Enhancement of megavoltage electronic portal images for markerless tumor tracking

Purpose The poor quality of megavoltage (MV) images from electronic portal imaging device (EPID) hinders visual verification of tumor targeting accuracy particularly during markerless tumor tracking. The aim of this study was to investigate the effect of a few representative image processing treatme...

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Veröffentlicht in:Journal of applied clinical medical physics 2018-09, Vol.19 (5), p.398-406
Hauptverfasser: Cheong, Kwang‐Ho, Yoon, Jai‐Woong, Park, Soah, Hwang, Taejin, Kang, Sei‐Kwon, Koo, Taeryool, Han, Tae Jin, Kim, Haeyoung, Lee, Me Yeon, Kim, Kyoung Ju, Bae, Hoonsik
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container_end_page 406
container_issue 5
container_start_page 398
container_title Journal of applied clinical medical physics
container_volume 19
creator Cheong, Kwang‐Ho
Yoon, Jai‐Woong
Park, Soah
Hwang, Taejin
Kang, Sei‐Kwon
Koo, Taeryool
Han, Tae Jin
Kim, Haeyoung
Lee, Me Yeon
Kim, Kyoung Ju
Bae, Hoonsik
description Purpose The poor quality of megavoltage (MV) images from electronic portal imaging device (EPID) hinders visual verification of tumor targeting accuracy particularly during markerless tumor tracking. The aim of this study was to investigate the effect of a few representative image processing treatments on visual verification and detection capability of tumors under auto tracking. Methods Images of QC‐3 quality phantom, a single patient's setup image, and cine images of two‐lung cancer patients were acquired. Three image processing methods were individually employed to the same original images. For each deblurring, contrast enhancement, and denoising, a total variation deconvolution, contrast‐limited adaptive histogram equalization (CLAHE), and median filter were adopted, respectively. To study the effect of image enhancement on tumor auto‐detection, a tumor tracking algorithm was adopted in which the tumor position was determined as the minimum point of the mean of the sum of squared pixel differences (MSSD) between two images. The detectability and accuracy were compared. Results Deblurring of a quality phantom image yielded sharper edges, while the contrast‐enhanced image was more readable with improved structural differentiation. Meanwhile, the denoising operation resulted in noise reduction, however, at the cost of sharpness. Based on comparison of pixel value profiles, contrast enhancement outperformed others in image perception. During the tracking experiment, only contrast enhancement resulted in tumor detection in all images using our tracking algorithm. Deblurring failed to determine the target position in two frames out of a total of 75 images. For original and denoised set, target location was not determined for the same five images. Meanwhile, deblurred image showed increased detection accuracy compared with the original set. The denoised image resulted in decreased accuracy. In the case of contrast‐improved set, the tracking accuracy was nearly maintained as that of the original image. Conclusions Considering the effect of each processing on tumor tracking and the visual perception in a limited time, contrast enhancement would be the first consideration to visually verify the tracking accuracy of tumors on MV EPID without sacrificing tumor detectability and detection accuracy.
doi_str_mv 10.1002/acm2.12411
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The aim of this study was to investigate the effect of a few representative image processing treatments on visual verification and detection capability of tumors under auto tracking. Methods Images of QC‐3 quality phantom, a single patient's setup image, and cine images of two‐lung cancer patients were acquired. Three image processing methods were individually employed to the same original images. For each deblurring, contrast enhancement, and denoising, a total variation deconvolution, contrast‐limited adaptive histogram equalization (CLAHE), and median filter were adopted, respectively. To study the effect of image enhancement on tumor auto‐detection, a tumor tracking algorithm was adopted in which the tumor position was determined as the minimum point of the mean of the sum of squared pixel differences (MSSD) between two images. The detectability and accuracy were compared. Results Deblurring of a quality phantom image yielded sharper edges, while the contrast‐enhanced image was more readable with improved structural differentiation. Meanwhile, the denoising operation resulted in noise reduction, however, at the cost of sharpness. Based on comparison of pixel value profiles, contrast enhancement outperformed others in image perception. During the tracking experiment, only contrast enhancement resulted in tumor detection in all images using our tracking algorithm. Deblurring failed to determine the target position in two frames out of a total of 75 images. For original and denoised set, target location was not determined for the same five images. Meanwhile, deblurred image showed increased detection accuracy compared with the original set. The denoised image resulted in decreased accuracy. In the case of contrast‐improved set, the tracking accuracy was nearly maintained as that of the original image. Conclusions Considering the effect of each processing on tumor tracking and the visual perception in a limited time, contrast enhancement would be the first consideration to visually verify the tracking accuracy of tumors on MV EPID without sacrificing tumor detectability and detection accuracy.