Pediatric rheumatology

Canakinumab dosing intervals in pediatric colchicine-resistant familial Mediterranean fever (FMF): outcomes and predictors of successful extension in a real-world cohort

Rheumatology (Oxford)Published Retrospective cohort study

Authors' conclusion

Although canakinumab achieves sustained inflammatory suppression, biochemical improvement does not ensure comparable clinical control.

Study context

Population
Pediatric patients with colchicine-resistant FMF treated with canakinumab
Participants
60 patients
Exposure
Canakinumab dosing interval groups: stable interval vs successful vs unsuccessful interval extension
  • Group 1n = 14reference
  • Group 2n = 24
  • Group 3n = 22
Outcome
Clinical and inflammatory outcomes across dosing interval groups; predictors of successful interval extension
Methodological detailssingle-centre, linear mixed-effects models, multivariable logistic regression, Firth's penalized method as sensitivity analysis
  • Single-centre
  • Linear mixed-effects models
  • Multivariable logistic regression
  • Firth's penalized method as sensitivity analysis

Main finding

As reported in the abstract

Complete remission rate

P = 0.005

Observational data: associations, not effects.

Further findings

OutcomeEstimateP value
Arthritis at disease onset as predictor of successful interval extension (multivariable logistic regression)Arthritis at onsetvs No arthritis at onsetIndependently associated · Firth's penalized method as sensitivity analysisOR for successful interval extension 7.14 (95% CI 1.26–40.41)P = 0.026
Arthritis at disease onset as predictor of successful interval extension (multivariable logistic regression)Arthritis at onsetvs No arthritis at onsetConsistent direction · Firth's penalized method as sensitivity analysisOR for successful interval extension (Firth sensitivity analysis) 5.51 (95% CI 1.08–28.23)P = 0.081

Annual attack rate after canakinumab initiation, median (all patients)

Median annual attack rate before canakinumab, attacks per patient-year
7 (4-12)
Median annual attack rate after canakinumab, attacks per patient-year
1.1 (0.5-2.1)

C-reactive protein (CRP) trajectories

CRP declined rapidly and stabilized after month 3; inflammatory trajectories did not differ across groups

Original publication

Canakinumab dosing intervals in pediatric colchicine-resistant FMF: outcomes and predictors of successful extension in a real-world cohort. Rheumatology (Oxford). Published 19 August 2026. doi:10.1093/rheumatology/keag437

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