Abstract:Colorectal cancer is the third most aggressive cancer worldwide. Polyps, as the main biomarker of the disease, are detected, localized, and characterized through colonoscopy procedures. Nonetheless, during the examination, up to 25% of polyps are missed, because of challenging conditions (camera movements, lighting changes), and the close similarity of polyps and intestinal folds. Besides, there is a remarked subjectivity and expert dependency to observe and detect abnormal regions along the intestinal tract. Currently, publicly available polyp datasets have allowed significant advances in computational strategies dedicated to characterizing non-parametric polyp shapes. These computational strategies have achieved remarkable scores of up to 90% in segmentation tasks. Nonetheless, these strategies operate on cropped and expert-selected frames that always observe polyps. In consequence, these computational approximations are far from clinical scenarios and real applications, where colonoscopies are redundant on intestinal background with high textural variability. In fact, the polyps typically represent less than 1% of total observations in a complete colonoscopy record. This work introduces COLON: the largest COlonoscopy LONg sequence dataset with around of 30 thousand polyp labeled frames and 400 thousand background frames. The dataset was collected from a total of 30 complete colonoscopies with polyps at different stages, variations in preparation procedures, and some cases the observation of surgical instrumentation. Additionally, 10 full intestinal background video control colonoscopies were integrated in order to achieve a robust polyp-background frame differentiation. The COLON dataset is open to the scientific community to bring new scenarios to propose computational tools dedicated to polyp detection and segmentation over long sequences, being closer to real colonoscopy scenarios.
Abstract:Stroke is the second leading cause of mortality worldwide. Immediate attention and diagnosis play a crucial role regarding patient prognosis. The key to diagnosis consists in localizing and delineating brain lesions. Standard stroke examination protocols include the initial evaluation from a non-contrast CT scan to discriminate between hemorrhage and ischemia. However, non-contrast CTs may lack sensitivity in detecting subtle ischemic changes in the acute phase. As a result, complementary diffusion-weighted MRI studies are captured to provide valuable insights, allowing to recover and quantify stroke lesions. This work introduced APIS, the first paired public dataset with NCCT and ADC studies of acute ischemic stroke patients. APIS was presented as a challenge at the 20th IEEE International Symposium on Biomedical Imaging 2023, where researchers were invited to propose new computational strategies that leverage paired data and deal with lesion segmentation over CT sequences. Despite all the teams employing specialized deep learning tools, the results suggest that the ischemic stroke segmentation task from NCCT remains challenging. The annotated dataset remains accessible to the public upon registration, inviting the scientific community to deal with stroke characterization from NCCT but guided with paired DWI information.