A clinical and genetic analysis of multiple primary cancer referrals to genetics services

Eur J Hum Genet. 2015 May;23(5):581-7. doi: 10.1038/ejhg.2014.157. Epub 2014 Sep 24.

Abstract

Multiple primary malignant tumours (MPMT) are frequently taken as an indicator of potential inherited cancer susceptibility and occur at appreciable frequency both among unselected cancer patients and, particularly, among referrals to cancer genetics services. However, there is a paucity of information on the clinical genetic evaluation of cohorts of MPMT patients representing a variety of tumour types. We ascertained a referral-based series of MPMT cases and describe the patterns of tumours observed. Service-based molecular genetic testing had demonstrated a pathogenic germline variant in an inherited cancer gene in fewer than one in four unselected referrals. To assess for evidence of thus far unidentified variants in those who tested negative, comparisons were made with those who tested positive. This revealed considerable overlap between the two groups with respect to clinical characteristics indicative of an inherited cancer syndrome. We therefore proceeded to test a subset of unexplained MPMT cases (n=62) for pathogenic germline variants in TP53 and PTEN but none were detected. Individuals with MPMT may receive negative genetic test results for a number of reasons, which are discussed. Many of these may be addressed by the increasing application of next generation sequencing techniques such as inherited cancer gene panels.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • DNA Mismatch Repair / genetics
  • Exons
  • Female
  • Genetic Predisposition to Disease
  • Genetic Testing*
  • Germ-Line Mutation
  • Humans
  • Male
  • Neoplasms, Multiple Primary / diagnosis*
  • Neoplasms, Multiple Primary / genetics*
  • PTEN Phosphohydrolase / genetics
  • Referral and Consultation*
  • Sequence Analysis, DNA
  • Tumor Suppressor Protein p53 / genetics

Substances

  • Tumor Suppressor Protein p53
  • PTEN Phosphohydrolase
  • PTEN protein, human