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A nomogram for risk stratification of protein-energy malnutrition in pediatric cancer patients: development and
Hong Zhang1, Ka Yan Ho2, Janelle Yorke2
1Department of Pediatrics, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, 830000, Xinjiang, China.
Insights
A new nomogram effectively predicts protein-energy malnutrition (PEM) risk in pediatric cancer patients, identifying key protective and risk factors for early intervention.
Area of Science:
- Pediatric Oncology
- Clinical Nutrition
- Biostatistics
Background:
- Protein-energy malnutrition (PEM) is a significant concern in pediatric cancer patients, impacting treatment outcomes.
- Early identification of PEM risk is crucial for timely nutritional support and intervention.
Purpose of the Study:
- To develop and validate a nomogram for predicting PEM risk in pediatric cancer patients.
- To assess the clinical utility of the developed nomogram.
Main Methods:
- A cohort of 375 pediatric cancer patients was analyzed using WHO BMI-for-age Z-scores.
- A prediction model was constructed using LASSO and multivariate logistic regression.
- Model performance was evaluated using AUC, calibration plots, and DCA.
Main Results:
- Six variables were identified: protective factors included being an only child, diagnosis duration (0-6 or >12 months), caregiver education, and income (≥1,000 yuan).
- Risk factors included rural residence and ≥6 chemotherapy cycles.
- The nomogram showed robust discrimination (AUC=0.823 in modeling, 0.779 in validation) and good calibration.
Conclusions:
- The developed nomogram is an interpretable and clinically practical tool for early PEM risk identification in pediatric cancer patients.
- This tool supports targeted nutritional screening and timely interventions, potentially improving patient outcomes.
Abstract:
To develop and internally validate a nomogram for predicting the risk of protein-energy malnutrition (PEM) in pediatric cancer patients and to evaluate its clinical utility. A total of 375 pediatric cancer patients admitted to a tertiary hospital in Xinjiang (January-May 2025) were enrolled. Nutritional status was assessed using the WHO BMI-for-age Z-score. Candidate variables (P < 0.01 in univariate analysis) were entered into the least absolute shrinkage and selection operator (LASSO) model, and multivariate logistic regression was applied to construct the prediction model. Model performance was assessed using the area under the receiver operating characteristic curve (AUC), calibration plots with the Hosmer-Lemeshow test, and decision curve analysis (DCA). Six readily obtainable variables were retained in the final model. Protective factors included being an only child (OR = 0.278), time since diagnosis of 0-6 months (OR = 0.264) or > 12 months (OR = 0.351), caregiver education of high school or above (OR = 0.406), and household per-capita income ≥ 1,000 yuan (OR = 0.255). Rural residence (OR = 2.643) and ≥ 6 chemotherapy cycles (OR = 2.259) were risk factors for PEM. The nomogram demonstrated robust discrimination in both the modeling (AUC = 0.823, 95% CI: 0.767-0.868) and validation (AUC = 0.779, 95% CI: 0.685-0.859) cohorts. Calibration curves showed close agreement between predicted and observed probabilities, and Hosmer-Lemeshow tests indicated good fit (all P > 0.05). DCA confirmed meaningful net clinical benefit across a wide range of threshold probabilities. The nomogram provides an interpretable and clinically practical tool for early identification of PEM risk in pediatric cancer patients, supporting targeted nutritional screening and timely intervention.
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