11C-Acetate PET Imaging in Hepatocellular Carcinoma and Other Liver Masses

It is well known that (18)F-FDG PET has a high average false-negative rate of 40%-50% in the detection of hepatocellular carcinoma (HCC). This is not an acceptable accuracy, particularly in countries where this tumor is prevalent. In this study, we evaluated prospectively the characteristics of (11)...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The Journal of nuclear medicine (1978) 2003-02, Vol.44 (2), p.213-221
Hauptverfasser: Ho, Chi-Lai, Yu, Simon C.H, Yeung, David W.C
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 221
container_issue 2
container_start_page 213
container_title The Journal of nuclear medicine (1978)
container_volume 44
creator Ho, Chi-Lai
Yu, Simon C.H
Yeung, David W.C
description It is well known that (18)F-FDG PET has a high average false-negative rate of 40%-50% in the detection of hepatocellular carcinoma (HCC). This is not an acceptable accuracy, particularly in countries where this tumor is prevalent. In this study, we evaluated prospectively the characteristics of (11)C-acetate and (18)F-FDG metabolism in HCC and other liver masses. Fifty-seven patients were recruited into this study, with masses consisting of 39 HCC; 3 cholangiocarcinomas; 10 hepatic metastases from lung, breast, colon, and carcinoid primary malignancies; and 5 benign pathologies, including focal nodular hyperplasia (FNH), adenoma, and hemangioma. All patients, except 2 with typical findings of hemangioma and 3 clinically obvious metastases, were confirmed histopathologically by liver biopsy or resection. All patients fasted for at least 6 h and blood glucose concentration was measured before they underwent dual PET radiopharmaceutical evaluation of the upper abdomen with (11)C-acetate and (18)F-FDG. In the subgroup of HCC patients with the number of lesions < or = 3 (32 patients; 55 lesions; mean size +/- SD, 3.5 +/- 1.9 cm), the sensitivity of detection by (11)C-acetate is 87.3% ((11)C-acetate maximum SUV [SUV(max)] = 7.32 +/- 2.02, with a lesion-to-normal liver ratio of 1.96 +/- 0.63), whereas the sensitivity of detection by (18)F-FDG is only 47.3%, and 34% lesions show uptake of both tracers. None of the lesions was negative for both tracers (100% sensitivity using both tracers). In some lesions and in the subgroup of HCC patients (n = 7) with multifocal or diffuse disease, dual-tracer uptake by different parts of the tumor is demonstrated. Histopathologic correlation suggests that the well-differentiated HCC tumors are detected by (11)C-acetate and the poorly differentiated types are detected by (18)F-FDG. All 16 non-HCC malignant (cholangiocarcinoma and metastatic) liver lesions do not show abnormal (11)C-acetate metabolism. Of the benign liver lesions, only FNH shows mildly increased (11)C-acetate activities ((11)C-acetate SUV(max) = 3.59, with a lesion-to-normal liver ratio of 1.25). (11)C-Acetate has a high sensitivity and specificity as a radiotracer complementary to (18)F-FDG in PET imaging of HCC and evaluation of other liver masses.
