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Profiling of rectal cancers MRI in pathological complete remission states after neoadjuvant concurrent chemoradiation therapy

DC Field Value Language
dc.contributor.author금웅섭-
dc.contributor.author김한솔-
dc.contributor.author김혜민-
dc.contributor.author김호근-
dc.contributor.author임준석-
dc.contributor.author허혁-
dc.contributor.author김남규-
dc.contributor.author김명진-
dc.date.accessioned2017-02-24T03:30:03Z-
dc.date.available2017-02-24T03:30:03Z-
dc.date.issued2016-
dc.identifier.issn0009-9260-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/146359-
dc.description.abstractAIM: To fully characterise the magnetic resonance imaging (MRI) traits of rectal cancers in a large sample of patients, each experiencing pathological complete remission (pCR) after neoadjuvant concurrent chemoradiation therapy (CCRT). MATERIALS AND METHODS: A total of 120 patients (77 male, 43 female; median age, 59.5 years; range, 32-81 years) with rectal cancers in CCRT-induced pCR states who underwent pre- and post-CCRT MRI and eventual surgery between July, 2005 and September, 2014 were retrospectively reviewed. In most (n=100), diffusion-weighted imaging was also performed. Tumour volume, tumour regression grade (TRG), T-stage, mesorectal fascia (MRF) status, and T2 signal intensity (T2-SI) were analysed. Paired t-test and McNemar's test were applied for statistical comparisons. RESULTS: Tumour volume declined sharply after CCRT (pre-CCRT, 21.5 ± 22.4 cm(3); post-CCRT, 6.6 ± 8.4 cm(3); p<0.001). TRG distribution was as follows: G1 (clinical CR), 3; G2, 38; G3, 78; G4, 1; and G5 (marked progression), 0. Downstaging of T-stage (34%,16/47) and MRF status (19.7%,13/66) did occur; but on post-CCRT MRI, 25.8% (31/120) remained at T3 ≥ 5 mm or T4 stage, and 44.2% (53/120) were MRF-positive. A majority (88.3%, 106/120) of patients displayed intermediate T2-SI prior to CCRT. Most converted to dark T2-SI after CCRT, with 12.5% (15/120) unchanged. On post-CCRT MRI, 11% (11/100) of patients showed diffusion restriction. CONCLUSION: MRI findings in CCRT-induced pCR-status rectal cancers were highly variable. Tumour volume and T2-SI mostly decreased; however, such lesions occasionally presented with unexpected atypical features, such as large residual volume and/or intermediate T2-SI.-
dc.description.statementOfResponsibilityrestriction-
dc.format.extent250~257-
dc.languageEnglish-
dc.publisherBlackwell Scientific Publications Ltd-
dc.relation.isPartOfCLINICAL RADIOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAged, 80 and over-
dc.subject.MESHChemoradiotherapy*-
dc.subject.MESHDiffusion Magnetic Resonance Imaging-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHLymphatic Metastasis-
dc.subject.MESHMagnetic Resonance Imaging/methods*-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHNeoadjuvant Therapy-
dc.subject.MESHNeoplasm Grading-
dc.subject.MESHNeoplasm Staging-
dc.subject.MESHRectal Neoplasms/pathology*-
dc.subject.MESHRectal Neoplasms/therapy*-
dc.subject.MESHRemission Induction-
dc.subject.MESHTreatment Outcome-
dc.subject.MESHTumor Burden-
dc.titleProfiling of rectal cancers MRI in pathological complete remission states after neoadjuvant concurrent chemoradiation therapy-
dc.typeArticle-
dc.publisher.locationEngland-
dc.contributor.collegeCollege of Medicine-
dc.contributor.departmentDept. of Radiation Oncology-
dc.contributor.googleauthorH. Kim-
dc.contributor.googleauthorH.M. Kim-
dc.contributor.googleauthorW.S. Koom-
dc.contributor.googleauthorN.K. Kim-
dc.contributor.googleauthorM.-J. Kim-
dc.contributor.googleauthorH. Hur-
dc.contributor.googleauthorJ.S. Lim-
dc.identifier.doi10.1016/j.crad.2015.11.011-
dc.contributor.localIdA00273-
dc.contributor.localIdA01099-
dc.contributor.localIdA04553-
dc.contributor.localIdA01183-
dc.contributor.localIdA03408-
dc.contributor.localIdA04373-
dc.contributor.localIdA00353-
dc.contributor.localIdA00426-
dc.relation.journalcodeJ00610-
dc.identifier.eissn1365-229X-
dc.identifier.pmid26747329-
dc.identifier.urlhttp://www.sciencedirect.com/science/article/pii/S0009926015004481-
dc.contributor.alternativeNameKoom, Woong Sub-
dc.contributor.alternativeNameKim, Hon Soul-
dc.contributor.alternativeNameKim, Hye Min-
dc.contributor.alternativeNameKim, Ho Keun-
dc.contributor.alternativeNameLim, Joon Seok-
dc.contributor.alternativeNameHur, Hyuk-
dc.contributor.alternativeNameKim, Nam Kyu-
dc.contributor.alternativeNameKim, Myeong Jin-
dc.contributor.affiliatedAuthorKoom, Woong Sub-
dc.contributor.affiliatedAuthorKim, Hon Soul-
dc.contributor.affiliatedAuthorKim, Hye Min-
dc.contributor.affiliatedAuthorKim, Ho Keun-
dc.contributor.affiliatedAuthorLim, Joon Seok-
dc.contributor.affiliatedAuthorHur, Hyuk-
dc.contributor.affiliatedAuthorKim, Nam Kyu-
dc.contributor.affiliatedAuthorKim, Myeong Jin-
dc.citation.volume71-
dc.citation.number3-
dc.citation.startPage250-
dc.citation.endPage257-
dc.identifier.bibliographicCitationCLINICAL RADIOLOGY, Vol.71(3) : 250-257, 2016-
dc.date.modified2017-02-24-
dc.identifier.rimsid47868-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Radiation Oncology (방사선종양학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Radiology (영상의학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Surgery (외과학교실) > 1. Journal Papers

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