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: 1891

Early MRI Endpoints Provide a Valid Measure of Structural Damage While Reducing Study Duration and Participant Numbers in Rheumatoid Arthritis Clinical Trials

Joshua Baker1, Philip G. Conaghan2, Paul Emery3, Daniel Baker4 and Mikkel Østergaard5, 1Medicine/Rheumatology, Philadelphia VA Medical Center, Philadelphia, PA, 2University of Leeds and NIHR Leeds Musculoskeletal Biomedical Research Unit, Leeds, United Kingdom, 3NIHR-Leeds Musculoskeletal Biomedical Research Unit and Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, United Kingdom, 4Janseen R&D, Spring House, PA, 5Copenhagen Center for Arthritis Research, Copenhagen University Hospital at Glostrup, Glostrup, Denmark

Meeting: 2014 ACR/ARHP Annual Meeting

Keywords: clinical trials, magnetic resonance imaging (MRI) and rheumatoid arthritis (RA)

  • 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: Imaging of Rheumatic Diseases: X-ray, MRI and CT

Session Type: Abstract Submissions (ACR)

Background/Purpose

We used data from a large randomized controlled clinical trial of an effective biologic (golimumab, GO-BEFORE study) to compare the associations of disease activity and disease severity with two imaging techniques to measure joint erosion: 1) early progression in rheumatoid arthritis magnetic resonance imaging scores (RAMRIS) and 2) radiographic progression. We subsequently assessed the potential impact of incorporating these MRI scores in clinical trial design.

Methods

MRI of the dominant hand was performed and RAMRIS scores were determined at baseline, week 12 and week 24. van der Heijde-Sharp (vdHS) scores were determined for x-rays at baseline and week 52. Progression in vdHS and RAMRIS erosion scores were defined as a change of >0.5. Associations between X-ray and MRI outcomes with clinical features associated with severe disease and structural damage were evaluated to assess convergent validity. Iterative Wilcoxon ranksum tests assessed the sample size requirements to detect a significant difference in the change in structural damage score between combination therapy (methotrexate+golimumab) and methotrexate monotherapy. Sample size calculations were also performed based on dichotomous progression outcomes.

Results

MRI progression at 12 and 24 weeks was associated with greater DAS28(CRP), CRP, and vdHS at baseline, and greater HAQ scores at 2-years (Table 1). These associations were similar in magnitude to those seen with X-ray progression at 1-year. Ranksum testing for differences in the change in structural damage between treatment and controls arms achieved significance (p<0.05) with fewer total study subjects when MRI erosion score was the outcome assessed (175 for MRI at 12/24 weeks v. 300 subjects for ΔvdHS at 52 weeks) (Figure 1). When the study sample was enriched with subjects with a synovitis score >5 (a level previously associated with MRI progression) at baseline, the study sample further decreased to 125. Sample size calculations demonstrated that a study enriched with 117 subjects with synovitis scores >5 would have 80% power to detect a difference in the proportion of subjects progressing on MRI at 12 weeks. A sample size calculation based on an unenriched population and using 1-year x-ray progression as the outcome estimated a study size of 470 subjects.

Conclusion

Early MRI erosion score outcomes have convergent validity comparable to that of 52-week x-ray progression. Use of MRI in clinical trials would decrease sample sizes and reduce length of follow-up for studies assessing differences in structural damage progression between groups.

Table 1:  Clinical characteristics of MRI/x-ray progressors and non-progressors within the MRI sub-study (convergent validity).

MRI 24 Weeks (N=238)

X-ray 52 Weeks (N=238)

Progression

(N=52)

No Progression

(N=186)

P Value

Progression

(N=62)

No Progression

(N=176)

P Value

Baseline DAS28(CRP)

5.81 (1.13)

5.53 (1.06)

0.1

5.79 (1.10)

5.52 (1.06)

0.09

Baseline CRP

1.8 (0.95, 3.4)

1 (0.4, 2.5)

0.002

2 (0.8, 4.2)

1 (0.4, 2.4)

0.001

Baseline vdHS

15 (3.25, 29.8)

4.5 (2, 13)

0.002

9 (2.9, 26)

4.5 (2, 15)

0.01

ΔHAQ Score (2-years)*

0.036 (0.78)

-0.14 (0.59)

0.08

-0.054 (0.74)

-0.12 (0.61)

0.5

24 Week ACR50, N (%)

14 (28%)

86 (47%)

0.01

21 (34%)

79 (45%)

0.1

* Adjusted for baseline HAQ


Disclosure:

J. Baker,
None;

P. G. Conaghan,

Abbvie,

8,

Merck Human Health,

8,

Novartis Pharmaceutical Corporation,

8,

Pfizer Inc,

8,

Roche Pharmaceuticals,

8,

UCB,

8;

P. Emery,

AbbVie, Bristol-Myers Squibb (BMS), MSD, Novartis, Pfizer Inc, Roche, and UCB Pharma,

2,

AbbVie, Bristol-Myers Squibb (BMS), MSD, Novartis, Pfizer Inc, Roche, and UCB Pharma,

5;

D. Baker,

Janssen Research & Development, LLC.,

3;

M. Østergaard,
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/early-mri-endpoints-provide-a-valid-measure-of-structural-damage-while-reducing-study-duration-and-participant-numbers-in-rheumatoid-arthritis-clinical-trials/

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