Calculating biological dose distributions in hadrontherapy using GATE: the BioDose actor

Abstract Objective
The BioDoseActor, a new tool implemented in the GATE Monte Carlo platform, aims to calculate the biological dose and its associated uncertainty for hadrontherapy treatment plans. This tool is designed to facilitate the validation of biophysical models and optimize clinical treatment planning by providing accurate biological dose distributions.
Approach
The BioDoseActor utilizes pre-calculated databases of the linear-quadratic coefficients α and β of cell survival curves, derived from biophysical models such as the modified MicroKinetic Model (mMKM) and the Nanodosimetry and Oxidative Stress (NanOx) model. These databases cover hydrogen, helium, lithium, carbon, and oxygen ions, with energy ranges from 0.1 MeV/u to 1000 MeV/u. The algorithm computes the biological dose using the linear-quadratic coefficients and their uncertainties, while optimizing Monte Carlo simulation parameters. Two step-size limitation methods in Geant4 (StepLimiter and StepFunction) were evaluated to balance accuracy and computation time in Spread Out Bragg Peak (SOBP) dose distributions for proton and carbon-ion beams.
Main Results
The StepFunction method proved more efficient than the StepLimiter, achieving a 30.6-fold acceleration factor for protons and a 2-fold acceleration factor for carbon ions while maintaining a maximum relative difference of 2% in SOBP. Optimal parameters for StepFunction were identified as α r = 8 .10 -5 , ρ r = 1 um for the clinical proton beam and (α r = 8.10 -4 , ρ r = 10 um) for the clinical carbon-ion beam. The calculated α and β coefficients and RBE values (1.2–1.5 for protons, 2–3 for carbon ions) aligned with literature. Application to a clinical carbon-ion treatment plan created by Raystation allowed us to validate the BioDoseActor and to demonstrate the tool’s capability to generate physical and biological dose maps and Dose Volume Histograms (DVHs).
Significance 
The BioDoseActor enables direct comparison of biophysical models, supporting the integration of biological dose calculations into clinical practice. By optimizing simulation parameters, it reduces computation time without compromising accuracy, thus enhancing the feasibility of biological dose-based treatment planning in hadrontherapy.

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Publication Details

Journal
Physics in Medicine and Biology
Published
2026-06-26
DOI
https://doi.org/10.1088/1361-6560/ae8358
Primary Topic
Radiation Therapy and Dosimetry
Type
article
Field-Weighted Citation Impact
0.00

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article

Calculating biological dose distributions in hadrontherapy using GATE: the BioDose actor

Michaël Beuve, Dietmar Georg, Barbara Knäusl, Étienne Testa et al.
Physics in Medicine and Biology
Radiation Therapy and Dosimetry
article

Calculating biological dose distributions in hadrontherapy using GATE: the BioDose actor

Michaël Beuve, Dietmar Georg, Barbara Knäusl, Étienne Testa, Lydia Maigne, Jean Michel Létang, H. Fuchs, Alexis Pereda, Thomas Berger
article en

Abstract

Abstract Objective
The BioDoseActor, a new tool implemented in the GATE Monte Carlo platform, aims to calculate the biological dose and its associated uncertainty for hadrontherapy treatment plans. This tool is designed to facilitate the validation of biophysical models and optimize clinical treatment planning by providing accurate biological dose distributions.
Approach
The BioDoseActor utilizes pre-calculated databases of the linear-quadratic coefficients α and β of cell survival curves, derived from biophysical models such as the modified MicroKinetic Model (mMKM) and the Nanodosimetry and Oxidative Stress (NanOx) model. These databases cover hydrogen, helium, lithium, carbon, and oxygen ions, with energy ranges from 0.1 MeV/u to 1000 MeV/u. The algorithm computes the biological dose using the linear-quadratic coefficients and their uncertainties, while optimizing Monte Carlo simulation parameters. Two step-size limitation methods in Geant4 (StepLimiter and StepFunction) were evaluated to balance accuracy and computation time in Spread Out Bragg Peak (SOBP) dose distributions for proton and carbon-ion beams.
Main Results
The StepFunction method proved more efficient than the StepLimiter, achieving a 30.6-fold acceleration factor for protons and a 2-fold acceleration factor for carbon ions while maintaining a maximum relative difference of 2% in SOBP. Optimal parameters for StepFunction were identified as α r = 8 .10 -5 , ρ r = 1 um for the clinical proton beam and (α r = 8.10 -4 , ρ r = 10 um) for the clinical carbon-ion beam. The calculated α and β coefficients and RBE values (1.2–1.5 for protons, 2–3 for carbon ions) aligned with literature. Application to a clinical carbon-ion treatment plan created by Raystation allowed us to validate the BioDoseActor and to demonstrate the tool’s capability to generate physical and biological dose maps and Dose Volume Histograms (DVHs).
Significance 
The BioDoseActor enables direct comparison of biophysical models, supporting the integration of biological dose calculations into clinical practice. By optimizing simulation parameters, it reduces computation time without compromising accuracy, thus enhancing the feasibility of biological dose-based treatment planning in hadrontherapy.

Physics in Medicine and Biology
Université Claude Bernard Lyon 1 (FR), Université Clermont Auvergne (FR), Universitätszahnklinik Wien (AT), Institut National des Sciences Appliquées de Lyon (FR), Medical University of Vienna (AT)
LabEx PRIMES
Openalex Percentile: Top 7%
Radiation Therapy and Dosimetry
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