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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd
2014
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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. |
format | Online Article Text |
id | pubmed-4288974 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | John Wiley & Sons, Ltd |
record_format | MEDLINE/PubMed |
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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