肺腺癌:放射组学可改善预后声明

S. Lang
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摘要

目的开发并验证一个预测 I 期肺腺癌(LUAD)早期复发的模型,该模型结合了基于术前 CT 的放射组学特征和肿瘤通过气隙扩散(STAS)的特征。材料与方法:从术后病理诊断为 I 期 LUAD 的患者中回顾性收集最近的术前薄层胸部 CT 扫描和术后病理血红素和伊红染色切片。人工分割感兴趣区,提取肿瘤和瘤周区域的放射组学特征,分别以 3 个体素单位、6 个体素单位和 12 个体素单位扩展,并通过卷积神经网络提取二维和三维深度学习图像特征。然后,构建了 RAdiomics Integrated with STAS 模型(RAISm)。然后在开发队列和验证队列中评估了 RAISm 的性能。结果2015年1月至2018年12月,两个医疗中心共226名患者被回顾性纳入模型的开发队列,并随机分为训练集(72.6%,n = 164)和测试集(27.4%,n = 62)。从2019年6月至2019年12月,51名患者被纳入验证队列。在训练队列(AUC = 0.847,95% CI 0.762-0.932)和验证队列(AUC = 0.817,95% CI 0.625-1.000)中,RAISm在预测I期LUAD早期复发方面具有出色的分辨能力。RAISm 在鉴别力和临床净效益方面优于单一模式特征和其他组合特征。结论:我们开创性地将基于术前 CT 的放射组学与 STAS 结合起来预测 I 期 LUAD 术后复发,并在验证队列中证实了该模型的卓越效果,显示了其辅助术后治疗策略的潜力。
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Adenokarzinome der Lunge: Radiomics könnten prognostische Aussagen verbessern
Objective: To develop and validate a prediction model for early recurrence of stage I lung adenocarcinoma (LUAD) that combines radiomics features based on preoperative CT with tumour spread through air spaces (STAS). Materials and methods: The most recent preoperative thin-section chest CT scans and postoperative pathological haematoxylin and eosin-stained sections were retrospectively collected from patients with a postoperative pathological diagnosis of stage I LUAD. Regions of interest were manually segmented, and radiomics features were extracted from the tumour and peritumoral regions extended by 3 voxel units, 6 voxel units, and 12 voxel units, and 2D and 3D deep learning image features were extracted by convolutional neural networks. Then, the RAdiomics Integrated with STAS model (RAISm) was constructed. The performance of RAISm was then evaluated in a development cohort and validation cohort. Results: A total of 226 patients from two medical centres from January 2015 to December 2018 were retrospectively included as the development cohort for the model and were randomly split into a training set (72.6%, n = 164) and a test set (27.4%, n = 62). From June 2019 to December 2019, 51 patients were included in the validation cohort. RAISm had excellent discrimination in predicting the early recurrence of stage I LUAD in the training cohort (AUC = 0.847, 95% CI 0.762–0.932) and validation cohort (AUC = 0.817, 95% CI 0.625–1.000). RAISm outperformed single modality signatures and other combinations of signatures in terms of discrimination and clinical net benefits. Conclusion: We pioneered combining preoperative CT-based radiomics with STAS to predict stage I LUAD recurrence postoperatively and confirmed the superior effect of the model in validation cohorts, showing its potential to assist in postoperative treatment strategies.
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