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BIOMARKER:

EGFR G465R

i
Other names: EGFR, ERBB, ERBB1, Epidermal growth factor receptor
Entrez ID:
1year
Biomarkers of acquired resistance to sotorasib (soto) plus panitumumab (pani) in chemorefractory KRAS G12C-mutated metastatic colorectal cancer (mCRC) (AACR 2023)
"Of 21 pts with paired plasma samples, 17 (81%) had ≥1 acquired genomic alteration. RTK alterations and secondary (2°) RAS alterations were most common; each occurred in 57% of pts (Table). KRAS amplification was the most common single alteration (43%)."
Preclinical
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HER-2 (Human epidermal growth factor receptor 2) • KRAS (KRAS proto-oncogene GTPase) • BRAF (B-raf proto-oncogene) • NRAS (Neuroblastoma RAS viral oncogene homolog)
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BRAF V600E • KRAS mutation • EGFR mutation • KRAS G12C • BRAF V600 • EGFR amplification • RAS mutation • NRAS Q61K • HER-2 S310F • KRAS G12 • NRAS Q61 • NRAS Q61R • KRAS Q61H • KRAS amplification • NRAS Q61L • EGFR G465R • EGFR S464L • KRAS Q61L
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Guardant360® CDx
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Vectibix (panitumumab) • Lumakras (sotorasib)
over1year
Structure-guided and phage-assisted evolution of a therapeutic anti-EGFR antibody to reverse acquired resistance. (PubMed, Nat Commun)
The evolved cetuximab variants (Ctx-VY, Ctx-Y104D and Ctx-W52D) with one or two amino acid substitutions in the complementarity-determining region inherit the optimized physical and chemical properties of cetuximab to a great extent, thus ensuring their druggability. Our data collectively show that structure-guided and phage-assisted evolution is an efficient and general approach for reversing receptor mutation-mediated resistance to therapeutic antibody drugs.
Preclinical • Journal
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EGFR (Epidermal growth factor receptor)
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EGFR S492R • EGFR G465R
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Erbitux (cetuximab)