TY - JOUR
T1 - Development of nomograms to predict axillary lymph node status in breast cancer patients
AU - Chen, Kai
AU - Liu, Jieqiong
AU - Li, Shunrong
AU - Jacobs, Lisa
N1 - Funding Information:
The data used in the study was derived from a de-identified NCDB. The American College of Surgeons and the Commission on Cancer have not verified and are not responsible for the analytic or statistical methodology used or the conclusions drawn from these data by the investigator. This study was supported by the National Natural Science Foundation of China (Grant # 81402201, Grant # 81602673), and Grant [2013] 163 from the Key Laboratory of Malignant Tumor Molecular Mechanism and Translational Medicine of Guangzhou Bureau of Science and Information Technology.
Funding Information:
This study was supported by the National Natural Science Foundation of China (Grant # 81402201/81372817) and Grant [2013] 163 from Key Laboratory of Malignant Tumor Molecular Mechanism and Translational Medicine of Guangzhou Bureau of Science and Information Technology. All of the funding bodies did not have a role in the design of the study and data collection or analysis. Also they did not have a role in the interpretation of the data. The funding bodies supported the travel of the author (Kai Chen) to US to meet with Lisa Jacobs for discussion over this manuscript. Also, the funding bodies support the expense of the language editting of this manuscript, and the working allowance for the authors (Kai Chen, Jieqiong Liu and Shunrong Li).
Publisher Copyright:
© 2017 The Author(s).
PY - 2017/8/23
Y1 - 2017/8/23
N2 - Background: Prediction of axillary lymph node (ALN) status preoperatively is critical in the management of breast cancer patients. This study aims to develop a new set of nomograms to accurately predict ALN status. Methods: We searched the National Cancer Database to identify eligible female breast cancer patients with profiles containing critical information. Patients diagnosed in 2010-2011 and 2012-2013 were designated the training (n=99,618) and validation (n=101,834) cohorts, respectively. We used binary logistic regression to investigate risk factors for ALN status and to develop a new set of nomograms to determine the probability of having any positive ALNs and N2-3 disease. We used ROC analysis and calibration plots to assess the discriminative ability and accuracy of the nomograms, respectively. Results: In the training cohort, we identified age, quadrant of the tumor, tumor size, histology, ER, PR, HER2, tumor grade and lymphovascular invasion as significant predictors of ALNs status. Nomogram-A was developed to predict the probability of having any positive ALNs (P_any) in the full population with a C-index of 0.788 and 0.786 in the training and validation cohorts, respectively. In patients with positive ALNs, Nomogram-B was developed to predict the conditional probability of having N2-3 disease (P_con) with a C-index of 0.680 and 0.677 in the training and validation cohorts, respectively. The absolute probability of having N2-3 disease can be estimated by P_any*P_con. Both of the nomograms were well-calibrated. Conclusions: We developed a set of nomograms to predict the ALN status in breast cancer patients.
AB - Background: Prediction of axillary lymph node (ALN) status preoperatively is critical in the management of breast cancer patients. This study aims to develop a new set of nomograms to accurately predict ALN status. Methods: We searched the National Cancer Database to identify eligible female breast cancer patients with profiles containing critical information. Patients diagnosed in 2010-2011 and 2012-2013 were designated the training (n=99,618) and validation (n=101,834) cohorts, respectively. We used binary logistic regression to investigate risk factors for ALN status and to develop a new set of nomograms to determine the probability of having any positive ALNs and N2-3 disease. We used ROC analysis and calibration plots to assess the discriminative ability and accuracy of the nomograms, respectively. Results: In the training cohort, we identified age, quadrant of the tumor, tumor size, histology, ER, PR, HER2, tumor grade and lymphovascular invasion as significant predictors of ALNs status. Nomogram-A was developed to predict the probability of having any positive ALNs (P_any) in the full population with a C-index of 0.788 and 0.786 in the training and validation cohorts, respectively. In patients with positive ALNs, Nomogram-B was developed to predict the conditional probability of having N2-3 disease (P_con) with a C-index of 0.680 and 0.677 in the training and validation cohorts, respectively. The absolute probability of having N2-3 disease can be estimated by P_any*P_con. Both of the nomograms were well-calibrated. Conclusions: We developed a set of nomograms to predict the ALN status in breast cancer patients.
KW - Breast cancer
KW - Lymph node status
KW - Nomogram
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U2 - 10.1186/s12885-017-3535-7
DO - 10.1186/s12885-017-3535-7
M3 - Article
C2 - 28835223
AN - SCOPUS:85028305149
SN - 1471-2407
VL - 17
JO - BMC cancer
JF - BMC cancer
IS - 1
M1 - 561
ER -