Qi Yana, Hu Yanran, Lin Chengting, Song Ge, Shi Liting, Zhu Hui
Department of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, Shandong, China.
Department of Pathology, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, Shandong, China.
Front Immunol. 2025 Jan 27;16:1530279. doi: 10.3389/fimmu.2025.1530279. eCollection 2025.
This study aimed to develop a multi-modality model by incorporating pretreatment computed tomography (CT) radiomics and pathomics features along with clinical variables to predict pathologic complete response (pCR) to neoadjuvant chemoimmunotherapy in patients with locally advanced esophageal cancer (EC).
A total of 223 EC patients who underwent neoadjuvant chemoimmunotherapy followed by surgical intervention between August 2021 and December 2023 were included in this study. Radiomics features were extracted from contrast-enhanced CT images using PyrRadiomics, while pathomics features were derived from whole-slide images (WSIs) of pathological specimens using a fine-tuned deep learning model (ResNet-50). After feature selection, three single-modality prediction models and a combined multi-modality model integrating two radiomics features, 11 pathomics features, and two clinicopathological features were constructed using the support vector machine (SVM) algorithm. The performance of the models were evaluated using receiver operating characteristic (ROC) analysis, calibration plots, and decision curve analysis (DCA). Shapley values were also utilized to explain the prediction model.
The predictive capability of the multi-modality model in predicting pCR yielded an area under the curve (AUC) of 0.89 (95% confidence interval [CI], 0.75-1.00), outperforming the radiomics model (AUC 0.70 [95% CI 0.54-0.85]), pathomics model (AUC 0.77 [95% CI 0.53-1.00]), and clinical model (AUC 0.63 [95% CI 0.46-0.80]). Additionally, both the calibration plot and DCA curves support the clinical utility of the integrated multi-modality model.
The combined multi-modality model we propose can better predict the pCR status of esophageal cancer and help inform clinical treatment decisions.
本研究旨在通过整合治疗前计算机断层扫描(CT)影像组学和病理组学特征以及临床变量,开发一种多模态模型,以预测局部晚期食管癌(EC)患者对新辅助化疗免疫治疗的病理完全缓解(pCR)情况。
本研究纳入了2021年8月至2023年12月期间接受新辅助化疗免疫治疗并随后接受手术干预的223例EC患者。使用PyrRadiomics从增强CT图像中提取影像组学特征,同时使用微调后的深度学习模型(ResNet-50)从病理标本的全切片图像(WSIs)中获取病理组学特征。经过特征选择后,使用支持向量机(SVM)算法构建了三个单模态预测模型以及一个整合了两个影像组学特征、11个病理组学特征和两个临床病理特征的联合多模态模型。使用受试者操作特征(ROC)分析、校准图和决策曲线分析(DCA)对模型性能进行评估。还利用Shapley值来解释预测模型。
多模态模型预测pCR的能力产生的曲线下面积(AUC)为0.89(95%置信区间[CI],0.75 - 1.00),优于影像组学模型(AUC 0.70 [95% CI 0.54 - 0.85])、病理组学模型(AUC 0.77 [95% CI 0.53 - 1.00])和临床模型(AUC 0.63 [95% CI 0.46 - 0.80])。此外,校准图和DCA曲线均支持整合多模态模型的临床实用性。
我们提出的联合多模态模型能够更好地预测食管癌的pCR状态,并有助于为临床治疗决策提供参考。