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: 1292

Fatigue Is an Independent Variable Predicting Physical Function and Disease Activity Score-28 Remission for Patients with Rheumatoid Arthritis Treated with Intravenously Administered Golimumab: Results From Phase 3, Placebo Controlled Clinical Trial

Rene Westhovens1, Michael Weinblatt2, Chenglong Han3, Tim Gathany4, Lilianne Kim5, Michael Mack6, Jiandong Lu6, Daniel Baker7, Alan Mendelsohn7 and Clifton O. Bingham III8, 1Rheumatology, University Hospital KU Leuven, Leuven, Belgium, 2Rheumatology & Immunology, Brigham & Women's Hospital, Boston, MA, 3Outcomes Research, Johnson & Johnson Pharmaceutical Services, LLC, Malvern, PA, 4Janssen Global Services, LLC., Malvern, PA, 5Janssen Research & Development, a division of Pharmaceutical Research & Development LLC, Janssen Research & Development, LLC, Malvern, PA, 6Biostatistics, Janssen Research & Development, LLC., Spring House, PA, 7Immunology, Janssen Research & Development, LLC, Spring House, PA, 8Department of Medicine, Johns Hopkins University, Baltimore, MD

Meeting: 2012 ACR/ARHP Annual Meeting

Keywords: Fatigue 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: Rheumatoid Arthritis Treatment - Small Molecules, Biologics and Gene Therapy

Session Type: Abstract Submissions (ACR)

Background/Purpose: To evaluate the association of fatigue with physical function and disease activity in patients with rheumatoid arthritis (RA), and the impact of treatment with intravenously administered golimumab (GLM) on fatigue using data from the Phase III clinical trial GO- FURTHER.

Methods: GO-FURTHER was a multicenter, randomized, placebo-controlled study. Adult patients with active RA despite MTX therapy were randomized to placebo + MTX (placebo group) or GLM 2mg/kg plus MTX (GLM group) at week 0, 2, and every 8 week thereafter. Patients in placebo group with <10% improvement in tender and swollen joint count from baseline at week 16 entered early escape and received a 2 mg/kg GLM infusion at Weeks 16 and 20.  Impact on physical function was assessed using the disability index of the Health Assessment Questionnaire (HAQ). Fatigue was measured using the Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-F) questionnaire, and clinically meaningful improvement in FACIT-Fatigue was defined as ≥ 4 points increase in the scores. Correlation of FACIT-Fatigue with HAQ and disease activity and remission (DAS28 using CRP<2.6) were analyzed using Pearson correlation, or multiple linear and logistic regression models to adjust for other confounding variables (age, CRP, swollen and tender joints counts). Comparisons between groups were performed using ANOVA on van der Waerden normal scores for continuous outcomes or Chi-square test for binary outcomes. 

Results: At baseline, mean (SD) FACIT-Fatigue score was 25.5 (10.54), indicating significant fatigue.  Significant correlations of FACIT-Fatigue with HAQ (r=-0.62, p<0.01) and DAS28 score (r=-0.42, p<0.01) were observed at baseline.  In multiple regression models, baseline FACIT-Fatigue score or change in FACIT-Fatigue at week 24 were correlated with change in HAQ and DAS28 score. Patients with higher FACIT-Fatigue scores at baseline were more likely to achieve DAS28 remission at week 24 (p=0.024). Compared to the placebo group, GLM-treated patients had significantly greater improvement in FACIT-fatigue at week 12 (5.4 ± 10.3 vs. 2.1 ± 9.0), which was sustained through week 16 (7.5 ± 10.5 vs. 2.2 ± 9.7) and 24 (8.0 ± 10.8 vs. 2.5 ± 10.2) (all p-values<0.001). Compared with the placebo group, a greater proportion of patients in the GLM group achieved clinically meaningful improvement in FACIT-Fatigue score at week 12 (57.5% vs. 42.8%) and at week 24 (65.8% vs. 40.3) (all p-values<0.001).

Conclusion: RA patients inadequately responsive to MTX experienced severe fatigue. Fatigue was a significant independent predictor of physical function and disease activity in patients with RA.  Treatment with intravenously administered GLM significantly improved clinical symptoms of fatigue in patients with RA inadequately responsive to MTX.


Disclosure:

R. Westhovens,

Janssen Research and Development, LLC,

9;

M. Weinblatt,

Janssen Research and Development, LLC,

9;

C. Han,

Johnson Johnson Pharmaceutical Services, LLC,

3;

T. Gathany,

Johnson & Johnson Pharmaceutical Services, LLC,

3;

L. Kim,

Janssen Research & Development, LLC,

3;

M. Mack,

Janssen Research & Development, LLC,

3;

J. Lu,

Janssen Research & Development, LLC,

3;

D. Baker,

Janssen Research & Development, LLC,

3;

A. Mendelsohn,

Janssen Research & Development, LLC,

3;

C. O. Bingham III,

Janssen Research & Development, LLC,

9.

  • 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/fatigue-is-an-independent-variable-predicting-physical-function-and-disease-activity-score-28-remission-for-patients-with-rheumatoid-arthritis-treated-with-intravenously-administered-golimumab-result/

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