Guanchao Ye, Guangyao Wu, Chunyang Zhang, Mingliang Wang, Hong Liu, Enmin Song, Yuzhou Zhuang, Kuo Li, Yu Qi, Yongde Liao
{"title":"基于 CT 的瘤内异质性量化用于预测非小细胞肺癌新辅助免疫化疗的病理完全反应","authors":"Guanchao Ye, Guangyao Wu, Chunyang Zhang, Mingliang Wang, Hong Liu, Enmin Song, Yuzhou Zhuang, Kuo Li, Yu Qi, Yongde Liao","doi":"10.3389/fimmu.2024.1414954","DOIUrl":null,"url":null,"abstract":"To investigate the prediction of pathologic complete response (pCR) in patients with non-small cell lung cancer (NSCLC) undergoing neoadjuvant immunochemotherapy (NAIC) using quantification of intratumoral heterogeneity from pre-treatment CT image.This retrospective study included 178 patients with NSCLC who underwent NAIC at 4 different centers. The training set comprised 108 patients from center A, while the external validation set consisted of 70 patients from center B, center C, and center D. The traditional radiomics model was contrasted using radiomics features. The radiomics features of each pixel within the tumor region of interest (ROI) were extracted. The optimal division of tumor subregions was determined using the K-means unsupervised clustering method. The internal tumor heterogeneity habitat model was developed using the habitats features from each tumor sub-region. The LR algorithm was employed in this study to construct a machine learning prediction model. The diagnostic performance of the model was evaluated using criteria such as area under the receiver operating characteristic curve (AUC), accuracy, specificity, sensitivity, positive predictive value (PPV), and negative predictive value (NPV).In the training cohort, the traditional radiomics model achieved an AUC of 0.778 [95% confidence interval (CI): 0.688-0.868], while the tumor internal heterogeneity habitat model achieved an AUC of 0.861 (95% CI: 0.789-0.932). The tumor internal heterogeneity habitat model exhibits a higher AUC value. It demonstrates an accuracy of 0.815, surpassing the accuracy of 0.685 achieved by traditional radiomics models. In the external validation cohort, the AUC values of the two models were 0.723 (CI: 0.591-0.855) and 0.781 (95% CI: 0.673-0.889), respectively. The habitat model continues to exhibit higher AUC values. In terms of accuracy evaluation, the tumor heterogeneity habitat model outperforms the traditional radiomics model, achieving a score of 0.743 compared to 0.686.The quantitative analysis of intratumoral heterogeneity using CT to predict pCR in NSCLC patients undergoing NAIC holds the potential to inform clinical decision-making for resectable NSCLC patients, prevent overtreatment, and enable personalized and precise cancer management.","PeriodicalId":505785,"journal":{"name":"Frontiers in Immunology","volume":"83 22","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-06-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"CT-based quantification of intratumoral heterogeneity for predicting pathologic complete response to neoadjuvant immunochemotherapy in non-small cell lung cancer\",\"authors\":\"Guanchao Ye, Guangyao Wu, Chunyang Zhang, Mingliang Wang, Hong Liu, Enmin Song, Yuzhou Zhuang, Kuo Li, Yu Qi, Yongde Liao\",\"doi\":\"10.3389/fimmu.2024.1414954\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"To investigate the prediction of pathologic complete response (pCR) in patients with non-small cell lung cancer (NSCLC) undergoing neoadjuvant immunochemotherapy (NAIC) using quantification of intratumoral heterogeneity from pre-treatment CT image.This retrospective study included 178 patients with NSCLC who underwent NAIC at 4 different centers. The training set comprised 108 patients from center A, while the external validation set consisted of 70 patients from center B, center C, and center D. The traditional radiomics model was contrasted using radiomics features. The radiomics features of each pixel within the tumor region of interest (ROI) were extracted. The optimal division of tumor subregions was determined using the K-means unsupervised clustering method. The internal tumor heterogeneity habitat model was developed using the habitats