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Background: In clinical proton radiotherapy, a constant relative biological effectiveness (RBE) of 1.1 is typically applied. Due to abundant evidence of variable RBE effects from in vitro data, multiple variable RBE models have been suggested, typically by describing the and parameters in the linear quadratic (LQ) model as a function of dose averaged linear energy transfer ( ).
Purpose: This work introduces a new variable RBE model based on the dirty dose concept, where dose deposited in voxels with a corresponding LET exceeding a specific threshold is considered "dirty" in the sense that it has a biological effect above the one predicted by a constant RBE of 1.1. As only one LET level, corresponding to a specific energy for a given particle in a given medium, needs to be monitored, this offers several advantages, such as simplified calculations by removing the need for intricate end of range LET calculations and averaging procedures, as well as opening up for more efficient experimental assessment of the cell specific model parameters.
Methods: Previously published in vitro data were utilized, where surviving fraction (SF), dose and were reported for a pristine proton beam with varying physical PMMA thicknesses placed upstream of the cells. The setup was re-simulated to extract dirty dose metrics for the corresponding reported -values. Models were created by setting the parameter of the LQ model as a function of the fraction of dirty dose and subsequently benchmarked against models based on other radiation quality metrics by comparing the root-mean-square-error (RMSE) of the predicted and actual cell surviving fraction.
Results: Variable RBE models based on dirty dose perform on par with conventional radiation quality metrics with a RMSE of 0.38 for a dirty dose-based model with a threshold of 7 , compared to 0.42 and 0.36 for a -based and -based model, respectively. Higher chosen LET thresholds typically performed better and lower performed worse.
Conclusion: The results indicate that models based on dirty dose metrics perform equally well as conventional radiation quality metrics. Due to the simplified calculations involved and the potential for more efficient measurement techniques for data generation, dirty dose-based models might be the most conservative and practical approach for creating future proton variable RBE models.
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http://dx.doi.org/10.1002/mp.17519 | DOI Listing |
Med Phys
September 2025
Department of Accelerator and Medical Physics, National Institutes for Quantum Science and Technology (QST), Chiba, Japan.
Background: Multi-ion radiotherapy using carbon, oxygen, and neon ions aims to improve local control by increasing dose-averaged linear energy transfer (LET) in the target. However, there has been limited understanding of how to utilize variables for multi-ion treatment planning such as the selection and arrangement of ion species.
Purpose: An in silico study was conducted to explore the feasibility of increasing a minimum LET, and the optimal selection and arrangement of ion species in multi-ion therapy for increasing LET in tumors of varying sizes mimicking bone and soft tissue sarcomas (BSTS).
Oral Dis
September 2025
Clinical Department, Radiation Oncology Unit, National Center for Oncological Hadrontherapy (CNAO), Pavia, Italy.
Aim: To evaluate the outcomes of combining carbon ion radiotherapy boost (CIRTb) with photons (Ph) or protons (PT) for locally advanced salivary gland and sinonasal cancers (SGCs and SNCs).
Materials And Methods: Sixty-nine patients with SGCs and SNCs received CIRTb to high-risk CTV and Ph or PT to low-risk CTV (LR-CTV) from October 2014 to September 2022. Two-year local relapse-free survival (LRFS) was analyzed with Kaplan-Meier.
Phys Med Biol
August 2025
Department of Radiation Oncology, The First Affiliated Hospital of Soochow University, State Key Laboratory of Radiation Medicine and Protection, School of Radiation Medicine and Protection, Collaborative Innovation Center of Radiological Medicine of Jiangsu Higher Education Institutions, Soochow Un
In examining the biological effects of proton radiation, DNA is the primary sensitive target. This study utilizes Monte Carlo simulations to efficiently calculate DNA damage yields at various proton depths to analyze the biological effects of protons and their variability on different scales.A new method, the 'Coefficient Method' is used to replace the complete chemical processes by adjusting parameters to obtain suitable values for simulating DNA damage yields at different spread-out Bragg peak (SOBP) depths of low-energy protons, and these parameters are then applied to high-energy proton simulations based on a mesh-type cell model.
View Article and Find Full Text PDFComput Biol Med
September 2025
Institute of Nuclear Physics Polish Academy of Sciences, Krakow, PL-31342, Poland.
Purpose: This work aims at implementation, validation, and proof of application of fast, voxel-based single proton linear energy transfer (LET) spectra scoring for clinical proton therapy. The LET spectra provide more comprehensive information on the mixed radiation field produced by protons in heterogeneous patient geometry in comparison to the dose-averaged LET (LET), commonly investigated pre-clinically and clinically.
Materials And Methods: We implemented single particle spectra scoring methods for LET and other physics quantities, e.
Adv Radiat Oncol
August 2025
Department of Medical Physics in Radiation Oncology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Purpose: To determine the relative biological effectiveness (RBE) in the rat spinal cord after 6 fractions of protons as a function of linear energy transfer (LET) and dose.
Methods And Materials: The rat spinal cord was irradiated at 4 different positions of a 6 cm spread-out Bragg peak using 6 fractions of protons (LET: 1.4, 2.