Extraction Of Quantitative Imaging Features Research Articles

A multi-scale deep residual network-based guided wave imaging evaluation method for fatigue crack quantification

Abstract As a promising structural health monitoring (SHM) technology, guided wave (GW) imaging is gaining increasing attention for crack monitoring of aircraft structures. However, actual fatigue crack propagation is a complex dynamically evolving process affected by various variabilities. It is still challenging to accurately track and quantify the dynamic fatigue crack propagation with GW imaging methods. Therefore, in order to achieve more accurate fatigue crack quantification, this paper proposes a multi-scale deep residual network-based GW imaging evaluation method. A convolutional neural network (CNN) is utilized to evaluate the entire pixel distribution of GW imaging maps to fuse damage-related information from multiple GW monitoring paths. By designing multi-scale convolutional kernels and deep residual learning, a robust quantitative image feature extraction is ensured with the dynamic evolution process of fatigue crack growth and the performance degradation is avoided as the CNN goes deeper, thereby improving the quantification accuracy. The method is validated on a fatigue test of landing gear beams, which are important load-carrying aircraft structural components. The results demonstrate that the proposed method can extract multi-scale crack length-related features and accurately track fatigue crack propagations. For batch specimens, the maximum quantification error is reduced from the original 6.1mm to 1.6mm, marking a significant improvement.

CDPNet: a radiomic feature learning method with epigenetic application to estimating MGMT promoter methylation status in glioblastoma.

Radiomics has been widely recognized for its effectiveness in decoding tumor phenotypes through the extraction of quantitative imaging features. However, the robustness of radiomic methods to estimate clinically relevant biomarkers non-invasively remains largely untested. In this study, we propose Cascaded Data Processing Network (CDPNet), a radiomic feature learning method to predict tumor molecular status from medical images. We apply CDPNet to an epigenetic case, specifically targeting the estimation of O6-methylguanine-DNA-methyltransferase (MGMT) promoter methylation from Magnetic Resonance Imaging (MRI) scans of glioblastoma patients. CDPNet has three components: 1) Principal Component Analysis (PCA), 2) Fisher Linear Discriminant (FLD), and 3) a combination of hashing and blockwise histograms. The outlined architectural framework capitalizes on PCA to reconstruct input image patches, followed by FLD to extract discriminative filter banks, and finally using binary hashing and blockwise histogram module for indexing, pooling, and feature generation. To validate the effectiveness of CDPNet, we conducted an exhaustive evaluation on a comprehensive retrospective cohort comprising 484 IDH-wildtype glioblastoma patients with pre-operative multi-parametric MRI scans (T1, T1-Gd, T2, and T2-FLAIR). The prediction of MGMT promoter methylation status was cast as a binary classification problem. The developed model underwent rigorous training via 10-fold cross-validation on a discovery cohort of 446 patients. Subsequently, the model's performance was evaluated on a distinct and previously unseen replication cohort of 38 patients. Our method achieved an accuracy of 70.11% and an area under the curve of 0.71 (95% CI: 0.65 - 0.74).

Radiomics in CT and MR imaging of the liver and pancreas: tools with potential for clinical application.

