Role of machine learning in early diagnosis of kidney diseases.

Machine learning (ML) and deep learning (DL) approaches have been used as indispensable tools in modern artificial intelligence-based computer-aided diagnostic (AIbased CAD) systems that can provide non-invasive, early, and accurate diagnosis of a given medical condition. These AI-based CAD systems have proven themselves to be reproducible and have the generalization ability to diagnose new unseen cases with several diseases and medical conditions in different organs (e.g., kidneys, prostate, brain, liver, lung, breast, and bladder). In this dissertation, we will focus on the role of such AI-based CAD systems in early diagnosis of two kidney diseases, namely: acute rejection (AR) post kidney transplantation and renal cancer (RC). A new renal computer-assisted diagnostic (Renal-CAD) system was developed to precisely diagnose AR post kidney transplantation at an early stage. The developed Renal-CAD system perform the following main steps: (1) auto-segmentation of the renal allograft from surrounding tissues from diffusion weighted magnetic resonance imaging (DW-MRI) and blood oxygen level-dependent MRI (BOLD-MRI), (2) extraction of image markers, namely: voxel-wise apparent diffusion coefficients (ADCs) are calculated from DW-MRI scans at 11 different low and high b-values and then represented as cumulative distribution functions (CDFs) and extraction of the transverse relaxation rate (R2*) values from the segmented kidneys using BOLD-MRI scans at different echotimes, (3) integration of multimodal image markers with the associated clinical biomarkers, serum creatinine (SCr) and creatinine clearance (CrCl), and (4) diagnosing renal allograft status as nonrejection (NR) or AR by utilizing these integrated biomarkers and the developed deep learning classification model built on stacked auto-encoders (SAEs). Using a leaveone- subject-out cross-validation approach along with SAEs on a total of 30 patients with transplanted kidney (AR = 10 and NR = 20), the Renal-CAD system demonstrated 93.3% accuracy, 90.0% sensitivity, and 95.0% specificity in differentiating AR from NR. Robustness of the Renal-CAD system was also confirmed by the area under the curve value of 0.92. Using a stratified 10-fold cross-validation approach, the Renal-CAD system demonstrated its reproduciblity and robustness with a diagnostic accuracy of 86.7%, sensitivity of 80.0%, specificity of 90.0%, and AUC of 0.88. In addition, a new renal cancer CAD (RC-CAD) system for precise diagnosis of RC at an early stage was developed, which incorporates the following main steps: (1) estimating the morphological features by applying a new parametric spherical harmonic technique, (2) extracting appearance-based features, namely: first order textural features are calculated and second order textural features are extracted after constructing the graylevel co-occurrence matrix (GLCM), (3) estimating the functional features by constructing wash-in/wash-out slopes to quantify the enhancement variations across different contrast enhanced computed tomography (CE-CT) phases, (4) integrating all the aforementioned features and modeling a two-stage multilayer perceptron artificial neural network (MLPANN) classifier to classify the renal tumor as benign or malignant and identify the malignancy subtype. On a total of 140 RC patients (malignant = 70 patients (ccRCC = 40 and nccRCC = 30) and benign angiomyolipoma tumors = 70), the developed RC-CAD system was validated using a leave-one-subject-out cross-validation approach. The developed RC-CAD system achieved a sensitivity of 95.3% ± 2.0%, a specificity of 99.9% ± 0.4%, and Dice similarity coefficient of 0.98 ± 0.01 in differentiating malignant from benign renal tumors, as well as an overall accuracy of 89.6% ± 5.0% in the sub-typing of RCC. The diagnostic abilities of the developed RC-CAD system were further validated using a randomly stratified 10-fold cross-validation approach. The results obtained using the proposed MLP-ANN classification model outperformed other machine learning classifiers (e.g., support vector machine, random forests, and relational functional gradient boosting) as well as other different approaches from the literature. In summary, machine and deep learning approaches have shown potential abilities to be utilized to build AI-based CAD systems. This is evidenced by the promising diagnostic performance obtained by both Renal-CAD and RC-CAD systems. For the Renal- CAD, the integration of functional markers extracted from multimodal MRIs with clinical biomarkers using SAEs classification model, potentially improved the final diagnostic results evidenced by high accuracy, sensitivity, and specificity. The developed Renal-CAD demonstrated high feasibility and efficacy for early, accurate, and non-invasive identification of AR. For the RC-CAD, integrating morphological, textural, and functional features extracted from CE-CT images using a MLP-ANN classification model eventually enhanced the final results in terms of accuracy, sensitivity, and specificity, making the proposed RC-CAD a reliable noninvasive diagnostic tool for RC. The early and accurate diagnosis of AR or RC will help physicians to provide early intervention with the appropriate treatment plan to prolong the life span of the diseased kidney, increase the survival chance of the patient, and thus improve the healthcare outcome in the U.S. and worldwide

