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Characterization of bone only metastasis patients with respect to tumor subtypes

Metastatic breast cancer (MBC) patients with bone only metastasis (BOM) are a unique population with limited characterization. We identified patients followed at MD Anderson Cancer Center from 01/01/1997 to 12/31/2015 for at least 6 months with a BOM diagnosis as first site of metastasis. Tumor subt...

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Autores principales: Parkes, Amanda, Clifton, Katherine, Al-Awadhi, Aydah, Oke, Oluchi, Warneke, Carla L., Litton, Jennifer K., Hortobagyi, Gabriel N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5785511/
https://www.ncbi.nlm.nih.gov/pubmed/29387785
http://dx.doi.org/10.1038/s41523-018-0054-x
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author Parkes, Amanda
Clifton, Katherine
Al-Awadhi, Aydah
Oke, Oluchi
Warneke, Carla L.
Litton, Jennifer K.
Hortobagyi, Gabriel N.
author_facet Parkes, Amanda
Clifton, Katherine
Al-Awadhi, Aydah
Oke, Oluchi
Warneke, Carla L.
Litton, Jennifer K.
Hortobagyi, Gabriel N.
author_sort Parkes, Amanda
collection PubMed
description Metastatic breast cancer (MBC) patients with bone only metastasis (BOM) are a unique population with limited characterization. We identified patients followed at MD Anderson Cancer Center from 01/01/1997 to 12/31/2015 for at least 6 months with a BOM diagnosis as first site of metastasis. Tumor subtype (TS) was assessed by initial breast biopsy immunohistochemistry using hormonal receptor (HR) and HER2 status, with four subtypes identified: HR+/HER2−, HR+/HER2+, HR−/HER2−, HR−/HER2+. HR+ was defined as estrogen receptor or progesterone receptor ≥1%. We identified 1445 patients with BOM, 1048 with TS data available. Among these patients, the majority were HR+/HER2− (78%). Median time from breast cancer diagnosis to first bone metastasis was 2.3 years (95% CI 2.1, 2.5) and varied significantly by TS, with longer time to distant disease in HR+/HER2− patients relative to all other TS (p < .0001). Median overall survival (OS) from breast cancer diagnosis was 8.7 years (95% CI 8.0, 9.7) and varied significantly by TS with poorer OS for HR−/HER2− and HR-/HER2+ patients relative to HR+/HER2− TS (p < .0001). The 442 patients with de novo BOM disease, defined as bone metastasis diagnosis within 4 months of breast cancer diagnosis, had significantly shorter OS (p < .0001). Overall, several higher risk BOM subsets were identified in this analysis, most notably HR−/HER2+ and HR−/HER2− TS and de novo BOM patients.
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spelling pubmed-57855112018-01-31 Characterization of bone only metastasis patients with respect to tumor subtypes Parkes, Amanda Clifton, Katherine Al-Awadhi, Aydah Oke, Oluchi Warneke, Carla L. Litton, Jennifer K. Hortobagyi, Gabriel N. NPJ Breast Cancer Article Metastatic breast cancer (MBC) patients with bone only metastasis (BOM) are a unique population with limited characterization. We identified patients followed at MD Anderson Cancer Center from 01/01/1997 to 12/31/2015 for at least 6 months with a BOM diagnosis as first site of metastasis. Tumor subtype (TS) was assessed by initial breast biopsy immunohistochemistry using hormonal receptor (HR) and HER2 status, with four subtypes identified: HR+/HER2−, HR+/HER2+, HR−/HER2−, HR−/HER2+. HR+ was defined as estrogen receptor or progesterone receptor ≥1%. We identified 1445 patients with BOM, 1048 with TS data available. Among these patients, the majority were HR+/HER2− (78%). Median time from breast cancer diagnosis to first bone metastasis was 2.3 years (95% CI 2.1, 2.5) and varied significantly by TS, with longer time to distant disease in HR+/HER2− patients relative to all other TS (p < .0001). Median overall survival (OS) from breast cancer diagnosis was 8.7 years (95% CI 8.0, 9.7) and varied significantly by TS with poorer OS for HR−/HER2− and HR-/HER2+ patients relative to HR+/HER2− TS (p < .0001). The 442 patients with de novo BOM disease, defined as bone metastasis diagnosis within 4 months of breast cancer diagnosis, had significantly shorter OS (p < .0001). Overall, several higher risk BOM subsets were identified in this analysis, most notably HR−/HER2+ and HR−/HER2− TS and de novo BOM patients. Nature Publishing Group UK 2018-01-25 /pmc/articles/PMC5785511/ /pubmed/29387785 http://dx.doi.org/10.1038/s41523-018-0054-x Text en © The Author(s) 2018 Open Access 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 http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Parkes, Amanda
Clifton, Katherine
Al-Awadhi, Aydah
Oke, Oluchi
Warneke, Carla L.
Litton, Jennifer K.
Hortobagyi, Gabriel N.
Characterization of bone only metastasis patients with respect to tumor subtypes
title Characterization of bone only metastasis patients with respect to tumor subtypes
title_full Characterization of bone only metastasis patients with respect to tumor subtypes
title_fullStr Characterization of bone only metastasis patients with respect to tumor subtypes
title_full_unstemmed Characterization of bone only metastasis patients with respect to tumor subtypes
title_short Characterization of bone only metastasis patients with respect to tumor subtypes
title_sort characterization of bone only metastasis patients with respect to tumor subtypes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5785511/
https://www.ncbi.nlm.nih.gov/pubmed/29387785
http://dx.doi.org/10.1038/s41523-018-0054-x
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