Background and Purpose: The manual delineation of Organs-at-Risk (OARs) in radiotherapy planning is a labor-intensive process characterized by significant inter-observer variability and substantial time consumption. This study developed and clinically validated Pelvic U-Net, a 3D U-Net deep learning architecture designed to automate the segmentation of 13 pelvic OARs. The primary objective was to evaluate whether an AI-driven workflow could maintain clinical gold-standard accuracy while significantly increasing departmental efficiency. Materials and Methods: The model was trained and evaluated using a gender-diverse dataset of 250 patients using CT modality (160 male, 90 female). A robust preprocessing pipeline and an intensive 3D data augmentation strategy were implemented to handle anatomical variability. Model performance was rigorously assessed across 50 independent test patients using geometric metrics (DSC, IoU, HD95), statistical analysis (P-value, T-tests), and dosimetric comparisons (Dmean, Dmax, Vx). Furthermore, a clinical qualitative assessment was performed via a blinded Turing test, where a radiation oncologist graded 50 sets of contours on a 4-point Likert scale (Grade 1: Usable as-is to Grade 4: Unusable). Results: Geometric evaluation showed expert-level accuracy, with Dice Similarity Coefficients (DSC) exceeding 0.94 for high-contrast structures like the bladder and pelvic bones. Dosimetric validation confirmed that VMAT plans optimized on AI contours were clinically equivalent to manual plans, with no statistically significant differences (P > 0.05) in critical dose parameters. In the qualitative Turing test, 94% of the AI-generated contours were deemed clinically acceptable (56% Grade 1; 38% Grade 2), requiring only minor or no manual refinements. The automated workflow reduced active contouring time from 45 minutes to approximately 8 minutes per patient an 82.2% reduction in professional workload. Conclusion: The Pelvic U-Net serves as a robust and reliable supportive tool for radiation oncology. By providing high-fidelity automated contours that meet stringent clinical and dosimetric safety requirements, the model effectively standardizes the planning process and significantly accelerates clinical throughput. The results support the implementation of an "edit-and-approve" hybrid workflow to facilitate faster transitions from patient simulation to treatment delivery.
Rifat Ijaj Ahamed (Wed,) studied this question.
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