Across rheumatic diseases

Oral glucocorticoid treatment for checkpoint inhibitor-associated inflammatory arthritis does not affect cancer progression-free survival: a RADIOS Registry study

Ann Rheum DisPublished Prospective cohort study

Main finding · PFS, GC exposure (time-varying Cox model)Result — go to the resultAdjusted hazard ratio 2.64 95% CI 0.36–19.61

Authors' conclusion

In this prospective ICI-IA cohort, low doses of glucocorticoids (median dose 13 mg [IQR: 7.5, 25] in the first month of treatment) did not adversely affect PFS.

Study context

Population
Patients with cancer with immune checkpoint inhibitor-associated inflammatory arthritis (ICI-IA), RADIOS registry; mean age 64.85 years, 48.3% female, 32% melanoma, 56.4% stage IV
Participants
269 patients
Exposure
GC exposure vs no GC / lower dose
Outcome
Cancer progression-free survival (PFS)
Methodological detailsmulticentre, registry, time-varying and landmark multivariable Cox regression
  • Multicentre
  • Registry
  • Time-varying and landmark multivariable Cox regression

Main finding

PFS, GC exposure (time-varying Cox model)

Adjusted hazard ratio

2.64

95% CI 0.36–19.61

Glucocorticoids
aHR 2.64 (95% CI 0.36–19.61)

As reported in the abstract

Observational data: associations, not effects.

Further findings

OutcomeaHR (95% CI)
PFS, GC dose abovevs below median in first month · first month of ICI-IA treatmentAdjusted Cox models; not associated with worse PFS1.15 (0.59–2.25)

Cancer progression (all participants)

Cancer progression
67 (24.9%)

GC dose in first month (prednisone equivalent) · first month of treatment

Median GC dose, mg daily
13
IQR
7.5, 25
Received immunomodulatory DMARD
7.8%

Original publication

Oral glucocorticoid treatment for checkpoint inhibitor-associated inflammatory arthritis does not affect cancer progression-free survival: a RADIOS Registry study. Ann Rheum Dis. Published 10 April 2026. doi:10.1016/j.ard.2026.02.017

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