ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2025
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • 2020-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstract Number: 2268

Differential Impact of Certolizumab Pegol, Etanercept, and Adalimumab on Rheumatoid Factor Reduction and Seroconversion in Rheumatoid Arthritis: A Propensity Score–Matched Study

Clementina López Medina1, Rafaela Ortega-Castro2, Francisco Jose Cepas3, Montserrat Robustillo-Villarino4, Andres Zuniga-Vera4, Ana Martinez-Feito5, Ester Costa-Moya6, Delia Taverner-Torrent6, Luis Sainz Comas7, Cesar Diaz-Torne7, Virginia Ruiz-Esquide8, Cynthia Rojas9, Lourdes Martin-de la Sierra Lopez10, Laura Jimenez-Rodriguez10, David Velasco-Sanchez10, Regina Fará Garcia11, Antonio Juan-Mas12, Marina soledad Moreno Garcia13, Ana Valeria Acosta Alfaro14, Santiago Muñoz15, Maria Martín López16, Raquel Zas17, FRANCISCO JAVIER GODOY NAVARRETE18, Isabel Anon Onate19, Fernando Ortiz-Márquez20, Natalia Mena Vázquez21, Paula Estrada-Alarcón22, Jerusalén Calvo23, Alejandro Escudero Contreras23 and Chamaida Plasencia-Rodríguez24, 1Department of Medicine, Hospital Universitario Reina Sofia, University of Cordoba, IMIBIC, Cordoba, Spain, 2Rheumatology service/Maimonides Institute for Research in Biomedicine of Cordoba (IMIBIC)/ Reina Sofia University Hospital/ University of Cordoba, Spain, Cordoba, Andalucia, Spain, 3University of Cordoba, Cordoba, Spain, 4Department of Rheumatology, Hospital Universitario de la Plana, Vila-real, Castellón, Spain, Vila-real, Castellón, Spain, 5Hospital Universitario La Paz, Madrid, Madrid, Spain, 6Hospital Sant Joan Reus, Reus, Spain, 7Hospital de la Santa Creu i Sant Pau, Barcelona, Spain, 8Hospital Clínic de Barcelona, Barcelona, Catalonia, Spain, 9Hospital Clinic, Barcelona, Spain, 10Hospital General Universitario de Ciudad Real, Ciudad Real, Spain, 11Hospital Son Llàtzer, Palma, Spain, 12Son Llazter University Hospital, Madrid, Spain, 13Hospital Universitario Miguel Servet, Zaragoza, Spain, 14Hospital Universitario Infanta Sofia; Universidad Europea de Madrid; FIIB HUIS-HUHEN, Madrid, Spain, 15Hospital Universitario Infanta Sofía;Universidad Europea de Madrid. Faculty of Medicine, Health and Sports. Department of Medicine; FIIB HUIS-HUHEN, Madrid, Spain, 16Hospital 12 de Octubre, Madrid, Spain, 17Hospital Universitario Doce de Octubre, Madrid, Spain, 18Jaen University Hospital, Spain, Jaen, Spain, 19Hospital Universitario de Jaén, Jaén, Spain, 20Department of Rheumatology, Hospital Regional Universitario de Málaga, Málaga, Spain, Malaga, Spain, 21Hospital Regional Universitario de Malaga, Malaga, Spain, Málaga, Spain, 22Hospital de San Juan Despí Moisès Broggi, Barcelona, Spain, 23IMIBIC / Reina Sofia Hospital / University of Cordoba, Córdoba, Spain, 24Hospital Universitario La Paz, MADRID, Spain

Meeting: ACR Convergence 2025

Keywords: Anti-TNF Drugs, rheumatoid arthritis, Rheumatoid Factor

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

Date: Tuesday, October 28, 2025

Title: (2265–2289) Rheumatoid Arthritis – Treatment Poster III

Session Type: Poster Session C

Session Time: 10:30AM-12:30PM

Background/Purpose: Rheumatoid factor (RF) is an antibody that contributes to the development of rheumatoid arthritis (RA) and is associated with greater disease severity. Seroconversion of RF after biological DMARD (bDMARD) treatment has been reported as infrequent. However, little is known about changes in serological status and their association with disease activity across different TNF inhibitors (TNFi).The objectives of this study were: a) To compare the change in RF levels and the rate of seroconversion over 6 months of treatment with certolizumab pegol (CZP), etanercept (ETN), and adalimumab (ADA); and b) To evaluate the association between the reduction in RF levels and the change in disease activity.

Methods: Longitudinal, retrospective, multicentre study including RA patients treated with CZP, ETN, or ADA between 2010 and 2024. RF levels and DAS28-ESR scores before TNFi initiation and after 6 months were collected. Two propensity score (PS) matching approaches (CZP vs. ETN and CZP vs. ADA) were used to balance the groups based on baseline imbalances. Paired t-tests evaluated changes in RF levels within treatments groups, and Pearson correlations assessed association between RF and DAS28 changes after confirming data normality. The proportions of seropositive patients who converted to seronegative and those achieving >50% reduction in RF after 6 months were compared using chi-square tests.

