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Updated: Sep 6, 2025

Expedited Radiation Biodosimetry by Automated Dicentric Chromosome Identification ADCI and Dose Estimation
Published on: September 4, 2017
Impact of Interfractional Error on Dosiomic Features
Chanon Puttanawarut1,2, Nat Sirirutbunkajorn3, Narisara Tawong3
1Chakri Naruebodindra Medical Institute, Ramathibodi Hospital, Mahidol University, Samutprakarn, Thailand.
Interfractional error impacts the stability of dosiomic features, particularly with fewer fractions. Understanding this variability is crucial for reproducible results in lung cancer treatment planning.
Area of Science:
- Medical Physics
- Radiation Oncology
- Radiomics
Background:
- Dose and image-based features (dosiomic features) are increasingly used in radiation oncology.
- Interfractional errors, or variations in patient positioning during treatment, can affect the accuracy and reliability of these features.
- Assessing the stability of dosiomic features under such errors is critical for their clinical application.
Purpose of the Study:
- To investigate the stability of dosiomic features under random interfractional error in lung cancer patients.
- To evaluate how the number of fractions influences the stability and values of dosiomic features.
- To identify dosiomic features that are sensitive to interfractional errors.
Main Methods:
- Dose distributions were simulated for 15 lung cancer patients with introduced interfractional errors (±3 mm).
- Dosiomic features were extracted from four regions of interest (GTV, PTV, heart, lungs) across different fraction number groups (2, 10, 20, 30).
- Stability was assessed using coefficient of variation (CV) and intraclass correlation coefficient (ICC); percent differences (PD) were calculated.
Main Results:
- Eleven of 93 dosiomic features showed high variability (CV ≥ 20%), with greatest variability in the Gross Tumor Volume (GTV).
- Feature stability decreased with fewer fractions; five features exhibited poor stability (ICC < 0.75).
- Mean dosiomic feature values remained consistent across fraction groups (ICC ≥ 0.9), though some showed >50% PD.
Conclusions:
- Certain dosiomic features demonstrate low stability under interfractional error, influenced by the total number of fractions.
- These findings highlight the need to consider interfractional error effects for reproducible radiomics in lung cancer.
- Further research should focus on robust dosiomic feature selection and error mitigation strategies.
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