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Updated: Jul 10, 2026

Expedited Radiation Biodosimetry by Automated Dicentric Chromosome Identification (ADCI) and Dose Estimation
Published on: September 4, 2017
A global calibration model for a-Si EPIDs used for transit dosimetry
S M J J G Nijsten1, W J C van Elmpt, M Jacobs
1Department of Radiation Oncology (MAASTRO), Research Institute for Growth and Development, University Hospital of Maastricht, Maastricht, The Netherlands. bas.nijsten@maastro.nl
Accurate transit dosimetry is achievable using amorphous silicon electronic portal imaging devices (a-Si EPIDs). A new calibration model corrects for EPID response variations, ensuring precise dose distribution verification in radiation therapy.
Area of Science:
- Medical Physics
- Radiation Oncology
- Imaging Technology
Background:
- Electronic portal imaging devices (EPIDs) are evolving beyond patient setup verification.
- Their application is expanding into dosimetric verification, particularly for transit dosimetry.
- Amorphous silicon (a-Si) EPIDs offer potential for accurate in-vivo dose measurements.
Purpose of the Study:
- To develop and validate a global calibration model for amorphous silicon EPIDs (a-Si EPIDs).
- To enable accurate dose distribution measurements for transit dosimetry applications.
- To assess the long-term stability and optimize buildup material for a-Si EPIDs.
Main Methods:
- A global calibration model was created, incorporating corrections for ghosting, field size, and energy dependence.
- Long-term stability and additional buildup effects were evaluated.
- Transit dose measurements were compared against ionization chamber data in a water tank using gamma analysis (3%/3mm).
Main Results:
- The calibration model effectively corrected for field size and energy dependence, reducing response variations from 30-40% to under 3%.
- Transit dose distributions consistently met gamma evaluation criteria for various treatment fields and phantoms.
- The developed model demonstrated high accuracy for dosimetric verification across diverse treatment conditions.
Conclusions:
- Amorphous silicon EPIDs can be accurately calibrated for transit dosimetry.
- The proposed global calibration model enhances the reliability of EPID-based dose verification.
- This advancement supports improved quality assurance in radiation therapy.
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