Positron emission tomography with F‐18‐fluorodeoxyglucose to evaluate the results of hepatic chemoembolization

BACKGROUND Positron emission tomography (PET) using F‐18‐fluorodeoxyglucose (18FDG) is an imaging modality allowing direct evaluation of cellular glucose metabolism. The purpose of this study was to examine the role of 18FDG‐PET in monitoring chemoembolization therapy of patients with liver metastas...

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Veröffentlicht in:Cancer 1996-11, Vol.78 (10), p.2216-2222
Hauptverfasser: Vitola, João V., Delbeke, Dominique, Meranze, Steven G., Mazer, Murray J., Pinson, C. Wright
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container_end_page 2222
container_issue 10
container_start_page 2216
container_title Cancer
container_volume 78
creator Vitola, João V.
Delbeke, Dominique
Meranze, Steven G.
Mazer, Murray J.
Pinson, C. Wright
description BACKGROUND Positron emission tomography (PET) using F‐18‐fluorodeoxyglucose (18FDG) is an imaging modality allowing direct evaluation of cellular glucose metabolism. The purpose of this study was to examine the role of 18FDG‐PET in monitoring chemoembolization therapy of patients with liver metastases from adenocarcinoma. METHODS Thirty‐four hepatic lesions in 4 patients were evaluated with 18FDG‐PET before and 2–3 months after interventional therapy. All patients underwent transcatheter arterial chemoembolization. A total of nine PET studies were performed. Semiquantitative measurement of the metabolic activity of the lesions was performed using the standard uptake value (SUV) of 18FDG. Comparison was performed between sequential PET scans using Student's t test for paired data analysis. The PET findings were also compared with tumor marker levels measured at the time of the PET scans. RESULTS Twenty‐five of 34 lesions had decreased 18FDG uptake (SUV = 8 ± 2 vs. 3 ± 1; P < 0.00001), as expected in successful tumor chemoembolization. These findings were associated with a significant decrease in serum tumor marker levels (86 ± 4%; P < 0.05) after treatment. However, there were 3 new lesions, and 6 of the 34 lesions demonstrated persistent or increased 18FDG uptake after treatment (SUV = 8 ± 2 vs. 13 ± 3; P < 0.05), consistent with the presence of residual viable tumor. These findings led to further interventional therapy in all patients. CONCLUSIONS 18FDG‐PET allows monitoring of response to treatment with hepatic chemoembolization in patients with liver metastases from adenocarcinoma. PET is a useful diagnostic tool and has the potential to be used to guide further interventional therapy. Cancer 1996;78:2216‐22.
doi_str_mv 10.1002/(SICI)1097-0142(19961115)78:10<2216::AID-CNCR25>3.0.CO;2-0
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Wright</creator><creatorcontrib>Vitola, João V. ; Delbeke, Dominique ; Meranze, Steven G. ; Mazer, Murray J. ; Pinson, C. Wright</creatorcontrib><description>BACKGROUND Positron emission tomography (PET) using F‐18‐fluorodeoxyglucose (18FDG) is an imaging modality allowing direct evaluation of cellular glucose metabolism. The purpose of this study was to examine the role of 18FDG‐PET in monitoring chemoembolization therapy of patients with liver metastases from adenocarcinoma. METHODS Thirty‐four hepatic lesions in 4 patients were evaluated with 18FDG‐PET before and 2–3 months after interventional therapy. All patients underwent transcatheter arterial chemoembolization. A total of nine PET studies were performed. Semiquantitative measurement of the metabolic activity of the lesions was performed using the standard uptake value (SUV) of 18FDG. Comparison was performed between sequential PET scans using Student's t test for paired data analysis. The PET findings were also compared with tumor marker levels measured at the time of the PET scans. RESULTS Twenty‐five of 34 lesions had decreased 18FDG uptake (SUV = 8 ± 2 vs. 3 ± 1; P &lt; 0.00001), as expected in successful tumor chemoembolization. These findings were associated with a significant decrease in serum tumor marker levels (86 ± 4%; P &lt; 0.05) after treatment. However, there were 3 new lesions, and 6 of the 34 lesions demonstrated persistent or increased 18FDG uptake after treatment (SUV = 8 ± 2 vs. 13 ± 3; P &lt; 0.05), consistent with the presence of residual viable tumor. These findings led to further interventional therapy in all patients. CONCLUSIONS 18FDG‐PET allows monitoring of response to treatment with hepatic chemoembolization in patients with liver metastases from adenocarcinoma. PET is a useful diagnostic tool and has the potential to be used to guide further interventional therapy. Cancer 1996;78:2216‐22.