Cohort profile: a nationwide study in Dutch CHEK2 c.1100delC families using the infrastructure of the HEreditary Breast and Ovarian cancer study Netherlands - Hebon-CHEK2

Maartje A C Schreurs, Muriel A Adank, Antoinette Hollestelle, Rosa de Groot, Denise J Stommel-Jenner, Christi J Van Asperen, Margreet G E M Ausems, Lieke P V Berger, Marinus J Blok, Klaartje van Engelen, Frans B L Hogervorst, Willemina Geurts-Giele, Johan J P Gille, Marijke R Wevers, Marjanka K Schmidt, Maartje J Hooning*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

PURPOSE: CHEK2 c.1100delC is associated with an increased breast cancer risk in women. While this variant is prevalent in the Netherlands (1% in the general population), knowledge of aetiology and prognosis of breast cancer and other tumours in CHEK2 c.1100delC carriers is lacking. The nationwide HEreditary Breast and Ovarian cancer study the Netherlands (Hebon) cohort aims to answer study questions in families with an increased risk of breast cancer and ovarian cancer. While initially focusing on BRCA1/2-variant families, Hebon gradually expanded to include pathogenic variants in other genes associated with breast and/or ovarian cancer over time. This provides an excellent setting to establish a cohort to ultimately study the impact of CHEK2 c.1100delC on cancer risk prediction and surveillance, breast cancer treatment and prognosis. PARTICIPANTS: We invited all heterozygous and homozygous CHEK2 c.1100delC indexes and tested female relatives. 1802 women were included, of whom 1374 were heterozygotes and 938 were breast cancer cases. Pedigrees were collected from all clinical genetic departments. Furthermore, participants completed a detailed questionnaire on hormonal and lifestyle factors, family history, cancer diagnosis and treatment. FINDINGS TO DATE: Mean age at study inclusion was 53 years. Linkage with the Netherlands Cancer Registry showed a younger age at diagnosis in homozygotes (mean age 41.7 years) and heterozygotes (47.9 years) than non-carriers (51.2 years). Furthermore, carriers were more often diagnosed with grade 2, oestrogen receptor-positive breast cancer and more often developed contralateral breast cancer than non-carriers. Most women consumed alcohol regularly and about half never smoked. FUTURE PLANS: Further data linkages with the Netherlands Cancer Registry will allow prospective follow-up and breast cancer risk assessment in unaffected women at the time of genetic testing, risk of contralateral breast cancer and survival in patients with breast cancer. Also, linkage with the nationwide network and registry of histopathology and cytopathology in The Netherlands (PALGA) allows us to retrieve tumour samples to study tumourigenesis.

Original languageEnglish
Article numbere086688
Pages (from-to)e086688
Number of pages11
JournalBMJ Open
Volume14
Issue number10
DOIs
Publication statusPublished - 9 Oct 2024

Keywords

  • Breast tumours
  • Cancer genetics
  • Epidemiology
  • Humans
  • Checkpoint Kinase 2/genetics
  • Female
  • Netherlands/epidemiology
  • Breast Neoplasms/genetics
  • Middle Aged
  • Genetic Predisposition to Disease
  • Ovarian Neoplasms/genetics epidemiology
  • Adult
  • Pedigree
  • Aged
  • Cohort Studies
  • Heterozygote

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