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: 1552

Effective Prevention Of New Osteitis On Magnetic Resonance Imaging In Patients With Early Axial Spondyloarthritis During 3 Years Of Continous Treatment With Etanercept – Data Of The Esther Trial

In-Ho Song1, Kay-Geert A. Hermann2, Hildrun Haibel3, Christian Althoff4, Denis Poddubnyy3, Joachim Listing5, Anja Weiss6, Ekkehard Lange7, Bruce Freundlich8, Martin Rudwaleit9 and Joachim Sieper10, 1Medical Department I, Rheumatology, Charité Universitätsmedizin Berlin, Campus Benjamin Franklin, Berlin, Germany, 2Radiology, Charité Universitätsmedizin Berlin, Campus Mitte, Berlin, Germany, 3Charité Universitätsmedizin Berlin, Berlin, Germany, 4Radiology, Charite Universitätsmedizin Berlin, Campus Mitte, Berlin, Germany, 5German Rheumatism Research Center, Berlin, Germany, 6German Rheumatism Research Centre, Berlin, Germany, 7BU Specialty Care, Pfizer Pharma AG, Berlin, Germany, 8University of Pennsylvania, Philadelphia, PA, 9Endokrinologikum, Berlin, Germany, 10Medical Department I, Rheumatology, Charité Universitätsmedizin Berlin, Campus Benjamin-Franklin, Berlin, Germany

Meeting: 2013 ACR/ARHP Annual Meeting

Keywords: Ankylosing spondylitis (AS), etanercept, spondylarthritis and treatment

  • 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: Spondylarthropathies and Psoriatic Arthritis: Clinical Aspects and Treatment: II

Session Type: Abstract Submissions (ACR)

Background/Purpose:   In patients with early axial spondyloarthritis (SpA) with a disease duration of < 5 years and evidence of active inflammation on whole-body magnetic resonance imaging (wb-MRI) in the spine and/or sacroiliac (SI-) joints at baseline [1] we assessed the degree of fluctuation of active inflammation (bone marrow edema/ osteitis) on MRI during treatment with 3 consecutive years with etanercept (ETN).

Methods:

In the previously reported ESTHER trial axial SpA patients were treated with ETN (n= 40) versus sulfasalazine (SSZ) (n= 36) in the first year [1]. All patients who were not in remission at week 48 (n=48) were either continuously treated with ETN, or sulfasalazine treatment was switched to ETN treatment. Wb-MRIs of those 40 patients who reached the end of year 4 were scored for active inflammation (osteitis) in the SI-joint quadrants and spine vertebral units (VUs). We here analysed MRI data in terms of osteitis in the pooled data set of 40 patients who were continously treated with ETN for 3 consecutive years. Data were analysed as observed. Scoring was performed by two radiologists, blinded for treatment arm and MRI time point. For this analysis, the presence or absence of osteitis were only counted if both scorers agreed.

Results:

At baseline there were 136 SI-joint quadrants with osteitis (according to both scorers). At year 2 osteitis disappeared in 50% of quadrants (68/136), at year 3 osteitis disappeared in 41% (56/136) of quadrants and osteitis disappeared at both year 2 and 3 in 32% (44/136).

In the spine at baseline 37 vertebral units (VUs) showed osteitis. Of these at year 2 osteitis disappeared in 65% (24/37), at year 3 in 57% (21/37) and in both year 2 and 3 in 51% (19/37).

Of the SI-joint quadrants which did not show osteitis (according to both scorers) at baseline (n= 131) the rate of new development of osteitis was 4% (5/131) at year 2; 7% (9/131) at year 3 and only 1.5% (2/131) at both year 2 and 3.

Of the spine vertebral units which did not show osteitis at baseline (n= 843) the rate of new development of osteitis was 0.8% (7/843) at year 2; 1.3% (11/843) at year 3 and 0.4% both at year 2 and 3.

The mean osteitis spine score (range 0-69) decreased from 1.6 (standard deviation 3.4) at baseline to 0.7 (1.4) at year 2 and 0.9 (1.8) at year 2. The mean SI-joint score (range 0-24) decreased from 6.8 (6.1) at baseline to 2.0 (2.2) at year 2 and 2.2 (2.5) at year 3. 

Conclusion:

There was a consistently effective suppression of osteitis on MRI in patients with early axial SpA and only a very low rate of new onset of osteitis during 3 years of continous treatment with etanercept. Whether this also prevents the occurrence of bone proliferation has to be proven by longer follow-ups.

References:

  1. Song I.-H. Ann Rheum Dis. 2011;70 (4):590-596.

Disclosure:

I. H. Song,

Pfizer, Merck Sharp Dohme/Schering Plough, AbbVie ,

5;

K. G. A. Hermann,
None;

H. Haibel,

AbbVie,MSD, Chugai,

8,

AbbVie, MSD,

5;

C. Althoff,
None;

D. Poddubnyy,

Merck Sharp Dohme/Schering Plough, AbbVie,

5;

J. Listing,
None;

A. Weiss,
None;

E. Lange,

Pfizer Inc,

3;

B. Freundlich,

Pfizer Inc,

9;

M. Rudwaleit,

Pfizer, Merck Sharp Dohme/Schering Plough, AbbVie, UCB,

5;

J. Sieper,

Pfizer, Merck Sharp Dohme/Schering Plough, AbbVie, UCB,

5.

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

« Back to 2013 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/effective-prevention-of-new-osteitis-on-magnetic-resonance-imaging-in-patients-with-early-axial-spondyloarthritis-during-3-years-of-continous-treatment-with-etanercept-data-of-the-esther-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