Abstract
BACKGROUND: This study aimed to evaluate the clinical feasibility and performance of CT-based auto-segmentation models integrated into an All-in-One radiotherapy workflow for rectal cancer. METHODS: This study included 312 rectal cancer patients, with 272 used to train three nnU-Net models for CTV45, CTV50, and GTV segmentation, and 40 for evaluation across one internal (n = 10), one clinical AIO (n = 10), and two external cohorts (n = 10 each). Segmentation accuracy (DSC, HD, HD95, ASSD, ASD) and time efficiency were assessed. RESULTS: In the internal testing set, mean DSC of CTV45, CTV50, and GTV were 0.90, 0.86, and 0.71; HD were 17.08, 25.48, and 79.59 mm; HD 95 were 4.89, 7.33, and 56.49 mm; ASSD were 1.23, 1.90, and 6.69 mm; and ASD were 1.24, 1.58, and 11.61 mm. Auto-segmentation reduced manual delineation time by 63.3–88.3% (p < 0.0001). In clinical practice, average DSC of CTV45, CTV50 and GTV were 0.93, 0.88, and 0.78; HD were 13.56, 23.84, and 35.38 mm; HD 95 were 3.33, 6.46, and 21.34 mm; ASSD were 0.78, 1.49, and 3.30 mm; and ASD were 0.74, 1.18, and 2.13 mm. The results from the multi-center testing also showed applicability of these models, since the average DSC of CTV45 and GTV were 0.84 and 0.80 respectively. CONCLUSIONS: The models demonstrated high accuracy and clinical utility, effectively streamlining target volume delineation and reducing manual workload in routine practice. TRIAL REGISTRATION: The study protocol was approved by the Institutional Review Board of Peking University Third Hospital (Approval No. (2024) Medical Ethics Review No. 182-01).