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Nomograms predicting survival for all four subtypes of breast cancer: a SEER-based population study

BACKGROUND: The prognosis of female breast cancer (BC) patients is determined by many clinicopathological factors. In this study, we aimed to identify prognostic factors for BC and develop reliable nomograms to predict the 1-, 3-, and 5-year overall survival (OS) and breast cancer-specific survival...

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Autores principales: Chu, Jianli, Yang, Dehong, Wang, Ling, Xia, Jielai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7214914/
https://www.ncbi.nlm.nih.gov/pubmed/32411767
http://dx.doi.org/10.21037/atm-20-2808
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author Chu, Jianli
Yang, Dehong
Wang, Ling
Xia, Jielai
author_facet Chu, Jianli
Yang, Dehong
Wang, Ling
Xia, Jielai
author_sort Chu, Jianli
collection PubMed
description BACKGROUND: The prognosis of female breast cancer (BC) patients is determined by many clinicopathological factors. In this study, we aimed to identify prognostic factors for BC and develop reliable nomograms to predict the 1-, 3-, and 5-year overall survival (OS) and breast cancer-specific survival (BCSS). METHODS: The Surveillance, Epidemiology, and End Results (SEER) database was used to screen 227,989 eligible patients as the study cohort. The whole cohort was randomly divided into a training cohort (n=113,996) and a testing cohort (n=113,993). The log-rank test and Cox proportional hazards analysis were applied to select variables and build nomogram models based on the training cohort. Internal and external validation were performed to evaluate the performance of the models by calculating the C-index and generating calibration plots in the training cohort and testing cohort. RESULTS: The following factors were included in both the OS and BCSS nomograms: subtypes of BC, metastasis (bone, liver, lung, and brain), age at diagnosis, race, tumor size, grade, number of positive lymph nodes, and marital status. The calibration plots presented excellent consistency between the actual and nomogram-predicted survival probabilities in both the training cohort and testing cohort. The C-index values of the nomograms were 0.796 and 0.793 for OS and 0.856 and 0.853 for BCSS in the training and testing cohorts, respectively. CONCLUSIONS: The established nomograms provide a visualization of the risk of each prognostic factor and can assist clinicians in predicting the 1-, 3-, and 5-year OS and BCSS for all 4 subtypes of BC.
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spelling pubmed-72149142020-05-14 Nomograms predicting survival for all four subtypes of breast cancer: a SEER-based population study Chu, Jianli Yang, Dehong Wang, Ling Xia, Jielai Ann Transl Med Original Article BACKGROUND: The prognosis of female breast cancer (BC) patients is determined by many clinicopathological factors. In this study, we aimed to identify prognostic factors for BC and develop reliable nomograms to predict the 1-, 3-, and 5-year overall survival (OS) and breast cancer-specific survival (BCSS). METHODS: The Surveillance, Epidemiology, and End Results (SEER) database was used to screen 227,989 eligible patients as the study cohort. The whole cohort was randomly divided into a training cohort (n=113,996) and a testing cohort (n=113,993). The log-rank test and Cox proportional hazards analysis were applied to select variables and build nomogram models based on the training cohort. Internal and external validation were performed to evaluate the performance of the models by calculating the C-index and generating calibration plots in the training cohort and testing cohort. RESULTS: The following factors were included in both the OS and BCSS nomograms: subtypes of BC, metastasis (bone, liver, lung, and brain), age at diagnosis, race, tumor size, grade, number of positive lymph nodes, and marital status. The calibration plots presented excellent consistency between the actual and nomogram-predicted survival probabilities in both the training cohort and testing cohort. The C-index values of the nomograms were 0.796 and 0.793 for OS and 0.856 and 0.853 for BCSS in the training and testing cohorts, respectively. CONCLUSIONS: The established nomograms provide a visualization of the risk of each prognostic factor and can assist clinicians in predicting the 1-, 3-, and 5-year OS and BCSS for all 4 subtypes of BC. AME Publishing Company 2020-04 /pmc/articles/PMC7214914/ /pubmed/32411767 http://dx.doi.org/10.21037/atm-20-2808 Text en 2020 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Chu, Jianli
Yang, Dehong
Wang, Ling
Xia, Jielai
Nomograms predicting survival for all four subtypes of breast cancer: a SEER-based population study
title Nomograms predicting survival for all four subtypes of breast cancer: a SEER-based population study
title_full Nomograms predicting survival for all four subtypes of breast cancer: a SEER-based population study
title_fullStr Nomograms predicting survival for all four subtypes of breast cancer: a SEER-based population study
title_full_unstemmed Nomograms predicting survival for all four subtypes of breast cancer: a SEER-based population study
title_short Nomograms predicting survival for all four subtypes of breast cancer: a SEER-based population study
title_sort nomograms predicting survival for all four subtypes of breast cancer: a seer-based population study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7214914/
https://www.ncbi.nlm.nih.gov/pubmed/32411767
http://dx.doi.org/10.21037/atm-20-2808
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