</description><identifier>ISSN: 1526-9914</identifier><identifier>EISSN: 1526-9914</identifier><identifier>DOI: 10.1002/acm2.12411</identifier><identifier>PMID: 29984883</identifier><language>eng</language><publisher>United States: John Wiley &amp; Sons, Inc</publisher><subject>Accuracy ; Algorithms ; contrast enhancement ; deblurring ; denoising ; Humans ; Image Enhancement ; Image Processing, Computer-Assisted ; image quality ; Lung cancer ; megavoltage electronic portal imaging device ; Neoplasms - diagnostic imaging ; Noise ; Phantoms, Imaging ; Radiation Oncology Physics ; Radiography ; Regularization methods ; tumor tracking ; Visual perception</subject><ispartof>Journal of applied clinical medical physics, 2018-09, Vol.19 (5), p.398-406</ispartof><rights>2018 The Authors. published by Wiley Periodicals, Inc. on behalf of American Association of Physicists in Medicine.</rights><rights>2018 The Authors. Journal of Applied Clinical Medical Physics published by Wiley Periodicals, Inc. on behalf of American Association of Physicists in Medicine.</rights><rights>2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3911-7ec6de2cb37ae201ce75848c25fbebffd0d357f13be6ad20b5519bd6a1facd7e3</citedby><cites>FETCH-LOGICAL-c3911-7ec6de2cb37ae201ce75848c25fbebffd0d357f13be6ad20b5519bd6a1facd7e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123147/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123147/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,1411,11541,27901,27902,45550,45551,46027,46451,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29984883$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cheong, Kwang‐Ho</creatorcontrib><creatorcontrib>Yoon, Jai‐Woong</creatorcontrib><creatorcontrib>Park, Soah</creatorcontrib><creatorcontrib>Hwang, Taejin</creatorcontrib><creatorcontrib>Kang, Sei‐Kwon</creatorcontrib><creatorcontrib>Koo, Taeryool</creatorcontrib><creatorcontrib>Han, Tae Jin</creatorcontrib><creatorcontrib>Kim, Haeyoung</creatorcontrib><creatorcontrib>Lee, Me Yeon</creatorcontrib><creatorcontrib>Kim, Kyoung Ju</creatorcontrib><creatorcontrib>Bae, Hoonsik</creatorcontrib><title>Enhancement of megavoltage electronic portal images for markerless tumor tracking</title><title>Journal of applied clinical medical physics</title><addtitle>J Appl Clin Med Phys</addtitle><description>Purpose The poor quality of megavoltage (MV) images from electronic portal imaging device (EPID) hinders visual verification of tumor targeting accuracy particularly during markerless tumor tracking. The aim of this study was to investigate the effect of a few representative image processing treatments on visual verification and detection capability of tumors under auto tracking. Methods Images of QC‐3 quality phantom, a single patient's setup image, and cine images of two‐lung cancer patients were acquired. Three image processing methods were individually employed to the same original images. For each deblurring, contrast enhancement, and denoising, a total variation deconvolution, contrast‐limited adaptive histogram equalization (CLAHE), and median filter were adopted, respectively. To study the effect of image enhancement on tumor auto‐detection, a tumor tracking algorithm was adopted in which the tumor position was determined as the minimum point of the mean of the sum of squared pixel differences (MSSD) between two images. The detectability and accuracy were compared. 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The aim of this study was to investigate the effect of a few representative image processing treatments on visual verification and detection capability of tumors under auto tracking. Methods Images of QC‐3 quality phantom, a single patient's setup image, and cine images of two‐lung cancer patients were acquired. Three image processing methods were individually employed to the same original images. For each deblurring, contrast enhancement, and denoising, a total variation deconvolution, contrast‐limited adaptive histogram equalization (CLAHE), and median filter were adopted, respectively. To study the effect of image enhancement on tumor auto‐detection, a tumor tracking algorithm was adopted in which the tumor position was determined as the minimum point of the mean of the sum of squared pixel differences (MSSD) between two images. The detectability and accuracy were compared. Results Deblurring of a quality phantom image yielded sharper edges, while the contrast‐enhanced image was more readable with improved structural differentiation. Meanwhile, the denoising operation resulted in noise reduction, however, at the cost of sharpness. Based on comparison of pixel value profiles, contrast enhancement outperformed others in image perception. During the tracking experiment, only contrast enhancement resulted in tumor detection in all images using our tracking algorithm. Deblurring failed to determine the target position in two frames out of a total of 75 images. For original and denoised set, target location was not determined for the same five images. Meanwhile, deblurred image showed increased detection accuracy compared with the original set. The denoised image resulted in decreased accuracy. In the case of contrast‐improved set, the tracking accuracy was nearly maintained as that of the original image. Conclusions Considering the effect of each processing on tumor tracking and the visual perception in a limited time, contrast enhancement would be the first consideration to visually verify the tracking accuracy of tumors on MV EPID without sacrificing tumor detectability and detection accuracy.</abstract><cop>United States</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>29984883</pmid><doi>10.1002/acm2.12411</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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subjects Accuracy
Algorithms
contrast enhancement
deblurring
denoising
Humans
Image Enhancement
Image Processing, Computer-Assisted
image quality
Lung cancer
megavoltage electronic portal imaging device
Neoplasms - diagnostic imaging
Noise
Phantoms, Imaging
Radiation Oncology Physics
Radiography
Regularization methods
tumor tracking
Visual perception
title Enhancement of megavoltage electronic portal images for markerless tumor tracking
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