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Updated: Apr 26, 2026

Irradiator Commissioning and Dosimetry for Assessment of LQ α and β Parameters, Radiation Dosing Schema, and in vivo Dose Deposition
Published on: March 11, 2021
Deep Learning Blood Dosimetry Predicts Severe Lymphopenia and Survival After Craniospinal Irradiation
Nalee Kim1, Sang Hoon Seo2, Jee Suk Chang3
1Department of Radiation Oncology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Purpose:
Craniospinal irradiation (CSI) is a standard treatment for pediatric brain tumors and is increasingly used for leptomeningeal metastases. Although effective, CSI often causes radiation-induced severe lymphopenia (RISL), which is associated with poor outcomes across various cancer types. We developed and validated a novel platform for personalized dosimetry of circulating blood cells (CBCs) and assessed its predictive value for RISL.
Methods And Materials:
We combined a prospective pediatric CSI registry (initiated April 2018; n = 48) and retrospectively collected patients (January 2010-November 2024; n = 168). RISL was defined as grade 4 lymphopenia (<200/µL) during or within 1 week after CSI. The platform integrated deep learning-based whole-body segmentation, individualized blood volume modeling (HEDOS), patient-specific hemodynamics (cardiac output), and treatment delivery parameters to estimate CBC dose-volume histograms, which quantify the cumulative radiation dose distribution to circulating blood during CSI. CBC dose metrics were analyzed using LASSO, Random Forest, and XGBoost models, with and without cross-validation and Synthetic Minority Over-sampling Technique, to identify RISL predictors.
Results:
Among 216 patients (median age 12 years; range, 2-68), proton beam therapy was used in 163 (75.5%). RISL occurred in 92 patients (42.6%). Among various CBC dosimetric parameters, CBC D5% consistently emerged as the most important predictor of RISL across all machine learning models. Stratification by CBC D5% with 3.0 GyE effectively differentiated overall survival and event-free survival outcomes (all P < .05).
Conclusions:
The current deep learning-based personalized blood dosimetry platform enables personalized CBC dosimetry during CSI. CBC D5% is associated with the development of RISL and survival outcomes. Personalized blood dosimetry may serve as a potential tool to identify patients at high risk for RISL, which may inform future efforts to optimize CSI planning.
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