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/(SICI)1097-0142(19961115)78:10&lt;2216::AID-CNCR25&gt;3.0.CO;2-0</identifier><identifier>PMID: 8918417</identifier><identifier>CODEN: CANCAR</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adenocarcinoma - diagnostic imaging ; Adenocarcinoma - secondary ; Adenocarcinoma - therapy ; Biological and medical sciences ; chemoembolization ; Chemoembolization, Therapeutic ; colorectal metastasis ; Colorectal Neoplasms - pathology ; Deoxyglucose - analogs &amp; derivatives ; emission computed tomography ; Female ; Fluorine Radioisotopes ; Fluorodeoxyglucose F18 ; F‐18‐fluorodeoxyglucose ; Gastroenterology. Liver. Pancreas. Abdomen ; hepatic metastasis ; Humans ; Liver Neoplasms - diagnostic imaging ; Liver Neoplasms - secondary ; Liver Neoplasms - therapy ; Liver. 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Wright</creatorcontrib><title>Positron emission tomography with F‐18‐fluorodeoxyglucose to evaluate the results of hepatic chemoembolization</title><title>Cancer</title><addtitle>Cancer</addtitle><description>BACKGROUND Positron emission tomography (PET) using F‐18‐fluorodeoxyglucose (18FDG) is an imaging modality allowing direct evaluation of cellular glucose metabolism. The purpose of this study was to examine the role of 18FDG‐PET in monitoring chemoembolization therapy of patients with liver metastases from adenocarcinoma. METHODS Thirty‐four hepatic lesions in 4 patients were evaluated with 18FDG‐PET before and 2–3 months after interventional therapy. All patients underwent transcatheter arterial chemoembolization. A total of nine PET studies were performed. Semiquantitative measurement of the metabolic activity of the lesions was performed using the standard uptake value (SUV) of 18FDG. Comparison was performed between sequential PET scans using Student's t test for paired data analysis. The PET findings were also compared with tumor marker levels measured at the time of the PET scans. RESULTS Twenty‐five of 34 lesions had decreased 18FDG uptake (SUV = 8 ± 2 vs. 3 ± 1; P &lt; 0.00001), as expected in successful tumor chemoembolization. These findings were associated with a significant decrease in serum tumor marker levels (86 ± 4%; P &lt; 0.05) after treatment. However, there were 3 new lesions, and 6 of the 34 lesions demonstrated persistent or increased 18FDG uptake after treatment (SUV = 8 ± 2 vs. 13 ± 3; P &lt; 0.05), consistent with the presence of residual viable tumor. These findings led to further interventional therapy in all patients. CONCLUSIONS 18FDG‐PET allows monitoring of response to treatment with hepatic chemoembolization in patients with liver metastases from adenocarcinoma. PET is a useful diagnostic tool and has the potential to be used to guide further interventional therapy. Cancer 1996;78:2216‐22.</description><subject>Adenocarcinoma - diagnostic imaging</subject><subject>Adenocarcinoma - secondary</subject><subject>Adenocarcinoma - therapy</subject><subject>Biological and medical sciences</subject><subject>chemoembolization</subject><subject>Chemoembolization, Therapeutic</subject><subject>colorectal metastasis</subject><subject>Colorectal Neoplasms - pathology</subject><subject>Deoxyglucose - analogs &amp; derivatives</subject><subject>emission computed tomography</subject><subject>Female</subject><subject>Fluorine Radioisotopes</subject><subject>Fluorodeoxyglucose F18</subject><subject>F‐18‐fluorodeoxyglucose</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>hepatic metastasis</subject><subject>Humans</subject><subject>Liver Neoplasms - diagnostic imaging</subject><subject>Liver Neoplasms - secondary</subject><subject>Liver Neoplasms - therapy</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Tomography, Emission-Computed</subject><subject>Tumors</subject><issn>0008-543X</issn><issn>1097-0142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc2O0zAQxy0EWsrCIyDlgNDuIcUfcewUhLQEFiqtKOJDQgjJStzxJiunLnbCUk48As_Ik-CooRc4cLHHMz__PZ4_Qs8InhOM6aOTd8tyeUpwIVJMMnpCiiInhPBTIRcEP6GU5IvF2fJ5Wr4u31L-lM3xvFw9pim-gWaHazfRDGMsU56xj7fRnRCu4lFQzo7QkSyIzIiYIf_Ghbb3bpNA14bQxqB3nbv01bbZJddt3yTnv378JDIuxg7OuzW4b7tLO2gXILIJfK3sUPUxbiDxEAbbh8SZpIFt1bc60Q10Drra2fZ7TLjNXXTLVDbAvWk_Rh_OX7wvX6UXq5fL8uwi1ZnkPK1rqWX8ORdcaM2Z0YRka8YM0JowivPMUFwTiHCudQZE5nktzRoXGIMwwI7Rw73u1rsvA4RexR9qsLbagBuCEpIzKbCM4Kc9qL0LwYNRW992ld8pgtVoiFKjIWqcrBonq_4YEjVGZjREqWiI2huimMKqXCmqcBS_P3Ux1B2sD9KTA7H-YKpXQVfW-Gqj23DAaCaK-FrEPu-x69bC7q8G_6O_f7Y3ZdhvHzm4aw</recordid><startdate>19961115</startdate><enddate>19961115</enddate><creator>Vitola, João V.</creator><creator>Delbeke, Dominique</creator><creator>Meranze, Steven G.</creator><creator>Mazer, Murray J.