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dc.contributor.author김규보*
dc.contributor.author박경란*
dc.date.accessioned2018-12-07T16:30:20Z-
dc.date.available2018-12-07T16:30:20Z-
dc.date.issued2017*
dc.identifier.issn1598-2998*
dc.identifier.otherOAK-21498*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/247281-
dc.description.abstractPurpose The purpose of this study was to evaluate the impact of postmastectomy radiotherapy (PMRT) on loco-regional recurrence-free survival (LRRFS), disease-free survival (DFS), and overall survival (OS) in pT1-2N1 patients treated with taxane-based chemotherapy. Materials and Methods We retrospectively reviewed the medical data of pathological N1 patients who were treated with modified radical mastectomy and adjuvant taxane-based chemotherapy in 12 hospitals between January 2006 and December 2010. Results We identified 714 consecutive patients. The median follow-up duration was 69 months (range, 1 to 114 months) and the 5-year LRRFS, DFS, and OS rates were 97%, 94%, and 98%, respectively, in patients who received PMRT (PMRT [+]). The corresponding figures were 96%, 90%, and 96%, respectively, in patients who did not receive PMRT (PMRT [-]). PMRT had no significant impact on survival. Upon multivariable analysis, only the histological grade (HG) was statistically significant as a prognostic factor for LRRFS and DFS. In a subgroup analysis of HG 3 patients, PMRT (+) showed better DFS (p=0.081). Conclusion PMRT had no significant impact on LRRFS, DFS, or OS in pT1-2N1 patients treated with taxane- based chemotherapy. PMRT showed a marginal benefit for DFS in HG 3 patients. Randomized studies are needed to confirm the benefit of PMRT in high risk patients, such as those with HG 3. © 2017 by the Korean Cancer Association.*
dc.languageEnglish*
dc.publisherKorean Cancer Association*
dc.subjectBreast neoplasms*
dc.subjectDisease-free survival*
dc.subjectRadiotherapy*
dc.subjectRecurrence*
dc.subjectSurvival*
dc.subjectTaxane*
dc.titlePostmastectomy radiotherapy in patients with pT1-2N1 breast cancer treated with taxane-based chemotherapy: A retrospective multicenter analysis (KROG 1418)*
dc.typeArticle*
dc.relation.issue4*
dc.relation.volume49*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.indexKCI*
dc.relation.startpage927*
dc.relation.lastpage936*
dc.relation.journaltitleCancer Research and Treatment*
dc.identifier.doi10.4143/crt.2016.508*
dc.identifier.wosidWOS:000413001500008*
dc.identifier.scopusid2-s2.0-85030762872*
dc.author.googleKim Y.-J.*
dc.author.googlePark W.*
dc.author.googleHa B.*
dc.author.googlePark B.*
dc.author.googleJoo J.*
dc.author.googleKim T.H.*
dc.author.googlePark I.H.*
dc.author.googleLee K.S.*
dc.author.googleLee E.S.*
dc.author.googleShin K.H.*
dc.author.googleKim H.*
dc.author.googleYu J.I.*
dc.author.googleChoi D.H.*
dc.author.googleHuh S.J.*
dc.author.googleWee C.W.*
dc.author.googleKim K.*
dc.author.googlePark K.R.*
dc.author.googleKim Y.B.*
dc.author.googleAhn S.J.*
dc.author.googleLee J.H.*
dc.author.googleKim J.H.*
dc.author.googleChun M.*
dc.author.googleLee H.-S.*
dc.author.googleKim J.S.*
dc.author.googleCha J.*
dc.contributor.scopusid김규보(8213302900)*
dc.contributor.scopusid박경란(14040340300;57203047823;57207108839;57308917900)*
dc.date.modifydate20240222162403*
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