Dynamic And Quantitative Radiomics Analysis In Interventional Radiology

Abstract

Interventional Radiology (IR) is a subspecialty of radiology that performs invasive procedures driven by diagnostic imaging for predictive and therapeutic purpose. The development of artificial intelligence (AI) has revolutionized the industry of IR. Researchers have created sophisticated models backed by machine learning algorithms and optimization methodologies for image registration, cellular structure detection and computer-aided disease diagnosis and prognosis predictions. However, due to the incapacity of the human eye to detect tiny structural characteristics and inter-radiologist heterogeneity, conventional experience-based IR visual evaluations may have drawbacks. Radiomics, a technique that utilizes machine learning, offers a practical and quantifiable solution to this issue. This technology has been used to evaluate the heterogeneity of malignancies that are difficult to detect by the human eye by creating an automated pipeline for the extraction and analysis of high throughput computational imaging characteristics from radiological medical pictures. However, it is a demanding task to directly put radiomics into applications in IR because of the heterogeneity and complexity of medical imaging data. Furthermore, recent radiomics studies are based on static images, while many clinical applications (such as detecting the occurrence and development of tumors and assessing patient response to chemotherapy and immunotherapy) is a dynamic process. Merely incorporating static features cannot comprehensively reflect the metabolic characteristics and dynamic processes of tumors or soft tissues. To address these issues, we proposed a robust feature selection framework to manage the high-dimensional small-size data. Apart from that, we explore and propose a descriptor in the view of computer vision and physiology by integrating static radiomics features with time-varying information in tumor dynamics. The major contributions to this study include: Firstly, we construct a result-driven feature selection framework, which could efficiently reduce the dimension of the original feature set. The framework integrates different feature selection techniques to ensure the distinctiveness, uniqueness, and generalization ability of the output feature set. In the task of classification hepatocellular carcinoma (HCC) and intrahepatic cholangiocarcinoma (ICC) in primary liver cancer, only three radiomics features (chosen from more than 1, 800 features of the proposed framework) can obtain an AUC of 0.83 in the independent dataset. Besides, we also analyze features’ pattern and contributions to the results, enhancing clinical interpretability of radiomics biomarkers. Secondly, we explore and build a pulmonary perfusion descriptor based on 18F-FDG whole-body dynamic PET images. Our major novelties include: 1) propose a physiology-and-computer-vision-interpretable descriptor construction framework by the decomposition of spatiotemporal information into three dimensions: shades of grey levels, textures, and dynamics. 2) The spatio-temporal comparison of pulmonary descriptor intra and inter patients is feasible, making it possible to be an auxiliary diagnostic tool in pulmonary function assessment. 3) Compared with traditional PET metabolic biomarker analysis, the proposed descriptor incorporates image’s temporal information, which enables a better understanding of the time-various mechanisms and detection of visual perfusion abnormalities among different patients. 4) The proposed descriptor eliminates the impact of vascular branching structure and gravity effect by utilizing time warping algorithms. Our experimental results showed that our proposed framework and descriptor are promising tools to medical imaging analysis