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Due to its predominantly asymptomatic or mildly symptomatic progression, lung cancer is often diagnosed in advanced stages, resulting in poorer survival rates for patients. As with other cancers, early detection significantly improves the chances of successful treatment. Early diagnosis can be facilitated through screening programs designed to detect lung tissue tumors when they are still small, typically around 3mm in size. However, the analysis of extensive screening program data is hampered by limited access to medical experts. In this study, we developed a procedure for identifying potential malignant neoplastic lesions within lung parenchyma. The system leverages machine learning (ML) techniques applied to two types of measurements: low-dose Computed Tomography-based radiomics and metabolomics. Using data from two Polish screening programs, two ML algorithms were tested, along with various integration methods, to create a final model that combines both modalities to support lung cancer screening.

Segmentation of the bronchovascular bundle within the lung parenchyma is a key step for the proper analysis and planning of many pulmonary diseases. It might also be considered the preprocessing step when the goal is to segment the nodules from the lung parenchyma. We propose a segmentation pipeline for the bronchovascular bundle based on the Computed Tomography images, returning either binary or labelled masks of vessels and bronchi situated in the lung parenchyma. The method consists of two modules, modeling of the bronchial tree and vessels. The core revolves around a similar pipeline, the determination of the initial perimeter by the GMM method, skeletonization, and hierarchical analysis of the created graph. We tested our method on both low-dose CT and standard-dose CT, with various pathologies, reconstructed with various slice thicknesses, and acquired from various machines. We conclude that the method is invariant with respect to the origin and parameters of the CT series. Our pipeline is best suited for studies with healthy patients, patients with lung nodules, and patients with emphysema.

The outbreak of the SARS-CoV-2 pandemic has put healthcare systems worldwide to their limits, resulting in increased waiting time for diagnosis and required medical assistance. With chest radiographs (CXR) being one of the most common COVID-19 diagnosis methods, many artificial intelligence tools for image-based COVID-19 detection have been developed, often trained on a small number of images from COVID-19-positive patients. Thus, the need for high-quality and well-annotated CXR image databases increased. This paper introduces POLCOVID dataset, containing chest X-ray (CXR) images of patients with COVID-19 or other-type pneumonia, and healthy individuals gathered from 15 Polish hospitals. The original radiographs are accompanied by the preprocessed images limited to the lung area and the corresponding lung masks obtained with the segmentation model. Moreover, the manually created lung masks are provided for a part of POLCOVID dataset and the other four publicly available CXR image collections. POLCOVID dataset can help in pneumonia or COVID-19 diagnosis, while the set of matched images and lung masks may serve for the development of lung segmentation solutions., Comment: 13 pages, 3 figures

Due to the large accumulation of patients requiring hospitalization, the COVID-19 pandemic disease caused a high overload of health systems, even in developed countries. Deep learning techniques based on medical imaging data can help in the faster detection of COVID-19 cases and monitoring of disease progression. Regardless of the numerous proposed solutions for lung X-rays, none of them is a product that can be used in the clinic. Five different datasets (POLCOVID, AIforCOVID, COVIDx, NIH, and artificially generated data) were used to construct a representative dataset of 23 799 CXRs for model training; 1 050 images were used as a hold-out test set, and 44 247 as independent test set (BIMCV database). A U-Net-based model was developed to identify a clinically relevant region of the CXR. Each image class (normal, pneumonia, and COVID-19) was divided into 3 subtypes using a 2D Gaussian mixture model. A decision tree was used to aggregate predictions from the InceptionV3 network based on processed CXRs and a dense neural network on radiomic features. The lung segmentation model gave the Sorensen-Dice coefficient of 94.86% in the validation dataset, and 93.36% in the testing dataset. In 5-fold cross-validation, the accuracy for all classes ranged from 91% to 93%, keeping slightly higher specificity than sensitivity and NPV than PPV. In the hold-out test set, the balanced accuracy ranged between 68% and 100%. The highest performance was obtained for the subtypes N1, P1, and C1. A similar performance was obtained on the independent dataset for normal and COVID-19 class subtypes. Seventy-six percent of COVID-19 patients wrongly classified as normal cases were annotated by radiologists as with no signs of disease. Finally, we developed the online service (https://circa.aei.polsl.pl) to provide access to fast diagnosis support tools.