Precursor lesions in familial and hereditary pancreatic cancer

Research output: Contribution to journalReview articlepeer-review

Abstract

Infiltrating ductal adenocarcinoma of the pancreas, referred to here as "pancreatic cancer," is one of the deadliest of all of the solid malignancies. The five-year survival rate in the United States for individuals diagnosed today with pancreatic cancer is a dismal 12%. Many invasive cancers, including pancreatic cancer, however, arise from histologically and genetically well-characterized precursor lesions, and these precancers are curable. Precursor lesions therefore are an attractive target for early detection and treatment. This is particularly true for individuals with an increased risk of developing invasive cancer, such as individuals with a strong family history of pancreatic cancer, and individuals with a germline variant known to increase the risk of developing pancreatic cancer. There is therefore a need to understand the precursor lesions that can give rise to invasive pancreatic cancer in these individuals.

Original languageEnglish
Pages (from-to)267–278
Number of pages12
JournalFamilial cancer
Volume23
Issue number3
Early online date6 Feb 2024
DOIs
Publication statusPublished - Aug 2024

Keywords

  • BRCA
  • CDKN2A
  • Familial
  • Germline
  • Intraductal papillary mucinous neoplasm
  • Pancreatic cancer
  • Precancer
  • Precursor

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