features from each tumor sub-region. The LR algorithm was employed in this study to construct a machine learning prediction model. The diagnostic performance of the model was evaluated using criteria such as area under the receiver operating characteristic curve (AUC), accuracy, specificity, sensitivity, positive predictive value (PPV), and negative predictive value (NPV).In the training cohort, the traditional radiomics model achieved an AUC of 0.778 [95% confidence interval (CI): 0.688-0.868], while the tumor internal heterogeneity habitat model achieved an AUC of 0.861 (95% CI: 0.789-0.932). The tumor internal heterogeneity habitat model exhibits a higher AUC value. It demonstrates an accuracy of 0.815, surpassing the accuracy of 0.685 achieved by traditional radiomics models. In the external validation cohort, the AUC values of the two models were 0.723 (CI: 0.591-0.855) and 0.781 (95% CI: 0.673-0.889), respectively. The habitat model continues to exhibit higher AUC values. 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引用次数: 0
摘要
这项回顾性研究纳入了178名在4个不同中心接受新辅助免疫化疗(NAIC)的非小细胞肺癌(NSCLC)患者。训练集由来自 A 中心的 108 名患者组成,外部验证集由来自 B 中心、C 中心和 D 中心的 70 名患者组成。提取肿瘤感兴趣区(ROI)内每个像素的放射组学特征。使用 K-means 无监督聚类方法确定肿瘤子区域的最佳划分。利用每个肿瘤子区域的生境特征建立肿瘤内部异质性生境模型。本研究采用 LR 算法构建机器学习预测模型。在训练队列中,传统放射组学模型的 AUC 为 0.778 [95% 置信区间 (CI):0.688-0.868],而肿瘤内部异质性生境模型的 AUC 为 0.861 (95% CI:0.789-0.932)。肿瘤内部异质性生境模型的 AUC 值更高。它的准确度为 0.815,超过了传统放射组学模型的准确度 0.685。在外部验证队列中,两个模型的 AUC 值分别为 0.723(CI:0.591-0.855)和 0.781(95% CI:0.673-0.889)。生境模型的 AUC 值仍然较高。在准确性评估方面,肿瘤异质性生境模型优于传统的放射组学模型,得分为0.743,而传统的放射组学模型为0.686。利用CT定量分析瘤内异质性来预测接受NAIC的NSCLC患者的pCR,有望为可切除的NSCLC患者的临床决策提供依据,防止过度治疗,实现个性化和精确的癌症管理。
CT-based quantification of intratumoral heterogeneity for predicting pathologic complete response to neoadjuvant immunochemotherapy in non-small cell lung cancer
To investigate the prediction of pathologic complete response (pCR) in patients with non-small cell lung cancer (NSCLC) undergoing neoadjuvant immunochemotherapy (NAIC) using quantification of intratumoral heterogeneity from pre-treatment CT image.This retrospective study included 178 patients with NSCLC who underwent NAIC at 4 different centers. The training set comprised 108 patients from center A, while the external validation set consisted of 70 patients from center B, center C, and center D. The traditional radiomics model was contrasted using radiomics features. The radiomics features of each pixel within the tumor region of interest (ROI) were extracted. The optimal division of tumor subregions was determined using the K-means unsupervised clustering method. The internal tumor heterogeneity habitat model was developed using the habitats features from each tumor sub-region. The LR algorithm was employed in this study to construct a machine learning prediction model. The diagnostic performance of the model was evaluated using criteria such as area under the receiver operating characteristic curve (AUC), accuracy, specificity, sensitivity, positive predictive value (PPV), and negative predictive value (NPV).In the training cohort, the traditional radiomics model achieved an AUC of 0.778 [95% confidence interval (CI): 0.688-0.868], while the tumor internal heterogeneity habitat model achieved an AUC of 0.861 (95% CI: 0.789-0.932). The tumor internal heterogeneity habitat model exhibits a higher AUC value. It demonstrates an accuracy of 0.815, surpassing the accuracy of 0.685 achieved by traditional radiomics models. In the external validation cohort, the AUC values of the two models were 0.723 (CI: 0.591-0.855) and 0.781 (95% CI: 0.673-0.889), respectively. The habitat model continues to exhibit higher AUC values. In terms of accuracy evaluation, the tumor heterogeneity habitat model outperforms the traditional radiomics model, achieving a score of 0.743 compared to 0.686.The quantitative analysis of intratumoral heterogeneity using CT to predict pCR in NSCLC patients undergoing NAIC holds the potential to inform clinical decision-making for resectable NSCLC patients, prevent overtreatment, and enable personalized and precise cancer management.