Targeting BRCA-mutant biliary tract cancer: Current evidence and future perspectives

J Dig Dis. 2023 Feb;24(2):85-97. doi: 10.1111/1751-2980.13168. Epub 2023 May 5.

Abstract

Biliary tract cancers (BTCs) are aggressive tumors of the biliary system, which are often diagnosed at the advanced stage with a dismal prognosis. Among BTC patients, germline or somatic breast cancer-related gene 1/2 (BRCA1/2) mutation has been reported and the use of poly(ADP-ribose) polymerase inhibitor (PARPi) has achieved a certain effect, with no obvious severe side effects. The frequencies and mutated types of BRCA1/2 in advanced BTCs vary among studies. BRCA1 and BRCA2 play distinct roles in the development of BTC regardless of age or gender difference. Surprisingly, some BTC patients with germline BRCA mutation can achieve better therapeutic effects than those with a somatic mutation, and patients who carry BRCA mutation are more likely to benefit from immunotherapy alone or in combination. Herein, we provide an overview of the targeted therapies in BRCA-mutant BTCs, with a particular focus on the differences between germline and somatic BRCA1/2 mutations, as well as review the current status and perspectives.

Keywords: BRCA1/2; biliary tract neoplasms; germline; poly(ADP-ribose) polymerase inhibitor; somatic.

Publication types

  • Review

MeSH terms

  • Antineoplastic Agents* / therapeutic use
  • BRCA1 Protein / genetics
  • BRCA2 Protein / genetics
  • Biliary Tract Neoplasms* / drug therapy
  • Humans
  • Mutation
  • Poly(ADP-ribose) Polymerase Inhibitors / pharmacology
  • Poly(ADP-ribose) Polymerase Inhibitors / therapeutic use

Substances

  • BRCA1 protein, human
  • BRCA1 Protein
  • BRCA2 protein, human
  • BRCA2 Protein
  • Antineoplastic Agents
  • Poly(ADP-ribose) Polymerase Inhibitors