Literature DB >> 32728836

Comparison of the efficacy and safety of biologic agents between elderly-onset and young-onset RA patients: the ANSWER cohort study.

Sadao Jinno1, Akira Onishi2, Maureen Dubreuil3,4, Kengo Akashi2, Motomu Hashimoto5, Wataru Yamamoto5, Koichi Murata5, Tohru Takeuchi6, Takuya Kotani6, Yuichi Maeda7, Kosuke Ebina8, Yonsu Son9, Hideki Amuro9, Ryota Hara10, Masaki Katayama11, Jun Saegusa2, Akio Morinobu2.   

Abstract

The objective of the study was to compare the efficacy and safety of biological disease-modifying antirheumatic drugs (bDMARDs) between elderly-onset rheumatoid arthritis (EORA) and young-onset rheumatoid arthritis (YORA) patients. Patients with rheumatoid arthritis (RA) aged ≧18 years enrolled in a Japanese multicenter observational registry between 2009 and 2018 who had moderate or high disease activity when initiating bDMARDs were included. EORA was defined as RA with onset at 60 or over. After propensity score weighting for differences in confounding factors, generalized estimating equations were used to assess the relationship between the age of RA onset and bDMARD clinical effectiveness at 48 weeks after starting a bDMARD. Among a total of 7183 patients in the registry, 2815 (39.2%) were identified as EORA. The proportion of patients on bDMARDs was lower in the EORA as compared to the YORA (18.3% vs 28.0%, p < 0.001). Of the 989 bDMARD initiators, 364 (36.8%) were identified as EORA. The median follow-up duration was 48 weeks both in the EORA and in the YORA. After adjusting for differences in baseline characteristics between the two age groups, there was no significant difference in Clinical Disease Activity Index scores at 48 weeks (mean difference 1.01, 95% CI = - 0.62 to 2.64, p = 0.22). There was a non-significant trend toward lower remission in EORA (OR = 0.52, 95% CI = 0.24-1.14, p = 0.10), and low disease activity/remission was similar (OR = 0.86, 95% CI = 0.29-2.52, p = 0.77). Drug retention (HR = 0.95, 95% CI = 0.55-1.35, p = 0.78) and discontinuations due to adverse events (HR = 0.78, 95% CI = 0.38-1.18, p = 0.22) were similar between the two age groups after adjustment for confounders. In RA patients initiating bDMARDs, improvements in clinical disease at 48 weeks were similar between EORA and YORA. Drug retention and adverse events discontinuation were similar between the two age groups.

Entities:  

Keywords:  Adult; Age of onset; Aged; Antirheumatic agents/therapeutic use; Arthritis; Biological products/therapeutic use; Disease progression; Health care; Outcome and process assessment; Registries; Rheumatoid/drug therapy; Rheumatoid/epidemiology

Year:  2020        PMID: 32728836     DOI: 10.1007/s00296-020-04660-y

Source DB:  PubMed          Journal:  Rheumatol Int        ISSN: 0172-8172            Impact factor:   2.631


  2 in total

1.  Risk of Severe Infection among Rheumatoid Arthritis Patients on Biological DMARDs: A Population-Based Cohort Study.

Authors:  Mattia Bellan; Lorenza Scotti; Daniela Ferrante; Elisa Calzaducca; Giulia Francesca Manfredi; Pier Paolo Sainaghi; Francesco Barone-Adesi
Journal:  J Clin Med       Date:  2022-05-24       Impact factor: 4.964

2.  Comparison of efficacy between anti-IL-6 receptor antibody and other biological disease-modifying antirheumatic drugs in the patients with rheumatoid arthritis who have knee joint involvement: the ANSWER cohort, retrospective study.

Authors:  Yuichi Maeda; Toru Hirano; Kosuke Ebina; Ryota Hara; Motomu Hashimoto; Wataru Yamamoto; Kosaku Murakami; Takuya Kotani; Kenichiro Hata; Yonsu Son; Hideki Amuro; Akira Onishi; Sadao Jinno; Masaki Katayama; Atsushi Kumanogoh
Journal:  Rheumatol Int       Date:  2021-04-26       Impact factor: 2.631

  2 in total

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