Metabolic Tumor Volume and Total Lesion Glycolysis in Oropharyngeal Cancer Treated With Definitive Radiotherapy: Which Threshold Is the Best Predictor of Local Control?
PURPOSEIn the context of oropharyngeal cancer treated with definitive radiotherapy, the aim of this retrospective study was to identify the best threshold value to compute metabolic tumor volume (MTV) and/or total lesion glycolysis to predict local-regional control (LRC) and disease-free survival. M...
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Veröffentlicht in: | Clinical nuclear medicine 2017-06, Vol.42 (6), p.e281-e285 |
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creator | Castelli, Joël Depeursinge, Adrien de Bari, Berardino Devillers, Anne de Crevoisier, Renaud Bourhis, Jean Prior, John O |
description | PURPOSEIn the context of oropharyngeal cancer treated with definitive radiotherapy, the aim of this retrospective study was to identify the best threshold value to compute metabolic tumor volume (MTV) and/or total lesion glycolysis to predict local-regional control (LRC) and disease-free survival.
METHODSOne hundred twenty patients with a locally advanced oropharyngeal cancer from 2 different institutions treated with definitive radiotherapy underwent FDG PET/CT before treatment. Various MTVs and total lesion glycolysis were defined based on 2 segmentation methods(i) an absolute threshold of SUV (0–20 g/mL) or (ii) a relative threshold for SUVmax (0%–100%). The parameters’ predictive capabilities for disease-free survival and LRC were assessed using the Harrell C-index and Cox regression model.
RESULTSRelative thresholds between 40% and 68% and absolute threshold between 5.5 and 7 had a similar predictive value for LRC (C-index = 0.65 and 0.64, respectively). Metabolic tumor volume had a higher predictive value than gross tumor volume (C-index = 0.61) and SUVmax (C-index = 0.54). Metabolic tumor volume computed with a relative threshold of 51% of SUVmax was the best predictor of disease-free survival (hazard ratio, 1.23 [per 10 mL], P = 0.009) and LRC (hazard ratio1.22 [per 10 mL], P = 0.02).
CONCLUSIONSThe use of different thresholds within a reasonable range (between 5.5 and 7 for an absolute threshold and between 40% and 68% for a relative threshold) seems to have no major impact on the predictive value of MTV. This parameter may be used to identify patient with a high risk of recurrence and who may benefit from treatment intensification. |
doi_str_mv | 10.1097/RLU.0000000000001614 |
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METHODSOne hundred twenty patients with a locally advanced oropharyngeal cancer from 2 different institutions treated with definitive radiotherapy underwent FDG PET/CT before treatment. Various MTVs and total lesion glycolysis were defined based on 2 segmentation methods(i) an absolute threshold of SUV (0–20 g/mL) or (ii) a relative threshold for SUVmax (0%–100%). The parameters’ predictive capabilities for disease-free survival and LRC were assessed using the Harrell C-index and Cox regression model.
RESULTSRelative thresholds between 40% and 68% and absolute threshold between 5.5 and 7 had a similar predictive value for LRC (C-index = 0.65 and 0.64, respectively). Metabolic tumor volume had a higher predictive value than gross tumor volume (C-index = 0.61) and SUVmax (C-index = 0.54). Metabolic tumor volume computed with a relative threshold of 51% of SUVmax was the best predictor of disease-free survival (hazard ratio, 1.23 [per 10 mL], P = 0.009) and LRC (hazard ratio1.22 [per 10 mL], P = 0.02).
CONCLUSIONSThe use of different thresholds within a reasonable range (between 5.5 and 7 for an absolute threshold and between 40% and 68% for a relative threshold) seems to have no major impact on the predictive value of MTV. This parameter may be used to identify patient with a high risk of recurrence and who may benefit from treatment intensification.</description><identifier>ISSN: 0363-9762</identifier><identifier>EISSN: 1536-0229</identifier><identifier>DOI: 10.1097/RLU.0000000000001614</identifier><identifier>PMID: 28288042</identifier><language>eng</language><publisher>United States: Copyright Wolters Kluwer Health, Inc. All rights reserved</publisher><subject>Adult ; Aged ; Bioengineering ; Disease-Free Survival ; Female ; Fluorodeoxyglucose F18 - metabolism ; Glycolysis ; Humans ; Life Sciences ; Male ; Middle Aged ; Oropharyngeal Neoplasms - diagnostic imaging ; Oropharyngeal Neoplasms - metabolism ; Oropharyngeal Neoplasms - pathology ; Oropharyngeal Neoplasms - radiotherapy ; Positron Emission Tomography Computed Tomography ; Positron-Emission Tomography ; Proportional Hazards Models ; Retrospective Studies ; Tumor Burden</subject><ispartof>Clinical nuclear medicine, 2017-06, Vol.42 (6), p.e281-e285</ispartof><rights>Copyright © 2017 Wolters Kluwer Health, Inc. All rights reserved.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3394-dd7674512343d1427cb825d167c279a7d88850a56f5f0cb39c11380633acd7253</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28288042$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://univ-rennes.hal.science/hal-01534147$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Castelli, Joël</creatorcontrib><creatorcontrib>Depeursinge, Adrien</creatorcontrib><creatorcontrib>de Bari, Berardino</creatorcontrib><creatorcontrib>Devillers, Anne</creatorcontrib><creatorcontrib>de Crevoisier, Renaud</creatorcontrib><creatorcontrib>Bourhis, Jean</creatorcontrib><creatorcontrib>Prior, John O</creatorcontrib><title>Metabolic Tumor Volume and Total Lesion Glycolysis in Oropharyngeal Cancer Treated With Definitive Radiotherapy: Which Threshold Is the Best Predictor of Local Control?</title><title>Clinical nuclear medicine</title><addtitle>Clin Nucl Med</addtitle><description>PURPOSEIn the context of oropharyngeal cancer treated with definitive radiotherapy, the aim of this retrospective study was to identify the best threshold value to compute metabolic tumor volume (MTV) and/or total lesion glycolysis to predict local-regional control (LRC) and disease-free survival.