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_73016762</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>73016762</sourcerecordid><originalsourceid>FETCH-LOGICAL-h153t-c31b0f5941371d3d4cb01797ec9cd1fb9247932d7127c926e27f4ab5645ec2ca3</originalsourceid><addsrcrecordid>eNpFj8tOwzAURC0EoqXwC8grdpH8drOsokKLisqirC3HuWlc5VHsBMTfNxVFbGY2R6MzV2hKJZeJVEpfoymhiiZSEjlBdzEeCCFqPp_fogllUlNG2RS9UpolCwe97QG_L3d43di9b_fYt3gFR9t3Dup6qG3AmQ3Ot11jsW0LvO0rCHjjv8Z8szFCvEc3pa0jPFx6hj6el7tslWy2L-tssUmq0a1PHKc5KWUqKNe04IVwOaE61eBSV9AyT5nQKWfFKKhdyhQwXQqbSyUkOOYsn6Gn391j6D4HiL1pfDxb2ha6IRrNx99asRF8vIBD3kBhjsE3NvyYv_f_S5XfV98-gGkHV4MNZ_rQNkIYZhjl_ASRf2J8</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>73016762</pqid></control><display><type>article</type><title>11C-Acetate PET Imaging in Hepatocellular Carcinoma and Other Liver Masses</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>Ho, Chi-Lai ; Yu, Simon C.H ; Yeung, David W.C</creator><creatorcontrib>Ho, Chi-Lai ; Yu, Simon C.H ; Yeung, David W.C</creatorcontrib><description>It is well known that (18)F-FDG PET has a high average false-negative rate of 40%-50% in the detection of hepatocellular carcinoma (HCC). This is not an acceptable accuracy, particularly in countries where this tumor is prevalent. In this study, we evaluated prospectively the characteristics of (11)C-acetate and (18)F-FDG metabolism in HCC and other liver masses. Fifty-seven patients were recruited into this study, with masses consisting of 39 HCC; 3 cholangiocarcinomas; 10 hepatic metastases from lung, breast, colon, and carcinoid primary malignancies; and 5 benign pathologies, including focal nodular hyperplasia (FNH), adenoma, and hemangioma. All patients, except 2 with typical findings of hemangioma and 3 clinically obvious metastases, were confirmed histopathologically by liver biopsy or resection. All patients fasted for at least 6 h and blood glucose concentration was measured before they underwent dual PET radiopharmaceutical evaluation of the upper abdomen with (11)C-acetate and (18)F-FDG. In the subgroup of HCC patients with the number of lesions &lt; or = 3 (32 patients; 55 lesions; mean size +/- SD, 3.5 +/- 1.9 cm), the sensitivity of detection by (11)C-acetate is 87.3% ((11)C-acetate maximum SUV [SUV(max)] = 7.32 +/- 2.02, with a lesion-to-normal liver ratio of 1.96 +/- 0.63), whereas the sensitivity of detection by (18)F-FDG is only 47.3%, and 34% lesions show uptake of both tracers. None of the lesions was negative for both tracers (100% sensitivity using both tracers). In some lesions and in the subgroup of HCC patients (n = 7) with multifocal or diffuse disease, dual-tracer uptake by different parts of the tumor is demonstrated. Histopathologic correlation suggests that the well-differentiated HCC tumors are detected by (11)C-acetate and the poorly differentiated types are detected by (18)F-FDG. All 16 non-HCC malignant (cholangiocarcinoma and metastatic) liver lesions do not show abnormal (11)C-acetate metabolism. Of the benign liver lesions, only FNH shows mildly increased (11)C-acetate activities ((11)C-acetate SUV(max) = 3.59, with a lesion-to-normal liver ratio of 1.25). (11)C-Acetate has a high sensitivity and specificity as a radiotracer complementary to (18)F-FDG in PET imaging of HCC and evaluation of other liver masses.</description><identifier>ISSN: 0161-5505</identifier><identifier>EISSN: 1535-5667</identifier><identifier>PMID: 12571212</identifier><language>eng</language><publisher>United States: Soc Nuclear Med</publisher><subject>Acetates - pharmacokinetics ; Adult ; Aged ; Aged, 80 and over ; Breast Neoplasms - pathology ; Carbon Radioisotopes ; Carcinoma, Hepatocellular - diagnosis ; Carcinoma, Hepatocellular - diagnostic imaging ; Carcinoma, Hepatocellular - metabolism ; Carcinoma, Hepatocellular - secondary ; Cholangiocarcinoma - diagnostic imaging ; Cholangiocarcinoma - metabolism ; Cholangiocarcinoma - pathology ; Cholangiocarcinoma - secondary ; Colonic Neoplasms - pathology ; False Negative Reactions ; Female ; Fluorodeoxyglucose F18 - pharmacokinetics ; Humans ; Liver Neoplasms - diagnosis ; Liver Neoplasms - diagnostic imaging ; Liver Neoplasms - metabolism ; Liver Neoplasms - secondary ; Lung Neoplasms - pathology ; Male ; Middle Aged ; Prospective Studies ; Radionuclide Imaging ; Radiopharmaceuticals - pharmacokinetics ; Reproducibility of Results ; Sensitivity and Specificity</subject><ispartof>The Journal of nuclear medicine (1978), 2003-02, Vol.44 (2), p.213-221</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12571212$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ho, Chi-Lai</creatorcontrib><creatorcontrib>Yu, Simon C.H</creatorcontrib><creatorcontrib>Yeung, David W.C</creatorcontrib><title>11C-Acetate PET Imaging in Hepatocellular Carcinoma and Other Liver Masses</title><title>The Journal of nuclear medicine (1978)</title><addtitle>J Nucl Med</addtitle><description>It is well known that (18)F-FDG PET has a high average false-negative rate of 40%-50% in the detection of hepatocellular carcinoma (HCC). This is not an acceptable accuracy, particularly in countries where this tumor is prevalent. In this study, we evaluated prospectively the characteristics of (11)C-acetate and (18)F-FDG metabolism in HCC and other liver masses. Fifty-seven patients were recruited into this study, with masses consisting of 39 HCC; 3 cholangiocarcinomas; 10 hepatic metastases from lung, breast, colon, and carcinoid primary malignancies; and 5 benign pathologies, including focal nodular hyperplasia (FNH), adenoma, and hemangioma. All patients, except 2 with typical findings of hemangioma and 3 clinically obvious metastases, were confirmed histopathologically by liver biopsy or resection. All patients fasted for at least 6 h and blood glucose concentration was measured before they underwent dual PET radiopharmaceutical evaluation of the upper abdomen with (11)C-acetate and (18)F-FDG. In the subgroup of HCC patients with the number of lesions &lt; or = 3 (32 patients; 55 lesions; mean size +/- SD, 3.5 +/- 1.9 cm), the sensitivity of detection by (11)C-acetate is 87.3% ((11)C-acetate maximum SUV [SUV(max)] = 7.32 +/- 2.02, with a lesion-to-normal liver ratio of 1.96 +/- 0.63), whereas the sensitivity of detection by (18)F-FDG is only 47.3%, and 34% lesions show uptake of both tracers. None of the lesions was negative for both tracers (100% sensitivity using both tracers). In some lesions and in the subgroup of HCC patients (n = 7) with multifocal or diffuse disease, dual-tracer uptake by different parts of the tumor is demonstrated. Histopathologic correlation suggests that the well-differentiated HCC tumors are detected by (11)C-acetate and the poorly differentiated types are detected by (18)F-FDG. All 16 non-HCC malignant (cholangiocarcinoma and metastatic) liver lesions do not show abnormal (11)C-acetate metabolism. Of the benign liver lesions, only FNH shows mildly increased (11)C-acetate activities ((11)C-acetate SUV(max) = 3.59, with a lesion-to-normal liver ratio of 1.25). (11)C-Acetate has a high sensitivity and specificity as a radiotracer complementary to (18)F-FDG in PET imaging of HCC and evaluation of other liver masses.</description><subject>Acetates - pharmacokinetics</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Breast Neoplasms - pathology</subject><subject>Carbon Radioisotopes</subject><subject>Carcinoma, Hepatocellular - diagnosis</subject><subject>Carcinoma, Hepatocellular - diagnostic imaging</subject><subject>Carcinoma, Hepatocellular - metabolism</subject><subject>Carcinoma, Hepatocellular - secondary</subject><subject>Cholangiocarcinoma - diagnostic imaging</subject><subject>Cholangiocarcinoma - metabolism</subject><subject>Cholangiocarcinoma - pathology</subject><subject>Cholangiocarcinoma - secondary</subject><subject>Colonic