Radiomics allows the extraction of quantitative imaging features from clinical magnetic resonance imaging (MRI) and computerized tomography (CT) studies. The advantages of radiomics have primarily been exploited in oncological applications, including better characterization and staging of oncological lesions and prediction of patient outcomes and treatment response. The potential introduction of radiomics in the clinical setting requires the establishment of a standardized radiomics pipeline and a quality assurance program. Radiomics and texture analysis of the liver have improved the differentiation of hypervascular lesions such as adenomas, focal nodular hyperplasia, and hepatocellular carcinoma (HCC) during the arterial phase, and in the pretreatment determination of HCC prognostic factors (e.g., tumor grade, microvascular invasion, Ki-67 proliferation index). Radiomics of pancreatic CT and MR images has enhanced pancreatic ductal adenocarcinoma detection and its differentiation from pancreatic neuroendocrine tumors, mass-forming chronic pancreatitis, or autoimmune pancreatitis. Radiomics can further help to better characterize incidental pancreatic cystic lesions, accurately discriminating benign from malignant intrapancreatic mucinous neoplasms. Nonetheless, despite their encouraging results and exciting potential, these tools have yet to be implemented in the clinical setting. This non-systematic review will describe the essential steps in the implementation of the radiomics and feature extraction workflow from liver and pancreas CT and MRI studies for their potential clinical application. A succinct overview of reported radiomics applications in the liver and pancreas and the challenges and limitations of their implementation in the clinical setting is also discussed, concluding with a brief exploration of the future perspectives of radiomics in the gastroenterology field.

Deep Learning-Based Radiomics for Prognostic Stratification of Low-Grade Gliomas Using a Multiple-Gene Signature

Low-grade gliomas are a heterogeneous group of infiltrative neoplasms. Radiomics allows the characterization of phenotypes with high-throughput extraction of quantitative imaging features from radiologic images. Deep learning models, such as convolutional neural networks (CNNs), offer well-performing models and a simplified pipeline by automatic feature learning. In our study, MRI data were retrospectively obtained from The Cancer Imaging Archive (TCIA), which contains MR images for a subset of the LGG patients in The Cancer Genome Atlas (TCGA). Corresponding molecular genetics and clinical information were obtained from TCGA. Three genes included in the genetic signatures were WEE1, CRTAC1, and SEMA4G. A CNN-based deep learning model was used to classify patients into low and high-risk groups, with the median gene signature risk score as the cut-off value. The data were randomly split into training and test sets, with 61 patients in the training set and 20 in the test set. In the test set, models using T1 and T2 weighted images had an area under the receiver operating characteristic curve of 73% and 79%, respectively. In conclusion, we developed a CNN-based model to predict non-invasively the risk stratification provided by the prognostic gene signature in LGGs. Numerous previously discovered gene signatures and novel genetic identifiers that will be developed in the future may be utilized with this method.

Radiomics analysis of contrast-enhanced T1W MRI: predicting the recurrence of acute pancreatitis

To investigate the predictive value of radiomics based on T1-weighted contrast-enhanced MRI (CE-MRI) in forecasting the recurrence of acute pancreatitis (AP). A total of 201 patients with first-episode of acute pancreatitis were enrolled retrospectively (140 in the training cohort and 61 in the testing cohort), with 69 and 30 patients who experienced recurrence in each cohort, respectively. Quantitative image feature extraction was obtained from MR contrast-enhanced late arterial-phase images. The optimal radiomics features retained after dimensionality reduction were used to construct the radiomics model through logistic regression analysis, and the clinical characteristics were collected to construct the clinical model. The nomogram model was established by linearly integrating the clinically independent risk factor with the optimal radiomics signature. The five best radiomics features were determined by dimensionality reduction. The radiomics model had a higher area under the receiver operating characteristic curve (AUC) than the clinical model for estimating the recurrence of acute pancreatitis for both the training cohort (0.915 vs. 0.811, p = 0.020) and testing cohort (0.917 vs. 0.681, p = 0.002). The nomogram model showed good performance, with an AUC of 0.943 in the training cohort and 0.906 in the testing cohort. The radiomics model based on CE-MRI showed good performance for optimizing the individualized prediction of recurrent acute pancreatitis, which provides a reference for the prevention and treatment of recurrent pancreatitis.

Deep Learning With Radiomics for Disease Diagnosis and Treatment: Challenges and Potential.

