Intrahepatic cholangiocarcinoma patient with epidermal growth factor receptor exon 19 deletion unresponsive to

Caijiu Deng1,2, Junming Huang3, Qian Yu4

  • 1Department of Oncology, The Affiliated Panyu Central Hospital, Guangzhou Medical University, No. 8 Fuyu Road East, Panyu, Guangzhou, 511400, Guangdong, People's Republic of China.

Discover Oncology
|April 10, 2025
PubMed
Abstract

Insights

This case study found that a cholangiocarcinoma patient with an EGFR exon 19 deletion did not respond to afatinib treatment. Genetic testing is recommended for cholangiocarcinoma patients to explore potential treatment options.

Area of Science:

  • Oncology
  • Genetics

Background:

  • The effectiveness of epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) in cholangiocarcinoma (CCA) remains unclear.
  • This report details a case of a 67-year-old CCA patient with an EGFR exon 19 deletion treated with afatinib.

Purpose of the Study:

  • To evaluate the efficacy of afatinib in a CCA patient with a specific EGFR mutation.
  • To highlight the potential role of genetic testing in identifying treatment options for CCA.

Main Methods:

  • A 67-year-old male diagnosed with intrahepatic cholangiocarcinoma (CCA) with liver metastases.
  • The patient received afatinib as first-line treatment due to refusal of standard chemotherapy.
  • Subsequent treatment with apatinib was administered upon disease progression.

Main Results:

  • The patient exhibited no response to afatinib treatment.
  • The patient experienced disease progression and ultimately succumbed to hepatic failure.
  • Overall survival was limited to 1.8 months.

Conclusions:

  • The CCA patient with an EGFR exon 19 deletion was unresponsive to afatinib.
  • Genetic testing may be beneficial for cholangiocarcinoma patients to identify potential therapeutic targets and expand treatment choices.