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The prognostic and predictive value of ESR1 fusion gene transcripts in primary breast cancer

BACKGROUND: In breast cancer (BC), recurrent fusion genes of estrogen receptor alpha (ESR1) and AKAP12, ARMT1 and CCDC170 have been reported. In these gene fusions the ligand binding domain of ESR1 has been replaced by the transactivation domain of the fusion partner constitutively activating the re...

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Autores principales: Vitale, Silvia R., Ruigrok-Ritstier, Kirsten, Timmermans, A. Mieke, Foekens, Renée, Trapman-Jansen, Anita M. A. C., Beaufort, Corine M., Vigneri, Paolo, Sleijfer, Stefan, Martens, John W. M., Sieuwerts, Anieta M., Jansen, Maurice P. H. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8840267/
https://www.ncbi.nlm.nih.gov/pubmed/35151276
http://dx.doi.org/10.1186/s12885-022-09265-1
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author Vitale, Silvia R.
Ruigrok-Ritstier, Kirsten
Timmermans, A. Mieke
Foekens, Renée
Trapman-Jansen, Anita M. A. C.
Beaufort, Corine M.
Vigneri, Paolo
Sleijfer, Stefan
Martens, John W. M.
Sieuwerts, Anieta M.
Jansen, Maurice P. H. M.
author_facet Vitale, Silvia R.
Ruigrok-Ritstier, Kirsten
Timmermans, A. Mieke
Foekens, Renée
Trapman-Jansen, Anita M. A. C.
Beaufort, Corine M.
Vigneri, Paolo
Sleijfer, Stefan
Martens, John W. M.
Sieuwerts, Anieta M.
Jansen, Maurice P. H. M.
author_sort Vitale, Silvia R.
collection PubMed
description BACKGROUND: In breast cancer (BC), recurrent fusion genes of estrogen receptor alpha (ESR1) and AKAP12, ARMT1 and CCDC170 have been reported. In these gene fusions the ligand binding domain of ESR1 has been replaced by the transactivation domain of the fusion partner constitutively activating the receptor. As a result, these gene fusions can drive tumor growth hormone independently as been shown in preclinical models, but the clinical value of these fusions have not been reported. Here, we studied the prognostic and predictive value of different frequently reported ESR1 fusion transcripts in primary BC. METHODS: We evaluated 732 patients with primary BC (131 ESR1-negative and 601 ESR1-positive cases), including two ER-positive BC patient cohorts: one cohort of 322 patients with advanced disease who received first-line endocrine therapy (ET) (predictive cohort), and a second cohort of 279 patients with lymph node negative disease (LNN) who received no adjuvant systemic treatment (prognostic cohort). Fusion gene transcript levels were measured by reverse transcriptase quantitative PCR. The presence of the different fusion transcripts was associated, in uni- and multivariable Cox regression analysis taking along current clinico-pathological characteristics, to progression free survival (PFS) during first-line endocrine therapy in the predictive cohort, and disease- free survival (DFS) and overall survival (OS) in the prognostic cohort. RESULTS: The ESR1-CCDC170 fusion transcript was present in 27.6% of the ESR1-positive BC subjects and in 2.3% of the ESR1-negative cases. In the predictive cohort, none of the fusion transcripts were associated with response to first-line ET. In the prognostic cohort, the median DFS and OS were respectively 37 and 93 months for patients with an ESR1-CCDC170 exon 8 gene fusion transcript and respectively 91 and 212 months for patients without this fusion transcript. In a multivariable analysis, this ESR1-CCDC170 fusion transcript was an independent prognostic factor for DFS (HR) (95% confidence interval (CI): 1.8 (1.2–2.8), P = 0.005) and OS (HR (95% CI: 1.7 (1.1–2.7), P = 0.023). CONCLUSIONS: Our study shows that in primary BC only ESR1-CCDC170 exon 8 gene fusion transcript carries prognostic value. None of the ESR1 fusion transcripts, which are considered to have constitutive ER activity, was predictive for outcome in BC with advanced disease treated with endocrine treatment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-022-09265-1.
