Biomechanical imaging biomarker during chemoradiotherapy predicts treatment response in head and neck squamous cell carcinoma
. For response-adapted adaptive radiotherapy (R-ART), promising biomarkers are needed to predict post-radiotherapy (post-RT) responses using routine clinical information obtained during RT. In this study, a patient-specific biomechanical model (BM) of the head and neck squamous cell carcinoma (HNSCC...
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creator | Fujimoto, Koya Shiinoki, Takehiro Kawazoe, Yusuke Yuasa, Yuki Mukaidani, Wataru Manabe, Yuki Kajima, Miki Tanaka, Hidekazu |
description | . For response-adapted adaptive radiotherapy (R-ART), promising biomarkers are needed to predict post-radiotherapy (post-RT) responses using routine clinical information obtained during RT. In this study, a patient-specific biomechanical model (BM) of the head and neck squamous cell carcinoma (HNSCC) was proposed using the pre-RT maximum standardized uptake value (SUV
) of
F-fluorodeoxyglucose (FDG) and tumor structural changes during RT as evaluated using computed tomography (CT). In addition, we evaluated the predictive performance of BM-driven imaging biomarkers for the treatment response of patients with HNSCC who underwent concurrent chemoradiotherapy (CCRT).
. Patients with histologically confirmed HNSCC treated with definitive CCRT were enrolled in this study. All patients underwent CT two times as follows: before the start of RT (pre-RT) and 3 weeks after the start of RT (mid-RT). Among these patients, 67 patients who underwent positron emission tomography/CT during the pre-RT period were included in the final analysis. The locoregional control (LC), progression-free survival (PFS), and overall survival (OS) prediction performances of whole tumor stress change (TS) between pre- and mid-RT computed using BM were assessed using univariate, multivariate, and Kaplan-Meier survival curve analyses, respectively. Furthermore, performance was compared with the pre and post-RT SUV
, tumor volume reduction rate (TVRR) during RT, and other clinical prognostic factors.
. For both univariate, multivariate, and survival curve analyses, the significant prognostic factors were as follows (
< 0.05): TS and TVRR for LC; TS and pre-RT FDG-SUV
for PFS; and TS only for OS. In addition, for 2 year LC, PFS, and OS prediction, TS showed a comparable predictive performance to post-RT FDG-SUV
.
. BM-driven TS is an effective prognostic factor for tumor treatment response after CCRT. The proposed method can be a feasible functional imaging biomarker that can be acquired during RT using only routine clinical data and may provide useful information for decision-making during R-ART. |
doi_str_mv | 10.1088/1361-6560/ad29b9 |
format | Article |
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) of
F-fluorodeoxyglucose (FDG) and tumor structural changes during RT as evaluated using computed tomography (CT). In addition, we evaluated the predictive performance of BM-driven imaging biomarkers for the treatment response of patients with HNSCC who underwent concurrent chemoradiotherapy (CCRT).
. Patients with histologically confirmed HNSCC treated with definitive CCRT were enrolled in this study. All patients underwent CT two times as follows: before the start of RT (pre-RT) and 3 weeks after the start of RT (mid-RT). Among these patients, 67 patients who underwent positron emission tomography/CT during the pre-RT period were included in the final analysis. The locoregional control (LC), progression-free survival (PFS), and overall survival (OS) prediction performances of whole tumor stress change (TS) between pre- and mid-RT computed using BM were assessed using univariate, multivariate, and Kaplan-Meier survival curve analyses, respectively. Furthermore, performance was compared with the pre and post-RT SUV
, tumor volume reduction rate (TVRR) during RT, and other clinical prognostic factors.
. For both univariate, multivariate, and survival curve analyses, the significant prognostic factors were as follows (
< 0.05): TS and TVRR for LC; TS and pre-RT FDG-SUV
for PFS; and TS only for OS. In addition, for 2 year LC, PFS, and OS prediction, TS showed a comparable predictive performance to post-RT FDG-SUV
.