Neoplasms - pathology</subject><subject>False Negative Reactions</subject><subject>Female</subject><subject>Fluorodeoxyglucose F18 - pharmacokinetics</subject><subject>Humans</subject><subject>Liver Neoplasms - diagnosis</subject><subject>Liver Neoplasms - diagnostic imaging</subject><subject>Liver Neoplasms - metabolism</subject><subject>Liver Neoplasms - secondary</subject><subject>Lung Neoplasms - pathology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Prospective Studies</subject><subject>Radionuclide Imaging</subject><subject>Radiopharmaceuticals - pharmacokinetics</subject><subject>Reproducibility of Results</subject><subject>Sensitivity and Specificity</subject><issn>0161-5505</issn><issn>1535-5667</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFj8tOwzAURC0EoqXwC8grdpH8drOsokKLisqirC3HuWlc5VHsBMTfNxVFbGY2R6MzV2hKJZeJVEpfoymhiiZSEjlBdzEeCCFqPp_fogllUlNG2RS9UpolCwe97QG_L3d43di9b_fYt3gFR9t3Dup6qG3AmQ3Ot11jsW0LvO0rCHjjv8Z8szFCvEc3pa0jPFx6hj6el7tslWy2L-tssUmq0a1PHKc5KWUqKNe04IVwOaE61eBSV9AyT5nQKWfFKKhdyhQwXQqbSyUkOOYsn6Gn391j6D4HiL1pfDxb2ha6IRrNx99asRF8vIBD3kBhjsE3NvyYv_f_S5XfV98-gGkHV4MNZ_rQNkIYZhjl_ASRf2J8</recordid><startdate>200302</startdate><enddate>200302</enddate><creator>Ho, Chi-Lai</creator><creator>Yu, Simon C.H</creator><creator>Yeung, David W.C</creator><general>Soc Nuclear Med</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>200302</creationdate><title>11C-Acetate PET Imaging in Hepatocellular Carcinoma and Other Liver Masses</title><author>Ho, Chi-Lai ; Yu, Simon C.H ; Yeung, David W.C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h153t-c31b0f5941371d3d4cb01797ec9cd1fb9247932d7127c926e27f4ab5645ec2ca3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Acetates - pharmacokinetics</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Breast Neoplasms - pathology</topic><topic>Carbon Radioisotopes</topic><topic>Carcinoma, Hepatocellular - diagnosis</topic><topic>Carcinoma, Hepatocellular - diagnostic imaging</topic><topic>Carcinoma, Hepatocellular - metabolism</topic><topic>Carcinoma, Hepatocellular - secondary</topic><topic>Cholangiocarcinoma - diagnostic imaging</topic><topic>Cholangiocarcinoma - metabolism</topic><topic>Cholangiocarcinoma - pathology</topic><topic>Cholangiocarcinoma - secondary</topic><topic>Colonic Neoplasms - pathology</topic><topic>False Negative Reactions</topic><topic>Female</topic><topic>Fluorodeoxyglucose F18 - pharmacokinetics</topic><topic>Humans</topic><topic>Liver Neoplasms - diagnosis</topic><topic>Liver Neoplasms - diagnostic imaging</topic><topic>Liver Neoplasms - metabolism</topic><topic>Liver Neoplasms - secondary</topic><topic>Lung Neoplasms - pathology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Prospective Studies</topic><topic>Radionuclide Imaging</topic><topic>Radiopharmaceuticals - pharmacokinetics</topic><topic>Reproducibility of Results</topic><topic>Sensitivity and Specificity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ho, Chi-Lai</creatorcontrib><creatorcontrib>Yu, Simon C.H</creatorcontrib><creatorcontrib>Yeung, David W.C</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of nuclear medicine (1978)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ho, Chi-Lai</au><au>Yu, Simon C.H</au><au>Yeung, David W.C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>11C-Acetate PET Imaging in Hepatocellular Carcinoma and Other Liver Masses</atitle><jtitle>The Journal of nuclear medicine (1978)</jtitle><addtitle>J Nucl Med</addtitle><date>2003-02</date><risdate>2003</risdate><volume>44</volume><issue>2</issue><spage>213</spage><epage>221</epage><pages>213-221</pages><issn>0161-5505</issn><eissn>1535-5667</eissn><abstract>It is well known that (18)F-FDG PET has a high average false-negative rate of 40%-50% in the detection of hepatocellular carcinoma (HCC). This is not an acceptable accuracy, particularly in countries where this tumor is