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Published in: Breast Cancer Research and Treatment 3/2013

01-02-2013 | Clinical Trial

Which nomogram is best for predicting non-sentinel lymph node metastasis in breast cancer patients? A meta-analysis

Authors: Liling Zhu, Liang Jin, Shunrong Li, Kai Chen, Weijuan Jia, Quanyuan Shan, Stephen Walter, Erwei Song, Fengxi Su

Published in: Breast Cancer Research and Treatment | Issue 3/2013

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Abstract

To present a systemic review and meta-analysis to evaluate the nomograms developed to predict non-sentinel lymph node (NSLN) metastasis in breast cancer patients. We focused on the six nomograms (Cambridge, MSKCC, Mayo, MDA, Tenon, and Stanford) that are the most widely validated. The AUCs were converted to odds ratios for the meta-analysis. In total, the Cambridge, Mayo, MDA, MSKCC, Stanford, and Tenon models were validated in 2,156, 2,431, 843, 8,143, 3,700, and 3,648 patients, respectively. The pooled AUCs for the Cambridge, MDA, MSKCC, Mayo, Tenon, and Stanford models were 0.721, 0.706, 0.715, 0.728, 0.720, and 0.688, respectively. Subgroup analysis revealed that in populations with a higher micrometastasis rate in the SLNs, the Tenon and Stanford models had a significantly higher predictive accuracy. A meta-regression analysis revealed that the SLN micrometastasis rate, but not the NSLN-positivity rate, was associated with improved predictive accuracy in the Tenon and Stanford models. The performance of the MSKCC and Cambridge models was not influenced by these two factors. All of these prediction models perform better than random chance. The Stanford model seems to be relatively inferior to the other models. The accuracy of the Tenon and Stanford models is influenced by the tumor burden in the SLNs.
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Metadata
Title
Which nomogram is best for predicting non-sentinel lymph node metastasis in breast cancer patients? A meta-analysis
Authors
Liling Zhu
Liang Jin
Shunrong Li
Kai Chen
Weijuan Jia
Quanyuan Shan
Stephen Walter
Erwei Song
Fengxi Su
Publication date
01-02-2013
Publisher
Springer US
Published in
Breast Cancer Research and Treatment / Issue 3/2013
Print ISSN: 0167-6806
Electronic ISSN: 1573-7217
DOI
https://doi.org/10.1007/s10549-012-2360-6

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