Rheumatoid arthritis

Progressive interstitial lung disease associated with rheumatoid arthritis and abatacept: data from a multicentre cohort of 526 patients

Rheumatology (Oxford)Published Multicentre cohort study

Authors' conclusion

Despite ABA therapy, progressive ILD occurred in nearly one-quarter of RA patients.

Study context

Population
RA-associated interstitial lung disease (ILD) patients treated with abatacept in clinical practice, with serial pulmonary function testsfrom cohort of 526
Participants
343 patients
Exposure
Progressive vs stable or improved ILD in RA-ILD treated with abatacept
  • Progressive ILDn = 80
  • Stable or improvedn = 263reference
Outcome
Progressive ILD (absolute decline in FVC ≥10% or relative decline of 5-9% with clinical and/or radiological progression)
Follow-up
24 months after starting ABA
Methodological detailsnational multicentre, multivariable analysis
  • National multicentre
  • Multivariable analysis

Main finding

As reported in the abstract

Progressive ILD · 24 months

Observational data: associations, not effects.

Further findings

Prior MTX exposure, progressive ILD vs stable or improved

Prior MTX exposure, progressive cases vs stable/improved (p = 0.02)
63% vs 76%
  • Lower prior exposure among progressive cases

Prior tocilizumab exposure, progressive ILD vs stable or improved

Prior tocilizumab exposure, progressive cases vs stable/improved (p = 0.048)
4 vs 34
  • Lower prior exposure among progressive cases

Predictors of ILD progression (multivariable analysis)

Prior MTX treatment (protective), OR
0.453
Previous golimumab exposure, OR
10.009
Higher DAS28-ESR, OR
1.284
  • Multivariable analysis

ILD progression by ILD radiologic pattern or time from ABA initiation

No significant differences according to ILD radiologic pattern or time from ABA initiation

Original publication

Progressive interstitial lung disease associated with rheumatoid arthritis and abatacept: data from a multicentre cohort of 526 patients. Rheumatology (Oxford). Published 18 January 2026. doi:10.1093/rheumatology/keag023

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