The high-throughput extraction of quantitative imaging features from medical images for the purpose of radiomic analysis, i.e., radiomics in a broad sense, is a rapidly developing and emerging research field that has been attracting increasing interest, particularly in multimodality and multi-omics studies. In this context, the quantitative analysis of multidimensional data plays an essential role in assessing the spatio-temporal characteristics of different tissues and organs and their microenvironment. Herein, recent developments in this method, including manually defined features, data acquisition and preprocessing, lesion segmentation, feature extraction, feature selection and dimension reduction, statistical analysis, and model construction, are reviewed. In addition, deep learning-based techniques for automatic segmentation and radiomic analysis are being analyzed to address limitations such as rigorous workflow, manual/semi-automatic lesion annotation, and inadequate feature criteria, and multicenter validation. Furthermore, a summary of the current state-of-the-art applications of this technology in disease diagnosis, treatment response, and prognosis prediction from the perspective of radiology images, multimodality images, histopathology images, and three-dimensional dose distribution data, particularly in oncology, is presented. The potential and value of radiomics in diagnostic and therapeutic strategies are also further analyzed, and for the first time, the advances and challenges associated with dosiomics in radiotherapy are summarized, highlighting the latest progress in radiomics. Finally, a robust framework for radiomic analysis is presented and challenges and recommendations for future development are discussed, including but not limited to the factors that affect model stability (medical big data and multitype data and expert knowledge in medical), limitations of data-driven processes (reproducibility and interpretability of studies, different treatment alternatives for various institutions, and prospective researches and clinical trials), and thoughts on future directions (the capability to achieve clinical applications and open platform for radiomics analysis).

Quantitative imaging feature pipeline: a web-based tool for utilizing, sharing, and building image-processing pipelines.

.Quantitative image features that can be computed from medical images are proving to be valuable biomarkers of underlying cancer biology that can be used for assessing treatment response and predicting clinical outcomes. However, validation and eventual clinical implementation of these tools is challenging due to the absence of shared software algorithms, architectures, and the tools required for computing, comparing, evaluating, and disseminating predictive models. Similarly, researchers need to have programming expertise in order to complete these tasks. The quantitative image feature pipeline (QIFP) is an open-source, web-based, graphical user interface (GUI) of configurable quantitative image-processing pipelines for both planar (two-dimensional) and volumetric (three-dimensional) medical images. This allows researchers and clinicians a GUI-driven approach to process and analyze images, without having to write any software code. The QIFP allows users to upload a repository of linked imaging, segmentation, and clinical data or access publicly available datasets (e.g., The Cancer Imaging Archive) through direct links. Researchers have access to a library of file conversion, segmentation, quantitative image feature extraction, and machine learning algorithms. An interface is also provided to allow users to upload their own algorithms in Docker containers. The QIFP gives researchers the tools and infrastructure for the assessment and development of new imaging biomarkers and the ability to use them for single and multicenter clinical and virtual clinical trials.

PET/MRI Radiomics in Patients With Brain Metastases.

Although a variety of imaging modalities are used or currently being investigated for patients with brain tumors including brain metastases, clinical image interpretation to date uses only a fraction of the underlying complex, high-dimensional digital information from routinely acquired imaging data. The growing availability of high-performance computing allows the extraction of quantitative imaging features from medical images that are usually beyond human perception. Using machine learning techniques and advanced statistical methods, subsets of such imaging features are used to generate mathematical models that represent characteristic signatures related to the underlying tumor biology and might be helpful for the assessment of prognosis or treatment response, or the identification of molecular markers. The identification of appropriate, characteristic image features as well as the generation of predictive or prognostic mathematical models is summarized under the term radiomics. This review summarizes the current status of radiomics in patients with brain metastases.

