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Metastatic progression of breast cancer: insights from 50 years of autopsies

There remain no clear guidelines for the optimal management of patients with metastatic breast cancer. To better understand its natural history, we undertook a detailed examination of 197 autopsies performed on women who died of breast cancer. We reviewed clinical, treatment and pathological aspects...

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Autores principales: Cummings, Margaret C, Simpson, Peter T, Reid, Lynne E, Jayanthan, Janani, Skerman, Joanna, Song, Sarah, McCart Reed, Amy E, Kutasovic, Jamie R, Morey, Adrienne L, Marquart, Louise, O'Rourke, Peter, Lakhani, Sunil R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4288974/
https://www.ncbi.nlm.nih.gov/pubmed/24122263
http://dx.doi.org/10.1002/path.4288
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author Cummings, Margaret C
Simpson, Peter T
Reid, Lynne E
Jayanthan, Janani
Skerman, Joanna
Song, Sarah
McCart Reed, Amy E
Kutasovic, Jamie R
Morey, Adrienne L
Marquart, Louise
O'Rourke, Peter
Lakhani, Sunil R
author_facet Cummings, Margaret C
Simpson, Peter T
Reid, Lynne E
Jayanthan, Janani
Skerman, Joanna
Song, Sarah
McCart Reed, Amy E
Kutasovic, Jamie R
Morey, Adrienne L
Marquart, Louise
O'Rourke, Peter
Lakhani, Sunil R
author_sort Cummings, Margaret C
collection PubMed
description There remain no clear guidelines for the optimal management of patients with metastatic breast cancer. To better understand its natural history, we undertook a detailed examination of 197 autopsies performed on women who died of breast cancer. We reviewed clinical, treatment and pathological aspects of all cases and, additionally, pathological features and biomarker expression (ER, PgR, HER2, EGFR, p53, Ki67, c-Kit, CK AE1/AE3) were assessed in detail for the primary tumour and matched metastases for 55 of the cases. Genomes of the primary tumour and multiple metastases were analysed by array-based comparative genomic hybridization for six cases(##). 945 metastatic deposits were identified, with a median of four/patient. The most common organs involved were lung/pleura (80%), bone (74%), liver (71%) and non-axillary lymph nodes (55%). Major findings included: (a) patients with CNS metastases were more likely to have bone metastases (p < 0.013); (b) younger age was associated with metastasis to the liver (≤ 49 years; p < 0.001) and to gynaecological organs (≤ 49 years; p = 0.001); (c) surgical excision of the primary tumour was associated with metastasis to the liver (p = 0.002); and (d) ER and PgR showed down-regulation during progression in a non-random manner, particularly in lung/pleura (ER; p < 0.001), liver and bone metastases. Genomic analysis revealed DNA copy number variation between the primary tumour and metastases (e.g. amplification of 2q11.2–q12.1 and 10q22.2–q22.3) but little variation between metastases from the same patient. In summary, the association of CNS and bone metastases, liver and gynaecological metastases in young women and the risk of liver metastases following surgery have important implications for the management of patients with breast cancer. Clonal heterogeneity of the primary tumour is important in developing metastatic propensity and the change in tumour phenotype during progression/colonization highlights the importance of sampling metastatic disease for optimal treatment strategies. © 2013 The Authors. Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland.
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spelling pubmed-42889742015-01-20 Metastatic progression of breast cancer: insights from 50 years of autopsies Cummings, Margaret C Simpson, Peter T Reid, Lynne E Jayanthan, Janani Skerman, Joanna Song, Sarah McCart Reed, Amy E Kutasovic, Jamie R Morey, Adrienne L Marquart, Louise O'Rourke, Peter Lakhani, Sunil R J Pathol Original Papers There remain no clear guidelines for the optimal management of patients with metastatic breast cancer. To better understand its natural history, we undertook a detailed examination of 197 autopsies performed on women who died of breast cancer. We reviewed clinical, treatment and pathological aspects of all cases and, additionally, pathological features and biomarker expression (ER, PgR, HER2, EGFR, p53, Ki67, c-Kit, CK AE1/AE3) were assessed in detail for the primary tumour and matched metastases for 55 of the cases. Genomes of the primary tumour and multiple metastases were analysed by array-based comparative genomic hybridization for six cases(##). 945 metastatic deposits were identified, with a median of four/patient. The most common organs involved were lung/pleura (80%), bone (74%), liver (71%) and non-axillary lymph nodes (55%). Major findings included: (a) patients with CNS metastases were more likely to have bone metastases (p < 0.013); (b) younger age was associated with metastasis to the liver (≤ 49 years; p < 0.001) and to gynaecological organs (≤ 49 years; p = 0.001); (c) surgical excision of the primary tumour was associated with metastasis to the liver (p = 0.002); and (d) ER and PgR showed down-regulation during progression in a non-random manner, particularly in lung/pleura (ER; p < 0.001), liver and bone metastases. Genomic analysis revealed DNA copy number variation between the primary tumour and metastases (e.g. amplification of 2q11.2–q12.1 and 10q22.2–q22.3) but little variation between metastases from the same patient. In summary, the association of CNS and bone metastases, liver and gynaecological metastases in young women and the risk of liver metastases following surgery have important implications for the management of patients with breast cancer. Clonal heterogeneity of the primary tumour is important in developing metastatic propensity and the change in tumour phenotype during progression/colonization highlights the importance of sampling metastatic disease for optimal treatment strategies. © 2013 The Authors. Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland. John Wiley & Sons, Ltd 2014-01 2013-12-06 /pmc/articles/PMC4288974/ /pubmed/24122263 http://dx.doi.org/10.1002/path.4288 Text en © 2013 The Authors. Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland. http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Papers
Cummings, Margaret C
Simpson, Peter T
Reid, Lynne E
Jayanthan, Janani
Skerman, Joanna
Song, Sarah
McCart Reed, Amy E
Kutasovic, Jamie R
Morey, Adrienne L
Marquart, Louise
O'Rourke, Peter
Lakhani, Sunil R
Metastatic progression of breast cancer: insights from 50 years of autopsies
title Metastatic progression of breast cancer: insights from 50 years of autopsies
title_full Metastatic progression of breast cancer: insights from 50 years of autopsies
title_fullStr Metastatic progression of breast cancer: insights from 50 years of autopsies
title_full_unstemmed Metastatic progression of breast cancer: insights from 50 years of autopsies
title_short Metastatic progression of breast cancer: insights from 50 years of autopsies
title_sort metastatic progression of breast cancer: insights from 50 years of autopsies
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4288974/
https://www.ncbi.nlm.nih.gov/pubmed/24122263
http://dx.doi.org/10.1002/path.4288
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