Personalized drug screening in patient-derived organoids of biliary tract cancer and its clinical application

Cell Rep Med. 2023 Nov 21;4(11):101277. doi: 10.1016/j.xcrm.2023.101277. Epub 2023 Nov 8.

Abstract

Patients with biliary tract cancer (BTC) show different responses to chemotherapy, and there is no effective way to predict chemotherapeutic response. We have generated 61 BTC patient-derived organoids (PDOs) from 82 tumors (74.4%) that show similar histological and genetic characteristics to the corresponding primary BTC tissues. BTC tumor tissues with enhanced stemness- and proliferation-related gene expression by RNA sequencing can more easily form organoids. As expected, BTC PDOs show different responses to the chemotherapies of gemcitabine, cisplatin, 5-fluoruracil, oxaliplatin, etc. The drug screening results in PDOs are further validated in PDO-based xenografts and confirmed in 92.3% (12/13) of BTC patients with actual clinical response. Moreover, we have identified gene expression signatures of BTC PDOs with different drug responses and established gene expression panels to predict chemotherapy response in BTC patients. In conclusion, BTC PDO is a promising precision medicine tool for anti-cancer therapy in BTC patients.

Keywords: biliary tract cancer; chemotherapy; organoids; personalized drug screening.

MeSH terms

  • Biliary Tract Neoplasms* / drug therapy
  • Biliary Tract Neoplasms* / genetics
  • Biliary Tract Neoplasms* / pathology
  • Drug Evaluation, Preclinical
  • Early Detection of Cancer*
  • Gemcitabine
  • Humans
  • Organoids / pathology

Substances

  • Gemcitabine