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Clinical characteristics of pancreatic and biliary tract cancers associated with Lynch syndrome

  • Shigemasa Takamizawa
  • , Chigusa Morizane
  • , Noriko Tanabe
  • , Yuta Maruki
  • , Shunsuke Kondo
  • , Susumu Hijioka
  • , Hideki Ueno
  • , Kokichi Sugano
  • , Nobuyoshi Hiraoka
  • , Takuji Okusaka

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

Abstract

Background/Purpose: Pancreatic and biliary tract cancers are one of the Lynch syndrome-associated malignancies. There are few reports describing the patients’ backgrounds and clinical characteristics. Methods: We retrospectively reviewed the medical records of patients with Lynch syndrome-associated pancreatic or biliary tract malignant tumors at National Cancer Center Hospital between March 1992 and October 2019. Results: Fourteen patients were included. They had a history of multiple cancers and a family history of cancer. For the six patients with pancreatic malignant tumor, the median age was 63 years. The primary tumor site of 5/6 patients with pancreatic cancer was the body or tail. Only one patient had pancreatic head cancer. The median overall survival (OS) was 68 (range, 17-198) months. For the eight patients with biliary tract malignant tumor, the median age was 65.5 years. The primary tumor site of 5/8 patients was the intrahepatic bile duct, whereas the primary site of 2/8 was the hilar bile duct. The median OS was 62 (range, 3-183) months. Conclusions: This study brought out several observations on tumor location, late development, and favorable long-term outcomes. Additional studies are needed to identify the characteristics.

Original languageEnglish
Pages (from-to)377-384
Number of pages8
JournalJournal of Hepato-Biliary-Pancreatic Sciences
Volume29
Issue number3
DOIs
StatePublished - Mar 2022
Externally publishedYes

Keywords

  • Lynch syndrome
  • biliary tract cancer
  • hereditary cancer
  • history of cancer
  • pancreatic cancer

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