Pediatric hemophagocytic lymphohistiocytosis (HLH) lacks reliable risk models for personalized treatment. We aimed to develop a survival nomogram to address this gap. We retrospectively analyzed 404 pediatric HLH patients from multiple centers. Independent prognostic variables identified by Cox regression were incorporated into a nomogram. Five predictors of mortality were identified: central nervous system involvement, gastrointestinal bleeding, WBC 69pg/mL. The nomogram demonstrated strong predictive accuracy, with validation cohort AUCs of 0.83, 0.78, and 0.79 for 1-, 2-, and 3-year overall survival (OS). Calibration and decision curve analysis confirmed accuracy. Using an X-tile-determined cutoff of 261, patients were stratified into low- and high-risk groups with significantly different 3-year OS (training cohort: 94.0% vs. 47.2%; validation cohort: 88.2% vs. 43.2%; p < 0.0001). This multicenter study established and externally validated a nomogram-based model that enables early risk stratification and may inform individualized therapy for pediatric HLH.
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Shu-yi Guo
Sun Yat-sen University
Tang Ru
Sun Yat-sen University
Shilin Liu
Qingdao University
Annals of Hematology
Sun Yat-sen University
Southern Medical University
The First Affiliated Hospital, Sun Yat-sen University
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Guo et al. (Thu,) studied this question.
synapsesocial.com/papers/68f19f20de32064e504ddd83 — DOI: https://doi.org/10.1007/s00277-025-06676-5