Methotrexate Reduces the Probability of Discontinuation of TNF Inhibitors in Seropositive Patients With Rheumatoid Arthritis. A Real-World Data Analysis.

TNF inhibitor drug survival methotrexate rheumatoid arthritis seropositivity

Journal

Frontiers in medicine
ISSN: 2296-858X
Titre abrégé: Front Med (Lausanne)
Pays: Switzerland
ID NLM: 101648047

Informations de publication

Date de publication:
2021
Historique:
received: 08 04 2021
accepted: 07 06 2021
entrez: 16 7 2021
pubmed: 17 7 2021
medline: 17 7 2021
Statut: epublish

Résumé

Tumor necrosis factor inhibitors (TNFi) are widely used for the treatment of patients with rheumatoid arthritis (RA), however a considerable percentage of patients discontinued the therapy. The aim of this study is to explore real-world TNFi survival, stratified for seropositivity, and to determine the factors that may influence it. This is a retrospective, observational and longitudinal study, using real-world data of patients, who started their first TNFi therapy between 1999 and 2018 from the RA-PAZ cohort. Patients were considered seropositive if they showed positive serum levels of either RF, ACPA, or both. Treatment survival was analyzed using Kaplan-Meier curves, and Cox proportional hazards models were used to compare the risks of TNFi discontinuation for seronegative and seropositive patients. Of the included 250 patients, 213 (85%) were seropositive. Results showed that TNFi survival did not depend on seropositivity status. However, median survival time was significant longer for seropositive patients who received concomitant MTX compared to patients who did not receive it (median [95% CI]: 3.3 yr. [2.3-4.2] vs. 2.6 yr. [1.7-3.6], respectively;

Identifiants

pubmed: 34268325
doi: 10.3389/fmed.2021.692557
pmc: PMC8275858
doi:

Types de publication

Journal Article

Langues

eng

Pagination

692557

Informations de copyright

Copyright © 2021 Hernández-Breijo, Brenis, Plasencia-Rodríguez, Martínez-Feito, Novella-Navarro, Pascual-Salcedo and Balsa.

Déclaration de conflit d'intérêts

CP-R has received research grants/honoraria from AbbVie, Lilly, Novartis, Pfizer, Sanofi, Biogen and UCB. DP-S reports speaker fees and grants from Abbvie, Grifols, Menarini, Novartis, Pfizer and Takeda during the conduct of the study. AB reports grants, consultancies and speaker fees from Abbvie, BMS, Nordic, Novartis, Pfizer, Sandoz, Sanofi, Roche and UCB during the conduct of the study. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Borja Hernández-Breijo (B)

Immuno-Rheumatology Research Group, Hospital La Paz Institute for Health Research-IdiPAZ, Madrid, Spain.

Claudia M Brenis (CM)

Immuno-Rheumatology Research Group, Hospital La Paz Institute for Health Research-IdiPAZ, Madrid, Spain.

Chamaida Plasencia-Rodríguez (C)

Immuno-Rheumatology Research Group, Hospital La Paz Institute for Health Research-IdiPAZ, Madrid, Spain.
Rheumatology, La Paz University Hospital, Madrid, Spain.

Ana Martínez-Feito (A)

Immuno-Rheumatology Research Group, Hospital La Paz Institute for Health Research-IdiPAZ, Madrid, Spain.
Immunology, La Paz University Hospital, Madrid, Spain.

Marta Novella-Navarro (M)

Immuno-Rheumatology Research Group, Hospital La Paz Institute for Health Research-IdiPAZ, Madrid, Spain.
Rheumatology, La Paz University Hospital, Madrid, Spain.

Dora Pascual-Salcedo (D)

Immuno-Rheumatology Research Group, Hospital La Paz Institute for Health Research-IdiPAZ, Madrid, Spain.

Alejandro Balsa (A)

Immuno-Rheumatology Research Group, Hospital La Paz Institute for Health Research-IdiPAZ, Madrid, Spain.
Rheumatology, La Paz University Hospital, Madrid, Spain.

Classifications MeSH