prevalent. In this study, we evaluated prospectively the characteristics of (11)C-acetate and (18)F-FDG metabolism in HCC and other liver masses. Fifty-seven patients were recruited into this study, with masses consisting of 39 HCC; 3 cholangiocarcinomas; 10 hepatic metastases from lung, breast, colon, and carcinoid primary malignancies; and 5 benign pathologies, including focal nodular hyperplasia (FNH), adenoma, and hemangioma. All patients, except 2 with typical findings of hemangioma and 3 clinically obvious metastases, were confirmed histopathologically by liver biopsy or resection. All patients fasted for at least 6 h and blood glucose concentration was measured before they underwent dual PET radiopharmaceutical evaluation of the upper abdomen with (11)C-acetate and (18)F-FDG. In the subgroup of HCC patients with the number of lesions &lt; or = 3 (32 patients; 55 lesions; mean size +/- SD, 3.5 +/- 1.9 cm), the sensitivity of detection by (11)C-acetate is 87.3% ((11)C-acetate maximum SUV [SUV(max)] = 7.32 +/- 2.02, with a lesion-to-normal liver ratio of 1.96 +/- 0.63), whereas the sensitivity of detection by (18)F-FDG is only 47.3%, and 34% lesions show uptake of both tracers. None of the lesions was negative for both tracers (100% sensitivity using both tracers). In some lesions and in the subgroup of HCC patients (n = 7) with multifocal or diffuse disease, dual-tracer uptake by different parts of the tumor is demonstrated. Histopathologic correlation suggests that the well-differentiated HCC tumors are detected by (11)C-acetate and the poorly differentiated types are detected by (18)F-FDG. All 16 non-HCC malignant (cholangiocarcinoma and metastatic) liver lesions do not show abnormal (11)C-acetate metabolism. Of the benign liver lesions, only FNH shows mildly increased (11)C-acetate activities ((11)C-acetate SUV(max) = 3.59, with a lesion-to-normal liver ratio of 1.25). (11)C-Acetate has a high sensitivity and specificity as a radiotracer complementary to (18)F-FDG in PET imaging of HCC and evaluation of other liver masses.</abstract><cop>United States</cop><pub>Soc Nuclear Med</pub><pmid>12571212</pmid><tpages>9</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0161-5505
ispartof The Journal of nuclear medicine (1978), 2003-02, Vol.44 (2), p.213-221
issn 0161-5505
1535-5667
language eng
recordid cdi_proquest_miscellaneous_73016762
source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects Acetates - pharmacokinetics
Adult
Aged
Aged, 80 and over
Breast Neoplasms - pathology
Carbon Radioisotopes
Carcinoma, Hepatocellular - diagnosis
Carcinoma, Hepatocellular - diagnostic imaging
Carcinoma, Hepatocellular - metabolism
Carcinoma, Hepatocellular - secondary
Cholangiocarcinoma - diagnostic imaging
Cholangiocarcinoma - metabolism
Cholangiocarcinoma - pathology
Cholangiocarcinoma - secondary
Colonic Neoplasms - pathology
False Negative Reactions
Female
Fluorodeoxyglucose F18 - pharmacokinetics
Humans
Liver Neoplasms - diagnosis
Liver Neoplasms - diagnostic imaging
Liver Neoplasms - metabolism
Liver Neoplasms - secondary
Lung Neoplasms - pathology
Male
Middle Aged
Prospective Studies
Radionuclide Imaging
Radiopharmaceuticals - pharmacokinetics
Reproducibility of Results
Sensitivity and Specificity
title 11C-Acetate PET Imaging in Hepatocellular Carcinoma and Other Liver Masses
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T06%3A51%3A23IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=11C-Acetate%20PET%20Imaging%20in%20Hepatocellular%20Carcinoma%20and%20Other%20Liver%20Masses&rft.jtitle=The%20Journal%20of%20nuclear%20medicine%20(1978)&rft.au=Ho,%20Chi-Lai&rft.date=2003-02&rft.volume=44&rft.issue=2&rft.spage=213&rft.epage=221&rft.pages=213-221&rft.issn=0161-5505&rft.eissn=1535-5667&rft_id=info:doi/&rft_dat=%3Cproquest_pubme%3E73016762%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=73016762&rft_id=info:pmid/12571212&rfr_iscdi=true