Vasculitis & polymyalgia rheumatica

Effectiveness and safety of interleukin 6 receptor inhibitors versus conventional immunomodulatory therapy in steroid-refractory polymyalgia rheumatica

RMD OpenPublished Retrospective cohort study

Main finding · GC discontinuationResult — go to the resultAdjusted hazard ratio 1.28 95% CI 1.02–1.60

Authors' conclusion

IL-6Ri therapy was more effective as a steroid-sparing agent than csIM for PMR with no new safety findings.

Study context

Population
Patients with PMR on glucocorticoids (GC), without prior IL-6Ri exposure, initiating IL-6Ri/conventional synthetic immunomodulators (csIM) therapy; US Medicare fee-for-service claims; csIM-naïve and csIM-experienced cohorts415 matched pairs (187/228)
Exposure
IL-6R inhibitors vs conventional synthetic immunomodulators in PMR on GC
Outcome
Time-to-GC discontinuation and time-to-minimal GC use (≤2 mg/day or stop GC)
Follow-up
Year 1
Methodological detailscomparative cohort, matched using direct methods and propensity score methods, US Medicare claims data
  • Comparative cohort
  • Matched using direct methods and propensity score methods
  • US Medicare claims data

Main finding

GC discontinuation

Adjusted hazard ratio

1.28

95% CI 1.02–1.60

P = 0.031

IL-6Rivs csIM
aHR 1.28 (95% CI 1.02–1.60); P = 0.031

As reported in the abstract

Observational data: associations, not effects.

Further findings

OutcomeaHR (95% CI)P value
Co-primary: minimal GC use (≤2 mg/day or stop GC) · year 11.28 (1.03–1.58)P = 0.025

Safety

Primary hospitalised infections, IR/100 patient-years · year 1

Primary hospitalised infections, IR/100 patient-years · year 2

Primary hospitalised infections, IR/100 patient-years · year 2

Similar for year 2

Other adverse events of special interest

Incidence rates (IRs) low and comparable in both groups

Original publication

Effectiveness and safety of interleukin 6 receptor inhibitors versus conventional immunomodulatory therapy in steroid-refractory polymyalgia rheumatica. RMD Open. Published 3 August 2026. doi:10.1136/rmdopen-2026-006850

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