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Gene Regulation and Targeted Therapy in Gastric Cancer Peritoneal Metastasis: Radiological Findings from Dual Energy CT and PET/CT
Published on: January 22, 2018
CT Radiomics for Predicting Outcomes in HER2-Positive Surgically Resectable Advanced Gastric Cancer: A Preliminary
Huiping Zhao1, Jianbo Gao2, Jing Li3
1Department of CT, Shaanxi Provincial People's Hospital, No. 256, Youyi West Road, Xi'an 710068, Shaanxi Province, China (H.Z.); National Engineering Research Center for Miniaturized Detection Systems, School of Life Sciences, Northwest University, No. 229 North Taibai Road, Xi'an 710069, Shaanxi Province, China (H.Z.).
Rationale And Objectives:
Accurate risk stratification in human epidermal growth factor receptor 2-positive surgically resectable advanced gastric cancer (HER2-p SRAGC) can strengthen monitoring for high-risk patients, allowing timely HER2-specific treatment and potentially improving prognosis. Therefore, we aimed to develop a CT radiomics model for predicting outcomes in HER2-p SRAGC and compare it with the 8th edition TNM staging system.
Materials And Methods:
621 HER2-p SRAGC patients who received either radical gastrectomy or radical gastrectomy after neoadjuvant therapy or chemotherapy were retrospectively enrolled in two hospitals and assigned to a training (n=330), an internal validation (n=143) and an external validation (n=148) cohorts. A radiomics model incorporating Radscore and clinical scores was constructed. Model performance was assessed by Kaplan-Meier estimator, Log-rank test, and Harrell's C-index.
Results:
The radiomics model was correlated with the overall survival (OS) across all cohorts, with C-indexes of 0.711[95% confidence interval (CI): 0.666-0.756; p<0.001; training], 0.669 (95%CI: 0.585-0.753; p=0.009; internal validation) and 0.693 (95%CI: 0.597-0.789; p=0.015; external validation). In all study cohorts, the radiomics model successfully stratified patients into high-risk and low-risk groups, and outweighed individual scores, pathological staging (pTNM), and clinical staging (cTNM) but was inferior to post-neoadjuvant therapy staging (ypTNM). Additionally, the radiomics model had added value to the prognostic efficacy of pTNM and was unaffected by patient age and gender.
Conclusion:
The radiomics model delivers individualized prognosis prediction of HER2-p SRAGC, surpassing clinical scores, and both pTNM and cTNM in forecasting OS. It confers incremental benefit to pTNM and exhibits certain universality across patient types.
Trial Registration:
Retrospectively registered.
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