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Bone metastases from breast carcinoma: histopathological – radiological correlations and prognostic features

The aim of this study was to identify factors that may be associated with the development of bone metastases in patients with metastatic breast carcinoma and to see if any of these factors had a bearing on subsequent survival. In total, 492 patients presented to the Nottingham City Hospital with met...

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Autores principales: James, J J, Evans, A J, Pinder, S E, Gutteridge, E, Cheung, K L, Chan, S, Robertson, J F R
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2376918/
https://www.ncbi.nlm.nih.gov/pubmed/12915874
http://dx.doi.org/10.1038/sj.bjc.6601198
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author James, J J
Evans, A J
Pinder, S E
Gutteridge, E
Cheung, K L
Chan, S
Robertson, J F R
author_facet James, J J
Evans, A J
Pinder, S E
Gutteridge, E
Cheung, K L
Chan, S
Robertson, J F R
author_sort James, J J
collection PubMed
description The aim of this study was to identify factors that may be associated with the development of bone metastases in patients with metastatic breast carcinoma and to see if any of these factors had a bearing on subsequent survival. In total, 492 patients presented to the Nottingham City Hospital with metastatic breast carcinoma between July 1997 and December 2001. Of these, 267 patients had bone metastases at presentation with metastatic disease, 91 patients in this group had bone as their only site of metastatic disease. Sites of first presentation of metastatic disease were prospectively recorded, as were histological features of the primary tumour (tumour type, histological grade, lymph node stage, tumour size and oestrogen receptor (ER) status). The radiological features of the bone metastases, the metastasis-free interval and serological tumour marker levels at presentation with metastases were all recorded. There was a significant association between the development of bone metastases and lower grade tumours (P=0.019), ER-positive tumours (P<0.0001) and the lymph node stage of the primary tumour (P=0.047). A multivariate analysis found that metastasis-free interval, additional sites of metastatic disease other than bone, ER status and serological tumour marker levels all independently contributed to survival from time of presentation with bone metastases.
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spelling pubmed-23769182009-09-10 Bone metastases from breast carcinoma: histopathological – radiological correlations and prognostic features James, J J Evans, A J Pinder, S E Gutteridge, E Cheung, K L Chan, S Robertson, J F R Br J Cancer Molecular and Cellular Pathology The aim of this study was to identify factors that may be associated with the development of bone metastases in patients with metastatic breast carcinoma and to see if any of these factors had a bearing on subsequent survival. In total, 492 patients presented to the Nottingham City Hospital with metastatic breast carcinoma between July 1997 and December 2001. Of these, 267 patients had bone metastases at presentation with metastatic disease, 91 patients in this group had bone as their only site of metastatic disease. Sites of first presentation of metastatic disease were prospectively recorded, as were histological features of the primary tumour (tumour type, histological grade, lymph node stage, tumour size and oestrogen receptor (ER) status). The radiological features of the bone metastases, the metastasis-free interval and serological tumour marker levels at presentation with metastases were all recorded. There was a significant association between the development of bone metastases and lower grade tumours (P=0.019), ER-positive tumours (P<0.0001) and the lymph node stage of the primary tumour (P=0.047). A multivariate analysis found that metastasis-free interval, additional sites of metastatic disease other than bone, ER status and serological tumour marker levels all independently contributed to survival from time of presentation with bone metastases. Nature Publishing Group 2003-08-18 2003-08-12 /pmc/articles/PMC2376918/ /pubmed/12915874 http://dx.doi.org/10.1038/sj.bjc.6601198 Text en Copyright © 2003 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Molecular and Cellular Pathology
James, J J
Evans, A J
Pinder, S E
Gutteridge, E
Cheung, K L
Chan, S
Robertson, J F R
Bone metastases from breast carcinoma: histopathological – radiological correlations and prognostic features
title Bone metastases from breast carcinoma: histopathological – radiological correlations and prognostic features
title_full Bone metastases from breast carcinoma: histopathological – radiological correlations and prognostic features
title_fullStr Bone metastases from breast carcinoma: histopathological – radiological correlations and prognostic features
title_full_unstemmed Bone metastases from breast carcinoma: histopathological – radiological correlations and prognostic features
title_short Bone metastases from breast carcinoma: histopathological – radiological correlations and prognostic features
title_sort bone metastases from breast carcinoma: histopathological – radiological correlations and prognostic features
topic Molecular and Cellular Pathology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2376918/
https://www.ncbi.nlm.nih.gov/pubmed/12915874
http://dx.doi.org/10.1038/sj.bjc.6601198
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