Hyper-Dense_Lung_Seg: Multimodal-Fusion-Based Modified U-Net for Lung Tumour Segmentation Using Multimodality of CT-PET Scans
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Published:2023-11-20
Issue:22
Volume:13
Page:3481
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ISSN:2075-4418
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Container-title:Diagnostics
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language:en
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Short-container-title:Diagnostics
Author:
Alshmrani Goram Mufarah12, Ni Qiang1, Jiang Richard1, Muhammed Nada3
Affiliation:
1. School of Computing and Commutations, Lancaster University, Lancaster LA1 4YW, UK 2. College of Computing and Information Technology, University of Bisha, Bisha 67714, Saudi Arabia 3. Computers and Control Engineering Department, Faculty of Engineering, Tanta University, Tanta 31733, Egypt
Abstract
The majority of cancer-related deaths globally are due to lung cancer, which also has the second-highest mortality rate. The segmentation of lung tumours, treatment evaluation, and tumour stage classification have become significantly more accessible with the advent of PET/CT scans. With the advent of PET/CT scans, it is possible to obtain both functioning and anatomic data during a single examination. However, integrating images from different modalities can indeed be time-consuming for medical professionals and remains a challenging task. This challenge arises from several factors, including differences in image acquisition techniques, image resolutions, and the inherent variations in the spectral and temporal data captured by different imaging modalities. Artificial Intelligence (AI) methodologies have shown potential in the automation of image integration and segmentation. To address these challenges, multimodal fusion approach-based U-Net architecture (early fusion, late fusion, dense fusion, hyper-dense fusion, and hyper-dense VGG16 U-Net) are proposed for lung tumour segmentation. Dice scores of 73% show that hyper-dense VGG16 U-Net is superior to the other four proposed models. The proposed method can potentially aid medical professionals in detecting lung cancer at an early stage.
Funder
The Engineering and Physical Sciences Research Council Leverhulme Trust
Subject
Clinical Biochemistry
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