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A Case of Advanced Biliary Tract Cancer With EGFR Amplification That Responded to Necitumumab
Makoto Sugimori1,2,3, Masaki Nishimura2, Kazuya Sugimori2
1Division of Cancer Genome Medicine, Yokohama City University Medical Center, Yokohama, Japan.
Background:
Recent advances in cancer genome analysis and the practice of precision medicine have made it possible to identify fractions with rare genetic alterations. Among biliary tract cancers, EGFR-amplified cancers are known to be rare fractions across organs and have a poor prognosis. The use of anti-EGFR antibody for EGFR-amplified cancers has been promising; however, the evidence is not yet clear.
Case:
In this report, we describe the case of a 48-year-old man diagnosed with advanced gallbladder cancer. The patient was administered gemcitabine plus cisplatin, followed by S-1 monotherapy; however, disease progression was observed after two cycles of each regimen. Comprehensive genomic profiling test revealed EGFR-amplification, and the patient was treated with combination therapy with the anti-EGFR antibody necitumumab, gemcitabine, and cisplatin. After two cycles of treatment, tumor size reduced, and the treatment response was evaluated as partial response. On Day 90, after five cycles of treatment, tumor progression was confirmed. In addition, after disease progression, liquid biopsy revealed acquired pathogenic gene alterations suggesting anti-EGFR antibody resistance.
Conclusion:
This report supports the clinical benefit of anti-EGFR antibodies for EGFR-amplified biliary tract cancers and the importance of genomic analysis in personalized therapy and drug resistance research.
Insights
This case study highlights the potential of anti-EGFR antibodies in treating rare EGFR-amplified biliary tract cancers. Genomic analysis is crucial for identifying these alterations and understanding drug resistance mechanisms in precision medicine.
Area of Science:
- Oncology
- Genomics
- Precision Medicine
Background:
- Biliary tract cancers (BTCs) with EGFR-amplification are rare and associated with poor prognosis.
- Precision medicine enables identification of rare genetic alterations for targeted therapies.
- Anti-EGFR antibody efficacy in EGFR-amplified BTCs requires further clinical evidence.
Observation:
- A 48-year-old male with advanced gallbladder cancer progressed on standard chemotherapy (gemcitabine/cisplatin, S-1).
- Comprehensive genomic profiling revealed EGFR-amplification.
- Initial partial response was observed with necitumumab (anti-EGFR antibody) plus chemotherapy, followed by disease progression.
Findings:
- The patient developed acquired resistance to anti-EGFR antibody therapy, indicated by liquid biopsy findings.
- EGFR-amplification in BTC presents a targetable alteration for novel therapeutic strategies.
Implications:
- This case supports the clinical utility of anti-EGFR antibodies in EGFR-amplified BTC.
- Genomic analysis is vital for personalized therapy selection and investigating acquired resistance mechanisms.
- Further research into overcoming anti-EGFR antibody resistance is warranted for improved patient outcomes.
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