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Cited 23 time in webofscience Cited 22 time in scopus
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Clinical relevance of lymph node ratio in breast cancer patients with one to three positive lymph nodes

Authors
Kim, S. I.Cho, S-HLee, J. S.Moon, H-GNoh, W. C.Youn, H. J.Ko, B. K.Park, B-W
Issue Date
3-Sep-2013
Publisher
NATURE PUBLISHING GROUP
Keywords
breast neoplasms; lymph node ratio; pN1; prognostic factor; predictive factor; post-mastectomy radiation therapy
Citation
BRITISH JOURNAL OF CANCER, v.109, no.5, pp.1165 - 1171
Journal Title
BRITISH JOURNAL OF CANCER
Volume
109
Number
5
Start Page
1165
End Page
1171
URI
http://scholarworks.bwise.kr/ssu/handle/2018.sw.ssu/11172
DOI
10.1038/bjc.2013.465
ISSN
0007-0920
Abstract
Background: To test the hypotheses that breast cancer patients with one to three positive lymph nodes (pN1) consist of heterogeneous prognostic subsets and that the ratio of positive nodes to total nodes dissected (lymph node ratio, LNR) might discriminate patients with a higher risk as candidates for post-mastectomy radiation therapy (PMRT). Methods: Using information from 7741 node-positive patients, we first identified cutoff values of the LNR using the nonparametric bootstrap method. Focusing on 3477 patients with pN1 disease, we then evaluated the clinical relevance of the LNR categorised by the estimated cutoff values (categorised LNR, cLNR). Results: Among 3477 patients with pN1 disease, 3059 and 418 patients were assigned into the low and intermediate cLNR groups, respectively, based on a cutoff value of 0.18. The prognostic factors associated with poor overall survival (OS) included younger age, T2 stage, negative oestrogen/progesterone receptors, high histologic grade, and intermediate cLNR. Post-mastectomy radiation therapy significantly increased OS in patients assigned to the intermediate cLNR (hazard ratio, 0.39; 95% confidence interval, 0.17-0.89; P = 0.0248), whereas patients in the low cLNR group derived no additional survival benefit from PMRT. Conclusion: This study suggests that PMRT should be recommended for patients with pN1 disease and an intermediate cLNR.
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