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Updated: Jun 16, 2025

Dynamic Lung Tumor Tracking for Stereotactic Ablative Body Radiation Therapy
Published on: June 7, 2015
Predicting the 3-Dimensional Dose Distribution of Multilesion Lung Stereotactic Ablative Radiation Therapy With
Edward Wang1, Hassan Abdallah2, Jonatan Snir3
1Department of Medical Biophysics, Western University, London, Ontario, Canada; Schulich School of Medicine and Dentistry, London, Ontario, Canada.
Purpose:
Because SABR therapy is being used to treat greater numbers of lung metastases, selecting the optimal dose and fractionation to balance local failure and treatment toxicity becomes increasingly challenging. Multilesion lung SABR therapy plans include spatially diverse lesions with heterogeneous prescriptions and interacting dose distributions. In this study, we developed and evaluated a generative adversarial network (GAN) to provide real-time dosimetry predictions for these complex cases.
Methods And Materials:
A GAN was trained to predict dosimetry on a data set of patients who received SABR therapy for lung lesions at a tertiary center. Model input included the planning computed tomography scan, the organs at risk (OARs) and target structures, and an initial estimate of exponential dose fall-off. Multilesion plans were split 80/20 for training and evaluation. Models were evaluated on voxel-voxel, clinical dose-volume histogram, and conformality metrics. An out-of-sample validation and analysis of model variance were performed.
Results:
There were 125 multilesion plans from 102 patients with 357 lesions. Patients were treated for 2 to 7 lesions, with 19 unique dose-fractionation schemes over 1 to 3 courses of treatment. The out-of-sample validation set contained an additional 90 plans from 80 patients. The mean absolute difference and gamma pass fraction between the predicted and true dosimetry was <3 Gy and >90% for all OARs. The absolute differences in lung V20 and CV14 were 1.40% ± 0.99% and 75.8 ± 42.0 cc, respectively. The ratios of predicted to true R50%, R100%, and D2cm were 1.00 ± 0.16, 0.96 ± 0.32, and 1.01 ± 0.36, respectively. The out-of-sample validation set maintained mean absolute difference and gamma pass fraction of <3 Gy and >90%, respectively for all OARs. The median standard deviation of variance in V20 and CV14 prediction was 0.49% and 22.2 cc, respectively.
Conclusions:
A GAN for predicting the 3-D dosimetry of complex multilesion lung SABR therapy is presented. Rapid dosimetry prediction can be used to assess treatment feasibility and explore dosimetric differences between varying prescriptions.
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