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spelling pubmed-88402672022-02-16 The prognostic and predictive value of ESR1 fusion gene transcripts in primary breast cancer Vitale, Silvia R. Ruigrok-Ritstier, Kirsten Timmermans, A. Mieke Foekens, Renée Trapman-Jansen, Anita M. A. C. Beaufort, Corine M. Vigneri, Paolo Sleijfer, Stefan Martens, John W. M. Sieuwerts, Anieta M. Jansen, Maurice P. H. M. BMC Cancer Research BACKGROUND: In breast cancer (BC), recurrent fusion genes of estrogen receptor alpha (ESR1) and AKAP12, ARMT1 and CCDC170 have been reported. In these gene fusions the ligand binding domain of ESR1 has been replaced by the transactivation domain of the fusion partner constitutively activating the receptor. As a result, these gene fusions can drive tumor growth hormone independently as been shown in preclinical models, but the clinical value of these fusions have not been reported. Here, we studied the prognostic and predictive value of different frequently reported ESR1 fusion transcripts in primary BC. METHODS: We evaluated 732 patients with primary BC (131 ESR1-negative and 601 ESR1-positive cases), including two ER-positive BC patient cohorts: one cohort of 322 patients with advanced disease who received first-line endocrine therapy (ET) (predictive cohort), and a second cohort of 279 patients with lymph node negative disease (LNN) who received no adjuvant systemic treatment (prognostic cohort). Fusion gene transcript levels were measured by reverse transcriptase quantitative PCR. The presence of the different fusion transcripts was associated, in uni- and multivariable Cox regression analysis taking along current clinico-pathological characteristics, to progression free survival (PFS) during first-line endocrine therapy in the predictive cohort, and disease- free survival (DFS) and overall survival (OS) in the prognostic cohort. RESULTS: The ESR1-CCDC170 fusion transcript was present in 27.6% of the ESR1-positive BC subjects and in 2.3% of the ESR1-negative cases. In the predictive cohort, none of the fusion transcripts were associated with response to first-line ET. In the prognostic cohort, the median DFS and OS were respectively 37 and 93 months for patients with an ESR1-CCDC170 exon 8 gene fusion transcript and respectively 91 and 212 months for patients without this fusion transcript. In a multivariable analysis, this ESR1-CCDC170 fusion transcript was an independent prognostic factor for DFS (HR) (95% confidence interval (CI): 1.8 (1.2–2.8), P = 0.005) and OS (HR (95% CI: 1.7 (1.1–2.7), P = 0.023). CONCLUSIONS: Our study shows that in primary BC only ESR1-CCDC170 exon 8 gene fusion transcript carries prognostic value. None of the ESR1 fusion transcripts, which are considered to have constitutive ER activity, was predictive for outcome in BC with advanced disease treated with endocrine treatment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-022-09265-1. BioMed Central 2022-02-12 /pmc/articles/PMC8840267/ /pubmed/35151276 http://dx.doi.org/10.1186/s12885-022-09265-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Vitale, Silvia R.
Ruigrok-Ritstier, Kirsten
Timmermans, A. Mieke
Foekens, Renée
Trapman-Jansen, Anita M. A. C.
Beaufort, Corine M.
Vigneri, Paolo
Sleijfer, Stefan
Martens, John W. M.
Sieuwerts, Anieta M.
Jansen, Maurice P. H. M.
The prognostic and predictive value of ESR1 fusion gene transcripts in primary breast cancer
title The prognostic and predictive value of ESR1 fusion gene transcripts in primary breast cancer
title_full The prognostic and predictive value of ESR1 fusion gene transcripts in primary breast cancer
title_fullStr The prognostic and predictive value of ESR1 fusion gene transcripts in primary breast cancer
title_full_unstemmed The prognostic and predictive value of ESR1 fusion gene transcripts in primary breast cancer
title_short The prognostic and predictive value of ESR1 fusion gene transcripts in primary breast cancer
title_sort prognostic and predictive value of esr1 fusion gene transcripts in primary breast cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8840267/
https://www.ncbi.nlm.nih.gov/pubmed/35151276
http://dx.doi.org/10.1186/s12885-022-09265-1
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