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Risk, Timing, and Predictors of Disease Flare After Discontinuation of Anti–Tumor Necrosis Factor Therapy in Children With Polyarticular Forms of Juvenile Idiopathic Arthritis With Clinically Inactive Disease

  • Daniel J. Lovell
  • , Anne L. Johnson
  • , Bin Huang
  • , Beth S. Gottlieb
  • , Paula W. Morris
  • , Yukiko Kimura
  • , Karen Onel
  • , Suzanne C. Li
  • , Alexei A. Grom
  • , Janalee Taylor
  • , Hermine I. Brunner
  • , Jennifer L. Huggins
  • , James J. Nocton
  • , Kathleen A. Haines
  • , Barbara S. Edelheit
  • , Michael Shishov
  • , Lawrence K. Jung
  • , Calvin B. Williams
  • , Melissa S. Tesher
  • , Denise M. Costanzo
  • Lawrence S. Zemel, Jason A. Dare, Murray H. Passo, Kaleo C. Ede, Judyann C. Olson, Elaine A. Cassidy, Thomas A. Griffin, Linda Wagner-Weiner, Jennifer E. Weiss, Larry B. Vogler, Kelly A. Rouster-Stevens, Timothy Beukelman, Randy Q. Cron, Daniel Kietz, Kenneth Schikler, Kara M. Schmidt, Jay Mehta, Dawn M. Wahezi, Tracy V. Ting, James W. Verbsky, B. Anne Eberhard, Steven Spalding, Chen Chen, Edward H. Giannini
  • Cincinnati Children's Hospital Medical Center
  • Northwell Health System
  • University of Arkansas for Medical Sciences
  • Hospital for Special Surgery - New York
  • Joseph M. Sanzari Children's Hospital
  • Medical College of Wisconsin
  • Connecticut Children's Medical Center
  • Phoenix Children's Hospital
  • Children's National Medical Center
  • The University of Chicago
  • Medical University of South Carolina
  • University of Pittsburgh
  • Emory University
  • University of Alabama at Birmingham
  • University of Louisville
  • Albert Einstein College of Medicine
  • Cleveland Clinic Foundation

Research output: Contribution to journal › Article › peer-review

39 Scopus citations

Abstract

Objective: To determine the frequency, time to flare, and predictors of disease flare upon withdrawal of anti–tumor necrosis factor (anti-TNF) therapy in children with polyarticular forms of juvenile idiopathic arthritis (JIA) who demonstrated ≥6 months of continuous clinically inactive disease. Methods: In 16 centers 137 patients with clinically inactive JIA who were receiving anti-TNF therapy (42% of whom were also receiving methotrexate [MTX]) were prospectively followed up. If the disease remained clinically inactive for the initial 6 months of the study, anti-TNF was stopped and patients were assessed for flare at 1, 2, 3, 4, 6, and 8 months. Life-table analysis, t-tests, chi-square test, and Cox regression analysis were used to identify independent variables that could significantly predict flare by 8 months or time to flare. Results: Of 137 patients, 106 (77%) maintained clinically inactive disease while receiving anti-TNF therapy for the initial 6 months and were included in the phase of the study in which anti-TNF therapy was stopped. Stopping anti-TNF resulted in disease flare in 39 (37%) of 106 patients by 8 months. The mean/median ± SEM time to flare was 212/250 ± 9.77 days. Patients with shorter disease duration at enrollment, older age at onset and diagnosis, shorter disease duration prior to experiencing clinically inactive disease, and shorter time from onset of clinically inactive disease to enrollment were found to have significantly lower hazard ratios for likelihood of flare by 8 months (P < 0.05). Conclusion: Over one-third of patients with polyarticular JIA with sustained clinically inactive disease will experience a flare by 8 months after discontinuation of anti-TNF therapy. Several predictors of lower likelihood of flare were identified.

Original languageEnglish
Pages (from-to)1508-1518
Number of pages11
JournalArthritis and Rheumatology
Volume70
Issue number9
DOIs
StatePublished - Sep 2018

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