Automated quality control by application of machine learning techniques for quantitative liver MRI

Quantitative magnetic resonance imaging (qMRI) and multi-parametric MRI are being increasingly used to diagnose and monitor liver diseases such as non-alcoholic fatty liver disease (NAFLD). These acquisitions are comparably more complicated than traditional T1-weighted and T2-weighted MRI scans and are also more prone to image quality is- sues and artefacts. In order for the output of the qMRI scans to be useable, they must undergo a rigorous and often lengthy quality control (QC). This manual QC is prone to human error and subjective. Additionally, with the development of new qMRI tech- niques, this leads to the manifestation of new quality issues. This thesis focuses on the development and implementation of automated QC processes for liver qMRI scans, that is where possible tag-free such that the process can be adapted to different imag- ing techniques. These automated QC processes were implemented using a variety of machine learning (ML) and deep learning (DL) approaches. These methods, developed on T1 mapping in UKBiobank, were designed to output metrics from the MRI scans that could be used to identify a specific quality issue, such as in chapter 3, or give a more general indication of the image quality in chapter 4. Furthermore, it was hypothe- sised that the introduction of associated meta-data, such as patient factors and scanning parameters, into these deep learning models would increase overall performance. This was explored in chapter 5. Finally, in order to assess the utility of our developed al- gorithms in a wider setting except for T1 mapping in UKBiobank, we tested it in two settings. Pilot study one assessed the utility of the model in T1 mapping in a separate study (CoverScan). Pilot study two assessed the utility of the model in a different qMRI acquisition; proton density fat fraction (PDFF) acquisitions from UKBiobank

Frameworks in medical image analysis with deep neural networks

In recent years, deep neural network based medical image analysis has become quite powerful and achieved similar results performance-wise as experts. Consequently, the integration of these tools into the clinical routine as clinical decision support systems is highly desired. The benefits of automatic image analysis for clinicians are massive, ranging from improved diagnostic as well as treatment quality to increased time-efficiency through automated structured reporting. However, implementations in the literature revealed a significant lack of standardization in pipeline building resulting in low reproducibility, high complexity through extensive knowledge requirements for building state-of-the-art pipelines, and difficulties for application in clinical research. The main objective of this work is the standardization of pipeline building in deep neural network based medical image segmentation and classification. This is why the Python frameworks MIScnn for medical image segmentation and AUCMEDI for medical image classification are proposed which simplify the implementation process through intuitive building blocks eliminating the need for time-consuming and error-prone implementation of common components from scratch. The proposed frameworks include state-of-the-art methodology, follow outstanding open-source principles like extensive documentation as well as stability, offer rapid as well as simple application capabilities for deep learning experts as well as clinical researchers, and provide cutting-edge high-performance competitive with the strongest implementations in the literature. As secondary objectives, this work presents more than a dozen in-house studies as well as discusses various external studies utilizing the proposed frameworks in order to prove the capabilities of standardized medical image analysis. The presented studies demonstrate excellent predictive capabilities in applications ranging from COVID-19 detection in computed tomography scans to the integration into a clinical study workflow for Gleason grading of prostate cancer microscopy sections and advance the state-of-the-art in medical image analysis by simplifying experimentation setups for research. Furthermore, studies for increasing reproducibility in performance assessment of medical image segmentation are presented including an open-source metric library for standardized evaluation and a community guideline on proper metric usage. The proposed contributions in this work improve the knowledge representation of the field, enable rapid as well as high-performing applications, facilitate further research, and strengthen the reproducibility of future studies

Brainlesion: Glioma, Multiple Sclerosis, Stroke and Traumatic Brain Injuries

This two-volume set LNCS 12962 and 12963 constitutes the thoroughly refereed proceedings of the 7th International MICCAI Brainlesion Workshop, BrainLes 2021, as well as the RSNA-ASNR-MICCAI Brain Tumor Segmentation (BraTS) Challenge, the Federated Tumor Segmentation (FeTS) Challenge, the Cross-Modality Domain Adaptation (CrossMoDA) Challenge, and the challenge on Quantification of Uncertainties in Biomedical Image Quantification (QUBIQ). These were held jointly at the 23rd Medical Image Computing for Computer Assisted Intervention Conference, MICCAI 2020, in September 2021. The 91 revised papers presented in these volumes were selected form 151 submissions. Due to COVID-19 pandemic the conference was held virtually. This is an open access book

