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dc.contributor.author김규보*
dc.date.accessioned2018-12-07T16:30:22Z-
dc.date.available2018-12-07T16:30:22Z-
dc.date.issued2017*
dc.identifier.issn1949-2553*
dc.identifier.otherOAK-21351*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/247291-
dc.description.abstractPurpose: This study was conducted to evaluate the impact of radiation dose after margin involved resection in patients with extrahepatic bile duct cancer. Methods: Among the 251 patients who underwent curative resection followed by adjuvant chemoradiotherapy, 86 patients had either invasive carcinoma (n = 63) or carcinoma in situ (n = 23) at the resected margin. Among them, 54 patients received conventional radiation dose (40-50.4 Gy) and 32 patients received escalated radiation dose (54-56 Gy). Results: Escalated radiation dose was associated with improved locoregional control (5yr rate, 73.8% vs. 47.1%, p = 0.069), but not disease-free survival (5yr rate, 43.4% vs. 32.6%, p = 0.490) and overall survival (5yr rate, 40.6% vs. 29.6%, p = 0.348). In multivariate analysis for locoregional control, invasive carcinoma at the margin (HR 2.957, p = 0.032) and escalated radiation dose (HR 0.394, p = 0.047) were independent prognostic factors. No additional gastrointestinal toxicity was observed in escalated dose group. Conclusions: Delivery of radiation dose ≥ 54 Gy was well tolerated and associated with improved locoregional control, but not with overall survival after margin involved resection. Further validation study is warranted. © Kim et al.*
dc.languageEnglish*
dc.publisherImpact Journals LLC*
dc.subjectExtrahepatic bile duct cancer*
dc.subjectPostoperative radiotherapy*
dc.subjectR1 resection*
dc.subjectRadiation dose*
dc.titleImpact of radiation dose in postoperative radiotherapy after R1 resection for extrahepatic bile duct cancer: Long term results from a single institution*
dc.typeArticle*
dc.relation.issue44*
dc.relation.volume8*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage78076*
dc.relation.lastpage78085*
dc.relation.journaltitleOncotarget*
dc.identifier.doi10.18632/oncotarget.17368*
dc.identifier.wosidWOS:000412066700182*
dc.identifier.scopusid2-s2.0-85030315119*
dc.author.googleKim B.H.*
dc.author.googleChie E.K.*
dc.author.googleKim K.*
dc.author.googleJang J.-Y.*
dc.author.googleKim S.W.*
dc.author.googleOh D.-Y.*
dc.author.googleBang Y.-J.*
dc.author.googleHa S.W.*
dc.contributor.scopusid김규보(8213302900)*
dc.date.modifydate20240222162403*


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