Predictors of Effectiveness of Anakinra in Systemic Juvenile Idiopathic Arthritis

Benedetta Saccomanno1,2, Jessica Tibaldi1,2, Francesca Minoia1,2

  • 1From the Università degli Studi di Genova, and the Istituto Giannina Gaslini, Genoa; Fondazione Institute for Research and Health Care (IRCCS) Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy; Instituto de Criança - Faculty of Medicine of the University of São Paulo (FMUSP), São Paulo, Brazil.

Insights

Predictors of treatment success for anakinra in children with systemic-onset juvenile idiopathic arthritis (sJIA) include shorter disease duration and higher ferritin levels. Early interleukin-1 (IL-1) inhibition may benefit specific patient profiles.

Area of Science:

  • Pediatric Rheumatology
  • Immunology
  • Pharmacology

Background:

  • Systemic-onset juvenile idiopathic arthritis (sJIA) is a severe autoimmune disease.
  • Interleukin-1 (IL-1) inhibitors like anakinra offer therapeutic options for sJIA.
  • Predicting response to anakinra is crucial for optimizing treatment strategies.

Purpose of the Study:

  • To identify predictors of therapeutic response to anakinra in pediatric patients with sJIA.
  • To delineate the clinical profile of children likely to benefit from IL-1 blockade.

Main Methods:

  • Retrospective review of clinical charts for sJIA patients treated with anakinra (2004-2017).
  • Analysis of demographic, clinical, and laboratory variables as potential predictors.
  • Assessment of anakinra effectiveness at 1 year, defining complete clinical response (CCR).

Main Results:

  • Of 62 sJIA patients, 39% achieved CCR at 1 year.
  • Multivariable analysis identified shorter disease duration, lower active joint count, higher ferritin, and greater systemic activity as predictors of CCR.
  • The predictive model demonstrated an area under the curve of 0.83.

Conclusions:

  • Shorter disease duration, fewer active joints, higher ferritin, and more active systemic disease predict anakinra response in sJIA.
  • Findings support early IL-1 inhibition for select sJIA patients.
  • Further research is needed to identify biomarkers for IL-1 and IL-6 antagonist response.
Abstract

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