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Impact of respiratory motion on 18F‐FDG PET radiomics stability: Clinical evaluation with a digital PET scanner
Purpose 18F‐FDG PET quantitative features are susceptible to respiratory motion. However, studies using clinical patient data to explore the impact of respiratory motion on 18F‐FDG PET radiomic features are limited. In this study, we investigated the impact of respiratory motion on radiomics stabili...
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Published in: | Journal of applied clinical medical physics 2023-12, Vol.24 (12), p.n/a |
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creator | Chen, Yu‐Hung Kan, Kuo‐Yi Liu, Shu‐Hsin Lin, Hsin‐Hon Lue, Kun‐Han |
description | Purpose
18F‐FDG PET quantitative features are susceptible to respiratory motion. However, studies using clinical patient data to explore the impact of respiratory motion on 18F‐FDG PET radiomic features are limited. In this study, we investigated the impact of respiratory motion on radiomics stability with clinical 18F‐FDG PET images using a data‐driven gating (DDG) algorithm on the digital PET scanner.
Materials and Methods
A total of 101 patients who underwent oncological 18F‐FDG PET scans were retrospectively included. A DDG algorithm combined with a motion compensation technique was used to extract the PET images with respiratory motion correction. 18F‐FDG‐avid lesions from the thorax to the upper abdomen were analyzed on the non‐DDG and DDG PET images. The lesions were segmented with a 40% threshold of the maximum standardized uptake. A total of 725 radiomic features were computed from the segmented lesions, including first‐order, shape, texture, and wavelet features. The intraclass correlation coefficient (ICC) and coefficient of variation (COV) were calculated to evaluate feature stability. An ICC above 0.9 and a COV below 5% were considered high stability.
Results
In total, 168 lesions with and without respiratory motion correction were analyzed. Our results indicated that most 18F‐FDG PET radiomic features are sensitive to respiratory motion. Overall, only 27 out of 725 (3.72%) radiomic features were identified as highly stable, including one from the first‐order features (entropy), one from the shape features (sphericity), four from the gray‐level co‐occurrence matrix features (normalized and unnormalized inverse difference moment, joint entropy, and sum entropy), one from the gray‐level run‐length matrix features (run entropy), and 20 from the wavelet filter‐based features.
Conclusion
Respiratory motion has a significant impact on 18F‐FDG PET radiomics stability. The highly stable features identified in our study may serve as potential candidates for further applications, such as machine learning modeling. |
doi_str_mv | 10.1002/acm2.14200 |
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fullrecord | <record><control><sourceid>proquest_wiley</sourceid><recordid>TN_cdi_proquest_journals_2895766174</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2895766174</sourcerecordid><originalsourceid>FETCH-LOGICAL-g2580-6161ffcc377a2f960004904c2692b855f10e5462ba34d651c36b1fef22768e7a3</originalsourceid><addsrcrecordid>eNpNkE1OwzAQhS0EEqWw4QSWWKd4nMRJ2FWhLZWKYFHWluPaxVX-artU2XGEnpGTkLYskEaaJ81786QPoXsgIyCEPgpZ0RFElJALNICYsiDLILr8p6_RjXMbQgDSMB2g7bxqhfS40dgq1xorfGM7XDXeNDXuB9Lpz_dh-jzD75MltmJlmspIh50XhSmN755wXpraSFFi9SXKnTgl98Z_YoFXZm18fzlmnRR1rewtutKidOrubw_Rx3SyzF-Cxdtsno8XwZrGKQkYMNBayjBJBNUZI4REGYkkZRkt0jjWQFQcMVqIMFqxGGTICtBKU5qwVCUiHKKH89_WNtudcp5vmp2t-0pO0yxOGIMk6l1wdu1NqTreWlMJ23Eg_MiTH3nyE08-zl_pSYW_HPFqAA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2895766174</pqid></control><display><type>article</type><title>Impact of respiratory motion on 18F‐FDG PET radiomics stability: Clinical evaluation with a digital PET scanner</title><source>Publicly Available Content Database</source><source>Wiley Open Access</source><source>PubMed Central</source><creator>Chen, Yu‐Hung ; Kan, Kuo‐Yi ; Liu, Shu‐Hsin ; Lin, Hsin‐Hon ; Lue, Kun‐Han</creator><creatorcontrib>Chen, Yu‐Hung ; Kan, Kuo‐Yi ; Liu, Shu‐Hsin ; Lin, Hsin‐Hon ; Lue, Kun‐Han</creatorcontrib><description>Purpose
18F‐FDG PET quantitative features are susceptible to respiratory motion. However, studies using clinical patient data to explore the impact of respiratory motion on 18F‐FDG PET radiomic features are limited. In this study, we investigated the impact of respiratory motion on radiomics stability with clinical 18F‐FDG PET images using a data‐driven gating (DDG) algorithm on the digital PET scanner.
