Rheumatoid arthritis

Drug retention of biologics and Janus kinase inhibitors in patients with rheumatoid arthritis: the ANSWER cohort study

RMD OpenPublished Retrospective cohort study

Authors' conclusion

TNFi (HR=1.52, 95% CI: 1.37 to 1.68) and CTLA4-Ig (HR=1.14, 95% CI: 1.00 to 1.30) showed a higher overall drug discontinuation rate, excluding non-toxicity and remission, than aIL-6R.

Study context

Population
Real-world cohort of patients with RA, multicentre, Japan (ANSWER cohort)
Participants
6,666 treatment courses
Exposure
Tumour necrosis factor inhibitors (TNFi), CTLA4-Ig and Janus kinase inhibitors (JAKi) vs aIL-6R
  • TNFin = 3,577
  • aIL-6Rn = 1,497reference
  • CTLA4-Ign = 1,139
  • JAKin = 453
Outcome
Drug retention; HRs of treatment discontinuation by reason (ineffectiveness, toxic adverse events, non-toxic reasons, remission)
Methodological detailsmulticentre, multivariate Cox proportional hazards modelling
  • Multicentre
  • Multivariate Cox proportional hazards modelling

Main finding

As reported in the abstract

Discontinuation due to ineffectiveness
Each group vs aIL-6RHazard ratio (95% CI)
TNFi
1.93(1.69–2.19)
CTLA4-Ig
1.42(1.20–1.67)
JAKi
1.29(1.03–1.63)

Observational data: associations, not effects.

Further findings

OutcomeHR for overall drug discontinuation (95% CI)
Overall drug discontinuation (excluding non-toxic reasons and remission)TNFivs aIL-6R1.52 (1.37–1.68)
Overall drug discontinuation (excluding non-toxic reasons and remission)CTLA4-Igvs aIL-6R1.14 (1.00–1.30)

Safety

OutcomeHR (95% CI)
Discontinuation due to toxic adverse eventsTNFivs CTLA4-Ig1.28 (1.05–1.56)
Discontinuation due to toxic adverse eventsaIL-6Rvs CTLA4-Ig1.27 (1.03–1.57)
Baseline oral GC use and discontinuation due to toxic adverse eventsJAKivs aIL-6RConcomitant oral GCs at baseline2.30 (1.23–4.28)
Baseline oral GC use and discontinuation due to toxic adverse eventsTNFivs aIL-6RConcomitant oral GCs at baseline1.29 (1.07–1.55)

Original publication

Drug retention of biologics and Janus kinase inhibitors in patients with rheumatoid arthritis: the ANSWER cohort study. RMD Open. Published 18 August 2023. doi:10.1136/rmdopen-2023-003160

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