Utilizing intratumoral and peritumoral ultrasound radiomics for predicting KRAS gene mutation status in rectal cancer patients

克拉斯 医学 接收机工作特性 结直肠癌 逻辑回归 曲线下面积 放射科 肿瘤科 癌症 内科学
作者
Yajiao Gan,Qiping Hu,Qingling Shen,Qingfu Qian,Lin Peng,Minling Zhuo,Ensheng Xue,Zhikui Chen
出处
期刊:Journal of Applied Clinical Medical Physics [Wiley]
卷期号:26 (7): e70153-e70153 被引量:1
标识
DOI:10.1002/acm2.70153
摘要

Abstract BACKGROUND KRAS mutations are associated with treatment and prognostic outcomes in colorectal cancer patients.There have been no studies on utilizing the peritumoral images to predict KRAS mutation status in rectal cancer patients. We aim to develop a radiomics model utilizing intratumoral and peritumoral ultrasound images for predicting KRAS mutation status in rectal cancer. METHODS This study retrospectively included 278 patients with pathologically confirmed rectal cancer following surgery, who were randomly divided into training group (194 cases) and test group (84 cases) at a 7:3 ratio. Radiomic features from both intratumoral and peritumoral regions were extracted from endorectal ultrasound images. A five‐step procedure was used to select robust features. Based on these, intratumoral, peritumoral, and combined models were created using logistic regression, support vector machine, and light gradient boosting machine. The predictive accuracy, calibration, and clinical utility of the models were evaluated using receiver operating characteristic curves, calibration curves, and decision curve analysis. The SHapley Additive exPlanation (SHAP) method was used to evaluate the importance of the features in the optimal models. RESULTS In the test set, the area under the curve of all three combined models exceeded that of the individual intratumoral and peritumoral models. According to area under the curve, decision curve analysis, and calibration curves, combine_LR demonstrated the best performance, with an area under the curve of 0.881. CONCLUSIONS The ultrasound radiomics model, incorporating both intratumoral and peritumoral features, effectively predicts KRAS status in rectal cancer patients, potentially guiding clinical targeted therapy selection.

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