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Proton Therapy Delivery and Its Clinical Application in Select Solid Tumor Malignancies
Published on: February 6, 2019
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FRoG dose computation meets Monte Carlo accuracy for proton therapy dose calculation in lung
Giuseppe Magro1, Stewart Mein2, Benedikt Kopp3
1National Centre for Oncological Hadrontherapy (CNAO), Clinical Department, Pavia, Italy.
Summary
Novel GPU-accelerated dose engines show clinical viability for lung cancer proton therapy. FRoG demonstrated accurate dose calculations, comparable to Monte Carlo methods, supporting improved thoracic treatments.
Area of Science:
- Medical Physics
- Radiation Oncology
- Computational Biology
Background:
- Proton therapy, particularly spot-scanning intensity-modulated proton therapy (IMPT), offers precise dose delivery.
- Accurate dose calculation is critical for effective and safe IMPT, especially in complex geometries like the lung.
- Existing analytical models may have limitations in capturing the full physics of proton interactions.
Purpose of the Study:
- To benchmark and evaluate novel analytical GPU-accelerated and CPU-based Monte Carlo (MC) dose-engines for IMPT.
- To assess the clinical viability of these dose-engines for lung cancer treatment.
- To compare the performance of FRoG, RayStation-MC (RS-MC), and general-purpose MC (gp-MC) dose calculation systems.
Main Methods:
- Nine patient cases from clinical experience and a public database were used for in-silico study.
- Plans were optimized using 2 orthogonal beams in RayStation v.8.
- Forward calculations were performed with FRoG (analytical PBA), RS-MC (CPU), and gp-MC. Dosimetric benchmarks were obtained using a lung-like phantom and ionization chambers.
Main Results:
- FRoG and RS-MC showed average GTV dose differences of 1.8% and 2.3% compared to gp-MC.
- FRoG and RS-MC achieved local γ-passing rates of approximately 96% and 93%, respectively.
- Phantom measurements confirmed FRoG's high accuracy with deviations under 0.1%.
Conclusions:
- GPU-accelerated analytical PBA, MC-TPS, and gp-MC dose calculations are within clinical tolerances.
- FRoG predictions closely matched gp-MC and experimental data for thoracic proton dose calculations.
- FRoG offers a viable solution for clinical treatment planning or as an auxiliary dose-engine for lung cancer patients.
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