. BM-driven TS is an effective prognostic factor for tumor treatment response after CCRT. The proposed method can be a feasible functional imaging biomarker that can be acquired during RT using only routine clinical data and may provide useful information for decision-making during R-ART.</description><identifier>ISSN: 0031-9155</identifier><identifier>EISSN: 1361-6560</identifier><identifier>DOI: 10.1088/1361-6560/ad29b9</identifier><identifier>PMID: 38359451</identifier><identifier>CODEN: PHMBA7</identifier><language>eng</language><publisher>England: IOP Publishing</publisher><subject>biomechanical model ; chemoradiotherapy ; head and neck cancer ; imaging biomarker ; response prediction</subject><ispartof>Physics in medicine & biology, 2024-03, Vol.69 (5), p.55033</ispartof><rights>2024 Institute of Physics and Engineering in Medicine</rights><rights>2024 Institute of Physics and Engineering in Medicine.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c321t-6edacb96136792f4b5043e3fb48a16e73cdad4b8045e7c8e4a4810babec4e64b3</cites><orcidid>0000-0002-0246-8489 ; 0000-0002-7498-1409</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://iopscience.iop.org/article/10.1088/1361-6560/ad29b9/pdf$$EPDF$$P50$$Giop$$H</linktopdf><link.rule.ids>314,776,780,27901,27902,53821,53868</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38359451$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fujimoto, Koya</creatorcontrib><creatorcontrib>Shiinoki, Takehiro</creatorcontrib><creatorcontrib>Kawazoe, Yusuke</creatorcontrib><creatorcontrib>Yuasa, Yuki</creatorcontrib><creatorcontrib>Mukaidani, Wataru</creatorcontrib><creatorcontrib>Manabe, Yuki</creatorcontrib><creatorcontrib>Kajima, Miki</creatorcontrib><creatorcontrib>Tanaka, Hidekazu</creatorcontrib><title>Biomechanical imaging biomarker during chemoradiotherapy predicts treatment response in head and neck squamous cell carcinoma</title><title>Physics in medicine & biology</title><addtitle>PMB</addtitle><addtitle>Phys. Med. Biol</addtitle><description>. For response-adapted adaptive radiotherapy (R-ART), promising biomarkers are needed to predict post-radiotherapy (post-RT) responses using routine clinical information obtained during RT. In this study, a patient-specific biomechanical model (BM) of the head and neck squamous cell carcinoma (HNSCC) was proposed using the pre-RT maximum standardized uptake value (SUV
) of
F-fluorodeoxyglucose (FDG) and tumor structural changes during RT as evaluated using computed tomography (CT). In addition, we evaluated the predictive performance of BM-driven imaging biomarkers for the treatment response of patients with HNSCC who underwent concurrent chemoradiotherapy (CCRT).
. Patients with histologically confirmed HNSCC treated with definitive CCRT were enrolled in this study. All patients underwent CT two times as follows: before the start of RT (pre-RT) and 3 weeks after the start of RT (mid-RT). Among these patients, 67 patients who underwent positron emission tomography/CT during the pre-RT period were included in the final analysis. The locoregional control (LC), progression-free survival (PFS), and overall survival (OS) prediction performances of whole tumor stress change (TS) between pre- and mid-RT computed using BM were assessed using univariate, multivariate, and Kaplan-Meier survival curve analyses, respectively. Furthermore, performance was compared with the pre and post-RT SUV
, tumor volume reduction rate (TVRR) during RT, and other clinical prognostic factors.
. For both univariate, multivariate, and survival curve analyses, the significant prognostic factors were as follows (
< 0.05): TS and TVRR for LC; TS and pre-RT FDG-SUV
for PFS; and TS only for OS. In addition, for 2 year LC, PFS, and OS prediction, TS showed a comparable predictive performance to post-RT FDG-SUV
.
. BM-driven TS is an effective prognostic factor for tumor treatment response after CCRT. The proposed method can be a feasible functional imaging biomarker that can be acquired during RT using only routine clinical data and may provide useful information for decision-making during R-ART.</description><subject>biomechanical model</subject><subject>chemoradiotherapy</subject><subject>head and neck cancer</subject><subject>imaging biomarker</subject><subject>response prediction</subject><issn>0031-9155</issn><issn>1361-6560</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp1kLtP3TAUh62KqtzS7kzIGx2aYsePm4yA-pKQurSzdWyfcA03drCTgaH_O44uZaLTkX76zusj5JSzL5x13QUXmjdaaXYBvu1t_4ZsXqIjsmFM8KbnSh2T96XcMcZ518p35Fh0QvVS8Q35exXSiG4HMTjY0zDCbYi31NYU8j1m6pe8Bm6HY8rgQ5p3mGF6pFNGH9xc6JwR5hHjTDOWKcWCNES6Q_AUoqcR3T0tDwuMaSnU4X5PHWQXYt3wgbwdYF_w43M9IX--ff19_aO5-fX95_XlTeNEy-dGowdne11_2_btIK1iUqAYrOyAa9wK58FL2zGpcOs6lCA7zixYdBK1tOKEfDrMnXJ6WLDMZgxlPQUi1qtM27dVjNKtqig7oC6nUjIOZsrVSn40nJlVulkNm9WwOUivLWfP0xc7on9p-Ge5AucHIKTJ3KUlx_qsmUZrdG-UYUoxIczkh0p-foX87-Yn6d2bzw</recordid><startdate>20240307</startdate><enddate>20240307</enddate><creator>Fujimoto, Koya</creator><creator>Shiinoki, Takehiro</creator><creator>Kawazoe, Yusuke</creator><creator>Yuasa, Yuki</creator><creator>Mukaidani, Wataru</creator><creator>Manabe, Yuki</creator><creator>Kajima, Miki</creator><creator>Tanaka, Hidekazu</creator><general>IOP