[A Case of Metastatic Colon Cancer Dramatically Affected by Anti-EGFR Antibody Therapy]
Ryoma Yagi1, Yoshifumi Shimada, Kohei Miura
1Division of Digestive and General Surgery, Niigata University Graduate School of Medical and Dental Sciences.
Abstract:
RAS mutation is an established predictive biomarker of resistance to anti-epidermal growth factor receptor(EGFR)therapy in metastatic colorectal cancer. In addition, previous studies identified mutations in ERBB2, FGFR1, PDGFRA, BRAF, MAP2K1, PTEN, and PIK3CA as potential mechanisms of resistance to anti-EGFR therapy. Testing for these mutations might be necessary to determine eligibility for anti-EGFR therapy in patients with metastatic colorectal cancer. CancerPlex®is a nextgeneration sequencer for 413 cancer genes. An analysis panel includes genes that may be associated with resistance to anti- EGFR therapy. A 65-year-old man with unresectable rectal cancer, multiple lung metastases, and a bulky liver metastasis was evaluated for expression of genes associated with resistance to anti-EGFR. The analysis found that all genes indicating resistance were wild-type genes. Cetuximab monotherapy was administered after rectal resection, with dramatic shrinkage of the metastatic tumors. A more accurate selection of patients according to tumor genetic status using CancerPlex®might improve the risk-benefit profile of anti-EGFR therapy.
Insights
RAS mutations predict resistance to anti-EGFR therapy in metastatic colorectal cancer. Comprehensive gene analysis identified no resistance markers, enabling successful cetuximab treatment in one patient.
Area of Science:
- Oncology
- Genetics
- Molecular Biology
Background:
- RAS mutations are established biomarkers for resistance to anti-epidermal growth factor receptor (EGFR) therapy in metastatic colorectal cancer (mCRC).
- Additional genes (ERBB2, FGFR1, PDGFRA, BRAF, MAP2K1, PTEN, PIK3CA) are implicated in anti-EGFR therapy resistance.
- Accurate patient selection based on genetic profiling is crucial for optimizing anti-EGFR therapy outcomes.
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