METHODSOne hundred twenty patients with a locally advanced oropharyngeal cancer from 2 different institutions treated with definitive radiotherapy underwent FDG PET/CT before treatment. Various MTVs and total lesion glycolysis were defined based on 2 segmentation methods(i) an absolute threshold of SUV (0–20 g/mL) or (ii) a relative threshold for SUVmax (0%–100%). The parameters’ predictive capabilities for disease-free survival and LRC were assessed using the Harrell C-index and Cox regression model.
RESULTSRelative thresholds between 40% and 68% and absolute threshold between 5.5 and 7 had a similar predictive value for LRC (C-index = 0.65 and 0.64, respectively). Metabolic tumor volume had a higher predictive value than gross tumor volume (C-index = 0.61) and SUVmax (C-index = 0.54). Metabolic tumor volume computed with a relative threshold of 51% of SUVmax was the best predictor of disease-free survival (hazard ratio, 1.23 [per 10 mL], P = 0.009) and LRC (hazard ratio1.22 [per 10 mL], P = 0.02).
CONCLUSIONSThe use of different thresholds within a reasonable range (between 5.5 and 7 for an absolute threshold and between 40% and 68% for a relative threshold) seems to have no major impact on the predictive value of MTV. This parameter may be used to identify patient with a high risk of recurrence and who may benefit from treatment intensification.</description><subject>Adult</subject><subject>Aged</subject><subject>Bioengineering</subject><subject>Disease-Free Survival</subject><subject>Female</subject><subject>Fluorodeoxyglucose F18 - metabolism</subject><subject>Glycolysis</subject><subject>Humans</subject><subject>Life Sciences</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Oropharyngeal Neoplasms - diagnostic imaging</subject><subject>Oropharyngeal Neoplasms - metabolism</subject><subject>Oropharyngeal Neoplasms - pathology</subject><subject>Oropharyngeal Neoplasms - radiotherapy</subject><subject>Positron Emission Tomography Computed Tomography</subject><subject>Positron-Emission Tomography</subject><subject>Proportional Hazards Models</subject><subject>Retrospective Studies</subject><subject>Tumor Burden</subject><issn>0363-9762</issn><issn>1536-0229</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kd9uFCEUhydGY7fVNzCGS72Yyp8ZYLwxda1tkzE1zdReEhYYQdlhBabNvpGPKevWxnghNyTwnd_h8FXVCwSPEezYm6v--hj-tRBFzaNqgVpCa4hx97haQEJJ3TGKD6rDlL79ZmjztDrAHHMOG7yofn4yWa6CdwoM8zpE8CX4eW2AnDQYQpYe9Ca5MIEzv1XBb5NLwE3gMoaNlXE7fTUFWcpJmQiGaGQ2Gty4bMEHM7rJZXdrwJXULmRrotxs34Ib65QFg40m2eA1uEig3IH3JmXwORrtVC7PCCPog9plhynH4N89q56M0ifz_H4_qq4_ng7L87q_PLtYnvS1IqRraq0ZZU2LMGmIRg1masVxqxFlCrNOMs05b6Fs6diOUK1IpxAiHFJCpNIMt-Soer3PtdKLTXTrMqUI0onzk17szmD54QY17BYV9tWe3cTwYy4DiLVLyngvJxPmJBBnrMWUMl7QZo-qGFKKZnzIRlDsfIriU_zrs5S9vO8wr9ZGPxT9EVgAvgfugs8mpu9-vjNR2KIl2_9n_wJREqxt</recordid><startdate>20170601</startdate><enddate>20170601</enddate><creator>Castelli, Joël</creator><creator>Depeursinge, Adrien</creator><creator>de Bari, Berardino</creator><creator>Devillers, Anne</creator><creator>de Crevoisier, Renaud</creator><creator>Bourhis, Jean</creator><creator>Prior, John O</creator><general>Copyright Wolters Kluwer Health, Inc. All rights reserved</general><general>Lippincott, Williams & Wilkins</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>1XC</scope></search><sort><creationdate>20170601</creationdate><title>Metabolic Tumor Volume and Total Lesion Glycolysis in Oropharyngeal Cancer Treated With Definitive Radiotherapy: Which Threshold Is the Best Predictor of Local Control?