Enhancing Precision in Rectal Cancer Radiotherapy: Localized Fine-Tuning of Deep-learning based Auto-segmentation (DLAS) Model for Clinical Target Volume and Organs-at-risk

Author:

Geng Jianhao1,Sui Xin1,Du Rongxu1,Feng Jialin1,Wang Ruoxi1,Wang Meijiao1,Yao Kaining1,Chen Qi2,Bai Lu2,Wang Shaobin2,Li Yongheng1,Wu Hao1,Hu Xiangmin3,Du Yi1

Affiliation:

1. Peking University Cancer Hospital & Institute

2. MedMind Technology Co., Ltd

3. Beijing Institute of Technology

Abstract

Abstract Background and Purpose Various deep learning auto-segmentation (DLAS) models have been proposed, some of which commercialized. However, the issue of performance degradation is notable when pretrained models are deployed in the clinic. This study aims to enhance precision of a popular commercial DLAS product in rectal cancer radiotherapy by localized fine-tuning, addressing challenges in practicality and generalizability in real-world clinical settings. Materials and Methods A total of 120 Stage II/III mid-low rectal cancer patients were retrospectively enrolled and divided into three datasets: training (n = 60), external validation (ExVal, n = 30), and generalizability evaluation (GenEva, n = 30) datasets respectively. The patients in the training and ExVal dataset were acquired on the same CT simulator, while those in GenEva were on a different CT simulator. The commercial DLAS software was first localized fine-tuned for clinical target volume (CTV) and organs-at-risk (OAR) using the training data, and then validated on ExVal and GenEva respectively. Performance evaluation involved comparing the localized fine-tuned model (LFT) with the vendor-provided pretrained model (VPM) against ground truth contours, using metrics like Dice similarity coefficient (DSC), 95th Hausdorff distance (95HD), sensitivity and specificity. Results Localized fine-tuning significantly improved CTV delineation accuracy (p < 0.05) with LFT outperforming VPM in target volume, DSC, 95HD and specificity. Both models exhibited adequate accuracy for bladder and femoral heads, and LFT demonstrated significant enhancement in segmenting the more complex small intestine. We did not identify performance degradation when LFT and VPM models were applied in the GenEva dataset. Conclusions The necessity and potential benefits of localized fine-tuning DLAS towards institution-specific model adaption is underscored. The commercial DLAS software exhibits superior accuracy once localized fine-tuned, and is highly robust to imaging equipment changes.

Publisher

Research Square Platform LLC

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