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Lunch and Poster Display session

161P - Cancer risks for other sites in addition to breast in CHEK2 c.1100delC families

Date

16 May 2024

Session

Lunch and Poster Display session

Presenters

Maartje Schreurs

Citation

Annals of Oncology (2024) 9 (suppl_4): 1-9. 10.1016/esmoop/esmoop103181

Authors

M.A.C. Schreurs1, M.K. Schmidt2, A. Hollestelle3, M. Schaapveld4, C. van Asperen5, M. Ausems6, I. van de Beek4, M. Broekema7, M. Collée3, A. van der Hout8, K. van Kaam9, F. Komdeur7, A. Mensenkamp10, M.A. Adank4, M.J. Hooning3

Author affiliations

  • 1 Erasmus MC - Daniel den Hoed Cancer Center, Rotterdam/NL
  • 2 NKI-AVL - Netherlands Cancer Institute/Antoni van Leeuwenhoek Hospital, 1066 CX - Amsterdam/NL
  • 3 Erasmus MC Cancer Institute, Rotterdam/NL
  • 4 Netherlands Cancer Institute, Amsterdam/NL
  • 5 LUMC-Leiden University Medical Center, Leiden/NL
  • 6 UMC - University Medical Center Utrecht, Utrecht/NL
  • 7 Amsterdam UMC, locatie AMC, Amsterdam/NL
  • 8 UMCG - University Medical Center Groningen, Groningen/NL
  • 9 Maastricht University Medical Center (MUMC), Maastricht/NL
  • 10 Radboud University Medical Center, Nijmegen/NL

Resources

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Abstract 161P

Background

Female CHEK2 c.1100delC carriers are eligible for additional breast surveillance due to an increased breast cancer risk. Increased risks for other cancers have been reported. We studied whether CHEK2 c.1100delC is associated with an increased risk for other types of cancer within these families.

Methods

Including 10,780 individuals from 609 CHEK2 c.1100delC families, we calculated standardized incidence rates (SIRs) and absolute excess risk (AER, per 10.000 person years) by comparing first-reported cancer derived from the pedigrees with general Dutch population rates from 1970 onwards. Attained-age analyses were performed for sites where significant increased risks were found.

Results

We found significant increased risks of colorectal cancer (CRC; SIR=1.43, 95%CI=1.14-1.76; AER=1.43 in women and SIR=1.47; 95%CI=1.22-1.77; AER=2.25 in men) and hematological cancers in women (SIR=1.32; 95%CI=1.02-1.67; AER=0.87). CRC was significantly more frequent in CHEK2 families from age 45 onwards.

Conclusions

A significantly increased risk of CRC, and hematological cancers in women was found, starting at a younger age than expected. Currently, colorectal surveillance starts at age 45 in high-risk individuals, independent of CHEK2 status. Our results suggest that some CHEK2 families might benefit from this surveillance as well, however, further research is needed to determine who may profit from this additional colorectal surveillance.

Legal entity responsible for the study

The authors.

Funding

Dutch Cancer Society.

Disclosure

All authors have declared no conflicts of interest.

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