</creator><creator>Pinson, C. Wright</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>IQODW</scope><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></search><sort><creationdate>19961115</creationdate><title>Positron emission tomography with F‐18‐fluorodeoxyglucose to evaluate the results of hepatic chemoembolization</title><author>Vitola, João V. ; Delbeke, Dominique ; Meranze, Steven G. ; Mazer, Murray J. ; Pinson, C. Wright</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4855-bb8c81995757cc53fc114d33fe2b132064f20b1e4856cc4e1866b8fd0900e7fe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Adenocarcinoma - diagnostic imaging</topic><topic>Adenocarcinoma - secondary</topic><topic>Adenocarcinoma - therapy</topic><topic>Biological and medical sciences</topic><topic>chemoembolization</topic><topic>Chemoembolization, Therapeutic</topic><topic>colorectal metastasis</topic><topic>Colorectal Neoplasms - pathology</topic><topic>Deoxyglucose - analogs &amp; derivatives</topic><topic>emission computed tomography</topic><topic>Female</topic><topic>Fluorine Radioisotopes</topic><topic>Fluorodeoxyglucose F18</topic><topic>F‐18‐fluorodeoxyglucose</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>hepatic metastasis</topic><topic>Humans</topic><topic>Liver Neoplasms - diagnostic imaging</topic><topic>Liver Neoplasms - secondary</topic><topic>Liver Neoplasms - therapy</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Tomography, Emission-Computed</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vitola, João V.</creatorcontrib><creatorcontrib>Delbeke, Dominique</creatorcontrib><creatorcontrib>Meranze, Steven G.</creatorcontrib><creatorcontrib>Mazer, Murray J.</creatorcontrib><creatorcontrib>Pinson, C. 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Wright</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Positron emission tomography with F‐18‐fluorodeoxyglucose to evaluate the results of hepatic chemoembolization</atitle><jtitle>Cancer</jtitle><addtitle>Cancer</addtitle><date>1996-11-15</date><risdate>1996</risdate><volume>78</volume><issue>10</issue><spage>2216</spage><epage>2222</epage><pages>2216-2222</pages><issn>0008-543X</issn><eissn>1097-0142</eissn><coden>CANCAR</coden><abstract>BACKGROUND Positron emission tomography (PET) using F‐18‐fluorodeoxyglucose (18FDG) is an imaging modality allowing direct evaluation of cellular glucose metabolism. The purpose of this study was to examine the role of 18FDG‐PET in monitoring chemoembolization therapy of patients with liver metastases from adenocarcinoma. METHODS Thirty‐four hepatic lesions in 4 patients were evaluated with 18FDG‐PET before and 2–3 months after interventional therapy. All patients underwent transcatheter arterial chemoembolization. A total of nine PET studies were performed. Semiquantitative measurement of the metabolic activity of the lesions was performed using the standard uptake value (SUV) of 18FDG. Comparison was performed between sequential PET scans using Student's t test for paired data analysis. The PET findings were also compared with tumor marker levels measured at the time of the PET scans. RESULTS Twenty‐five of 34 lesions had decreased 18FDG uptake (SUV = 8 ± 2 vs. 3 ± 1; P &lt; 0.00001), as expected in successful tumor chemoembolization. These findings were associated with a significant decrease in serum tumor marker levels (86 ± 4%; P &lt; 0.05) after treatment. However, there were 3 new lesions, and 6 of the 34 lesions demonstrated persistent or increased 18FDG uptake after treatment (SUV = 8 ± 2 vs. 13 ± 3; P &lt; 0.05), consistent with the presence of residual viable tumor. These findings led to further interventional therapy in all patients. CONCLUSIONS 18FDG‐PET allows monitoring of response to treatment with hepatic chemoembolization in patients with liver metastases from adenocarcinoma. PET is a useful diagnostic tool and has the potential to be used to guide further interventional therapy. Cancer 1996;78:2216‐22.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>8918417</pmid><doi>10.1002/(SICI)1097-0142(19961115)78:10&lt;2216::AID-CNCR25&gt;3.0.CO;2-0</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Wiley Online Library Journals Frontfile Complete; Wiley Free Content; Alma/SFX Local Collection
subjects Adenocarcinoma - diagnostic imaging
Adenocarcinoma - secondary
Adenocarcinoma - therapy
Biological and medical sciences
chemoembolization
Chemoembolization, Therapeutic
colorectal metastasis
Colorectal Neoplasms - pathology
Deoxyglucose - analogs & derivatives
emission computed tomography
Female
Fluorine Radioisotopes
Fluorodeoxyglucose F18
F‐18‐fluorodeoxyglucose
Gastroenterology. Liver. Pancreas. Abdomen
hepatic metastasis
Humans
Liver Neoplasms - diagnostic imaging
Liver Neoplasms - secondary
Liver Neoplasms - therapy
Liver. Biliary tract. Portal circulation. Exocrine pancreas
Male
Medical sciences
Middle Aged
Tomography, Emission-Computed
Tumors
title Positron emission tomography with F‐18‐fluorodeoxyglucose to evaluate the results of hepatic chemoembolization
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