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Prognostic Value of Metabolic Tumor Volume and Total Lesion Glycolysis on Preoperative 18F-FDG PET/CT in Patients With Very Early and Early Hepatocellular Carcinoma

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dc.contributor.author조호진-
dc.contributor.author김경식-
dc.contributor.author최기홍-
dc.contributor.author윤미진-
dc.contributor.author황상현-
dc.date.accessioned2020-07-16T16:47:53Z-
dc.date.available2020-07-16T16:47:53Z-
dc.date.issued2017-01-
dc.identifier.issn0363-9762-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/178318-
dc.description.abstractPurpose: The aim of this article was to evaluate the prognostic value of metabolic tumor volume (MTV) and total lesion glycolysis (TLG) on preoperative F-FDG PET/CT for predicting intrahepatic recurrence-free survival (IHRFS), extrahepatic metastasis-free survival (EHMFS), and overall survival (OS) in patients with very early/early hepatocellular carcinoma (HCC). Patients and methods: We retrospectively enrolled 132 patients with very early/early HCC who underwent F-FDG PET/CT followed by surgery. The maximum tumor SUV-to-mean normal liver SUV ratio, MTV, and TLG were measured for each patient. Prognostic significances of PET/CT parameters and clinicopathologic factors for IHRFS, EHMFS, and OS were evaluated. Cumulative IHRFS, EHMFS, and OS were calculated using the Kaplan-Meier method. Results: Thirty-three (25%) and 21 (15.9%) of 132 patients experienced intrahepatic and extrahepatic recurrence, respectively, during a median follow-up period of 38.1 months. In multivariate analysis, none of the factors were significant for IHRFS. Metabolic tumor volume and TLG were only significant factors for EHMFS and OS (P < 0.05). The 5-year EHMFS rates were 94.8% in patients with low MTV and TLG, and 62.1% and 63.2% in patients with high MTV and TLG, respectively (P < 0.001). The 5-year OS rates were 92.6% and 92.4% in patients with low MTV and TLG, and 63.3% and 64.3% in patients with high MTV and TLG, respectively (P < 0.001). Conclusions: Metabolic tumor volume and TLG on preoperative PET/CT were independent prognostic factors for EHMFS and OS but not IHRFS in patients with very early/early HCC. Therefore, patients with high MTV or TLG should be closely observed for extrahepatic metastasis using systemic evaluations.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherLippincott-
dc.relation.isPartOfCLINICAL NUCLEAR MEDICINE-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAged, 80 and over-
dc.subject.MESHCarcinoma, Hepatocellular / diagnostic imaging*-
dc.subject.MESHCarcinoma, Hepatocellular / metabolism-
dc.subject.MESHFemale-
dc.subject.MESHFluorodeoxyglucose F18* / metabolism-
dc.subject.MESHGlycolysis*-
dc.subject.MESHHumans-
dc.subject.MESHLiver Neoplasms / diagnostic imaging*-
dc.subject.MESHLiver Neoplasms / metabolism-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHPositron Emission Tomography Computed Tomography*-
dc.subject.MESHPredictive Value of Tests-
dc.subject.MESHRadiopharmaceuticals*-
dc.titlePrognostic Value of Metabolic Tumor Volume and Total Lesion Glycolysis on Preoperative 18F-FDG PET/CT in Patients With Very Early and Early Hepatocellular Carcinoma-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Nuclear Medicine (핵의학교실)-
dc.contributor.googleauthorSang Hyun Hwang-
dc.contributor.googleauthorJeong Won Lee-
dc.contributor.googleauthorHo Jin Cho-
dc.contributor.googleauthorKyung Sik Kim-
dc.contributor.googleauthorGi Hong Choi-
dc.contributor.googleauthorMijin Yun-
dc.identifier.doi10.1097/RLU.0000000000001449-
dc.contributor.localIdA03941-
dc.contributor.localIdA00299-
dc.contributor.localIdA04046-
dc.contributor.localIdA02550-
dc.relation.journalcodeJ00595-
dc.identifier.eissn1536-0229-
dc.identifier.pmid27775949-
dc.identifier.urlhttps://journals.lww.com/nuclearmed/Fulltext/2017/01000/Prognostic_Value_of_Metabolic_Tumor_Volume_and.6.aspx-
dc.contributor.alternativeNameCho, Ho Jin-
dc.contributor.affiliatedAuthor조호진-
dc.contributor.affiliatedAuthor김경식-
dc.contributor.affiliatedAuthor최기홍-
dc.contributor.affiliatedAuthor윤미진-
dc.citation.volume42-
dc.citation.number1-
dc.citation.startPage34-
dc.citation.endPage39-
dc.identifier.bibliographicCitationCLINICAL NUCLEAR MEDICINE, Vol.42(1) : 34-39, 2017-01-
dc.identifier.rimsid64718-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Nuclear Medicine (핵의학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Surgery (외과학교실) > 1. Journal Papers

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