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Metabolic tumour volume on 18 F-FDG PET/CT predicts extended pathological T stages in patients with renal cell carcinoma at staging

DC Field Value Language
dc.contributor.author김동우-
dc.contributor.author김현정-
dc.contributor.author박지수-
dc.contributor.author윤미진-
dc.contributor.author이승환-
dc.contributor.author조남훈-
dc.contributor.author최영득-
dc.contributor.author한웅규-
dc.contributor.author함원식-
dc.date.accessioned2022-02-23T01:22:45Z-
dc.date.available2022-02-23T01:22:45Z-
dc.date.issued2021-12-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/187667-
dc.description.abstractWe evaluated the predictive value of 18F-fluorodeoxyglucose (FDG) uptake on positron emission tomography/CT (PET/CT) for extended pathological T (pT) stages (≥ pT3a) in Renal cell carcinoma (RCC) patients at staging. Thirty-eight RCC patients who underwent 18F-FDG PET/CT at staging, followed by radical nephrectomy between September 2016 and September 2018, were included in this prospective study. Patients were classified into two groups (limited pT stage: stage T1/2, n = 17; extended pT stage: T3/4, n = 21). Univariate and multivariate logistic regression analyses were performed to identify clinicopathological and metabolic variables to predict extended pT stages. 18F-FDG metabolic parameters were compared in relation to International Society of Urological Pathology (ISUP) grade and lymphovascular invasion (LVI). In univariate analysis, maximum standardised uptake value, metabolic tumour volume (MTV), and ISUP grade were significant. In multivariate analysis, MTV was the only significant factor of extended pT stages. With a cut-off MTV of 21.2, an area under the curve was 0.944, which was higher than 0.824 for clinical T stages (p = 0.037). In addition, high MTV, but not tumour size, was significantly correlated with aggressive pathologic features (ISUP grade and LVI). High glycolytic tumour volume on 18F-FDG PET/CT in RCC patients at staging is predictive of extended pT stages which could aid decision-making regarding the best type of surgery-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherNature Publishing Group-
dc.relation.isPartOfSCIENTIFIC REPORTS-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHCarcinoma, Renal Cell / pathology*-
dc.subject.MESHFemale-
dc.subject.MESHFluorodeoxyglucose F18 / administration & dosage*-
dc.subject.MESHGlycolysis / physiology-
dc.subject.MESHHumans-
dc.subject.MESHKidney Neoplasms / pathology*-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHMultimodal Imaging / methods-
dc.subject.MESHNeoplasm Staging / methods-
dc.subject.MESHNephrectomy / methods-
dc.subject.MESHPositron Emission Tomography Computed Tomography / methods-
dc.subject.MESHPositron-Emission Tomography / methods-
dc.subject.MESHPrognosis-
dc.subject.MESHProspective Studies-
dc.subject.MESHTomography, X-Ray Computed / methods-
dc.subject.MESHTumor Burden / physiology*-
dc.titleMetabolic tumour volume on 18 F-FDG PET/CT predicts extended pathological T stages in patients with renal cell carcinoma at staging-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Nuclear Medicine (핵의학교실)-
dc.contributor.googleauthorDongwoo Kim-
dc.contributor.googleauthorNarae Lee-
dc.contributor.googleauthorSuk Hyun Lee-
dc.contributor.googleauthorHyun Jeong Kim-
dc.contributor.googleauthorHye-Suk Hong-
dc.contributor.googleauthorJee Soo Park-
dc.contributor.googleauthorNam-Hoon Cho-
dc.contributor.googleauthorYoung Deuk Choi-
dc.contributor.googleauthorWon Sik Ham-
dc.contributor.googleauthorSeung Hwan Lee-
dc.contributor.googleauthorWoong Kyu Han-
dc.contributor.googleauthorMijin Yun-
dc.identifier.doi10.1038/s41598-021-03023-2-
dc.contributor.localIdA05304-
dc.contributor.localIdA01129-
dc.contributor.localIdA05336-
dc.contributor.localIdA02550-
dc.contributor.localIdA02938-
dc.contributor.localIdA03812-
dc.contributor.localIdA04111-
dc.contributor.localIdA04308-
dc.contributor.localIdA04337-
dc.relation.journalcodeJ02646-
dc.identifier.eissn2045-2322-
dc.identifier.pmid34873277-
dc.contributor.alternativeNameKim, Dongwoo-
dc.contributor.affiliatedAuthor김동우-
dc.contributor.affiliatedAuthor김현정-
dc.contributor.affiliatedAuthor박지수-
dc.contributor.affiliatedAuthor윤미진-
dc.contributor.affiliatedAuthor이승환-
dc.contributor.affiliatedAuthor조남훈-
dc.contributor.affiliatedAuthor최영득-
dc.contributor.affiliatedAuthor한웅규-
dc.contributor.affiliatedAuthor함원식-
dc.citation.volume11-
dc.citation.number1-
dc.citation.startPage23486-
dc.identifier.bibliographicCitationSCIENTIFIC REPORTS, Vol.11(1) : 23486, 2021-12-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Nuclear Medicine (핵의학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Urology (비뇨의학교실) > 1. Journal Papers

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