Radiomics converts medical images into mineable data via a high-throughput extraction of quantitative features used for clinical decision support. However, these radiomic features are susceptible to variation across scanners, acquisition protocols, and reconstruction settings. Various investigations have assessed the reproducibility and validation of radiomic features across these discrepancies. In this narrative review, we combine systematic keyword searches with prior domain knowledge to discuss various harmonization solutions to make the radiomic features more reproducible across various scanners and protocol settings. Different harmonization solutions are discussed and divided into two main categories: image domain and feature domain. The image domain category comprises methods such as the standardization of image acquisition, post-processing of raw sensor-level image data, data augmentation techniques, and style transfer. The feature domain category consists of methods such as the identification of reproducible features and normalization techniques such as statistical normalization, intensity harmonization, ComBat and its derivatives, and normalization using deep learning. We also reflect upon the importance of deep learning solutions for addressing variability across multi-centric radiomic studies especially using generative adversarial networks (GANs), neural style transfer (NST) techniques, or a combination of both. We cover a broader range of methods especially GANs and NST methods in more detail than previous reviews.
Three-dimensional radiomics-based machine learning models can stratify women with endometrial carcinoma at preoperative multiparametric MRI based on high-risk histopathologic features and can ident... Background Stratifying high-risk histopathologic features in endometrial carcinoma is important for treatment planning. Radiomics analysis at preoperative MRI holds potential to identify high-risk ...
17 January 2019 in IEEE Transactions on Radiation and Plasma Medical Sciences
Purpose: The distribution of a radiomic feature can differ between two institutions due to, for example, different image acquisition parameters, imaging systems, and contouring (i.e., tumor delineation) variations between clinicians. We aimed to develop effective statistical methods to successfully apply a radiomics-based predictive model to an external dataset. Theory: Two common feature normalization methods, re-scaling and standardization, were evaluated for suitability in reducing feature variability between institutions. Standardization was chosen as the preferred approach, since re-scaling was more sensitive to statistical outliers, and potentially reduced the discrimination power of a feature. It was also demonstrated why a dataset needs to be balanced between positive and negative outcomes before standardization is applied to it. Methods: In this work, the novelty and power of the developed method for improved application of radiomics models on external datasets is tied to finding the normalization transformations separately for each independent set. The clinical effectiveness of the normalization method was shown using magnetic resonance images of primary uterine adenocarcinoma. Feature selection was done using 94 samples (Institution X), and feature testing was done using 63 samples (Institution Y). The outcomes studied were lymphovascular space invasion and cancer staging. Logistic regression was used to obtain the prediction accuracy of a feature. Promising radiomic features were defined as those with AUC > 0.75 in the training set. Results: When comparing the prediction accuracy, F-score, and Matthews Correlation Coefficient (MCC) of promising radiomic features in the testing set with and without standardization, there was an improvement due to standardization. For cancer stage prediction, average accuracy for all promising features rose from 0.64 to 0.72, average F-score from 0.48 to 0.71, and average MCC from 0.34 to 0.44 (p <10-5). Furthermore, when applying standardization, the ratio of sensitivity to specificity was close to unity in the testing set, comparable to the ratio in the training set. Without standardization, this ratio deviated significantly from unity in the testing set. Conclusions: Applying feature standardization separately for each independent set using imbalance adjustments was shown to improve the predictive ability of radiomic models when applied to a dataset from an external institution.
1 November 2017 in International Journal of Radiation Oncology, Biology, Physics
This retrospective study investigated the value of pretreatment contrast-enhanced Magnetic Resonance Imaging (MRI)-based radiomics for the prediction of pathologic complete tumor response to neoadjuvant systemic therapy in breast cancer patients. A total of 292 breast cancer patients, with 320 tumors, who were treated with neo-adjuvant systemic therapy and underwent a pretreatment MRI exam were enrolled. As the data were collected in two different hospitals with five different MRI scanners and varying acquisition protocols, three different strategies to split training and validation datasets were used. Radiomics, clinical, and combined models were developed using random forest classifiers in each strategy. The analysis of radiomics features had no added value in predicting pathologic complete tumor response to neoadjuvant systemic therapy in breast cancer patients compared with the clinical models, nor did the combined models perform significantly better than the clinical models. Further, the radiomics features selected for the models and their performance differed with and within the different strategies. Due to previous and current work, we tentatively attribute the lack of improvement in clinical models following the addition of radiomics to the effects of variations in acquisition and reconstruction parameters. The lack of reproducibility data (i.e., test-retest or similar) meant that this effect could not be analyzed. These results indicate the need for reproducibility studies to preselect reproducible features in order to properly assess the potential of radiomics.
Background: Searching through the COVID-19 research literature to gain actionable clinical insight is a formidable task, even for experts. The usefulness of this corpus in terms of improving patient care is tied to the ability to see the big picture that emerges when the studies are seen in conjunction rather than in isolation. When the answer to a search query requires linking together multiple pieces of information across documents, simple keyword searches are insufficient. To answer such complex information needs, an innovative artificial intelligence (AI) technology named a knowledge graph (KG) could prove to be effective. Methods: We conducted an exploratory literature review of KG applications in the context of COVID-19. The search term used was “covid-19 knowledge graph”. In addition to PubMed, the first five pages of search results for Google Scholar and Google were considered for inclusion. Google Scholar was used to include non-peer-reviewed or non-indexed articles such as pre-prints and conference proceedings. Google was used to identify companies or consortiums active in this domain that have not published any literature, peer-reviewed or otherwise. Results: Our search yielded 34 results on PubMed and 50 results each on Google and Google Scholar. We found KGs being used for facilitating literature search, drug repurposing, clinical trial mapping, and risk factor analysis. Conclusions: Our synopses of these works make a compelling case for the utility of this nascent field of research.