The Technome - A Predictive Internal Calibration Approach for Quantitative Imaging Biomarker Research

The goal of radiomics is to convert medical images into a minable data space by extraction of quantitative imaging features for clinically relevant analyses, e.g. survival time prediction of a patient. One problem of radiomics from computed tomography is the impact of technical variation such as reconstruction kernel variation within a study. Additionally, what is often neglected is the impact of inter-patient technical variation, resulting from patient characteristics, even when scan and reconstruction parameters are constant. In our approach, measurements within 3D regions-of-interests (ROI) are calibrated by further ROIs such as air, adipose tissue, liver, etc. that are used as control regions (CR). Our goal is to derive general rules for an automated internal calibration that enhance prediction, based on the analysed features and a set of CRs. We define qualification criteria motivated by status-quo radiomics stability analysis techniques to only collect information from the CRs which is relevant given a respective task. These criteria are used in an optimisation to automatically derive a suitable internal calibration for prediction tasks based on the CRs. Our calibration enhanced the performance for centrilobular emphysema prediction in a COPD study and prediction of patients’ one-year-survival in an oncological study.

Current applications and challenges of radiomics in urothelial cancer

New discoveries and technologies have begun to change paradigms of urothelial cancer therapy in recent years. One of the novel techniques which emerged in the imaging community is radiomics, which refers to the high-throughput extraction of quantitative image features from medical images. Radiomics, being noninvasive and easy to perform, has shown great potential in oncology by providing valuable information about tumor type, aggressiveness, progression, response to treatment and prognosis and enabling us to gain insights into the true utility of personalized medicine in the management of cancer in the near future. With rapid development in this area, radiomics has already been applied in urothelial cancer to predict pathological grade, clinical stage, lymph node metastasis and treatment response demonstrating promising results. In this review, we highlight advances in clinical applications of radiomics in urothelial cancer, discuss about the challenges and implications of radiomics for radiologists and suggest the future directions that we could move toward in order to fully realize the potentials of radiomics to improve personalized management of patients with urothelial cancer.

Radiomics in Brain Tumor: Image Assessment, Quantitative Feature Descriptors, and Machine-Learning Approaches.

Radiomics describes a broad set of computational methods that extract quantitative features from radiographic images. The resulting features can be used to inform imaging diagnosis, prognosis, and therapy response in oncology. However, major challenges remain for methodologic developments to optimize feature extraction and provide rapid information flow in clinical settings. Equally important, to be clinically useful, predictive radiomic properties must be clearly linked to meaningful biologic characteristics and qualitative imaging properties familiar to radiologists. Here we use a cross-disciplinary approach to highlight studies in radiomics. We review brain tumor radiologic studies (eg, imaging interpretation) through computational models (eg, computer vision and machine learning) that provide novel clinical insights. We outline current quantitative image feature extraction and prediction strategies with different levels of available clinical classes for supporting clinical decision-making. We further discuss machine-learning challenges and data opportunities to advance radiomic studies.

Multi-objective radiomics model for predicting distant failure in lung SBRT

Stereotactic body radiation therapy (SBRT) has demonstrated high local control rates in early stage non-small cell lung cancer patients who are not ideal surgical candidates. However, distant failure after SBRT is still common. For patients at high risk of early distant failure after SBRT treatment, additional systemic therapy may reduce the risk of distant relapse and improve overall survival. Therefore, a strategy that can correctly stratify patients at high risk of failure is needed. The field of radiomics holds great potential in predicting treatment outcomes by using high-throughput extraction of quantitative imaging features. The construction of predictive models in radiomics is typically based on a single objective such as overall accuracy or the area under the curve (AUC). However, because of imbalanced positive and negative events in the training datasets, a single objective may not be ideal to guide model construction. To overcome these limitations, we propose a multi-objective radiomics model that simultaneously considers sensitivity and specificity as objective functions. To design a more accurate and reliable model, an iterative multi-objective immune algorithm (IMIA) was proposed to optimize these objective functions. The multi-objective radiomics model is more sensitive than the single-objective model, while maintaining the same levels of specificity and AUC. The IMIA performs better than the traditional immune-inspired multi-objective algorithm.

