EnCoV, Institut Pascal, UMR 6602 CNRS, Université Clermont Auvergne, 28 place Henri Dunant, 63000, Clermont-Ferrand, France.
Department of Medical Imaging, CHU Clermont Ferrand, 1 place Lucie Aubrac, 63100, Clermont-Ferrand, France.
Int J Comput Assist Radiol Surg. 2022 Oct;17(10):1867-1877. doi: 10.1007/s11548-022-02662-8. Epub 2022 Jun 2.
Immunotherapy has dramatically improved the prognosis of patients with metastatic melanoma (MM). Yet, there is a lack of biomarkers to predict whether a patient will benefit from immunotherapy. Our aim was to create radiomics models on pretreatment computed tomography (CT) to predict overall survival (OS) and treatment response in patients with MM treated with anti-PD-1 immunotherapy.
We performed a monocentric retrospective analysis of 503 metastatic lesions in 71 patients with 46 radiomics features extracted following lesion segmentation. Predictive accuracies for OS < 1 year versus > 1 year and treatment response versus no response was compared for five feature selection methods (sequential forward selection, recursive, Boruta, relief, random forest) and four classifiers (support vector machine (SVM), random forest, K-nearest neighbor, logistic regression (LR)) used with or without SMOTE data augmentation. A fivefold cross-validation was performed at the patient level, with a tumour-based classification.
The highest accuracy level for OS predictions was obtained with 3D lesions (0.91) without clinical data integration when combining Boruta feature selection and the LR classifier, The highest accuracy for treatment response prediction was obtained with 3D lesions (0.88) without clinical data integration when combining Boruta feature selection, the LR classifier and SMOTE data augmentation. The accuracy was significantly higher concerning OS prediction with 3D segmentation (0.91 vs 0.86) while clinical data integration led to improved accuracy notably in 2D lesions (0.76 vs 0.87) regarding treatment response prediction. Skewness was the only feature found to be an independent predictor of OS (HR (CI 95%) 1.34, p-value 0.001).
This is the first study to investigate CT texture parameter selection and classification methods for predicting MM prognosis with treatment by immunotherapy. Combining pretreatment CT radiomics features from a single tumor with data selection and classifiers may accurately predict OS and treatment response in MM treated with anti-PD-1.
免疫疗法显著改善了转移性黑色素瘤(MM)患者的预后。然而,目前缺乏预测患者是否受益于免疫治疗的生物标志物。我们的目的是在接受 PD-1 免疫治疗的 MM 患者中建立治疗前 CT 的放射组学模型,以预测总生存期(OS)和治疗反应。
我们对 71 例患者的 503 个转移性病变进行了单中心回顾性分析,对病变分割后提取的 46 个放射组学特征进行了分析。使用五种特征选择方法(顺序前向选择、递归、Boruta、Relief、随机森林)和四种分类器(支持向量机(SVM)、随机森林、K-最近邻、逻辑回归(LR))对 OS<1 年与>1 年的预测准确率和治疗反应与无反应进行了比较,分类器使用或不使用 SMOTE 数据扩充。在患者水平上进行了五次交叉验证,采用基于肿瘤的分类。
在不结合临床数据的情况下,结合 Boruta 特征选择和 LR 分类器,3D 病变的 OS 预测准确率最高(0.91);在不结合临床数据的情况下,结合 Boruta 特征选择、LR 分类器和 SMOTE 数据扩充,3D 病变的治疗反应预测准确率最高(0.88)。3D 分割的 OS 预测准确率显著高于 2D 病变(0.91 与 0.86),而临床数据集成显著提高了 2D 病变的治疗反应预测准确率(0.76 与 0.87)。偏度是唯一被发现与 OS 相关的独立预测因素(HR(CI95%)1.34,p 值<0.001)。
这是第一项研究,探讨了 CT 纹理参数选择和分类方法,以预测免疫治疗治疗的 MM 预后。结合单一肿瘤的治疗前 CT 放射组学特征与数据选择和分类器,可能准确预测接受 PD-1 免疫治疗的 MM 的 OS 和治疗反应。