Voxel-Based Dose Prediction with Multi-Patient Atlas Selection for Automated Radiotherapy Treatment Planning

TL;DR

This paper presents a novel multi-patient atlas-based method for direct voxel-level dose prediction in radiotherapy planning, improving automation and accuracy without predefined dose objectives.

Contribution

It introduces an atlas selection mechanism combined with a conditional random field for optimized dose prediction across multiple treatment sites, advancing prior atlas-based approaches.

Findings

Improved dose prediction accuracy over previous methods.

Atlas selection enhances prediction quality for most treatment sites.

Potential for better automated planning in CNS Brain cases.

Abstract

Automating the radiotherapy treatment planning process is a technically challenging problem. The majority of automated approaches have focused on customizing and inferring dose volume objectives to used in plan optimization. In this work we outline a multi-patient atlas-based dose prediction approach that learns to predict the dose-per-voxel for a novel patient directly from the computed tomography (CT) planning scan without the requirement of specifying any objectives. Our method learns to automatically select the most effective atlases for a novel patient, and then map the dose from those atlases onto the novel patient. We extend our previous work to include a conditional random field for the optimization of a joint distribution prior that matches the complementary goals of an accurately spatially distributed dose distribution while still adhering to the desired dose volume histograms. The resulting distribution can then be used for inverse-planning with a new spatial dose objective, or to create typical dose volume objectives for the canonical optimization pipeline. We investigated six treatment sites (633 patients for training and 113 patients for testing) and evaluated the mean absolute difference (MAD) in all DVHs for the clinical and predicted dose distribution. The results on average are favorable in comparison to our previous approach (1.91 vs 2.57). Comparing our method with and without atlas-selection further validates that atlas-selection improved dose prediction on average in Whole Breast (0.64 vs 1.59), Prostate (2.13 vs 4.07), and Rectum (1.46 vs 3.29) while it is less important in Breast Cavity (0.79 vs 0.92) and Lung (1.33 vs 1.27) for which there is high conformity and minimal dose shaping. In CNS Brain, atlas-selection has the potential to be impactful (3.65 vs 5.09), but selecting the ideal atlas is the most challenging.