Zhang Jianyuan, Zhao Xinming, Zhao Yan, Zhang Jingmian, Zhang Zhaoqi, Wang Jianfang, Wang Yingchen, Dai Meng, Han Jingya
Department of Nuclear Medicine, The Fourth Hospital of Hebei Medical University, 12 Jiankang Road, Shijiazhuang, 050011, Hebei, China.
Department of Nuclear Medicine, Baoding No. 1 Central Hospital, Baoding, 071000, Hebei, China.
Eur J Nucl Med Mol Imaging. 2020 May;47(5):1137-1146. doi: 10.1007/s00259-019-04592-1. Epub 2019 Nov 14.
To assess the predictive power of pre-therapy F-FDG PET/CT-based radiomic features for epidermal growth factor receptor (EGFR) mutation status in non-small cell lung cancer.
Two hundred and forty-eight lung cancer patients underwent pre-therapy diagnostic F-FDG PET/CT scans and were tested for genetic mutations. The LIFEx package was used to extract 47 PET and 45 CT radiomic features reflecting tumor heterogeneity and phenotype. The least absolute shrinkage and selection operator (LASSO) algorithm was used to select radiomic features and develop a radiomics signature. We compared the predictive performance of models established by radiomics signature, clinical variables, and their combinations using receiver operating curves (ROCs). In addition, a nomogram based on the radiomics signature score (rad-score) and clinical variables was developed.
The patients were divided into a training set (n = 175) and a validation set (n = 73). Ten radiomic features were selected to build the radiomics signature model. The model showed a significant ability to discriminate between EGFR mutation and EGFR wild type, with area under the ROC curve (AUC) equal to 0.79 in the training set, and 0.85 in the validation set, compared with 0.75 and 0.69 for the clinical model. When clinical variables and radiomics signature were combined, the AUC increased to 0.86 (95% CI [0.80-0.91]) in the training set and 0.87 (95% CI [0.79-0.95]) in the validation set, thus showing better performance in the prediction of EGFR mutations.
The PET/CT-based radiomic features showed good performance in predicting EGFR mutation in non-small cell lung cancer, providing a useful method for the choice of targeted therapy in a clinical setting.
评估基于治疗前F-FDG PET/CT的影像组学特征对非小细胞肺癌表皮生长因子受体(EGFR)突变状态的预测能力。
248例肺癌患者接受了治疗前诊断性F-FDG PET/CT扫描,并进行了基因突变检测。使用LIFEx软件包提取47个PET和45个CT影像组学特征,以反映肿瘤的异质性和表型。采用最小绝对收缩和选择算子(LASSO)算法选择影像组学特征并建立影像组学特征模型。我们使用受试者工作特征曲线(ROC)比较了由影像组学特征模型、临床变量及其组合建立的模型的预测性能。此外,还基于影像组学特征评分(rad-score)和临床变量开发了列线图。
患者被分为训练集(n = 175)和验证集(n = 73)。选择了10个影像组学特征来构建影像组学特征模型。该模型显示出显著的区分EGFR突变和EGFR野生型的能力,训练集中ROC曲线下面积(AUC)为0.79,验证集中为0.85,而临床模型在训练集和验证集中的AUC分别为0.75和0.69。当临床变量和影像组学特征相结合时,训练集中的AUC增加到0.86(95%CI[0.80 - 0.91]),验证集中增加到0.87(95%CI[0.79 - 0.95]),从而在EGFR突变预测中表现出更好的性能。
基于PET/CT的影像组学特征在预测非小细胞肺癌EGFR突变方面表现良好,为临床靶向治疗的选择提供了一种有用的方法。