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Clinically determined type of 18F-fluoro-2-deoxyglucose uptake as an alternative prognostic marker in resectable pancreatic cancer

DC Field Value Language
dc.contributor.author강창무-
dc.contributor.author이우정-
dc.contributor.author정재욱-
dc.contributor.author황호경-
dc.contributor.author윤미진-
dc.date.accessioned2017-11-02T08:39:09Z-
dc.date.available2017-11-02T08:39:09Z-
dc.date.issued2017-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/154720-
dc.description.abstractPURPOSE: To investigate the association between clinical PET (positron emission tomography) type and oncologic outcome in resectable pancreatic cancer. METHODS: Between January 2008 and October 2012, patients who underwent potentially curative resection for resectable pancreatic ductal adenocarcinoma without neoadjuvant treatment were retrospectively investigated. Clinical PET type was defined as follows: pancreatic cancer with similar 18FDG uptake to renal calyx was determined as kidney-type (K-type), and relatively lower 18FDG uptake than that of renal calyx was regarded as Non-K type. RESULTS: A total of 53 patients were enrolled. After agreement-based reclassification, agreement based K-type (aK-type) was noted in 34 patients (64.2%), and agreement based Non-K type (aNon K-type) was found in 19 patients (35.8%). There was a significant difference between aK-type and aNon K-type pancreatic cancer (tumor size (P = 0.030), adjusted CA 19-9 (P = 0.007), maximum standard uptake value (SUVmax,P<0.001), metabolic tumor volume (MTV2.5, P<0.001), total lesion glycolysis (TLG, P<0.001)). K-type pancreatic cancer (n = 31) showed a significantly shorter disease-free time compared with Non-K type (n = 16) (10.8 vs. 24.1 months, P = 0.013). It was also noted that aK-type showed inferior disease-free survival to that of aNon-K type pancreatic cancer (11.9 vs. 28.6 months, P = 0.012). CONCLUSIONS: Clinical PET type is a reliable clinical marker to estimate aggressive tumor biology and can be utilized in predicting tumor recurrence and necessity for postoperative chemotherapy.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherPublic Library of Science-
dc.relation.isPartOfPLOS ONE-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAged-
dc.subject.MESHCarcinoma, Pancreatic Ductal/classification-
dc.subject.MESHCarcinoma, Pancreatic Ductal/diagnostic imaging*-
dc.subject.MESHCarcinoma, Pancreatic Ductal/mortality-
dc.subject.MESHCarcinoma, Pancreatic Ductal/surgery-
dc.subject.MESHDisease-Free Survival-
dc.subject.MESHFemale-
dc.subject.MESHFluorodeoxyglucose F18/metabolism-
dc.subject.MESHFluorodeoxyglucose F18/pharmacokinetics*-
dc.subject.MESHHumans-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHPancreatectomy*-
dc.subject.MESHPancreatic Neoplasms/classification-
dc.subject.MESHPancreatic Neoplasms/diagnostic imaging*-
dc.subject.MESHPancreatic Neoplasms/mortality-
dc.subject.MESHPancreatic Neoplasms/surgery-
dc.subject.MESHPositron-Emission Tomography/methods*-
dc.subject.MESHPrognosis-
dc.subject.MESHRadiopharmaceuticals/metabolism-
dc.subject.MESHRadiopharmaceuticals/pharmacokinetics*-
dc.subject.MESHRetrospective Studies-
dc.subject.MESHTumor Burden-
dc.titleClinically determined type of 18F-fluoro-2-deoxyglucose uptake as an alternative prognostic marker in resectable pancreatic cancer-
dc.typeArticle-
dc.publisher.locationUnited States-
dc.contributor.collegeCollege of Medicine-
dc.contributor.departmentDept. of Surgery-
dc.contributor.googleauthorJae Uk Chong-
dc.contributor.googleauthorHo Kyoung Hwang-
dc.contributor.googleauthorJin Ho Lee-
dc.contributor.googleauthorMijin Yun-
dc.contributor.googleauthorChang Moo Kang-
dc.contributor.googleauthorWoo Jung Lee-
dc.identifier.doi10.1371/journal.pone.0172606-
dc.contributor.localIdA02993-
dc.contributor.localIdA03710-
dc.contributor.localIdA04497-
dc.contributor.localIdA02550-
dc.contributor.localIdA00088-
dc.relation.journalcodeJ02540-
dc.identifier.eissn1932-6203-
dc.identifier.pmid28235029-
dc.contributor.alternativeNameKang, Chang Moo-
dc.contributor.alternativeNameLee, Woo Jung-
dc.contributor.alternativeNameChong, Jae Uk-
dc.contributor.alternativeNameHwang, Ho Kyoung-
dc.contributor.alternativeNameYun, Mi Jin-
dc.contributor.affiliatedAuthorLee, Woo Jung-
dc.contributor.affiliatedAuthorChong, Jae Uk-
dc.contributor.affiliatedAuthorHwang, Ho Kyoung-
dc.contributor.affiliatedAuthorYun, Mi Jin-
dc.contributor.affiliatedAuthorKang, Chang Moo-
dc.citation.titlePLoS One-
dc.citation.volume12-
dc.citation.number2-
dc.citation.startPagee0172606-
dc.identifier.bibliographicCitationPLOS ONE, Vol.12(2) : e0172606, 2017-
dc.date.modified2017-11-01-
dc.identifier.rimsid44201-
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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