Computational resources for radiomics

Radiomics has the potential to individualize patient treatment by using images that are already being routinely acquired. Defined as the extraction of quantitative imaging features from clinical images for use in statistical models, radiomics has had success in a variety of tumor sites and imaging modalities. Researchers new to the field must start by choosing software to segment tumors [or other regions of interest (ROI)], extract quantitative image features, and analyze the results. This review describes the various software programs available for these tasks and gives examples of the use of these programs in radiomics research.

A radiomic signature based on advanced tumor shape parameters (Spiculated-ness) to predict the outcome of locally advanced (LA) HNSCC patients.

11571Background: Tumor invasion patterns are known to be associated with HNSCC pts outcome. Radiomics is a rapidly-emerging field involving the extraction of quantitative imaging features from stan...

Robust Radiomics feature quantification using semiautomatic volumetric segmentation.

Due to advances in the acquisition and analysis of medical imaging, it is currently possible to quantify the tumor phenotype. The emerging field of Radiomics addresses this issue by converting medical images into minable data by extracting a large number of quantitative imaging features. One of the main challenges of Radiomics is tumor segmentation. Where manual delineation is time consuming and prone to inter-observer variability, it has been shown that semi-automated approaches are fast and reduce inter-observer variability. In this study, a semiautomatic region growing volumetric segmentation algorithm, implemented in the free and publicly available 3D-Slicer platform, was investigated in terms of its robustness for quantitative imaging feature extraction. Fifty-six 3D-radiomic features, quantifying phenotypic differences based on tumor intensity, shape and texture, were extracted from the computed tomography images of twenty lung cancer patients. These radiomic features were derived from the 3D-tumor volumes defined by three independent observers twice using 3D-Slicer, and compared to manual slice-by-slice delineations of five independent physicians in terms of intra-class correlation coefficient (ICC) and feature range. Radiomic features extracted from 3D-Slicer segmentations had significantly higher reproducibility (ICC = 0.85±0.15, p = 0.0009) compared to the features extracted from the manual segmentations (ICC = 0.77±0.17). Furthermore, we found that features extracted from 3D-Slicer segmentations were more robust, as the range was significantly smaller across observers (p = 3.819e-07), and overlapping with the feature ranges extracted from manual contouring (boundary lower: p = 0.007, higher: p = 5.863e-06). Our results show that 3D-Slicer segmented tumor volumes provide a better alternative to the manual delineation for feature quantification, as they yield more reproducible imaging descriptors. Therefore, 3D-Slicer can be employed for quantitative image feature extraction and image data mining research in large patient cohorts.

MO‐D‐WAB‐01: How OMICs Is Going to Impact Research Topics for Medical Physicists

The ongoing revolution in genomics provides many new research opportunities for physicists. Two crucial research areas to advance clinical oncology include the intersections between imaging and genomics, as well as the use of genomic analyses to improve patient management in radiation oncology. Confusingly, the term ‘radiogenomics’ is used for both applications. In the field of radiology, ‘radiogenomics’ refers to the underlying genomic correlates of image features, for example the correlation of tumor biopsies mRNA microarray signatures with image features. In radiation oncology and radiobiology, the term ‘radiogenomics’ refers to the impact of a patient's genotype on the relative radiosensitivity or radioresistance of normal tissues. Tumor biopsy mRNA signatures, for radiosensitivity, hypoxia, or proliferation, have been studied to predict response and to potentially individualize treatments. Blood proteomics has been applied to normal tissue responses such as radiation pneumonitis. Imaging radiogenomics can further be thought of as ‘radiomics’ + genomics, where radiomics is the extraction of quantitative image features that can be incorporated into disease classification schemes or predictive models. We will also touch on the general application of systems modeling that is so important to advancement in modern biology and response modeling. This session will emphasis new opportunities, as well as challenges and obstacles to progress. ‘Omic’ sciences will greatly impact the study and clinical use of tumor control probability and normal tissue complication probability models; the biological interpretation of image features; and the clinical implications of imaging and cancer screening.