基于MRI生境和US放射组学预测人表皮生长因子受体2在乳腺癌中的表达。

IF 3.4 4区 医学 Q2 ONCOLOGY
Breast Cancer : Targets and Therapy Pub Date : 2025-08-15 eCollection Date: 2025-01-01 DOI:10.2147/BCTT.S535697
Zikai Lin, Fangyi Huang, Liyan Wei, Xinhong Liao, Yong Gao
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引用次数: 0

摘要

目的:本研究旨在基于磁共振成像(MRI)栖息地和超声(US)放射组学预测人表皮生长因子受体2 (HER-2)在乳腺癌中的表达。患者和方法:回顾性研究纳入2019年5月25日至2025年4月15日病理证实的182例乳腺癌患者。数据集随机分为训练集(n=145)和测试集(n=37),比例为8:2。所有患者术前均行MRI和US检查。在第二阶段的动态对比增强t1加权成像上勾画出感兴趣的体积,并通过K-means聚类将其聚类到不同的栖息地区域。特征选择采用Spearman相关、贪婪递归消除策略、最小绝对收缩和选择算子回归。基于极端随机树的模型是使用从MRI栖息地提取的放射组学特征开发的,或者从美国感兴趣的区域。基于基线数据建立临床模型,然后将最佳栖息地模型和美国模型叠加,以及最佳栖息地模型、美国模型和临床模型的组合。通过曲线下面积(auc)和综合判别改进(IDI)来评价模型的性能。最佳生境模型和美国模型的可解释性采用Shapley加性解释分析。结果:选择model_h1_多参数模型为最佳生境模型(训练集和测试集的AUC分别为0.880和0.801)。Model_H1+US+Cli(训练集和测试集的AUC分别为0.945和0.835)优于model_h1_多参数模型、US模型和临床模型。IDI分析显示Model_H1+US+Cli进一步改善。结论:基于多参数MRI栖息地放射组学、US影像放射组学及临床特征的联合模型可有效预测HER-2在乳腺癌中的表达状况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Predicting Human Epidermal Growth Factor Receptor 2 Expression in Breast Cancer Based on Radiomics of MRI Habitat and US.

Predicting Human Epidermal Growth Factor Receptor 2 Expression in Breast Cancer Based on Radiomics of MRI Habitat and US.

Predicting Human Epidermal Growth Factor Receptor 2 Expression in Breast Cancer Based on Radiomics of MRI Habitat and US.

Predicting Human Epidermal Growth Factor Receptor 2 Expression in Breast Cancer Based on Radiomics of MRI Habitat and US.

Purpose: This study aims to predict human epidermal growth factor receptor-2 (HER-2) expression in breast cancer based on radiomics of magnetic resonance imaging (MRI) habitat and ultrasound (US).

Patients and methods: This retrospective study included 182 breast cancer patients confirmed by pathology from May 25, 2019 to April 15, 2025. The data set was randomly divided into a training set (n=145) and a testing set (n=37) with an 8:2 ratio. All patients underwent MRI and US before surgery. Volumes of interest were delineated on the second phase of dynamic contrast-enhanced T1-weighted imaging, which were clustered into different habitat regions via K-means clustering. Feature selection was using Spearman correlation, greedy recursive elimination strategy, least absolute shrinkage and selection operator regression. Models based on extremely randomized trees were developed using radiomics features extracted from MRI habitats, or from regions of interest on US. A clinical model was developed based on baseline data, followed by stacking the best habitat model and US model, as well as a combination of the best habitat, US, and clinical models. Model performance was evaluated by areas under the curve (AUCs) and integrated discrimination improvement (IDI). The interpretability of the best habitat model and US model was using Shapley Additive exPlanations analysis.

Results: Model_H1_multi-parametric was selected as the best habitat model (AUC was 0.880 and 0.801 in the training set and testing set). Model_H1+US+Cli (AUC was 0.945 and 0.835 in the training set and testing set) outperformed Model_H1_multi-parametric, the US model and the clinical model. The IDI analysis demonstrated further improvement by Model_H1+US+Cli.

Conclusion: A combined model based on multi-parametric MRI habitat radiomics, US imaging radiomics, and clinical features can effectively predict HER-2 expression status in breast cancer.

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