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Clinical Usefulness of 18F-Fluorodeoxyglucose-Positron Emission Tomography in Patients With Locally Advanced Pancreatic Cancer Planned to Undergo Concurrent Chemoradiation Therapy

DC Field Value Language
dc.contributor.author박정엽-
dc.contributor.author성진실-
dc.contributor.author송시영-
dc.contributor.author윤미진-
dc.contributor.author이종두-
dc.contributor.author조응혁-
dc.contributor.author장지석-
dc.contributor.author최서희-
dc.date.accessioned2015-01-06T17:04:34Z-
dc.date.available2015-01-06T17:04:34Z-
dc.date.issued2014-
dc.identifier.issn0360-3016-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/99305-
dc.description.abstractPurpose : To assess the role of coregistered 18F-fluorodeoxyglucose positron emission tomography (FDG-PET) in detecting radiographically occult distant metastasis (DM) at staging in patients with locally advanced pancreatic cancer (LAPC) and to study whether FDG-PET parameters can predict relatively long-term survival in patients who are more likely to benefit from chemoradiation therapy (CRT). Methods and Materials : From our institutional database, we identified 388 LAPC patients with M0 on conventional computed tomography (CT) who were planned to undergo CRT. Coregistered FDG-PET staging was offered to all patients, and follow-up FDG-PET was used at the clinical discretion of the physician. Results : FDG-PET detected unsuspected CT-occult DM in 33% of all 388 patients and allowed them to receive systemic therapy immediately. The remaining 260 patients (PET-M0) underwent CRT selectively as an initial treatment. Early DM arose in 13.1% of 260 patients, and the 1-year estimated locoregional recurrence rate was 5.4%. Median overall survival (OS) and progression-free survival (PFS) were 14.6 and 9.3 months, respectively, at a median follow-up time of 32.3 months (range, 10-99.1 months). Patients with a baseline standardized uptake value (SUV) <3.5 and/or SUV decline ≥60% had significantly better OS and PFS than those having none, even after adjustment for all potential confounding variables (all P<.001). Conclusions : FDG-PET can detect radiographically occult DM at staging in one-third of patients and spare them from the potentially toxic therapy. Additionally, FDG-PET parameters including baseline SUV and SUV changes may serve as useful clinical markers for predicting the prognosis in LAPC patients.-
dc.description.statementOfResponsibilityopen-
dc.relation.isPartOfINTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS-
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.MESHChemoradiotherapy*/mortality-
dc.subject.MESHDisease-Free Survival-
dc.subject.MESHFemale-
dc.subject.MESHFluorodeoxyglucose F18*/pharmacokinetics-
dc.subject.MESHFollow-Up Studies-
dc.subject.MESHHumans-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHNeoplasm Metastasis/diagnostic imaging-
dc.subject.MESHNeoplasm Recurrence, Local/diagnostic imaging-
dc.subject.MESHNeoplasm Recurrence, Local/mortality-
dc.subject.MESHPancreatic Neoplasms/diagnostic imaging*-
dc.subject.MESHPancreatic Neoplasms/mortality-
dc.subject.MESHPancreatic Neoplasms/pathology-
dc.subject.MESHPancreatic Neoplasms/surgery-
dc.subject.MESHPositron-Emission Tomography/methods*-
dc.subject.MESHRadiopharmaceuticals/pharmacokinetics*-
dc.titleClinical Usefulness of 18F-Fluorodeoxyglucose-Positron Emission Tomography in Patients With Locally Advanced Pancreatic Cancer Planned to Undergo Concurrent Chemoradiation Therapy-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학)-
dc.contributor.googleauthorJee Suk Chang-
dc.contributor.googleauthorSeo Hee Choi-
dc.contributor.googleauthorYoungin Lee-
dc.contributor.googleauthorKyung Hwan Kim-
dc.contributor.googleauthorJeong Youp Park-
dc.contributor.googleauthorSi Young Song-
dc.contributor.googleauthorArthur Cho-
dc.contributor.googleauthorMijin Yun-
dc.contributor.googleauthorJong Doo Lee-
dc.contributor.googleauthorJinsil Seong-
dc.identifier.doi10.1016/j.ijrobp.2014.05.030-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA01647-
dc.contributor.localIdA01956-
dc.contributor.localIdA02035-
dc.contributor.localIdA02550-
dc.contributor.localIdA03138-
dc.contributor.localIdA03887-
dc.contributor.localIdA04658-
dc.relation.journalcodeJ01157-
dc.identifier.eissn1879-355X-
dc.identifier.pmid25015206-
dc.identifier.urlhttp://www.sciencedirect.com/science/article/pii/S0360301614006798-
dc.contributor.alternativeNamePark, Jeong Youp-
dc.contributor.alternativeNameSeong, Jin Sil-
dc.contributor.alternativeNameSong, Si Young-
dc.contributor.alternativeNameYun, Mi Jin-
dc.contributor.alternativeNameLee, Jong Doo-
dc.contributor.alternativeNameCho, Arthur Eung Hyuck-
dc.contributor.affiliatedAuthorPark, Jeong Youp-
dc.contributor.affiliatedAuthorSeong, Jin Sil-
dc.contributor.affiliatedAuthorSong, Si Young-
dc.contributor.affiliatedAuthorYun, Mi Jin-
dc.contributor.affiliatedAuthorLee, Jong Doo-
dc.contributor.affiliatedAuthorCho, Arthur Eung Hyuck-
dc.rights.accessRightsfree-
dc.citation.volume90-
dc.citation.number1-
dc.citation.startPage126-
dc.citation.endPage133-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, Vol.90(1) : 126-133, 2014-
dc.identifier.rimsid55992-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Nuclear Medicine (핵의학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Radiation Oncology (방사선종양학교실) > 1. Journal Papers

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