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Evolution of Estrogen Receptor Status from Primary Tumors to Metastasis and Serially Collected Circulating Tumor Cells

Background: The estrogen receptor (ER) can change expression between primary tumor (PT) and distant metastasis (DM) in breast cancer. A tissue biopsy reflects a momentary state at one location, whereas circulating tumor cells (CTCs) reflect real-time tumor progression. We evaluated ER-status during...

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Autores principales: Forsare, Carina, Bendahl, Pär-Ola, Moberg, Eric, Levin Tykjær Jørgensen, Charlotte, Jansson, Sara, Larsson, Anna-Maria, Aaltonen, Kristina, Rydén, Lisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7215368/
https://www.ncbi.nlm.nih.gov/pubmed/32326116
http://dx.doi.org/10.3390/ijms21082885
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author Forsare, Carina
Bendahl, Pär-Ola
Moberg, Eric
Levin Tykjær Jørgensen, Charlotte
Jansson, Sara
Larsson, Anna-Maria
Aaltonen, Kristina
Rydén, Lisa
author_facet Forsare, Carina
Bendahl, Pär-Ola
Moberg, Eric
Levin Tykjær Jørgensen, Charlotte
Jansson, Sara
Larsson, Anna-Maria
Aaltonen, Kristina
Rydén, Lisa
author_sort Forsare, Carina
collection PubMed
description Background: The estrogen receptor (ER) can change expression between primary tumor (PT) and distant metastasis (DM) in breast cancer. A tissue biopsy reflects a momentary state at one location, whereas circulating tumor cells (CTCs) reflect real-time tumor progression. We evaluated ER-status during tumor progression from PT to DM and CTCs, and related the ER-status of CTCs to prognosis. Methods: In a study of metastatic breast cancer, blood was collected at different timepoints. After CellSearch(®) enrichment, CTCs were captured on DropMount slides and evaluated for ER expression at baseline (BL) and after 1 and 3 months of therapy. Comparison of the ER-status of PT, DM, and CTCs at different timepoints was performed using the McNemar test. The primary endpoint was progression-free survival (PFS). Results: Evidence of a shift from ER positivity to negativity between PT and DM was demonstrated (p = 0.019). We found strong evidence of similar shifts from PT to CTCs at different timepoints (p < 0.0001). ER-positive CTCs at 1 and 3 months were related to better prognosis. Conclusions: A shift in ER-status from PT to DM/CTCs was demonstrated. ER-positive CTCs during systemic therapy might reflect the retention of a favorable phenotype that still responds to therapy.
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spelling pubmed-72153682020-05-18 Evolution of Estrogen Receptor Status from Primary Tumors to Metastasis and Serially Collected Circulating Tumor Cells Forsare, Carina Bendahl, Pär-Ola Moberg, Eric Levin Tykjær Jørgensen, Charlotte Jansson, Sara Larsson, Anna-Maria Aaltonen, Kristina Rydén, Lisa Int J Mol Sci Article Background: The estrogen receptor (ER) can change expression between primary tumor (PT) and distant metastasis (DM) in breast cancer. A tissue biopsy reflects a momentary state at one location, whereas circulating tumor cells (CTCs) reflect real-time tumor progression. We evaluated ER-status during tumor progression from PT to DM and CTCs, and related the ER-status of CTCs to prognosis. Methods: In a study of metastatic breast cancer, blood was collected at different timepoints. After CellSearch(®) enrichment, CTCs were captured on DropMount slides and evaluated for ER expression at baseline (BL) and after 1 and 3 months of therapy. Comparison of the ER-status of PT, DM, and CTCs at different timepoints was performed using the McNemar test. The primary endpoint was progression-free survival (PFS). Results: Evidence of a shift from ER positivity to negativity between PT and DM was demonstrated (p = 0.019). We found strong evidence of similar shifts from PT to CTCs at different timepoints (p < 0.0001). ER-positive CTCs at 1 and 3 months were related to better prognosis. Conclusions: A shift in ER-status from PT to DM/CTCs was demonstrated. ER-positive CTCs during systemic therapy might reflect the retention of a favorable phenotype that still responds to therapy. MDPI 2020-04-20 /pmc/articles/PMC7215368/ /pubmed/32326116 http://dx.doi.org/10.3390/ijms21082885 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Forsare, Carina
Bendahl, Pär-Ola
Moberg, Eric
Levin Tykjær Jørgensen, Charlotte
Jansson, Sara
Larsson, Anna-Maria
Aaltonen, Kristina
Rydén, Lisa
Evolution of Estrogen Receptor Status from Primary Tumors to Metastasis and Serially Collected Circulating Tumor Cells
title Evolution of Estrogen Receptor Status from Primary Tumors to Metastasis and Serially Collected Circulating Tumor Cells
title_full Evolution of Estrogen Receptor Status from Primary Tumors to Metastasis and Serially Collected Circulating Tumor Cells
title_fullStr Evolution of Estrogen Receptor Status from Primary Tumors to Metastasis and Serially Collected Circulating Tumor Cells
title_full_unstemmed Evolution of Estrogen Receptor Status from Primary Tumors to Metastasis and Serially Collected Circulating Tumor Cells
title_short Evolution of Estrogen Receptor Status from Primary Tumors to Metastasis and Serially Collected Circulating Tumor Cells
title_sort evolution of estrogen receptor status from primary tumors to metastasis and serially collected circulating tumor cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7215368/
https://www.ncbi.nlm.nih.gov/pubmed/32326116
http://dx.doi.org/10.3390/ijms21082885
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