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      Enhancing Brain Tumor Segmentation Accuracy through Scalable Federated Learning with Advanced Data Privacy and Security Measures

      , , , , ,
      Mathematics
      MDPI AG

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          Abstract

          Brain tumor segmentation in medical imaging is a critical task for diagnosis and treatment while preserving patient data privacy and security. Traditional centralized approaches often encounter obstacles in data sharing due to privacy regulations and security concerns, hindering the development of advanced AI-based medical imaging applications. To overcome these challenges, this study proposes the utilization of federated learning. The proposed framework enables collaborative learning by training the segmentation model on distributed data from multiple medical institutions without sharing raw data. Leveraging the U-Net-based model architecture, renowned for its exceptional performance in semantic segmentation tasks, this study emphasizes the scalability of the proposed approach for large-scale deployment in medical imaging applications. The experimental results showcase the remarkable effectiveness of federated learning, significantly improving specificity to 0.96 and the dice coefficient to 0.89 with the increase in clients from 50 to 100. Furthermore, the proposed approach outperforms existing convolutional neural network (CNN)- and recurrent neural network (RNN)-based methods, achieving higher accuracy, enhanced performance, and increased efficiency. The findings of this research contribute to advancing the field of medical image segmentation while upholding data privacy and security.

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          Most cited references56

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          The 2016 World Health Organization Classification of Tumors of the Central Nervous System: a summary.

          The 2016 World Health Organization Classification of Tumors of the Central Nervous System is both a conceptual and practical advance over its 2007 predecessor. For the first time, the WHO classification of CNS tumors uses molecular parameters in addition to histology to define many tumor entities, thus formulating a concept for how CNS tumor diagnoses should be structured in the molecular era. As such, the 2016 CNS WHO presents major restructuring of the diffuse gliomas, medulloblastomas and other embryonal tumors, and incorporates new entities that are defined by both histology and molecular features, including glioblastoma, IDH-wildtype and glioblastoma, IDH-mutant; diffuse midline glioma, H3 K27M-mutant; RELA fusion-positive ependymoma; medulloblastoma, WNT-activated and medulloblastoma, SHH-activated; and embryonal tumour with multilayered rosettes, C19MC-altered. The 2016 edition has added newly recognized neoplasms, and has deleted some entities, variants and patterns that no longer have diagnostic and/or biological relevance. Other notable changes include the addition of brain invasion as a criterion for atypical meningioma and the introduction of a soft tissue-type grading system for the now combined entity of solitary fibrous tumor / hemangiopericytoma-a departure from the manner by which other CNS tumors are graded. Overall, it is hoped that the 2016 CNS WHO will facilitate clinical, experimental and epidemiological studies that will lead to improvements in the lives of patients with brain tumors.
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            Advances in functional and structural MR image analysis and implementation as FSL.

            The techniques available for the interrogation and analysis of neuroimaging data have a large influence in determining the flexibility, sensitivity, and scope of neuroimaging experiments. The development of such methodologies has allowed investigators to address scientific questions that could not previously be answered and, as such, has become an important research area in its own right. In this paper, we present a review of the research carried out by the Analysis Group at the Oxford Centre for Functional MRI of the Brain (FMRIB). This research has focussed on the development of new methodologies for the analysis of both structural and functional magnetic resonance imaging data. The majority of the research laid out in this paper has been implemented as freely available software tools within FMRIB's Software Library (FSL).
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              The Multimodal Brain Tumor Image Segmentation Benchmark (BRATS).

              In this paper we report the set-up and results of the Multimodal Brain Tumor Image Segmentation Benchmark (BRATS) organized in conjunction with the MICCAI 2012 and 2013 conferences. Twenty state-of-the-art tumor segmentation algorithms were applied to a set of 65 multi-contrast MR scans of low- and high-grade glioma patients-manually annotated by up to four raters-and to 65 comparable scans generated using tumor image simulation software. Quantitative evaluations revealed considerable disagreement between the human raters in segmenting various tumor sub-regions (Dice scores in the range 74%-85%), illustrating the difficulty of this task. We found that different algorithms worked best for different sub-regions (reaching performance comparable to human inter-rater variability), but that no single algorithm ranked in the top for all sub-regions simultaneously. Fusing several good algorithms using a hierarchical majority vote yielded segmentations that consistently ranked above all individual algorithms, indicating remaining opportunities for further methodological improvements. The BRATS image data and manual annotations continue to be publicly available through an online evaluation system as an ongoing benchmarking resource.
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                Author and article information

                Contributors
                Journal
                MBSAAR
                Mathematics
                Mathematics
                MDPI AG
                2227-7390
                October 2023
                October 07 2023
                : 11
                : 19
                : 4189
                Article
                10.3390/math11194189
                d18ead71-8fbe-43c2-8baf-a29675a525c7
                © 2023

                https://creativecommons.org/licenses/by/4.0/

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