Validation of prediction models for anti-tumor necrosis factor treatment response in pediatric Crohn's disease: a

Omer Rotem-Tryfus1,2, Ben Kang3, Esther Orlanski-Meyer1

  • 1Juliet Keidan Institute of Pediatric Gastroenterology Hepatology and Nutrition, Shaare Zedek Medical Center, The Eisenberg R&D Authority, Jerusalem, Israel.

Journal of Crohn'S & Colitis
|September 19, 2025
PubMed

Insights

Predicting anti-tumor necrosis factor (TNF) therapy success in children with Crohn's disease is challenging. Existing prediction models show limited generalizability, emphasizing the need for external validation in pediatric populations.

Area of Science:

  • Pediatric Gastroenterology
  • Immunology
  • Clinical Trial Methodology

Background:

  • External validation of predictors for anti-tumor necrosis factor (TNF) therapy outcomes is limited, especially in pediatric populations.
  • Predicting treatment success in children with Crohn's disease (CD) requires robust, validated tools.

Purpose of the Study:

  • To systematically review and identify predictors of anti-TNF therapeutic success in Crohn's disease.
  • To externally validate identified predictors in a prospective pediatric cohort.

Main Methods:

  • Systematic literature search of PubMed and Embase for anti-TNF outcome predictors in CD.
  • Evaluation of identified predictors in a cohort of 186 pediatric CD patients initiating anti-TNF therapy.
  • Validation of multivariable models using logistic regression and area under the curve (AUC).

Main Results:

  • 24 individual predictors and 5 multi-item models were identified; few studies focused on children.
  • Prior corticosteroid use and combination immunomodulator therapy increased primary non-response risk.
  • Post-induction disease activity and inflammatory markers predicted remission and loss of response; multivariable models showed variable performance (AUC 0.54-0.76).

Conclusions:

  • Few previously suggested predictors demonstrated acceptable performance in pediatric CD, particularly those relying on post-induction data.
  • Existing prediction rules have limited generalizability in pediatric CD.
  • External validation is crucial before implementing prediction rules in clinical practice for pediatric CD patients.
Abstract

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