A Statistical Modeling Approach to the Analysis of Spatial Patterns of FDG-PET Uptake in Human Sarcoma
Clinical experience with positron emission tomography (PET) scanning of sarcoma, using fluorodeoxyglucose (FDG), has established spatial heterogeneity in the standardized uptake values within the tumor mass as a key prognostic indicator of patient survival. But it may be that a more detailed quantit...
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description | Clinical experience with positron emission tomography (PET) scanning of sarcoma, using fluorodeoxyglucose (FDG), has established spatial heterogeneity in the standardized uptake values within the tumor mass as a key prognostic indicator of patient survival. But it may be that a more detailed quantitation of the tumor FDG uptake pattern could provide additional insights into risk. The present work develops a statistical model for this purpose. The approach is based on a tubular representation of the tumor mass with a simplified radial analysis of uptake, transverse to the tubular axis. The technique provides novel ways of characterizing the overall profile of the tumor, including the introduction of an approach for the measurement of its phase of development. The phase measure can distinguish between early phase tumors, in which the uptake is highest at the core, and later stage masses, in which there can often be central voids in FDG uptake. Biologically, these voids arise from necrosis and fluid, fat or cartilage accumulations. The tumor profiling technique is implemented using open-source software tools and illustrations are provided with clinically representative scans. A series of FDG-PET studies from 185 patients is used to formally evaluate the prognostic benefit. Significant ({ p} < 0.05) improvements in the prediction of patient survival and progression are obtained from the tumor profiling analysis. After adjustment for other factors including heterogeneity, a typical one standard deviation increase in phase (as determined by the analysis) is associated with close to 20% more risk of progression or death. The work confirms that more detailed quantitative assessments of the spatial pattern of PET imaging data of tumor masses, beyond the maximum FDG uptake ({\rm SUV}_{\rm max}) and previously considered measures of heterogeneity, provide improved prognostic information for potential input to treatment decisions for future patients. |
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U. ; Eary, J. F.</creator><creatorcontrib>O'Sullivan, F. ; Wolsztynski, E. ; O'Sullivan, J. ; Richards, T. ; Conrad, E. U. ; Eary, J. F.</creatorcontrib><description>Clinical experience with positron emission tomography (PET) scanning of sarcoma, using fluorodeoxyglucose (FDG), has established spatial heterogeneity in the standardized uptake values within the tumor mass as a key prognostic indicator of patient survival. But it may be that a more detailed quantitation of the tumor FDG uptake pattern could provide additional insights into risk. The present work develops a statistical model for this purpose. The approach is based on a tubular representation of the tumor mass with a simplified radial analysis of uptake, transverse to the tubular axis. The technique provides novel ways of characterizing the overall profile of the tumor, including the introduction of an approach for the measurement of its phase of development. The phase measure can distinguish between early phase tumors, in which the uptake is highest at the core, and later stage masses, in which there can often be central voids in FDG uptake. Biologically, these voids arise from necrosis and fluid, fat or cartilage accumulations. The tumor profiling technique is implemented using open-source software tools and illustrations are provided with clinically representative scans. A series of FDG-PET studies from 185 patients is used to formally evaluate the prognostic benefit. Significant ({ p} < 0.05) improvements in the prediction of patient survival and progression are obtained from the tumor profiling analysis. After adjustment for other factors including heterogeneity, a typical one standard deviation increase in phase (as determined by the analysis) is associated with close to 20% more risk of progression or death. The work confirms that more detailed quantitative assessments of the spatial pattern of PET imaging data of tumor masses, beyond the maximum FDG uptake ({\rm SUV}_{\rm max}) and previously considered measures of heterogeneity, provide improved prognostic information for potential input to treatment decisions for future patients.