C. Cozic,
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 2012 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/the-annualized-progression-of-radiologic-damage-in-placebo-arms-of-rheumatoid-arthritis-trials-is-much-lower-than-the-mean-annual-progression-since-disease-onset/

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