Towards Multiomics-Based Dissection of Anti-EGFR Sensitivity in Colorectal Cancer
- PMID: 37594733
- PMCID: PMC10570674
- DOI: 10.1158/1078-0432.CCR-23-1954
Towards Multiomics-Based Dissection of Anti-EGFR Sensitivity in Colorectal Cancer
Abstract
Overexpression of the EGFR ligands amphiregulin (AREG)/epiregulin (EREG) may be a surrogate of EGFR dependency regardless of sidedness in metastatic colorectal cancer. High AREG/EREG may be coupled with negative hyper-selection (i.e., lack of genomic drivers of primary resistance beyond RAS and BRAF) to identify patients with right-sided tumors and potential sensitivity to EGFR blockade. See related article by Williams et al., p. 4153.
©2023 The Authors; Published by the American Association for Cancer Research.
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Associations between AI-Assisted Tumor Amphiregulin and Epiregulin IHC and Outcomes from Anti-EGFR Therapy in the Routine Management of Metastatic Colorectal Cancer.Clin Cancer Res. 2023 Oct 13;29(20):4153-4165. doi: 10.1158/1078-0432.CCR-23-0859. Clin Cancer Res. 2023. PMID: 37363997 Free PMC article.
References
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- Seligmann JF, Elliott F, Richman SD, Jacobs B, Hemmings G, Brown S, et al. . Combined epiregulin and amphiregulin expression levels as a predictive biomarker for panitumumab therapy benefit or lack of benefit in patients with RAS wild-type advanced colorectal cancer. JAMA Oncol 2016;2:633–42. - PubMed
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