</description><identifier>ISSN: 0278-0062</identifier><identifier>EISSN: 1558-254X</identifier><identifier>DOI: 10.1109/TMI.2011.2160984</identifier><identifier>PMID: 21724502</identifier><identifier>CODEN: ITMID4</identifier><language>eng</language><publisher>United States: IEEE</publisher><subject>Biomedical optical imaging ; Boundary surface extraction ; Fluorodeoxyglucose F18 - pharmacokinetics ; human sarcoma ; Humans ; Kaplan-Meier Estimate ; Medical treatment ; Modeling ; Models, Biological ; phase assessment ; Positron emission tomography ; Positron-Emission Tomography - methods ; Principal component analysis ; Prognosis ; Proportional Hazards Models ; Radiopharmaceuticals - pharmacokinetics ; Regression Analysis ; Sarcoma - diagnostic imaging ; Sarcoma - metabolism ; spatial statistics ; Standard deviation ; tumor profiling ; Tumors</subject><ispartof>IEEE transactions on medical imaging, 2011-12, Vol.30 (12), p.2059-2071</ispartof><rights>Copyright The Institute of Electrical and Electronics Engineers, Inc. (IEEE) Dec 2011</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c508t-c1066198b84bd45c8bc15affbd7032b08a1d34fcb04362d95de90ac7af054ec3</citedby><cites>FETCH-LOGICAL-c508t-c1066198b84bd45c8bc15affbd7032b08a1d34fcb04362d95de90ac7af054ec3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://ieeexplore.ieee.org/document/5936120$$EHTML$$P50$$Gieee$$H</linktohtml><link.rule.ids>230,314,780,784,796,885,27924,27925,54758</link.rule.ids><linktorsrc>$$Uhttps://ieeexplore.ieee.org/document/5936120$$EView_record_in_IEEE$$FView_record_in_$$GIEEE</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21724502$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>O'Sullivan, F.</creatorcontrib><creatorcontrib>Wolsztynski, E.</creatorcontrib><creatorcontrib>O'Sullivan, J.</creatorcontrib><creatorcontrib>Richards, T.</creatorcontrib><creatorcontrib>Conrad, E. U.</creatorcontrib><creatorcontrib>Eary, J. F.</creatorcontrib><title>A Statistical Modeling Approach to the Analysis of Spatial Patterns of FDG-PET Uptake in Human Sarcoma</title><title>IEEE transactions on medical imaging</title><addtitle>TMI</addtitle><addtitle>IEEE Trans Med Imaging</addtitle><description>Clinical experience with positron emission tomography (PET) scanning of sarcoma, using fluorodeoxyglucose (FDG), has established spatial heterogeneity in the standardized uptake values within the tumor mass as a key prognostic indicator of patient survival. But it may be that a more detailed quantitation of the tumor FDG uptake pattern could provide additional insights into risk. The present work develops a statistical model for this purpose. The approach is based on a tubular representation of the tumor mass with a simplified radial analysis of uptake, transverse to the tubular axis. The technique provides novel ways of characterizing the overall profile of the tumor, including the introduction of an approach for the measurement of its phase of development. The phase measure can distinguish between early phase tumors, in which the uptake is highest at the core, and later stage masses, in which there can often be central voids in FDG uptake. Biologically, these voids arise from necrosis and fluid, fat or cartilage accumulations. The tumor profiling technique is implemented using open-source software tools and illustrations are provided with clinically representative scans. A series of FDG-PET studies from 185 patients is used to formally evaluate the prognostic benefit. Significant ({ p} < 0.05) improvements in the prediction of patient survival and progression are obtained from the tumor profiling analysis. After adjustment for other factors including heterogeneity, a typical one standard deviation increase in phase (as determined by the analysis) is associated with close to 20% more risk of progression or death. The work confirms that more detailed quantitative assessments of the spatial pattern of PET imaging data of tumor masses, beyond the maximum FDG uptake ({\rm SUV}_{\rm max}) and previously considered measures of heterogeneity, provide improved prognostic information for potential input to treatment decisions for future patients.