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F-18-FDG uptake in breast cancer correlates with immunohistochemically defined subtypes

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dc.contributor.authorKoo, Hye Ryoung-
dc.contributor.authorPark, Jeong Seon-
dc.contributor.authorKang, Keon Wook-
dc.contributor.authorCho, Nariya-
dc.contributor.authorChang, Jung Min-
dc.contributor.authorBae, Min Sun-
dc.contributor.authorKim, Won Hwa-
dc.contributor.authorLee, Su Hyun-
dc.contributor.authorKim, Mi Young-
dc.contributor.authorKim, Jin You-
dc.contributor.authorSeo, Mirinae-
dc.contributor.authorMoon, Woo Kyung-
dc.date.accessioned2022-07-16T05:42:07Z-
dc.date.available2022-07-16T05:42:07Z-
dc.date.created2021-05-12-
dc.date.issued2014-03-
dc.identifier.issn0938-7994-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/160502-
dc.description.abstractObjectives To determine whether a correlation exists between maximum standardized uptake value (SUVmax) on F-18-fluorodeoxyglucose positron emission tomography (FDG-PET) and the subtypes of breast cancer. Methods This retrospective study involved 548 patients (mean age 51.6 years, range 21-81 years) with 552 index breast cancers (mean size 2.57 cm, range 1.0-14.5 cm). The correlation between F-18-FDG uptake in PET/CT, expressed as SUVmax, and immunohistochemically defined subtypes (luminal A, luminal B, human epidermal growth factor receptor 2 (HER2) positive and triple negative) was analyzed. Results The mean SUVmax value of the 552 tumours was 6.07 +/- 4.63 (range 0.9-32.8). The subtypes of the 552 tumours were 334 (60 %) luminal A, 66 (12 %) luminal B, 60 (11 %) HER2 positive and 92 (17 %) triple negative, for which the mean SUVmax values were 4.69+/-3.45, 6.51+/-4.18, 7.44+/-4.73 and 9.83+/-6.03, respectively. In a multivariate regression analysis, triple-negative and HER2-positive tumours had 1.67-fold (P < 0.001) and 1.27-fold (P = 0.009) higher SUVmax values, respectively, than luminal A tumours after adjustment for invasive tumour size, lymph node involvement status and histologic grade. Conclusion FDG uptake was independently associated with subtypes of invasive breast cancer. Triple-negative and HER2-positive breast cancers showed higher SUVmax values than luminal A tumours. Key Points F-18-FDG PET demonstrates increased tissue glucose metabolism, a hallmark of cancers. Immunohistochemically defined subtypes appear significantly associated with FDG uptake (expressed as SUVmax). Triple-negative tumours had 1.67-fold higher SUVmax values than luminal A tumours. HER2-positive tumours had 1.27-fold higher SUVmax values than luminal A tumours.-
dc.language영어-
dc.language.isoen-
dc.publisherSPRINGER-
dc.titleF-18-FDG uptake in breast cancer correlates with immunohistochemically defined subtypes-
dc.typeArticle-
dc.contributor.affiliatedAuthorPark, Jeong Seon-
dc.identifier.doi10.1007/s00330-013-3037-1-
dc.identifier.scopusid2-s2.0-84896706288-
dc.identifier.wosid000332658100009-
dc.identifier.bibliographicCitationEUROPEAN RADIOLOGY, v.24, no.3, pp.610 - 618-
dc.relation.isPartOfEUROPEAN RADIOLOGY-
dc.citation.titleEUROPEAN RADIOLOGY-
dc.citation.volume24-
dc.citation.number3-
dc.citation.startPage610-
dc.citation.endPage618-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaRadiology, Nuclear Medicine & Medical Imaging-
dc.relation.journalWebOfScienceCategoryRadiology, Nuclear Medicine & Medical Imaging-
dc.subject.keywordPlusINTERNATIONAL EXPERT CONSENSUS-
dc.subject.keywordPlusFDG UPTAKE-
dc.subject.keywordPlusNEOADJUVANT CHEMOTHERAPY-
dc.subject.keywordPlusPRIMARY THERAPY-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusPET/CT-
dc.subject.keywordPlusHIGHLIGHTS-
dc.subject.keywordPlusRECURRENCE-
dc.subject.keywordPlusGRADE-
dc.subject.keywordAuthorBreast cancer-
dc.subject.keywordAuthorPET-
dc.subject.keywordAuthorFDG uptake-
dc.subject.keywordAuthorImmunohistochemistry-
dc.subject.keywordAuthorSubtype-
dc.identifier.urlhttps://link.springer.com/article/10.1007/s00330-013-3037-1-
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