Materials and Methods
A total of 101 patients who underwent oncological 18F‐FDG PET scans were retrospectively included. A DDG algorithm combined with a motion compensation technique was used to extract the PET images with respiratory motion correction. 18F‐FDG‐avid lesions from the thorax to the upper abdomen were analyzed on the non‐DDG and DDG PET images. The lesions were segmented with a 40% threshold of the maximum standardized uptake. A total of 725 radiomic features were computed from the segmented lesions, including first‐order, shape, texture, and wavelet features. The intraclass correlation coefficient (ICC) and coefficient of variation (COV) were calculated to evaluate feature stability. An ICC above 0.9 and a COV below 5% were considered high stability.
Results
In total, 168 lesions with and without respiratory motion correction were analyzed. Our results indicated that most 18F‐FDG PET radiomic features are sensitive to respiratory motion. Overall, only 27 out of 725 (3.72%) radiomic features were identified as highly stable, including one from the first‐order features (entropy), one from the shape features (sphericity), four from the gray‐level co‐occurrence matrix features (normalized and unnormalized inverse difference moment, joint entropy, and sum entropy), one from the gray‐level run‐length matrix features (run entropy), and 20 from the wavelet filter‐based features.
Conclusion
Respiratory motion has a significant impact on 18F‐FDG PET radiomics stability. The highly stable features identified in our study may serve as potential candidates for further applications, such as machine learning modeling.</description><identifier>ISSN: 1526-9914</identifier><identifier>EISSN: 1526-9914</identifier><identifier>DOI: 10.1002/acm2.14200</identifier><language>eng</language><publisher>Malden Massachusetts: John Wiley & Sons, Inc</publisher><subject>18F‐FDG ; Abdomen ; Algorithms ; digital PET ; Lung cancer ; Metabolism ; Nuclear medicine ; Open source software ; Patients ; Radiomics ; Reproducibility ; respiratory motion ; Scanners ; stability ; Thorax</subject><ispartof>Journal of applied clinical medical physics, 2023-12, Vol.24 (12), p.n/a</ispartof><rights>2023 The Authors. published by Wiley Periodicals LLC on behalf of American Association of Physicists in Medicine.</rights><rights>2023. 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></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2895766174/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2895766174?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,11562,25753,27924,27925,37012,44590,46052,46476,75126</link.rule.ids></links><search><creatorcontrib>Chen, Yu‐Hung</creatorcontrib><creatorcontrib>Kan, Kuo‐Yi</creatorcontrib><creatorcontrib>Liu, Shu‐Hsin</creatorcontrib><creatorcontrib>Lin, Hsin‐Hon</creatorcontrib><creatorcontrib>Lue, Kun‐Han</creatorcontrib><title>Impact of respiratory motion on 18F‐FDG PET radiomics stability: Clinical evaluation with a digital PET scanner</title><title>Journal of applied clinical medical physics</title><description>Purpose
18F‐FDG PET quantitative features are susceptible to respiratory motion. However, studies using clinical patient data to explore the impact of respiratory motion on 18F‐FDG PET radiomic features are limited. In this study, we investigated the impact of respiratory motion on radiomics stability with clinical 18F‐FDG PET images using a data‐driven gating (DDG) algorithm on the digital PET scanner.
