Abstract

PurposeHerein, we developed a deep learning algorithm to improve the segmentation of the clinical target volume (CTV) on daily cone-beam computed tomography (CBCT) scans in breast cancer radiotherapy. By leveraging the Intentional Deep Overfit Learning (IDOL) framework, we aimed to enhance personalized image-guided radiotherapy (IGRT) based on patient-specific learning. MethodsWe utilized 240 CBCT scans from 100 breast cancer patients and employed a two-stage training approach. The first stage involved training a novel general deep learning model (Swin UNETR, UNET, and SegResNET) on 90 patients. The second stage utilized intentional overfitting on the remaining 10 patients for patient-specific CBCT outputs. Quantitative evaluation was conducted using the Dice Similarity Coefficient (DSC), Hausdorff Distance (HD), mean surface distance (MSD), and independent samples t-test with expert contours on CBCT scans from the 1st to 15th fractions. ResultsIDOL integration significantly improved CTV segmentation, particularly with the Swin UNETR model (p-values <0.05). Using patient-specific data, IDOL enhanced the DSC, HD, and MSD metrics. The average DSC for the 15th fraction improved from 0.9611 to 0.9819, the average HD decreased from 4.0118 mm to 1.3935 mm, and the average MSD decreased from 0.8723 to 0.4603. Incorporating CBCT scans from the initial treatments and 1st to 3rd fractions further improved results, with an average DSC of 0.9850, an average HD of 1.2707 mm, and an average MSD of 0.4076 for the 15th fraction, closely aligned with physician-drawn contours. ConclusionCompared with a general model, our patient-specific deep learning-based training algorithm significantly improved CTV segmentation accuracy of CBCT scans in patients with breast cancer. This approach, coupled with continuous deep learning training using daily CBCT scans, demonstrated enhanced CTV delineation accuracy and efficiency. Future studies should explore the adaptability of the IDOL framework to diverse deep learning models, datasets, and cancer sites.

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