Abstract:Herein we propose a deep learning-based approach for the prediction of lung lesion response based on radiomic features extracted from clinical CT scans of patients in non-small cell lung cancer trials. The approach starts with the classification of lung lesions from the set of primary and metastatic lesions at various anatomic locations. Focusing on the lung lesions, we perform automatic segmentation to extract their 3D volumes. Radiomic features are then extracted from the lesion on the pre-treatment scan and the first follow-up scan to predict which lesions will shrink at least 30% in diameter during treatment (either Pembrolizumab or combinations of chemotherapy and Pembrolizumab), which is defined as a partial response by the Response Evaluation Criteria In Solid Tumors (RECIST) guidelines. A 5-fold cross validation on the training set led to an AUC of 0.84 +/- 0.03, and the prediction on the testing dataset reached AUC of 0.73 +/- 0.02 for the outcome of 30% diameter shrinkage.
Abstract:Volumetric segmentation of lesions on CT scans is important for many types of analysis, including lesion growth kinetic modeling in clinical trials and machine learning of radiomic features. Manual segmentation is laborious, and impractical for large-scale use. For routine clinical use, and in clinical trials that apply the Response Evaluation Criteria In Solid Tumors (RECIST), clinicians typically outline the boundaries of a lesion on a single slice to extract diameter measurements. In this work, we have collected a large-scale database, named LesionVis, with pixel-wise manual 2D lesion delineations on the RECIST-slices. To extend the 2D segmentations to 3D, we propose a volumetric progressive lesion segmentation (PLS) algorithm to automatically segment the 3D lesion volume from 2D delineations using a scale-invariant and boundary-aware deep convolutional network (SIBA-Net). The SIBA-Net copes with the size transition of a lesion when the PLS progresses from the RECIST-slice to the edge-slices, as well as when performing longitudinal assessment of lesions whose size change over multiple time points. The proposed PLS-SiBA-Net (P-SiBA) approach is assessed on the lung lesion cases from LesionVis. Our experimental results demonstrate that the P-SiBA approach achieves mean Dice similarity coefficients (DSC) of 0.81, which significantly improves 3D segmentation accuracy compared with the approaches proposed previously (highest mean DSC at 0.78 on LesionVis). In summary, by leveraging the limited 2D delineations on the RECIST-slices, P-SiBA is an effective semi-supervised approach to produce accurate lesion segmentations in 3D.