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: 1336

Systematic Literature Review and Meta-Analysis of DAS28 Clinical Response Rates Among Advanced Therapies in Biologic-Naïve Patients with Rheumatoid Arthritis

Daniel Aletaha1, Ruta Sawant 2, Patrick Zueger 3, Erin Cook 4, Fan Mu 4, Vishvas Garg 2 and Keith A. Betts 4, 1Medical University of Vienna, Vienna, Austria, 2AbbVie Inc., North Chicago, IL, 3AbbVie Inc., North Chicago, 4Analysis Group, Inc., Boston, MA

Meeting: 2019 ACR/ARP Annual Meeting

Keywords: Biologics and meta-analysis, Disease-modifying antirheumatic drugs, Rheumatoid arthritis (RA)

  • Tweet
  • Email
  • Print
Session Information

Date: Monday, November 11, 2019

Title: RA – Diagnosis, Manifestations, & Outcomes Poster II: Treatments, Outcomes, & Measures

Session Type: Poster Session (Monday)

Session Time: 9:00AM-11:00AM

Background/Purpose: Biologic (b) and targeted synthetic (ts) DMARDs have demonstrated efficacy for the treatment of rheumatoid arthritis (RA) in clinical trials; however, real-world evidence on the effectiveness of bDMARDs/tsDMARDs has demonstrated a high unmet need reaching remission or LDA, even for the non-stringent DAS28 definitions. This systematic literature review (SLR) and meta-analysis was conducted to quantify real-world DAS28 clinical response rates, due to its high frequency of DAS28 reporting in the past literature, among patients with moderate to severe RA after 6 months of their first bDMARD/tsDMARD treatment.

Methods: An SLR was conducted using the MEDLINE and EMBASE databases and ACR (2015–2017) and EULAR (2015–2018) congress databases. The SLR included single- and multi-arm real-world observational studies that reported DAS28 remission outcomes (DAS28 < 2.6) at 6 months after bDMARD/tsDMARD treatment initiation in biologic-naïve adults with RA (N ≥50 per treatment arm). A traditional random-effects meta-analysis was conducted to estimate the DAS28 remission rates overall. Heterogeneity of studies for each treatment was assessed using the Cochran’s Q statistic and I2 statistic. In addition to DAS28 remission, DAS28 LDA rates, SDAI and CDAI remission rates were summarized descriptively.

Results: A total of 20 studies reported 6-month DAS28 remission data and were included in the analysis; only studies using bDMARDs met the inclusion criteria. Based on the meta-analysis (8,637 patients from studies conducted in 11 countries), the overall DAS28 remission rate was 24.1% (95% credible interval [CrI]: 19.4%, 29.5%; Figure). Remission rates by DAS28 measurement type were similar: DAS28–CRP, 24.5% [CrI 20.2%, 29.4%]; DAS28–ESR, 29.8% [CrI 24.8%, 35.4%]. Among the 20 included studies, a total of 9 reported the percentage of patients with LDA at 6 months, with some studies defining LDA as DAS28 ≥2.6 to < 3.2 while others as DAS28 ≥2.3 to < 2.7. The LDA rates ranged between 15% and 60% for DAS28 ≥2.6 to < 3.2 and between 11% and 56% for DAS28 ≥2.3 to < 2.7.

Conclusion: Despite treatment with bDMARDs, a large proportion of patients with RA do not achieve remission, even by the least stringent definition of remission, as by the DAS28 criteria (the rates of which are often higher than ACR70 response rates). Results from stringent remission criteria, e.g. the ACR/EULAR remission, have been reported too infrequently, but would show even much lower numbers indicative of a high unmet need in the RA treatment landscape and call for better treatment strategies.

Medical writing services provided by Brandy Menges (Fishawack Group, US) and funded by AbbVie.


Disclosure: D. Aletaha, AbbVie, 2, 5, 8, AbbVie, Janssen, Lilly, Novartis, Pfizer, and Roche, 5, AbbVie, Merck Sharp and Dohme, and Roche., 2, Amgen, 5, 8, Bristol-Myers Squibb, 8, Bristol-Myers Squibb, Celgene, Merck Sharp and Dohme, and UCB, 8, Celgene, 5, 8, Janssen, 5, Lilly, 5, 8, Medac, 5, 8, Merck, 5, 8, Merck Sharp and Dohme, 2, 8, Novartis, 2, 5, 8, Pfizer, 5, 8, Roche, 2, 5, 8, Sandoz, 5, 8, Sanofi/Genzyme, 5, 8, UCB, 8; R. Sawant, AbbVie, 1, 3; P. Zueger, AbbVie, 1, 3; E. Cook, Analysis Group, Inc., 3, 9; F. Mu, Analysis Group, Inc., 3, 9; V. Garg, AbbVie, 1, 3; K. Betts, Analysis Group, Inc., 3, 9.

To cite this abstract in AMA style:

Aletaha D, Sawant R, Zueger P, Cook E, Mu F, Garg V, Betts K. Systematic Literature Review and Meta-Analysis of DAS28 Clinical Response Rates Among Advanced Therapies in Biologic-Naïve Patients with Rheumatoid Arthritis [abstract]. Arthritis Rheumatol. 2019; 71 (suppl 10). https://acrabstracts.org/abstract/systematic-literature-review-and-meta-analysis-of-das28-clinical-response-rates-among-advanced-therapies-in-biologic-naive-patients-with-rheumatoid-arthritis/. Accessed .
  • Tweet
  • Email
  • Print

« Back to 2019 ACR/ARP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/systematic-literature-review-and-meta-analysis-of-das28-clinical-response-rates-among-advanced-therapies-in-biologic-naive-patients-with-rheumatoid-arthritis/

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