Results: A total of 1,185 RA patients treated with TNFi (246 CZP, 343 ETN, and 513 ADA) were included. After PS matching, 203 CZP vs. 203 ETN and 224 CZP vs. 224 ADA were analyzed, achieving balance in age, sex, disease duration, concomitant MTX use, and TNFi treatment line.ETN showed no significant difference in mean RF change after 6 months, whereas CZP showed a significant reduction (Figure 1A-B). Among seropositive, CZP-treated patients more often achieved >50% RF reduction than those on ETN (21.7% vs. 8.6%, p=0.010) (Figure 2A), and showed a numerically higher rate of seroconversion (9.4% vs. 5.2%). After 6 months, a direct association between RF and DAS28 reductions was observed in CZP-treated patients, whereas an inverse association was found in ETN-treated patients (Figure 3A–B), suggesting RF reduction was linked with an increase DAS28 in the ETN group.In the ADA vs. CZP comparison (Figure 1C–D), CZP showed a significant reduction in RF levels, while ADA did not. Among seropositive patients, more CZP-treated patients achieved >50% RF reduction than those on ADA (24.4% vs. 11.1%, p=0.028), and showed a numerically higher seroconversion rate (9.4% vs. 5.9%) (Figure 2B). After 6 months, RF and DAS28 changes were not associated in ADA-treated patients, while a significant association was seen in CZP group (Figure 3C–D).

Conclusion: CZP treatment was associated with a significant reduction in absolute RF levels and in the proportion of patients achieving >50% RF reduction compared to both ETN and ADA after 6 months. In CZP-treated patients, RF reduction was positively associated with improved in disease activity, suggesting a potential biomarker role for RF in CZP therapy follow-up. These findings suggest that RF reduction and seroconversion may vary across TNFi, with CZP showing a more favorable serological and clinical profile.

Supporting image 1Figure 1. Paired t-Test Analysis of Rheumatoid Factor Changes at 6 Months in Propensity Score-Matched Comparisons Between ETN vs. CZP (A,B) and ADA vs. CZP (C,D).

Supporting image 2Figure 2. Proportion of Patients Achieving >50% Reduction in Rheumatoid Factor at 6 Months in Propensity Score–Matched Comparisons: ETN vs. CZP (A) and ADA vs. CZP (B)

Supporting image 3Figure 3. Correlation Analysis of Rheumatoid Factor Changes and DAS28-ESR changes at 6 Months in Propensity Score-Matched Comparisons Between ETN vs. CZP (A,B) and ADA vs. CZP (C,D).


Disclosures: C. López Medina: None; R. Ortega-Castro: None; F. Cepas: None; M. Robustillo-Villarino: None; A. Zuniga-Vera: None; A. Martinez-Feito: None; E. Costa-Moya: None; D. Taverner-Torrent: None; L. Sainz Comas: None; C. Diaz-Torne: None; V. Ruiz-Esquide: None; C. Rojas: None; L. Martin-de la Sierra Lopez: None; L. Jimenez-Rodriguez: None; D. Velasco-Sanchez: None; R. Fará Garcia: None; A. Juan-Mas: None; M. Moreno Garcia: None; A. Acosta Alfaro: None; S. Muñoz: Janssen, 1, 2, 5, 6, 7; M. Martín López: None; R. Zas: None; F. GODOY NAVARRETE: None; I. Anon Onate: None; F. Ortiz-Márquez: None; N. Mena Vázquez: None; P. Estrada-Alarcón: None; J. Calvo: None; A. Escudero Contreras: None; C. Plasencia-Rodríguez: AbbVie/Abbott, 5, 6, Eli Lilly, 6, Novartis, 6, Pfizer, 5, 6, UCB, 6.

To cite this abstract in AMA style:

López Medina C, Ortega-Castro R, Cepas F, Robustillo-Villarino M, Zuniga-Vera A, Martinez-Feito A, Costa-Moya E, Taverner-Torrent D, Sainz Comas L, Diaz-Torne C, Ruiz-Esquide V, Rojas C, Martin-de la Sierra Lopez L, Jimenez-Rodriguez L, Velasco-Sanchez D, Fará Garcia R, Juan-Mas A, Moreno Garcia M, Acosta Alfaro A, Muñoz S, Martín López M, Zas R, GODOY NAVARRETE F, Anon Onate I, Ortiz-Márquez F, Mena Vázquez N, Estrada-Alarcón P, Calvo J, Escudero Contreras A, Plasencia-Rodríguez C. Differential Impact of Certolizumab Pegol, Etanercept, and Adalimumab on Rheumatoid Factor Reduction and Seroconversion in Rheumatoid Arthritis: A Propensity Score–Matched Study [abstract]. Arthritis Rheumatol. 2025; 77 (suppl 9). https://acrabstracts.org/abstract/differential-impact-of-certolizumab-pegol-etanercept-and-adalimumab-on-rheumatoid-factor-reduction-and-seroconversion-in-rheumatoid-arthritis-a-propensity-score-matched-study/. Accessed .
  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print

« Back to ACR Convergence 2025

ACR Meeting Abstracts - https://acrabstracts.org/abstract/differential-impact-of-certolizumab-pegol-etanercept-and-adalimumab-on-rheumatoid-factor-reduction-and-seroconversion-in-rheumatoid-arthritis-a-propensity-score-matched-study/

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 »

Embargo Policy

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 CT on October 25. 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