Panitumumab

EGFR Inhibitor
DB01269
Approved Indication

For the treatment of EGFR-expressing, metastatic colorectal carcinoma that is refractory to fluoropyrimidine-, oxaliplatin-, and irinotecan- containing chemotherapy regimens.

1 Targets
13 Resistance Mutations
70 References
3D Structure No structure available
No co-crystal structure available
Protein Targets
Mechanism of Action

Panitumumab binds specifically to EGFR on both normal and tumor cells, and competitively inhibits the binding of ligands for EGFR. Nonclinical studies show that binding of panitumumab to the EGFR prevents ligand-induced receptor autophosphorylation and activation of receptor-associated kinases, resulting in inhibition of cell growth, induction of apoptosis, decreased pro-inflammatory cytokine and vascular growth factor production, and internalization of the EGFR.

Resistance Mutations — 79 resistance samples observed in COSMIC
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KRAS
p.G12A 5 p.G12C 5 p.G12D 5 p.G12R 5 p.G12S 5 p.G12V 5 p.G13D 5 p.Q61E 5 p.Q61H 5 p.Q61P 5
NRAS
p.Q61H 5 p.Q61K 5 p.Q61L 5

Resistance mutations sourced from COSMIC Drug Resistance database. Cyan = on-target · Amber = off-target · numbered badge = PubMed references for that mutation

Details
DrugBank ID DB01269 ↗
Approval Date 2006-10-10
Molecular Weight — g/mol
Drug Class EGFR Inhibitor
ATC Codes L01XC08
Synonyms ABX-EGF