Publishing</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0246-8489</orcidid><orcidid>https://orcid.org/0000-0002-7498-1409</orcidid></search><sort><creationdate>20240307</creationdate><title>Biomechanical imaging biomarker during chemoradiotherapy predicts treatment response in head and neck squamous cell carcinoma</title><author>Fujimoto, Koya ; Shiinoki, Takehiro ; Kawazoe, Yusuke ; Yuasa, Yuki ; Mukaidani, Wataru ; Manabe, Yuki ; Kajima, Miki ; Tanaka, Hidekazu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c321t-6edacb96136792f4b5043e3fb48a16e73cdad4b8045e7c8e4a4810babec4e64b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>biomechanical model</topic><topic>chemoradiotherapy</topic><topic>head and neck cancer</topic><topic>imaging biomarker</topic><topic>response prediction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fujimoto, Koya</creatorcontrib><creatorcontrib>Shiinoki, Takehiro</creatorcontrib><creatorcontrib>Kawazoe, Yusuke</creatorcontrib><creatorcontrib>Yuasa, Yuki</creatorcontrib><creatorcontrib>Mukaidani, Wataru</creatorcontrib><creatorcontrib>Manabe, Yuki</creatorcontrib><creatorcontrib>Kajima, Miki</creatorcontrib><creatorcontrib>Tanaka, Hidekazu</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Physics in medicine & biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fujimoto, Koya</au><au>Shiinoki, Takehiro</au><au>Kawazoe, Yusuke</au><au>Yuasa, Yuki</au><au>Mukaidani, Wataru</au><au>Manabe, Yuki</au><au>Kajima, Miki</au><au>Tanaka, Hidekazu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biomechanical imaging biomarker during chemoradiotherapy predicts treatment response in head and neck squamous cell carcinoma</atitle><jtitle>Physics in medicine & biology</jtitle><stitle>PMB</stitle><addtitle>Phys. Med. Biol</addtitle><date>2024-03-07</date><risdate>2024</risdate><volume>69</volume><issue>5</issue><spage>55033</spage><pages>55033-</pages><issn>0031-9155</issn><eissn>1361-6560</eissn><coden>PHMBA7</coden><abstract>. For response-adapted adaptive radiotherapy (R-ART), promising biomarkers are needed to predict post-radiotherapy (post-RT) responses using routine clinical information obtained during RT. In this study, a patient-specific biomechanical model (BM) of the head and neck squamous cell carcinoma (HNSCC) was proposed using the pre-RT maximum standardized uptake value (SUV
) of
F-fluorodeoxyglucose (FDG) and tumor structural changes during RT as evaluated using computed tomography (CT). In addition, we evaluated the predictive performance of BM-driven imaging biomarkers for the treatment response of patients with HNSCC who underwent concurrent chemoradiotherapy (CCRT).
. Patients with histologically confirmed HNSCC treated with definitive CCRT were enrolled in this study. All patients underwent CT two times as follows: before the start of RT (pre-RT) and 3 weeks after the start of RT (mid-RT). Among these patients, 67 patients who underwent positron emission tomography/CT during the pre-RT period were included in the final analysis. The locoregional control (LC), progression-free survival (PFS), and overall survival (OS) prediction performances of whole tumor stress change (TS) between pre- and mid-RT computed using BM were assessed using univariate, multivariate, and Kaplan-Meier survival curve analyses, respectively. Furthermore, performance was compared with the pre and post-RT SUV
, tumor volume reduction rate (TVRR) during RT, and other clinical prognostic factors.
. For both univariate, multivariate, and survival curve analyses, the significant prognostic factors were as follows (
< 0.05): TS and TVRR for LC; TS and pre-RT FDG-SUV
for PFS; and TS only for OS. In addition, for 2 year LC, PFS, and OS prediction, TS showed a comparable predictive performance to post-RT FDG-SUV
.
. BM-driven TS is an effective prognostic factor for tumor treatment response after CCRT. The proposed method can be a feasible functional imaging biomarker that can be acquired during RT using only routine clinical data and may provide useful information for decision-making during R-ART.</abstract><cop>England</cop><pub>IOP Publishing</pub><pmid>38359451</pmid><doi>10.1088/1361-6560/ad29b9</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-0246-8489</orcidid><orcidid>https://orcid.org/0000-0002-7498-1409</orcidid></addata></record> |
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subjects | biomechanical model chemoradiotherapy head and neck cancer imaging biomarker response prediction |
title | Biomechanical imaging biomarker during chemoradiotherapy predicts treatment response in head and neck squamous cell carcinoma |
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