</description><subject>Biomedical optical imaging</subject><subject>Boundary surface extraction</subject><subject>Fluorodeoxyglucose F18 - pharmacokinetics</subject><subject>human sarcoma</subject><subject>Humans</subject><subject>Kaplan-Meier Estimate</subject><subject>Medical treatment</subject><subject>Modeling</subject><subject>Models, Biological</subject><subject>phase assessment</subject><subject>Positron emission tomography</subject><subject>Positron-Emission Tomography - methods</subject><subject>Principal component analysis</subject><subject>Prognosis</subject><subject>Proportional Hazards Models</subject><subject>Radiopharmaceuticals - pharmacokinetics</subject><subject>Regression Analysis</subject><subject>Sarcoma - diagnostic imaging</subject><subject>Sarcoma - metabolism</subject><subject>spatial statistics</subject><subject>Standard deviation</subject><subject>tumor profiling</subject><subject>Tumors</subject><issn>0278-0062</issn><issn>1558-254X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>RIE</sourceid><sourceid>EIF</sourceid><recordid>eNpVkV1r2zAUhsXYWNOu94PBELt3diRLtnwzCF2_oGWFZNA7cSzLjTrHciVl0H8_tcnCdiWh87yvJB5CPjKYMwbN19Xt9ZwDY3POKmiUeENmTEpVcCnu35IZ8FoVABU_IscxPgIwIaF5T444q3ne8hnpF3SZMLmYnMGB3vrODm58oItpCh7NmiZP09rSxYjDc3SR-p4upxzI8B2mZMP4enbx_bK4O1_Rn1PCX5a6kV5tNzjSJQbjN_iBvOtxiPZ0v56Q1cX56uyquPlxeX22uCmMBJUKw6CqWKNaJdpOSKNawyT2fdvVUPIWFLKuFL1pQZQV7xrZ2QbQ1NiDFNaUJ-TbrnbathvbGTumgIOegttgeNYenf5_Mrq1fvC_tahlKWuRC77sC4J_2tqY9KPfhvz3qBuopARZqgzBDjLBxxhsf7iAgX7xorMX_eJF773kyOd_H3YI_BWRgU87wFlrD2PZlBXjUP4BgmySGQ</recordid><startdate>20111201</startdate><enddate>20111201</enddate><creator>O'Sullivan, F.</creator><creator>Wolsztynski, E.</creator><creator>O'Sullivan, J.</creator><creator>Richards, T.</creator><creator>Conrad, E. 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U.</au><au>Eary, J. F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Statistical Modeling Approach to the Analysis of Spatial Patterns of FDG-PET Uptake in Human Sarcoma</atitle><jtitle>IEEE transactions on medical imaging</jtitle><stitle>TMI</stitle><addtitle>IEEE Trans Med Imaging</addtitle><date>2011-12-01</date><risdate>2011</risdate><volume>30</volume><issue>12</issue><spage>2059</spage><epage>2071</epage><pages>2059-2071</pages><issn>0278-0062</issn><eissn>1558-254X</eissn><coden>ITMID4</coden><abstract>Clinical experience with positron emission tomography (PET) scanning of sarcoma, using fluorodeoxyglucose (FDG), has established spatial heterogeneity in the standardized uptake values within the tumor mass as a key prognostic indicator of patient survival. But it may be that a more detailed quantitation of the tumor FDG uptake pattern could provide additional insights into risk. The present work develops a statistical model for this purpose. The approach is based on a tubular representation of the tumor mass with a simplified radial analysis of uptake, transverse to the tubular axis. The technique provides novel ways of characterizing the overall profile of the tumor, including the introduction of an approach for the measurement of its phase of development. The phase measure can distinguish between early phase tumors, in which the uptake is highest at the core, and later stage masses, in which there can often be central voids in FDG uptake. Biologically, these voids arise from necrosis and fluid, fat or cartilage accumulations. The tumor profiling technique is implemented using open-source software tools and illustrations are provided with clinically representative scans. A series of FDG-PET studies from 185 patients is used to formally evaluate the prognostic benefit. Significant ({ p} < 0.05) improvements in the prediction of patient survival and progression are obtained from the tumor profiling analysis. After adjustment for other factors including heterogeneity, a typical one standard deviation increase in phase (as determined by the analysis) is associated with close to 20% more risk of progression or death. The work confirms that more detailed quantitative assessments of the spatial pattern of PET imaging data of tumor masses, beyond the maximum FDG uptake ({\rm SUV}_{\rm max}) and previously considered measures of heterogeneity, provide improved prognostic information for potential input to treatment decisions for future patients.</abstract><cop>United States</cop><pub>IEEE</pub><pmid>21724502</pmid><doi>10.1109/TMI.2011.2160984</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biomedical optical imaging Boundary surface extraction Fluorodeoxyglucose F18 - pharmacokinetics human sarcoma Humans Kaplan-Meier Estimate Medical treatment Modeling Models, Biological phase assessment Positron emission tomography Positron-Emission Tomography - methods Principal component analysis Prognosis Proportional Hazards Models Radiopharmaceuticals - pharmacokinetics Regression Analysis Sarcoma - diagnostic imaging Sarcoma - metabolism spatial statistics Standard deviation tumor profiling Tumors |
title | A Statistical Modeling Approach to the Analysis of Spatial Patterns of FDG-PET Uptake in Human Sarcoma |
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