Development and validation of a risk prediction model for acute chemotherapy-induced nausea and vomiting in pediatric

Luyan Yu1, Yiheng Wu2, Nan Lin3

  • 1Department of Neurosurgery, Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou, China.

PubMed

Insights

This study developed a risk prediction model for chemotherapy-induced nausea and vomiting (CINV) in pediatric cancer patients. The model identifies key predictors, enabling personalized interventions to reduce CINV occurrence in children.

Area of Science:

  • Pediatric Oncology
  • Clinical Pharmacology
  • Biostatistics

Background:

  • Acute chemotherapy-induced nausea and vomiting (CINV) is highly prevalent in pediatric cancer patients (80-95%).
  • Existing risk prediction models for CINV are scarce for pediatric populations, despite distinct risk patterns from adults.
  • There is a need for tools to guide CINV prophylaxis and reduce its occurrence in children.

Purpose of the Study:

  • To develop and validate a risk prediction model for acute CINV in pediatric cancer patients.
  • To provide a clinical tool for predicting CINV risk and guiding personalized prophylaxis.
  • To reduce the incidence and adverse events of CINV in pediatric oncology.

Main Methods:

  • A cohort of 378 hospitalized children undergoing chemotherapy was analyzed.
  • Multivariate logistic regression identified predictors including prior CINV, body weight, mood, chemotherapy cycle, drug emetogenicity, sleep, and tumor type.
  • Model performance was evaluated using nomograms, ROC curves, calibration, and decision curves, with external validation on 230 patients.

Main Results:

  • Independent predictors for chemotherapy-induced nausea (CIN) included prior CINV, body weight, and negative emotions.
  • Predictors for chemotherapy-induced vomiting (CIV) included chemotherapy cycle, drug emetogenicity, sleep duration, tumor type, and prior CINV experience.
  • The developed nomograms demonstrated good predictive performance for both CIN and CIV.

Conclusions:

  • This is the first risk prediction model for CINV specifically developed for pediatric cancer patients.
  • The validated models offer a practical tool for healthcare professionals to predict CINV risk.
  • Timely and personalized interventions can be implemented to prevent CINV and mitigate associated adverse events in children.
Abstract

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