Modeling prompt gamma (PG) emission, detection and imaging in real patient anatomy using a novel Compton camera for dose verification in proton therapy

<i>Objective</i>. Prompt gamma (PG) imaging is a promising modality for proton dose verification. Currently, there is a lack of effective tools to investigate the entire PG imaging process in patient anatomy, from PG emission to camera detection and image reconstruction, to evaluate and optimize its efficacy for dose verification in proton therapy.<i>Approach</i>. To address this gap, we developed a Monte-Carlo package, POLARIS J Monte Carlo (PJ-MC), that simulates the entire PG emission and imaging workflow in patient anatomy. We utilized Geant4 classes and G4-ancillary tools, employing the DCMTK external tool with G4PhantomParameterisation to convert patient CT data into voxelized geometries. Proton beams were modeled based on medical physics commissioning data. A novel two-stage POLARIS-J3 Compton-Camera was simulated under the patient couch for recording total, double, and triple scattered PG signals. Proton maximum range calculations from the PJ-MC are compared with dose calculations from a clinical treatment planning system. The detected PG signals data in the simulation were used to reconstruct PG images using Kernel- Weighted-Back-Projection algorithm.<i>Main results</i>. Analysis of gamma energy distribution showed a decay pattern with clear emission lines from nuclear reactions involving oxygen, carbon, nitrogen, and calcium. Neutron-induced reactions contribute significantly less-by an order of magnitude-compared to proton-induced reactions in various tissues. Mean absolute percentage error analysis showed that PG range verification was more stable when considering the range at 80%or 50%of<i>D</i><sub>max</sub>, as opposed to the range at the<i>D</i><sub>max</sub>, where energy gating slightly improves accuracy but may reduce localization due to photon loss. Results showed that patient anatomy can impact the location of hot spot in the PG images, affecting its accuracy for localizing Bragg peak.<i>Significance</i>. In summary, our simulation package provides additional insights into PG emission and imaging in patient anatomy and serves as a robust tool for evaluating and optimizing PG imaging, enhancing its precision for dose verification in proton therapy.

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Publication Details

Journal
Physics in Medicine and Biology
Published
2025-05-30
DOI
https://doi.org/10.1088/1361-6560/addf0d
Citations
1
Primary Topic
Radiation Therapy and Dosimetry
Type
article
Field-Weighted Citation Impact
1.52
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article

Modeling prompt gamma (PG) emission, detection and imaging in real patient anatomy using a novel Compton camera for dose verification in proton therapy

Matthias K. Gobbert, Sina Mossahebi, J Polf, Zhuoran Jiang et al.
1 citations
Physics in Medicine and Biology
Radiation Therapy and Dosimetry
1.52
article

Modeling prompt gamma (PG) emission, detection and imaging in real patient anatomy using a novel Compton camera for dose verification in proton therapy

Matthias K. Gobbert, Sina Mossahebi, J Polf, Zhuoran Jiang, Vijay R. Sharma, S Peterson, Ananta Raj Chalise, Lei Ren, Ehsaan Shakeri
article en
1 citations

Abstract

<i>Objective</i>. Prompt gamma (PG) imaging is a promising modality for proton dose verification. Currently, there is a lack of effective tools to investigate the entire PG imaging process in patient anatomy, from PG emission to camera detection and image reconstruction, to evaluate and optimize its efficacy for dose verification in proton therapy.<i>Approach</i>. To address this gap, we developed a Monte-Carlo package, POLARIS J Monte Carlo (PJ-MC), that simulates the entire PG emission and imaging workflow in patient anatomy. We utilized Geant4 classes and G4-ancillary tools, employing the DCMTK external tool with G4PhantomParameterisation to convert patient CT data into voxelized geometries. Proton beams were modeled based on medical physics commissioning data. A novel two-stage POLARIS-J3 Compton-Camera was simulated under the patient couch for recording total, double, and triple scattered PG signals. Proton maximum range calculations from the PJ-MC are compared with dose calculations from a clinical treatment planning system. The detected PG signals data in the simulation were used to reconstruct PG images using Kernel- Weighted-Back-Projection algorithm.<i>Main results</i>. Analysis of gamma energy distribution showed a decay pattern with clear emission lines from nuclear reactions involving oxygen, carbon, nitrogen, and calcium. Neutron-induced reactions contribute significantly less-by an order of magnitude-compared to proton-induced reactions in various tissues. Mean absolute percentage error analysis showed that PG range verification was more stable when considering the range at 80%or 50%of<i>D</i><sub>max</sub>, as opposed to the range at the<i>D</i><sub>max</sub>, where energy gating slightly improves accuracy but may reduce localization due to photon loss. Results showed that patient anatomy can impact the location of hot spot in the PG images, affecting its accuracy for localizing Bragg peak.<i>Significance</i>. In summary, our simulation package provides additional insights into PG emission and imaging in patient anatomy and serves as a robust tool for evaluating and optimizing PG imaging, enhancing its precision for dose verification in proton therapy.

Physics in Medicine and BiologyVol. 70(12)
University of Maryland, Baltimore (US), University of Maryland Medical Center (US), University of Cape Town (ZA), Michigan Medicine (US), Stanford Medicine (US), Ann Arbor Center for Independent Living (US), University of Baltimore (US), University of Maryland, Baltimore County (US), Stanford University (US)
Affordable and clean energy
Openalex Percentile: Top 18%
Radiation Therapy and Dosimetry
1.52
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