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A preoperative nomogram to predict the risk of synchronous distant metastases at diagnosis of primary breast cancer
BACKGROUND: The detection of synchronous metastases at primary diagnosis of breast cancer (BC) affects its initial management. A risk calculator that incorporates many factors to evaluate an individual's risk of harbouring synchronous metastases would be useful to adapt cancer management. PATIE...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4366891/ https://www.ncbi.nlm.nih.gov/pubmed/25668007 http://dx.doi.org/10.1038/bjc.2015.34 |
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author | Boutros, C Mazouni, C Lerebours, F Stevens, D Lei, X Gonzalez-Angulo, A M Delaloge, S |
author_facet | Boutros, C Mazouni, C Lerebours, F Stevens, D Lei, X Gonzalez-Angulo, A M Delaloge, S |
author_sort | Boutros, C |
collection | PubMed |
description | BACKGROUND: The detection of synchronous metastases at primary diagnosis of breast cancer (BC) affects its initial management. A risk calculator that incorporates many factors to evaluate an individual's risk of harbouring synchronous metastases would be useful to adapt cancer management. PATIENTS AND METHODS: Patients with primary diagnosis of BC were identified from three institutional databases sharing homogeneous work-up recommendations. A risk score for synchronous metastases was estimated and a nomogram was constructed using the first database. Its performance was assessed by receiver characteristic (ROC) analysis. The nomogram was externally validated in the two independent cohorts. RESULTS: A preoperative nomogram based on the clinical tumour size (P<0.001), clinical nodal status (P<0.001), oestrogen (P=0.17) and progesterone receptors (P=0.04) was developed. The nomogram accuracy was 87.3% (95% confidence interval (CI), 84.45–90.2%). Overall, the area under the ROC curve (AUC) was 86.1% for the validation set from the Institut Curie-René Huguenin, and 63.8% for the MD Anderson validation set. The negative predictive value (NPV) was high in the three cohorts (97–99%). CONCLUSIONS: We developed and validated a strong metastasis risk calculator that can evaluate with high accuracy an individual's risk of harbouring synchronous metastases at diagnosis of primary BC. CONDENSED ABSTRACT: A nomogram to predict synchronous metastases at diagnosis of breast cancer was developed and externally validated. This tool allows avoiding unnecessary expensive work-up. |
format | Online Article Text |
id | pubmed-4366891 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-43668912016-03-17 A preoperative nomogram to predict the risk of synchronous distant metastases at diagnosis of primary breast cancer Boutros, C Mazouni, C Lerebours, F Stevens, D Lei, X Gonzalez-Angulo, A M Delaloge, S Br J Cancer Clinical Study BACKGROUND: The detection of synchronous metastases at primary diagnosis of breast cancer (BC) affects its initial management. A risk calculator that incorporates many factors to evaluate an individual's risk of harbouring synchronous metastases would be useful to adapt cancer management. PATIENTS AND METHODS: Patients with primary diagnosis of BC were identified from three institutional databases sharing homogeneous work-up recommendations. A risk score for synchronous metastases was estimated and a nomogram was constructed using the first database. Its performance was assessed by receiver characteristic (ROC) analysis. The nomogram was externally validated in the two independent cohorts. RESULTS: A preoperative nomogram based on the clinical tumour size (P<0.001), clinical nodal status (P<0.001), oestrogen (P=0.17) and progesterone receptors (P=0.04) was developed. The nomogram accuracy was 87.3% (95% confidence interval (CI), 84.45–90.2%). Overall, the area under the ROC curve (AUC) was 86.1% for the validation set from the Institut Curie-René Huguenin, and 63.8% for the MD Anderson validation set. The negative predictive value (NPV) was high in the three cohorts (97–99%). CONCLUSIONS: We developed and validated a strong metastasis risk calculator that can evaluate with high accuracy an individual's risk of harbouring synchronous metastases at diagnosis of primary BC. CONDENSED ABSTRACT: A nomogram to predict synchronous metastases at diagnosis of breast cancer was developed and externally validated. This tool allows avoiding unnecessary expensive work-up. Nature Publishing Group 2015-03-17 2015-02-10 /pmc/articles/PMC4366891/ /pubmed/25668007 http://dx.doi.org/10.1038/bjc.2015.34 Text en Copyright © 2015 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Clinical Study Boutros, C Mazouni, C Lerebours, F Stevens, D Lei, X Gonzalez-Angulo, A M Delaloge, S A preoperative nomogram to predict the risk of synchronous distant metastases at diagnosis of primary breast cancer |
title | A preoperative nomogram to predict the risk of synchronous distant metastases at diagnosis of primary breast cancer |
title_full | A preoperative nomogram to predict the risk of synchronous distant metastases at diagnosis of primary breast cancer |
title_fullStr | A preoperative nomogram to predict the risk of synchronous distant metastases at diagnosis of primary breast cancer |
title_full_unstemmed | A preoperative nomogram to predict the risk of synchronous distant metastases at diagnosis of primary breast cancer |
title_short | A preoperative nomogram to predict the risk of synchronous distant metastases at diagnosis of primary breast cancer |
title_sort | preoperative nomogram to predict the risk of synchronous distant metastases at diagnosis of primary breast cancer |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4366891/ https://www.ncbi.nlm.nih.gov/pubmed/25668007 http://dx.doi.org/10.1038/bjc.2015.34 |
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