Email updates

Keep up to date with the latest news and content from BMC Cancer and BioMed Central.

Open Access Highly Accessed Research article

New models and online calculator for predicting non-sentinel lymph node status in sentinel lymph node positive breast cancer patients

Holbrook E Kohrt1, Richard A Olshen23, Honnie R Bermas4, William H Goodson5, Douglas J Wood2, Solomon Henry2, Robert V Rouse6, Lisa Bailey7, Vicki J Philben8, Frederick M Dirbas9, Jocelyn J Dunn9, Denise L Johnson9, Irene L Wapnir9, Robert W Carlson1, Frank E Stockdale1, Nora M Hansen4, Stefanie S Jeffrey9* and The Bay Area SLN Study

Author Affiliations

1 Department of Medicine, Stanford University School of Medicine, Stanford, CA, USA

2 Department of Health Research and Policy-Biostatistics, Stanford University School of Medicine, Stanford, CA, USA

3 Departments of Statistics and Electrical Engineering, Stanford University, Stanford, CA, USA

4 Department of Surgery, Northwestern University Feinberg School of Medicine and Lynn Sage Comprehensive Breast Center, Northwestern Memorial Hospital, Chicago, IL, USA

5 Department of Surgery, California Pacific Medical Center, San Francisco, CA, USA

6 Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA

7 Department of Surgery, Alta Bates Summit Medical Center, Berkeley, CA, USA

8 Department of Surgery, Mercy Medical Center, Redding, CA, USA

9 Department of Surgery, Stanford University School of Medicine, Stanford, CA, USA

For all author emails, please log on.

BMC Cancer 2008, 8:66  doi:10.1186/1471-2407-8-66

Published: 4 March 2008

Abstract

Background

Current practice is to perform a completion axillary lymph node dissection (ALND) for breast cancer patients with tumor-involved sentinel lymph nodes (SLNs), although fewer than half will have non-sentinel node (NSLN) metastasis. Our goal was to develop new models to quantify the risk of NSLN metastasis in SLN-positive patients and to compare predictive capabilities to another widely used model.

Methods

We constructed three models to predict NSLN status: recursive partitioning with receiver operating characteristic curves (RP-ROC), boosted Classification and Regression Trees (CART), and multivariate logistic regression (MLR) informed by CART. Data were compiled from a multicenter Northern California and Oregon database of 784 patients who prospectively underwent SLN biopsy and completion ALND. We compared the predictive abilities of our best model and the Memorial Sloan-Kettering Breast Cancer Nomogram (Nomogram) in our dataset and an independent dataset from Northwestern University.

Results

285 patients had positive SLNs, of which 213 had known angiolymphatic invasion status and 171 had complete pathologic data including hormone receptor status. 264 (93%) patients had limited SLN disease (micrometastasis, 70%, or isolated tumor cells, 23%). 101 (35%) of all SLN-positive patients had tumor-involved NSLNs. Three variables (tumor size, angiolymphatic invasion, and SLN metastasis size) predicted risk in all our models. RP-ROC and boosted CART stratified patients into four risk levels. MLR informed by CART was most accurate. Using two composite predictors calculated from three variables, MLR informed by CART was more accurate than the Nomogram computed using eight predictors. In our dataset, area under ROC curve (AUC) was 0.83/0.85 for MLR (n = 213/n = 171) and 0.77 for Nomogram (n = 171). When applied to an independent dataset (n = 77), AUC was 0.74 for our model and 0.62 for Nomogram. The composite predictors in our model were the product of angiolymphatic invasion and size of SLN metastasis, and the product of tumor size and square of SLN metastasis size.

Conclusion

We present a new model developed from a community-based SLN database that uses only three rather than eight variables to achieve higher accuracy than the Nomogram for predicting NSLN status in two different datasets.