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: 1999

Patient-Reported Outcomes in Rheumatoid Arthritis Correlate with Clinical Disease Activity Index Response in the Study to Accelerate Information of Molecular Signatures (AIMS)

Vibeke Strand1, Emelly Rusli2, Lixia Zhang2, Christina Le-Short2, Alix Arnaud2, Johanna Withers3 and Sam Asgarian2, 1Stanford University School of Medicine, Stanford, CA, 2Scipher Medicine Corporation, Waltham, MA, 3Scipher Medicine Corportaion, Waltham, MA

Meeting: ACR Convergence 2022

Keywords: Disease Activity, Outcome measures, Patient reported outcomes, registry, rheumatoid arthritis

  • Tweet
  • Email
  • Print
Session Information

Date: Monday, November 14, 2022

Title: RA – Treatment Poster IV

Session Type: Poster Session D

Session Time: 1:00PM-3:00PM

Background/Purpose: Rheumatoid arthritis (RA) treatment response is typically defined using clinician-reported scores and patient global assessments of disease activity (PtGA), but patients may have a broader conceptualization of outcome, including physical function (Health Assessment Questionnaire Disability Index: HAQ-DI), pain, and fatigue levels. Patient-reported outcomes (PRO) play a crucial role that not only compliments clinical measures but also demonstrates treatment-associated improvements in broader health status. This study explored the association between Clinical Disease Activity Index (CDAI) responses to low disease activity (LDA) and remission (REM) and improvements in PtGA, pain, and HAQ-DI in patients with moderate-to-severely active RA.

Methods: Data from the Study to Accelerate Information of Molecular Signatures (AIMS), a clinical study of real-world longitudinal data from patients with RA managed across a network of private and academic rheumatology practices in the contiguous US were analyzed. Patient management in AIMS focuses on the utilization of a commercially available MSRC test. Adjusted mean improvements in CDAI, PtGA, pain, and HAQ-DI from baseline to 6 months and percentages reporting scores ≥ minimum clinically important differences (MCID, defined as improvement in PtGA and pain VAS ≥10 and HAQ-DI ≥0.22) were compared. Generalized linear modeling was employed to assess the associations between PROs with CDAI responses adjusted for baseline covariates such as age, gender, baseline CDAI, tender and swollen joint counts, PtGA, and HAQ-DI.

Results: A total of 471 patients were included; the mean age was 56.4 (SD=13.2) years, the mean baseline CDAI was 33 (SD= 16.3), 80% were female and 77% were TNFi-naïve (Table 1). At 6 months, improvements in all PROs in responders were statistically significant. More patients achieving CDAI-LDA and REM reported improvements in PtGA ≥ MCID (70% and 93%, respectively) than non-responders (47%, Table 2). PtGA, pain, and HAQ-DI improvements from baseline were significantly associated with CDAI-LDA responses (p<0.0001, Table 2). Specific distributions of mean PRO improvements by CDAI-LDA and REM status are shown in Figure 1.

Conclusion: RA patients who achieved CDAI-LDA or REM reported lower impacts of disease, less pain, and improved physical function. This study further underscores the importance of helping RA patients select the most effective therapy to reach treat-to-target goals, an area where precision medicine can fill a large unmet need.

Supporting image 1

Supporting image 2

Supporting image 3

Figure 1. PRO association with CDAI response status. Left panels: Boxplots showing distributions of PRO (PtGA, pain score, HAQ-DI) score improvement according to CDAI status at 6 months. Sample size and least squares mean (lsmean) are reported. Right panels: Bar charts showing percentage of patients reporting PRO (PtGA, pain, HAQ-DI) score improvement ≥ clinically critical values according to CDAI status at 6 months, where critical values are defined as 10, 10, and 0.22 for PtGA, pain score, and HAQ-DI, respectively.


Disclosures: V. Strand, AbbVie, Amgen, AstraZeneca, Bayer, Bristol-Myers Squibb(BMS), Boehringer-Ingelheim, Chemocentryx, Celltrion, Genentech/Roche, Gilead, GlaxoSmithKlein(GSK), Inmedix, Janssen, Kiniksa, Merck/MSD, Novartis, Pfizer, Regeneron Pharmaceuticals, Rheos, R-Pharma, Samsung, Sandoz, Sanofi, Scipher, Setpoint, Spherix, Aria, Bioventus, Blackrock, Equilium, Glenmark, Horizon, Kypha, Lilly, MiMedx, Sorrento, Tonix, Priovant; E. Rusli, Scipher Medicine; L. Zhang, Scipher Medicine; C. Le-Short, Scipher Medicine Corporation; A. Arnaud, Scipher Medicine; J. Withers, Scipher Medicine Corporation; S. Asgarian, Scipher Medicine.

To cite this abstract in AMA style:

Strand V, Rusli E, Zhang L, Le-Short C, Arnaud A, Withers J, Asgarian S. Patient-Reported Outcomes in Rheumatoid Arthritis Correlate with Clinical Disease Activity Index Response in the Study to Accelerate Information of Molecular Signatures (AIMS) [abstract]. Arthritis Rheumatol. 2022; 74 (suppl 9). https://acrabstracts.org/abstract/patient-reported-outcomes-in-rheumatoid-arthritis-correlate-with-clinical-disease-activity-index-response-in-the-study-to-accelerate-information-of-molecular-signatures-aims/. Accessed .
  • Tweet
  • Email
  • Print

« Back to ACR Convergence 2022

ACR Meeting Abstracts - https://acrabstracts.org/abstract/patient-reported-outcomes-in-rheumatoid-arthritis-correlate-with-clinical-disease-activity-index-response-in-the-study-to-accelerate-information-of-molecular-signatures-aims/

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