Page 101 - AI for Good Innovate for Impact
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AI for Good Innovate for Impact



               2       Use Case Description


               2�1     Description                                                                                  4.1-Healthcare


               Context and Background

               Brain cancer is a grave malignancy type that is a consequence of unconstrained and unrestricted
               multiplication of cells in the brain, generally engendered by a malignant brain tumour.

               Meningiomas are among the most common tumours of the Central Nervous System (CNS).
               These sorts of tumours, which have a varied growth potential, emerge from the meninges, the
               membranes that coat the brain and spinal cord, and generally do not metastasize.
               Necrosis - It is a dead region, and there is an absence of nuclei. It consists of small, dust-like
               structures. The cells are broken down along with cell borders, and there is a larger quantity
               of cell debris. There are many cells and connective tissues are fewer. Texture changes occur
               slowly in necrosis.

               A biopsy involves examining a tissue under a microscope to determine the presence or extent
               of disease spread.


               Histopathological (biopsy) analysis is a painstaking, prolonged, and labour-intensive skilled job,
               dependent on the expertise of the pathologist. With the availability of high-resolution digital
               images of slides, referred to as Whole Slide Images (WSI), digital histopathology opens the
               potential to automate and improve parts of this analysis process, with the goal of more efficient
               and less error-prone diagnosis, and reducing the workload of pathologists.

               Analysis of histopathological (biopsy) slides by pathologists is considered the gold standard
               in determining the presence and nature of diseases such as cancer. Thin sections of tissue
               extracted during biopsies are fixed on a glass slide and stained with specific chemicals, e.g.,
               Haematoxylin and Eosin (H&E) stains, and then observed under a microscope at different levels
               of magnification.

               Different magnification levels are used for different types of analysis, from which are derived
               the final impressions and diagnosis, such as categorization of tumours as malignant or benign,
               and if cancerous, the grade of the disease. In our study, the selected glass slides, stained with
               H&E, were scanned using a Leica SCN400 microscopic whole-slide scanner with nominally
               20x magnification.

               Aims and Objectives


               It was observed that there is a lack of publicly accessible labelled datasets of meningioma whole
               slide images. Hence, the first objective in the current work was the generation of a sizable,
               high-quality, expert validated, ground truth dataset of pathology features of meningioma whole
               slide images, which could be used for this research, and would also form the basis of future
               work on neuropathology analysis.


               The second and primary objective was the development of ML pipelines for detecting regions of
               necrosis in whole slide images of meningioma. This includes a comparison of the performance
               of various ML and ensemble algorithms, as well as the evaluation of performance metrics such
               as specificity and sensitivity of such algorithms with varying sizes of necrotic regions.



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