Liu Boya, Gu Xiangrong, Xie Danling, Zhao Bing, Han Dong, Zhang Yuli, Li Tao, Fang Jingqin
Department of Ultrasound, Daping Hospital, Army Medical University, Chongqing, China.
Department of Ultrasound Diagnosis, Wanzhou District First People's Hospital, Chongqing, China.
Technol Cancer Res Treat. 2025 Jan-Dec;24:15330338251334453. doi: 10.1177/15330338251334453. Epub 2025 Apr 17.
IntroductionTumor-infiltrating lymphocytes (TILs) are key indicators of immune response and prognosis in breast cancer (BC). Accurate prediction of TIL levels is essential for guiding personalized treatment strategies. This study aimed to develop and evaluate machine learning models using ultrasound-derived radiomics and clinical features to predict TIL levels in BC.MethodsThis retrospective study included 256 BC patients between January 2019 and August 2023, who were randomly divided into training (n = 179) and test (n = 77) cohorts. Radiomics features were extracted from the intratumor and peritumor regions in ultrasound images. Feature selection was performed using the "Boruta" package in R to iteratively remove non-significant features. Extra Trees Classifier was used to construct radiomics and clinical models. A combined radiomics-clinical (R-C) model was also developed. Model performance was evaluated using the area under the receiver operating characteristic curve (AUC), accuracy, sensitivity, specificity, and decision curve analysis (DCA) to assess clinical utility. A nomogram was created based on the best-performing model.ResultsA total of 1712 radiomics features were extracted from the intratumor and peritumor regions. The Boruta method selected five key features (four from the peritumor and one from the intratumor) for model construction. Clinical features, including immunohistochemistry, tumor size, shape, and echo characteristics, showed significant differences between high (≥10%) and low (<10%) TIL groups. Both the R-C and radiomics models outperformed the clinical model in the test cohort (area under the curve values of 0.869/0.838 vs 0.627, < .05). Calibration curves and Brier scores demonstrated superior accuracy and calibration for the R-C and radiomics models. DCA revealed the highest net benefit of the R-C model at intermediate threshold probabilities.ConclusionUltrasound-derived radiomics effectively predicts TIL levels in BC, providing valuable insights for personalized treatment and surveillance strategies.
引言
肿瘤浸润淋巴细胞(TILs)是乳腺癌(BC)免疫反应和预后的关键指标。准确预测TIL水平对于指导个性化治疗策略至关重要。本研究旨在开发和评估使用超声衍生的放射组学和临床特征来预测BC中TIL水平的机器学习模型。
方法
这项回顾性研究纳入了2019年1月至2023年8月期间的256例BC患者,他们被随机分为训练组(n = 179)和测试组(n = 77)。从超声图像中的肿瘤内和肿瘤周围区域提取放射组学特征。使用R语言中的“Boruta”包进行特征选择,以迭代方式去除无显著意义的特征。使用极端随机树分类器构建放射组学和临床模型。还开发了一个联合放射组学-临床(R-C)模型。使用受试者操作特征曲线下面积(AUC)、准确性、敏感性、特异性和决策曲线分析(DCA)评估模型性能,以评估临床实用性。基于表现最佳的模型创建了列线图。
结果
从肿瘤内和肿瘤周围区域共提取了1712个放射组学特征。Boruta方法选择了五个关键特征(四个来自肿瘤周围,一个来自肿瘤内)用于模型构建。临床特征,包括免疫组织化学、肿瘤大小、形状和回声特征,在高(≥10%)和低(<10%)TIL组之间显示出显著差异。在测试队列中,R-C模型和放射组学模型均优于临床模型(曲线下面积值分别为0.869/0.838对0.627,P <.05)。校准曲线和Brier评分显示R-C模型和放射组学模型具有更高的准确性和校准度。DCA显示R-C模型在中等阈值概率下具有最高的净效益。
结论
超声衍生的放射组学可有效预测BC中的TIL水平,为个性化治疗和监测策略提供有价值的见解。