</title><author>Castelli, Joël ; Depeursinge, Adrien ; de Bari, Berardino ; Devillers, Anne ; de Crevoisier, Renaud ; Bourhis, Jean ; Prior, John O</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3394-dd7674512343d1427cb825d167c279a7d88850a56f5f0cb39c11380633acd7253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Bioengineering</topic><topic>Disease-Free Survival</topic><topic>Female</topic><topic>Fluorodeoxyglucose F18 - metabolism</topic><topic>Glycolysis</topic><topic>Humans</topic><topic>Life Sciences</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Oropharyngeal Neoplasms - diagnostic imaging</topic><topic>Oropharyngeal Neoplasms - metabolism</topic><topic>Oropharyngeal Neoplasms - pathology</topic><topic>Oropharyngeal Neoplasms - radiotherapy</topic><topic>Positron Emission Tomography Computed Tomography</topic><topic>Positron-Emission Tomography</topic><topic>Proportional Hazards Models</topic><topic>Retrospective Studies</topic><topic>Tumor Burden</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Castelli, Joël</creatorcontrib><creatorcontrib>Depeursinge, Adrien</creatorcontrib><creatorcontrib>de Bari, Berardino</creatorcontrib><creatorcontrib>Devillers, Anne</creatorcontrib><creatorcontrib>de Crevoisier, Renaud</creatorcontrib><creatorcontrib>Bourhis, Jean</creatorcontrib><creatorcontrib>Prior, John O</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Clinical nuclear medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Castelli, Joël</au><au>Depeursinge, Adrien</au><au>de Bari, Berardino</au><au>Devillers, Anne</au><au>de Crevoisier, Renaud</au><au>Bourhis, Jean</au><au>Prior, John O</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metabolic Tumor Volume and Total Lesion Glycolysis in Oropharyngeal Cancer Treated With Definitive Radiotherapy: Which Threshold Is the Best Predictor of Local Control?</atitle><jtitle>Clinical nuclear medicine</jtitle><addtitle>Clin Nucl Med</addtitle><date>2017-06-01</date><risdate>2017</risdate><volume>42</volume><issue>6</issue><spage>e281</spage><epage>e285</epage><pages>e281-e285</pages><issn>0363-9762</issn><eissn>1536-0229</eissn><abstract>PURPOSEIn the context of oropharyngeal cancer treated with definitive radiotherapy, the aim of this retrospective study was to identify the best threshold value to compute metabolic tumor volume (MTV) and/or total lesion glycolysis to predict local-regional control (LRC) and disease-free survival.
METHODSOne hundred twenty patients with a locally advanced oropharyngeal cancer from 2 different institutions treated with definitive radiotherapy underwent FDG PET/CT before treatment. Various MTVs and total lesion glycolysis were defined based on 2 segmentation methods(i) an absolute threshold of SUV (0–20 g/mL) or (ii) a relative threshold for SUVmax (0%–100%). The parameters’ predictive capabilities for disease-free survival and LRC were assessed using the Harrell C-index and Cox regression model.
RESULTSRelative thresholds between 40% and 68% and absolute threshold between 5.5 and 7 had a similar predictive value for LRC (C-index = 0.65 and 0.64, respectively). Metabolic tumor volume had a higher predictive value than gross tumor volume (C-index = 0.61) and SUVmax (C-index = 0.54). Metabolic tumor volume computed with a relative threshold of 51% of SUVmax was the best predictor of disease-free survival (hazard ratio, 1.23 [per 10 mL], P = 0.009) and LRC (hazard ratio1.22 [per 10 mL], P = 0.02).
CONCLUSIONSThe use of different thresholds within a reasonable range (between 5.5 and 7 for an absolute threshold and between 40% and 68% for a relative threshold) seems to have no major impact on the predictive value of MTV. This parameter may be used to identify patient with a high risk of recurrence and who may benefit from treatment intensification.</abstract><cop>United States</cop><pub>Copyright Wolters Kluwer Health, Inc. All rights reserved</pub><pmid>28288042</pmid><doi>10.1097/RLU.0000000000001614</doi><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Bioengineering Disease-Free Survival Female Fluorodeoxyglucose F18 - metabolism Glycolysis Humans Life Sciences Male Middle Aged Oropharyngeal Neoplasms - diagnostic imaging Oropharyngeal Neoplasms - metabolism Oropharyngeal Neoplasms - pathology Oropharyngeal Neoplasms - radiotherapy Positron Emission Tomography Computed Tomography Positron-Emission Tomography Proportional Hazards Models Retrospective Studies Tumor Burden |
title | Metabolic Tumor Volume and Total Lesion Glycolysis in Oropharyngeal Cancer Treated With Definitive Radiotherapy: Which Threshold Is the Best Predictor of Local Control? |
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