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Clinicopathologic Profile of Breast Cancer in Germline ATM and CHEK2 Mutation Carriers

The most common breast cancer (BC) susceptibility genes beyond BRCA1/2 are ATM and CHEK2. For the purpose of exploring the clinicopathologic characteristics of BC developed by ATM or CHEK2 mutation carriers, we reviewed the archive of our Family Cancer Clinic. Since 2018, 1185 multi-gene panel tests...

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Autores principales: Toss, Angela, Tenedini, Elena, Piombino, Claudia, Venturelli, Marta, Marchi, Isabella, Gasparini, Elisa, Barbieri, Elena, Razzaboni, Elisabetta, Domati, Federica, Caggia, Federica, Grandi, Giovanni, Combi, Francesca, Tazzioli, Giovanni, Dominici, Massimo, Tagliafico, Enrico, Cortesi, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8143279/
https://www.ncbi.nlm.nih.gov/pubmed/33919281
http://dx.doi.org/10.3390/genes12050616
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author Toss, Angela
Tenedini, Elena
Piombino, Claudia
Venturelli, Marta
Marchi, Isabella
Gasparini, Elisa
Barbieri, Elena
Razzaboni, Elisabetta
Domati, Federica
Caggia, Federica
Grandi, Giovanni
Combi, Francesca
Tazzioli, Giovanni
Dominici, Massimo
Tagliafico, Enrico
Cortesi, Laura
author_facet Toss, Angela
Tenedini, Elena
Piombino, Claudia
Venturelli, Marta
Marchi, Isabella
Gasparini, Elisa
Barbieri, Elena
Razzaboni, Elisabetta
Domati, Federica
Caggia, Federica
Grandi, Giovanni
Combi, Francesca
Tazzioli, Giovanni
Dominici, Massimo
Tagliafico, Enrico
Cortesi, Laura
author_sort Toss, Angela
collection PubMed
description The most common breast cancer (BC) susceptibility genes beyond BRCA1/2 are ATM and CHEK2. For the purpose of exploring the clinicopathologic characteristics of BC developed by ATM or CHEK2 mutation carriers, we reviewed the archive of our Family Cancer Clinic. Since 2018, 1185 multi-gene panel tests have been performed. Nineteen ATM and 17 CHEK2 mutation carriers affected by 46 different BCs were identified. A high rate of bilateral tumors was observed in ATM (26.3%) and CHEK2 mutation carriers (41.2%). While 64.3% of CHEK2 tumors were luminal A-like, 56.2% of ATM tumors were luminal B-like/HER2-negative. Moreover, 21.4% of CHEK2-related invasive tumors showed a lobular histotype. About a quarter of all ATM-related BCs and a third of CHEK2 BCs were in situ carcinomas and more than half of ATM and CHEK2-related BCs were diagnosed at stage I-II. Finally, 63.2% of ATM mutation carriers and 64.7% of CHEK2 mutation carriers presented a positive BC family history. The biological and clinical characteristics of ATM and CHEK2-related tumors may help improve diagnosis, prognostication and targeted therapeutic approaches. Contralateral mastectomy should be considered and discussed with ATM and CHEK2 mutation carriers at the first diagnosis of BC.
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spelling pubmed-81432792021-05-25 Clinicopathologic Profile of Breast Cancer in Germline ATM and CHEK2 Mutation Carriers Toss, Angela Tenedini, Elena Piombino, Claudia Venturelli, Marta Marchi, Isabella Gasparini, Elisa Barbieri, Elena Razzaboni, Elisabetta Domati, Federica Caggia, Federica Grandi, Giovanni Combi, Francesca Tazzioli, Giovanni Dominici, Massimo Tagliafico, Enrico Cortesi, Laura Genes (Basel) Article The most common breast cancer (BC) susceptibility genes beyond BRCA1/2 are ATM and CHEK2. For the purpose of exploring the clinicopathologic characteristics of BC developed by ATM or CHEK2 mutation carriers, we reviewed the archive of our Family Cancer Clinic. Since 2018, 1185 multi-gene panel tests have been performed. Nineteen ATM and 17 CHEK2 mutation carriers affected by 46 different BCs were identified. A high rate of bilateral tumors was observed in ATM (26.3%) and CHEK2 mutation carriers (41.2%). While 64.3% of CHEK2 tumors were luminal A-like, 56.2% of ATM tumors were luminal B-like/HER2-negative. Moreover, 21.4% of CHEK2-related invasive tumors showed a lobular histotype. About a quarter of all ATM-related BCs and a third of CHEK2 BCs were in situ carcinomas and more than half of ATM and CHEK2-related BCs were diagnosed at stage I-II. Finally, 63.2% of ATM mutation carriers and 64.7% of CHEK2 mutation carriers presented a positive BC family history. The biological and clinical characteristics of ATM and CHEK2-related tumors may help improve diagnosis, prognostication and targeted therapeutic approaches. Contralateral mastectomy should be considered and discussed with ATM and CHEK2 mutation carriers at the first diagnosis of BC. MDPI 2021-04-21 /pmc/articles/PMC8143279/ /pubmed/33919281 http://dx.doi.org/10.3390/genes12050616 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Toss, Angela
Tenedini, Elena
Piombino, Claudia
Venturelli, Marta
Marchi, Isabella
Gasparini, Elisa
Barbieri, Elena
Razzaboni, Elisabetta
Domati, Federica
Caggia, Federica
Grandi, Giovanni
Combi, Francesca
Tazzioli, Giovanni
Dominici, Massimo
Tagliafico, Enrico
Cortesi, Laura
Clinicopathologic Profile of Breast Cancer in Germline ATM and CHEK2 Mutation Carriers
title Clinicopathologic Profile of Breast Cancer in Germline ATM and CHEK2 Mutation Carriers
title_full Clinicopathologic Profile of Breast Cancer in Germline ATM and CHEK2 Mutation Carriers
title_fullStr Clinicopathologic Profile of Breast Cancer in Germline ATM and CHEK2 Mutation Carriers
title_full_unstemmed Clinicopathologic Profile of Breast Cancer in Germline ATM and CHEK2 Mutation Carriers
title_short Clinicopathologic Profile of Breast Cancer in Germline ATM and CHEK2 Mutation Carriers
title_sort clinicopathologic profile of breast cancer in germline atm and chek2 mutation carriers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8143279/
https://www.ncbi.nlm.nih.gov/pubmed/33919281
http://dx.doi.org/10.3390/genes12050616
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