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 |
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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 |
format | Article |
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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.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/(SICI)1097-0142(19961115)78:10<2216::AID-CNCR25>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 & 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</subject><ispartof>Cancer, 1996-11, Vol.78 (10), p.2216-2222</ispartof><rights>Copyright © 1996 American Cancer Society</rights><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4855-bb8c81995757cc53fc114d33fe2b132064f20b1e4856cc4e1866b8fd0900e7fe3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2F%28SICI%291097-0142%2819961115%2978%3A10%3C2216%3A%3AAID-CNCR25%3E3.0.CO%3B2-0$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2F%28SICI%291097-0142%2819961115%2978%3A10%3C2216%3A%3AAID-CNCR25%3E3.0.CO%3B2-0$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>309,310,314,777,781,786,787,1412,1428,23911,23912,25121,27905,27906,45555,45556,46390,46814</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2479199$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8918417$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vitola, João V.</creatorcontrib><creatorcontrib>Delbeke, Dominique</creatorcontrib><creatorcontrib>Meranze, Steven G.</creatorcontrib><creatorcontrib>Mazer, Murray J.</creatorcontrib><creatorcontrib>Pinson, C. 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 < 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.</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 & 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 & 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. Wright</creatorcontrib><collection>Pascal-Francis</collection><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><jtitle>Cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vitola, João V.</au><au>Delbeke, Dominique</au><au>Meranze, Steven G.</au><au>Mazer, Murray J.</au><au>Pinson, C. 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 < 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.</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<2216::AID-CNCR25>3.0.CO;2-0</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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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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