Towards Interpretable Machine Learning in Medical Image Analysis

Over the past few years, ML has demonstrated human expert level performance in many medical image analysis tasks. However, due to the black-box nature of classic deep ML models, translating these models from the bench to the bedside to support the corresponding stakeholders in the desired tasks brings substantial challenges. One solution is interpretable ML, which attempts to reveal the working mechanisms of complex models. From a human-centered design perspective, interpretability is not a property of the ML model but an affordance, i.e., a relationship between algorithm and user. Thus, prototyping and user evaluations are critical to attaining solutions that afford interpretability. Following human-centered design principles in highly specialized and high stakes domains, such as medical image analysis, is challenging due to the limited access to end users. This dilemma is further exacerbated by the high knowledge imbalance between ML designers and end users. To overcome the predicament, we first define 4 levels of clinical evidence that can be used to justify the interpretability to design ML models. We state that designing ML models with 2 levels of clinical evidence: 1) commonly used clinical evidence, such as clinical guidelines, and 2) iteratively developed clinical evidence with end users are more likely to design models that are indeed interpretable to end users. In this dissertation, we first address how to design interpretable ML in medical image analysis that affords interpretability with these two different levels of clinical evidence. We further highly recommend formative user research as the first step of the interpretable model design to understand user needs and domain requirements. We also indicate the importance of empirical user evaluation to support transparent ML design choices to facilitate the adoption of human-centered design principles. All these aspects in this dissertation increase the likelihood that the algorithms afford interpretability and enable stakeholders to capitalize on the benefits of interpretable ML. In detail, we first propose neural symbolic reasoning to implement public clinical evidence into the designed models for various routinely performed clinical tasks. We utilize the routinely applied clinical taxonomy for abnormality classification in chest x-rays. We also establish a spleen injury grading system by strictly following the clinical guidelines for symbolic reasoning with the detected and segmented salient clinical features. Then, we propose the entire interpretable pipeline for UM prognostication with cytopathology images. We first perform formative user research and found that pathologists believe cell composition is informative for UM prognostication. Thus, we build a model to analyze cell composition directly. Finally, we conduct a comprehensive user study to assess the human factors of human-machine teaming with the designed model, e.g., whether the proposed model indeed affords interpretability to pathologists. The human-centered design process is proven to be truly interpretable to pathologists for UM prognostication. All in all, this dissertation introduces a comprehensive human-centered design for interpretable ML solutions in medical image analysis that affords interpretability to end users

Cancer Outcome Prediction with Multiform Medical Data using Deep Learning

This thesis illustrated the work done for my PhD project, which aims to develop personalised cancer outcome prediction models using various types of medical data. A predictive modelling workflow that can analyse data with different forms and generate comprehensive outcome prediction was designed and implemented on a variety of datasets. The model development was accompanied by applying deep learning techniques for multivariate survival analysis, medical image analysis and sequential data processing. The modelling workflow was applied to three different tasks: 1. Deep learning models were developed for estimating the progression probability of patients with colorectal cancer after resection and after different lines of chemotherapy, which got significantly better predictive performance than the Cox regression models. Besides, CT-based models were developed for predicting the tumour local response after chemotherapy of patients with lung metastasis, which got an AUC of 0. 769 on disease progression detection and 0.794 on treatment response classification. 2. Deep learning models were developed for predicting the survival state of patients with non-small cell lung cancer after radiotherapy using CT scans, dose distribution and disease and treatment variables. The eventual model obtained by ensemble voting got an AUC of 0.678, which is significantly higher than the score achieved by the radiomics model (0.633). 3. Deep-learning-aided approaches were used for estimating the progression risk for patients with solitary fibrous tumours using digital pathology slides. The deep learning architecture was able to optimise the WHO risk assessment model using automatically identified levels of mitotic activity. Compared to manual counting given by pathologists, deep-learning-aided mitosis counting can re-grade the patients whose risks were underestimated. The applications proved that the predictive models based on hybrid neural networks were able to analyse multiform medical data for generating data-based cancer outcome prediction. The results can be used for realising personalised treatment planning, evaluating treatment quality, and aiding clinical decision-making

Advanced Computational Methods for Oncological Image Analysis

[Cancer is the second most common cause of death worldwide and encompasses highly variable clinical and biological scenarios. Some of the current clinical challenges are (i) early diagnosis of the disease and (ii) precision medicine, which allows for treatments targeted to specific clinical cases. The ultimate goal is to optimize the clinical workflow by combining accurate diagnosis with the most suitable therapies. Toward this, large-scale machine learning research can define associations among clinical, imaging, and multi-omics studies, making it possible to provide reliable diagnostic and prognostic biomarkers for precision oncology. Such reliable computer-assisted methods (i.e., artificial intelligence) together with clinicians’ unique knowledge can be used to properly handle typical issues in evaluation/quantification procedures (i.e., operator dependence and time-consuming tasks). These technical advances can significantly improve result repeatability in disease diagnosis and guide toward appropriate cancer care. Indeed, the need to apply machine learning and computational intelligence techniques has steadily increased to effectively perform image processing operations—such as segmentation, co-registration, classification, and dimensionality reduction—and multi-omics data integration.