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Calculation of Apparent Diffusion Coefficients in Prostate Cancer Using Deep Learning Algorithms: A Pilot Study

BACKGROUND: Apparent diffusion coefficients (ADCs) obtained with diffusion-weighted imaging (DWI) are highly valuable for the detection and staging of prostate cancer and for assessing the response to treatment. However, DWI suffers from significant anatomic distortions and susceptibility artifacts,...

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Autores principales: Hu, Lei, Zhou, Da Wei, Fu, Cai Xia, Benkert, Thomas, Xiao, Yun Feng, Wei, Li Ming, Zhao, Jun Gong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8458902/
https://www.ncbi.nlm.nih.gov/pubmed/34568027
http://dx.doi.org/10.3389/fonc.2021.697721
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author Hu, Lei
Zhou, Da Wei
Fu, Cai Xia
Benkert, Thomas
Xiao, Yun Feng
Wei, Li Ming
Zhao, Jun Gong
author_facet Hu, Lei
Zhou, Da Wei
Fu, Cai Xia
Benkert, Thomas
Xiao, Yun Feng
Wei, Li Ming
Zhao, Jun Gong
author_sort Hu, Lei
collection PubMed
description BACKGROUND: Apparent diffusion coefficients (ADCs) obtained with diffusion-weighted imaging (DWI) are highly valuable for the detection and staging of prostate cancer and for assessing the response to treatment. However, DWI suffers from significant anatomic distortions and susceptibility artifacts, resulting in reduced accuracy and reproducibility of the ADC calculations. The current methods for improving the DWI quality are heavily dependent on software, hardware, and additional scan time. Therefore, their clinical application is limited. An accelerated ADC generation method that maintains calculation accuracy and repeatability without heavy dependence on magnetic resonance imaging scanners is of great clinical value. OBJECTIVES: We aimed to establish and evaluate a supervised learning framework for synthesizing ADC images using generative adversarial networks. METHODS: This prospective study included 200 patients with suspected prostate cancer (training set: 150 patients; test set #1: 50 patients) and 10 healthy volunteers (test set #2) who underwent both full field-of-view (FOV) diffusion-weighted imaging (f-DWI) and zoomed-FOV DWI (z-DWI) with b-values of 50, 1,000, and 1,500 s/mm(2). ADC values based on f-DWI and z-DWI (f-ADC and z-ADC) were calculated. Herein we propose an ADC synthesis method based on generative adversarial networks that uses f-DWI with a single b-value to generate synthesized ADC (s-ADC) values using z-ADC as a reference. The image quality of the s-ADC sets was evaluated using the peak signal-to-noise ratio (PSNR), root mean squared error (RMSE), structural similarity (SSIM), and feature similarity (FSIM). The distortions of each ADC set were evaluated using the T2-weighted image reference. The calculation reproducibility of the different ADC sets was compared using the intraclass correlation coefficient. The tumor detection and classification abilities of each ADC set were evaluated using a receiver operating characteristic curve analysis and a Spearman correlation coefficient. RESULTS: The s-ADC(b1000) had a significantly lower RMSE score and higher PSNR, SSIM, and FSIM scores than the s-ADC(b50) and s-ADC(b1500) (all P < 0.001). Both z-ADC and s-ADC(b1000) had less distortion and better quantitative ADC value reproducibility for all the evaluated tissues, and they demonstrated better tumor detection and classification performance than f-ADC. CONCLUSION: The deep learning algorithm might be a feasible method for generating ADC maps, as an alternative to z-ADC maps, without depending on hardware systems and additional scan time requirements.
