Rheumatoid arthritis

Comparison of tofacitinib, baricitinib, upadacitinib and filgotinib: a 2-year observational study from FIRST registry

RMD OpenPublished Retrospective cohort study

Authors' conclusion

This real-world study found no clinically meaningful differences in 2-year effectiveness among four JAKis, although the study was not powerful enough to detect differences in safety.

Study context

Population
Patients with rheumatoid arthritis (RA) treated with Janus kinase inhibitors (JAKis) in real-world settings, FIRST registry
Participants
607 treatment courses
Exposure
Four JAKis compared: Tofacitinib (TOF) vs baricitinib (BAR) vs upadacitinib (UPA) vs filgotinib (FIL)
  • TOFn = 159
  • BARn = 262
  • UPAn = 122
  • FILn = 64
Outcome
Change in CDAI score
Follow-up
Year 2
Methodological detailsmulticentre registry, multivariable mixed-effects models adjusted for baseline characteristics
  • Multicentre registry
  • Multivariable mixed-effects models adjusted for baseline characteristics

Main finding

As reported in the abstract

Change in CDAI
  • Multivariable analysis: no significant differences in Clinical Disease Activity Index (CDAI) among the four JAKis
  • As-observed analysis: slower improvement in UPA and FIL

Observational data: associations, not effects.

Secondary outcomes

Patient-reported outcomes (PROs)

Multivariable analysis: no significant differences in PROs

CDAI components (tender joint count, evaluator's global assessment)

UPA showed greater improvement in tender joint count and evaluator's global assessment

Overall retention rate · 2 years

2-year overall retention rate
78%

Discontinuation for insufficient effectiveness (most common reason)

Rate
6.5/100 person-years

Safety

Discontinuation for adverse events

Rate
4.2/100 py
  • Study not powerful enough to detect differences in safety

Original publication

Comparison of tofacitinib, baricitinib, upadacitinib and filgotinib: a 2-year observational study from FIRST registry. RMD Open. Published 16 January 2026. doi:10.1136/rmdopen-2025-006503

Composed by AI from the published abstract and checked against it. How Briefs are made →

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