Visualized radio-clinical biomarker for predicting neoadjuvant chemotherapy response and prognosis from pretreatment oversampled CT images of LAGC patients: A multicenter study

Author:

Xu Zhiyuan1,Chen Wujie1,Li Feng2,Zhang Yanqiang1,Yu Pengfei1,Yang Litao1,Huang Ling1,Sun Jiancheng3,Chen Shangqi4,Shi Chengwei5,Sun Yuanshui6,Ye Zaisheng7,Yuan Li1,Chen Jiahui1,Wei Qin1,Xu Jingli1,Xu Handong1,Tong Yahan1,Bao Zhehan1,Huang Chencui8,Li Yiming9,Du Yian1,Hu Can1,Cheng Xiangdong1ORCID

Affiliation:

1. Zhejiang Cancer Hospital

2. R&D Center, Beijing Deepwise& League of PHD Technology Co.,Ltd

3. The First affiliated hospital of Wenzhou University

4. HwaMei Hospital, University of Chinese Academy of Science

5. The First Affiliated Hospital of Zhejiang chinese medical university

6. Tongde Hospital Of Zhejiang Province

7. Fujian Provincial Cancer Hospital

8. R&D Center, Beijing Deepwise & League of PHD technology Co.,Ltd

9. R&D Center, Beijing Deepwise&League of PHD Technology Co., Ltd

Abstract

Abstract Background: The early noninvasive screening of patients suitable for neoadjuvant chemotherapy (NCT) is essential for personalized treatment in locally advanced gastric cancer (LAGC). The aim of this study was to develop and visualized a radio-clinical biomarker from pretreatment oversampled CT images to predict the response and prognosis to NCT in LAGC patients.Methods: 1060 LAGC patients were retrospectively recruited from six hospitals from January 2008 to December 2021. The training (TC) and internal validation cohort (IVC) were randomly selected from center I. The external validation cohort (EVC) comprised 265 patients from 5 other centers. An SE-ResNet50-based chemotherapy response predicting system (DL signature) was developed from pretreatment CT images preprocessed with imaging oversampling method (i.e. DeepSMOTE). Then, DL signature and clinic-based features were fed into the deep learning radio-clinical signature (DLCS). The predictive performance was evaluated according to discrimination, calibration and clinical usefulness. Model for OS prediction were built to further explore the survival benefit of the proposed DL signatures and clinicopathological characteristic. Result: DLCS showed perfect performance in predicting the response to NCT in the IVC (AUC, 0.86) and EVC (AUC, 0.82), with good calibration in all cohorts (p > 0.05). In addition, the performance of DLCS was better than that of the clinical model (p<0.05). Finally, we found that the DL signature could also serve as an independent factor for prognosis (HR, 0.828, p = 0.004). The C-index, iAUC, IBS for the OS model were 0.64, 1.24 and 0.71 in the test set.Conclusion: We proposed the DLCS that links the imaging features to clinical risk factors to generate high accuracy classification of tumor response and risk identification of OS in LAGC patients prior to NCT that then can be used for guiding personalized treatment plans with the help of the visualization of computerized tumor-level characterization.

Publisher

Research Square Platform LLC

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