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spelling pubmed-84589022021-09-24 Calculation of Apparent Diffusion Coefficients in Prostate Cancer Using Deep Learning Algorithms: A Pilot Study Hu, Lei Zhou, Da Wei Fu, Cai Xia Benkert, Thomas Xiao, Yun Feng Wei, Li Ming Zhao, Jun Gong Front Oncol Oncology BACKGROUND: Apparent diffusion coefficients (ADCs) obtained with diffusion-weighted imaging (DWI) are highly valuable for the detection and staging of prostate cancer and for assessing the response to treatment. However, DWI suffers from significant anatomic distortions and susceptibility artifacts, resulting in reduced accuracy and reproducibility of the ADC calculations. The current methods for improving the DWI quality are heavily dependent on software, hardware, and additional scan time. Therefore, their clinical application is limited. An accelerated ADC generation method that maintains calculation accuracy and repeatability without heavy dependence on magnetic resonance imaging scanners is of great clinical value. OBJECTIVES: We aimed to establish and evaluate a supervised learning framework for synthesizing ADC images using generative adversarial networks. METHODS: This prospective study included 200 patients with suspected prostate cancer (training set: 150 patients; test set #1: 50 patients) and 10 healthy volunteers (test set #2) who underwent both full field-of-view (FOV) diffusion-weighted imaging (f-DWI) and zoomed-FOV DWI (z-DWI) with b-values of 50, 1,000, and 1,500 s/mm(2). ADC values based on f-DWI and z-DWI (f-ADC and z-ADC) were calculated. Herein we propose an ADC synthesis method based on generative adversarial networks that uses f-DWI with a single b-value to generate synthesized ADC (s-ADC) values using z-ADC as a reference. The image quality of the s-ADC sets was evaluated using the peak signal-to-noise ratio (PSNR), root mean squared error (RMSE), structural similarity (SSIM), and feature similarity (FSIM). The distortions of each ADC set were evaluated using the T2-weighted image reference. The calculation reproducibility of the different ADC sets was compared using the intraclass correlation coefficient. The tumor detection and classification abilities of each ADC set were evaluated using a receiver operating characteristic curve analysis and a Spearman correlation coefficient. RESULTS: The s-ADC(b1000) had a significantly lower RMSE score and higher PSNR, SSIM, and FSIM scores than the s-ADC(b50) and s-ADC(b1500) (all P < 0.001). Both z-ADC and s-ADC(b1000) had less distortion and better quantitative ADC value reproducibility for all the evaluated tissues, and they demonstrated better tumor detection and classification performance than f-ADC. CONCLUSION: The deep learning algorithm might be a feasible method for generating ADC maps, as an alternative to z-ADC maps, without depending on hardware systems and additional scan time requirements. Frontiers Media S.A. 2021-09-09 /pmc/articles/PMC8458902/ /pubmed/34568027 http://dx.doi.org/10.3389/fonc.2021.697721 Text en Copyright © 2021 Hu, Zhou, Fu, Benkert, Xiao, Wei and Zhao https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Hu, Lei
Zhou, Da Wei
Fu, Cai Xia
Benkert, Thomas
Xiao, Yun Feng
Wei, Li Ming
Zhao, Jun Gong
Calculation of Apparent Diffusion Coefficients in Prostate Cancer Using Deep Learning Algorithms: A Pilot Study
title Calculation of Apparent Diffusion Coefficients in Prostate Cancer Using Deep Learning Algorithms: A Pilot Study
title_full Calculation of Apparent Diffusion Coefficients in Prostate Cancer Using Deep Learning Algorithms: A Pilot Study
title_fullStr Calculation of Apparent Diffusion Coefficients in Prostate Cancer Using Deep Learning Algorithms: A Pilot Study
title_full_unstemmed Calculation of Apparent Diffusion Coefficients in Prostate Cancer Using Deep Learning Algorithms: A Pilot Study
title_short Calculation of Apparent Diffusion Coefficients in Prostate Cancer Using Deep Learning Algorithms: A Pilot Study
title_sort calculation of apparent diffusion coefficients in prostate cancer using deep learning algorithms: a pilot study
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8458902/
https://www.ncbi.nlm.nih.gov/pubmed/34568027
http://dx.doi.org/10.3389/fonc.2021.697721
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