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Published on: January 29, 2019
Semi-supervised learning for dose prediction in targeted radionuclide therapy: a synthetic data study.
Jing Zhang1, Alexandre Bousse1, Chi-Hieu Pham1
1LaTIM, INSERM-UMR1101, University of Brest, Brest, France.
Semi-supervised learning (SSL) reduces the need for extensive labeled data in deep learning (DL) for radiation dose prediction in Targeted Radionuclide Therapy (TRT). This approach achieves dosimetry accuracy comparable to fully supervised methods, even with limited clinical data.
Area of Science:
- Medical Physics
- Radiology
- Artificial Intelligence
Background:
- Accurate radiation dose estimation is vital for effective Targeted Radionuclide Therapy (TRT).
- Deep learning (DL) shows potential for dosimetry, but requires large labeled datasets, which are often unavailable in clinical settings.
- This limitation hinders the widespread adoption of DL-based dosimetry in TRT.
Purpose of the Study:
- To develop and evaluate a semi-supervised learning (SSL) framework for radiation dose prediction in TRT.
- To reduce the dependency on large-scale labeled datasets by leveraging readily available pretherapy PET data.
- To adapt and extend traditional classification-based SSL approaches for regression-based dose prediction.
Main Methods:
- Exploration of a semi-supervised learning (SSL) framework utilizing pretherapy PET data with a small subset of dose labels.
- Adaptation and extension of classification-based SSL methods for regression tasks in dose prediction.
- Development of a synthetic dataset simulating PET images and Monte Carlo dose calculations for validation.
Main Results:
- Evaluation of multiple regression-adapted SSL methods under varying proportions of labeled data.
- Achieved overall mean absolute percentage errors of 9%-11% for dose prediction across different organs.
- Demonstrated performance comparable to fully supervised methods.
Conclusions:
- Proposed SSL methods show promising results for organ-level dose prediction in TRT.
- SSL effectively addresses the challenge of limited labeled clinical data for DL-based dosimetry.
- This approach enhances the feasibility of personalized dosimetry in TRT.
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