Cited 5 times in
Profiling of rectal cancers MRI in pathological complete remission states after neoadjuvant concurrent chemoradiation therapy
DC Field | Value | Language |
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dc.contributor.author | 금웅섭 | - |
dc.contributor.author | 김한솔 | - |
dc.contributor.author | 김혜민 | - |
dc.contributor.author | 김호근 | - |
dc.contributor.author | 임준석 | - |
dc.contributor.author | 허혁 | - |
dc.contributor.author | 김남규 | - |
dc.contributor.author | 김명진 | - |
dc.date.accessioned | 2017-02-24T03:30:03Z | - |
dc.date.available | 2017-02-24T03:30:03Z | - |
dc.date.issued | 2016 | - |
dc.identifier.issn | 0009-9260 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/146359 | - |
dc.description.abstract | AIM: 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.statementOfResponsibility | restriction | - |
dc.format.extent | 250~257 | - |
dc.language | English | - |
dc.publisher | Blackwell Scientific Publications Ltd | - |
dc.relation.isPartOf | CLINICAL RADIOLOGY | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Aged | - |
dc.subject.MESH | Aged, 80 and over | - |
dc.subject.MESH | Chemoradiotherapy* | - |
dc.subject.MESH | Diffusion Magnetic Resonance Imaging | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Lymphatic Metastasis | - |
dc.subject.MESH | Magnetic Resonance Imaging/methods* | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Neoadjuvant Therapy | - |
dc.subject.MESH | Neoplasm Grading | - |
dc.subject.MESH | Neoplasm Staging | - |
dc.subject.MESH | Rectal Neoplasms/pathology* | - |
dc.subject.MESH | Rectal Neoplasms/therapy* | - |
dc.subject.MESH | Remission Induction | - |
dc.subject.MESH | Treatment Outcome | - |
dc.subject.MESH | Tumor Burden | - |
dc.title | Profiling of rectal cancers MRI in pathological complete remission states after neoadjuvant concurrent chemoradiation therapy | - |
dc.type | Article | - |
dc.publisher.location | England | - |
dc.contributor.college | College of Medicine | - |
dc.contributor.department | Dept. of Radiation Oncology | - |
dc.contributor.googleauthor | H. Kim | - |
dc.contributor.googleauthor | H.M. Kim | - |
dc.contributor.googleauthor | W.S. Koom | - |
dc.contributor.googleauthor | N.K. Kim | - |
dc.contributor.googleauthor | M.-J. Kim | - |
dc.contributor.googleauthor | H. Hur | - |
dc.contributor.googleauthor | J.S. Lim | - |
dc.identifier.doi | 10.1016/j.crad.2015.11.011 | - |
dc.contributor.localId | A00273 | - |
dc.contributor.localId | A01099 | - |
dc.contributor.localId | A04553 | - |
dc.contributor.localId | A01183 | - |
dc.contributor.localId | A03408 | - |
dc.contributor.localId | A04373 | - |
dc.contributor.localId | A00353 | - |
dc.contributor.localId | A00426 | - |
dc.relation.journalcode | J00610 | - |
dc.identifier.eissn | 1365-229X | - |
dc.identifier.pmid | 26747329 | - |
dc.identifier.url | http://www.sciencedirect.com/science/article/pii/S0009926015004481 | - |
dc.contributor.alternativeName | Koom, Woong Sub | - |
dc.contributor.alternativeName | Kim, Hon Soul | - |
dc.contributor.alternativeName | Kim, Hye Min | - |
dc.contributor.alternativeName | Kim, Ho Keun | - |
dc.contributor.alternativeName | Lim, Joon Seok | - |
dc.contributor.alternativeName | Hur, Hyuk | - |
dc.contributor.alternativeName | Kim, Nam Kyu | - |
dc.contributor.alternativeName | Kim, Myeong Jin | - |
dc.contributor.affiliatedAuthor | Koom, Woong Sub | - |
dc.contributor.affiliatedAuthor | Kim, Hon Soul | - |
dc.contributor.affiliatedAuthor | Kim, Hye Min | - |
dc.contributor.affiliatedAuthor | Kim, Ho Keun | - |
dc.contributor.affiliatedAuthor | Lim, Joon Seok | - |
dc.contributor.affiliatedAuthor | Hur, Hyuk | - |
dc.contributor.affiliatedAuthor | Kim, Nam Kyu | - |
dc.contributor.affiliatedAuthor | Kim, Myeong Jin | - |
dc.citation.volume | 71 | - |
dc.citation.number | 3 | - |
dc.citation.startPage | 250 | - |
dc.citation.endPage | 257 | - |
dc.identifier.bibliographicCitation | CLINICAL RADIOLOGY, Vol.71(3) : 250-257, 2016 | - |
dc.date.modified | 2017-02-24 | - |
dc.identifier.rimsid | 47868 | - |
dc.type.rims | ART | - |
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