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editorial
. 2008 Jan 7;14(1):1–14. doi: 10.3748/wjg.14.1

Table 1.

Agents for anti-EGFR-based therapy of solid tumours

Name Target Mechanism Current status
Small molecule inhibitors
Gefitinib (Iressa) EGFR Reversibly acting tyrosine kinase inhibitor Approved for NSCLC with restricted indications
PhaseIfor HCC[133]
Erlotinib (Tarceva) EGFR Reversibly acting tyrosine kinase inhibitor Approved for NSCLC and pancreatic cancer
Phase II for hepatocellular cancer[33]
EKB-569 EGFR Irreversibly acting tyrosine kinase inhibitor Phase I/II for colorectal cancer[134]
Phase II for NSCLC[135]
Lapatinib (Tykerb) EGFR, erbB2 Reversibly acting tyrosine kinase inhibitor Phase III for breast cancer
Phase II for HCC[136]
Canertinib (CI-1033) Pan-erbB Irreversibly acting tyrosine kinase inhibitor Phase II for SCC and ovarian cancer[137]
BMS-599626 EGFR, erbB2 Reversibly acting tyrosine kinase inhibitor Phase II for HCC [138]
Monoclonal antibodies
Cetuximab EGFR Approved for colorectal cancer
Phase III for head and neck cancer, NSCLC and pancreatic cancer
Phase II for HCC[139]
Trastuzumab erbB2 Approved for breast cancer
ABX-EGF EGFR Phase III for colorectal-, head and neck-, and renal cell cancer
Matuzumab (EMD 72 000) EGFR Phase I/II for NSCLC[140], ovarian-[141], pancreatic cancer[142]