Materials and Methods
A total of 101 patients who underwent oncological 18F‐FDG PET scans were retrospectively included. A DDG algorithm combined with a motion compensation technique was used to extract the PET images with respiratory motion correction. 18F‐FDG‐avid lesions from the thorax to the upper abdomen were analyzed on the non‐DDG and DDG PET images. The lesions were segmented with a 40% threshold of the maximum standardized uptake. A total of 725 radiomic features were computed from the segmented lesions, including first‐order, shape, texture, and wavelet features. The intraclass correlation coefficient (ICC) and coefficient of variation (COV) were calculated to evaluate feature stability. An ICC above 0.9 and a COV below 5% were considered high stability.
Results
In total, 168 lesions with and without respiratory motion correction were analyzed. Our results indicated that most 18F‐FDG PET radiomic features are sensitive to respiratory motion. Overall, only 27 out of 725 (3.72%) radiomic features were identified as highly stable, including one from the first‐order features (entropy), one from the shape features (sphericity), four from the gray‐level co‐occurrence matrix features (normalized and unnormalized inverse difference moment, joint entropy, and sum entropy), one from the gray‐level run‐length matrix features (run entropy), and 20 from the wavelet filter‐based features.
Conclusion
Respiratory motion has a significant impact on 18F‐FDG PET radiomics stability. The highly stable features identified in our study may serve as potential candidates for further applications, such as machine learning modeling.</description><subject>18F‐FDG</subject><subject>Abdomen</subject><subject>Algorithms</subject><subject>digital PET</subject><subject>Lung cancer</subject><subject>Metabolism</subject><subject>Nuclear medicine</subject><subject>Open source software</subject><subject>Patients</subject><subject>Radiomics</subject><subject>Reproducibility</subject><subject>respiratory motion</subject><subject>Scanners</subject><subject>stability</subject><subject>Thorax</subject><issn>1526-9914</issn><issn>1526-9914</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>PIMPY</sourceid><recordid>eNpNkE1OwzAQhS0EEqWw4QSWWKd4nMRJ2FWhLZWKYFHWluPaxVX-artU2XGEnpGTkLYskEaaJ81786QPoXsgIyCEPgpZ0RFElJALNICYsiDLILr8p6_RjXMbQgDSMB2g7bxqhfS40dgq1xorfGM7XDXeNDXuB9Lpz_dh-jzD75MltmJlmspIh50XhSmN755wXpraSFFi9SXKnTgl98Z_YoFXZm18fzlmnRR1rewtutKidOrubw_Rx3SyzF-Cxdtsno8XwZrGKQkYMNBayjBJBNUZI4REGYkkZRkt0jjWQFQcMVqIMFqxGGTICtBKU5qwVCUiHKKH89_WNtudcp5vmp2t-0pO0yxOGIMk6l1wdu1NqTreWlMJ23Eg_MiTH3nyE08-zl_pSYW_HPFqAA</recordid><startdate>202312</startdate><enddate>202312</enddate><creator>Chen, Yu‐Hung</creator><creator>Kan, Kuo‐Yi</creator><creator>Liu, Shu‐Hsin</creator><creator>Lin, Hsin‐Hon</creator><creator>Lue, Kun‐Han</creator><general>John Wiley & Sons, Inc</general><scope>24P</scope><scope>WIN</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88I</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0S</scope><scope>M2P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope></search><sort><creationdate>202312</creationdate><title>Impact of respiratory motion on 18F‐FDG PET radiomics stability: Clinical evaluation with a digital PET scanner</title><author>Chen, Yu‐Hung ; Kan, Kuo‐Yi ; Liu, Shu‐Hsin ; Lin, Hsin‐Hon ; Lue, Kun‐Han</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g2580-6161ffcc377a2f960004904c2692b855f10e5462ba34d651c36b1fef22768e7a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>18F‐FDG</topic><topic>Abdomen</topic><topic>Algorithms</topic><topic>digital PET</topic><topic>Lung cancer</topic><topic>Metabolism</topic><topic>Nuclear medicine</topic><topic>Open source