Tocilizumab for juvenile idiopathic arthritis: a single-center case series

Fatma Yazılıtaş1, Semanur Özdel2, Doğan Şimşek2

  • 1MD. Physician and Pediatric Nephrologist, Department of Pediatric Nephrology, Dr. Sami Ulus Kadin Doğum Çocuk Sağliği ve Hastaliklari Eğitim ve Araştirma Hastanesi, Sağlik Bilimleri Üniversitesi, Ankara, Turkey.

Insights

Tocilizumab effectively treated juvenile idiopathic arthritis (JIA) in patients refractory to other therapies, showing significant symptom improvement and disease control. This biologic therapy is a viable option for resistant cases of polyarticular JIA (pJIA) and systemic JIA (sJIA).

Area of Science:

  • Pediatric Rheumatology
  • Immunology
  • Pharmacology

Background:

  • Juvenile idiopathic arthritis (JIA) is a prevalent chronic childhood rheumatic disease.
  • Inadequate treatment of JIA can result in joint damage, functional disability, and long-term health issues.

Purpose of the Study:

  • To evaluate the efficacy, safety, and tolerability of tocilizumab in pediatric patients with JIA.
  • To assess tocilizumab's utility in polyarticular JIA (pJIA) and systemic JIA (sJIA) cases unresponsive to other treatments.

Main Methods:

  • Retrospective observational case series involving 11 JIA patients treated with tocilizumab.
  • Analysis of patient records for demographic data, clinical/laboratory findings, treatment response, and adverse events.
  • Efficacy assessment using American College of Rheumatology (ACR) pediatric (Pedi) response criteria (ACR Pedi 30, 50, 70, 90).

Main Results:

  • Tocilizumab was administered to seven sJIA and four pJIA patients.
  • Most patients experienced symptom improvement, reduced inflammation, and achieved inactive disease.
  • High response rates observed: 90.9% achieved ACR Pedi 30, 50, and 70 scores.
  • Minor side effects were reported in five patients.

Conclusions:

  • Tocilizumab is a beneficial treatment option for JIA patients.
  • Consider tocilizumab for pJIA and sJIA patients resistant to conventional disease-modifying anti-rheumatic drugs (DMARDs) and/or other biologics.
Abstract

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