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

Angela TossElena TenediniClaudia PiombinoMarta VenturelliIsabella MarchiElisa GaspariniElena BarbieriElisabetta RazzaboniFederica DomatiFederica CaggiaGiovanni GrandiFrancesca CombiGiovanni TazzioliMassimo DominiciEnrico TagliaficoLaura Cortesi
Published in: Genes (2021)
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.
Keyphrases
  • dna damage
  • dna repair
  • dna damage response
  • oxidative stress
  • squamous cell carcinoma
  • gene expression
  • genome wide
  • dna methylation
  • drug induced
  • copy number
  • genome wide identification