software</topic><topic>Patients</topic><topic>Radiomics</topic><topic>Reproducibility</topic><topic>respiratory motion</topic><topic>Scanners</topic><topic>stability</topic><topic>Thorax</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Yu‐Hung</creatorcontrib><creatorcontrib>Kan, Kuo‐Yi</creatorcontrib><creatorcontrib>Liu, Shu‐Hsin</creatorcontrib><creatorcontrib>Lin, Hsin‐Hon</creatorcontrib><creatorcontrib>Lue, Kun‐Han</creatorcontrib><collection>Wiley Open Access</collection><collection>Wiley Free Archive</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Science Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><jtitle>Journal of applied clinical medical physics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Yu‐Hung</au><au>Kan, Kuo‐Yi</au><au>Liu, Shu‐Hsin</au><au>Lin, Hsin‐Hon</au><au>Lue, Kun‐Han</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of respiratory motion on 18F‐FDG PET radiomics stability: Clinical evaluation with a digital PET scanner</atitle><jtitle>Journal of applied clinical medical physics</jtitle><date>2023-12</date><risdate>2023</risdate><volume>24</volume><issue>12</issue><epage>n/a</epage><issn>1526-9914</issn><eissn>1526-9914</eissn><abstract>Purpose
18F‐FDG PET quantitative features are susceptible to respiratory motion. However, studies using clinical patient data to explore the impact of respiratory motion on 18F‐FDG PET radiomic features are limited. In this study, we investigated the impact of respiratory motion on radiomics stability with clinical 18F‐FDG PET images using a data‐driven gating (DDG) algorithm on the digital PET scanner.
Materials and Methods
A total of 101 patients who underwent oncological 18F‐FDG PET scans were retrospectively included. A DDG algorithm combined with a motion compensation technique was used to extract the PET images with respiratory motion correction. 18F‐FDG‐avid lesions from the thorax to the upper abdomen were analyzed on the non‐DDG and DDG PET images. The lesions were segmented with a 40% threshold of the maximum standardized uptake. A total of 725 radiomic features were computed from the segmented lesions, including first‐order, shape, texture, and wavelet features. The intraclass correlation coefficient (ICC) and coefficient of variation (COV) were calculated to evaluate feature stability. An ICC above 0.9 and a COV below 5% were considered high stability.
Results
In total, 168 lesions with and without respiratory motion correction were analyzed. Our results indicated that most 18F‐FDG PET radiomic features are sensitive to respiratory motion. Overall, only 27 out of 725 (3.72%) radiomic features were identified as highly stable, including one from the first‐order features (entropy), one from the shape features (sphericity), four from the gray‐level co‐occurrence matrix features (normalized and unnormalized inverse difference moment, joint entropy, and sum entropy), one from the gray‐level run‐length matrix features (run entropy), and 20 from the wavelet filter‐based features.
Conclusion
Respiratory motion has a significant impact on 18F‐FDG PET radiomics stability. The highly stable features identified in our study may serve as potential candidates for further applications, such as machine learning modeling.</abstract><cop>Malden Massachusetts</cop><pub>John Wiley & Sons, Inc</pub><doi>10.1002/acm2.14200</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 18F‐FDG Abdomen Algorithms digital PET Lung cancer Metabolism Nuclear medicine Open source software Patients Radiomics Reproducibility respiratory motion Scanners stability Thorax |
title | Impact of respiratory motion on 18F‐FDG PET radiomics stability: Clinical evaluation with a digital PET scanner |
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