Molecular Targets in Cholangiocarcinoma

Hepatology. 2021 Jan:73 Suppl 1:62-74. doi: 10.1002/hep.31278. Epub 2020 Dec 3.

Abstract

Cholangiocarcinoma (CCA) encompasses a heterogeneous collection of malignancies for which diagnostic biomarkers are lacking and population screening is infeasible because of its status as a rare disease. Coupled with high postsurgical recurrence rates among the minority of patients diagnosed at resectable stages, systemic clinical management will inevitably be required for the majority of patients with CCA with recurrent and advanced disease. In this review, we discuss the therapeutic potential of different classes of molecular targets at various stages of development in CCA, including those targeted to the tumor epithelia (oncogenic, developmental, metabolic, epigenomic) and tumor microenvironment (angiogenesis, checkpoint regulation). Furthermore, we discuss the successes and failures of CCA-targeted therapies, emphasizing key lessons learned that should pave the way for future molecular target evaluation in this uncommon yet bona fide target-rich disease.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Bile Duct Neoplasms / drug therapy*
  • Cholangiocarcinoma / drug therapy*
  • Epigenome
  • ErbB Receptors / antagonists & inhibitors
  • Humans
  • Molecular Targeted Therapy*
  • Receptor, Fibroblast Growth Factor, Type 2 / antagonists & inhibitors
  • TOR Serine-Threonine Kinases / antagonists & inhibitors
  • Tumor Microenvironment / drug effects

Substances

  • ErbB Receptors
  • Receptor, Fibroblast Growth Factor, Type 2
  • TOR Serine-Threonine Kinases