Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2010 Jul;17 Suppl 1(Suppl 1):S3-17.
doi: 10.3747/co.v17is1.616.

Efficacy of the monoclonal antibody EGFR inhibitors for the treatment of metastatic colorectal cancer

Affiliations
Free PMC article

Efficacy of the monoclonal antibody EGFR inhibitors for the treatment of metastatic colorectal cancer

M Fakih et al. Curr Oncol. 2010 Jul.
Free PMC article

Abstract

Two anti-epidermal growth factor receptor (EGFR) monoclonal antibodies (MoAbs) have been approved in Canada for the treatment of metastatic colorectal cancer (mCRC) - cetuximab, a mouse-human chimeric MoAb, and panitumumab, a fully human MoAb. This paper reviews the efficacy of the anti-EGFR monoclonal antibodies cetuximab and panitumumab - both as monotherapy and in combination with cytotoxic chemotherapy - in the treatment of mCRC. Both cetuximab and panitumumab have demonstrated clinical efficacy in monotherapy in patients with mCRC, an advantage that has recently been found to be limited largely to those with wild-type KRAS tumors. Advantages of using these agents in monotherapy include reduced cost and toxicity. While the addition of cetuximab to irinotecan has shown superior progression-free survival and response compared with cetuximab monotherapy, there is currently no evidence for a benefit of panitumumab in combination with irinotecan.

Keywords: BRAF; EGFR; KRAS; cetuximab; colorectal carcinoma; panitumumab.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Time to disease progression in patients treated with cetuximab alone or cetuximab plus irinotecan in the BOND trial
Figure 2
Figure 2
Overall survival in patients treated with cetuximab alone or cetuximab plus irinotecan in the BOND trial
Figure 3
Figure 3
Association between progression-free survival and severity of rash in patients with colorectal cancer treated with cetuximab

Similar articles

Cited by

References

    1. Canadian Cancer Society’s Steering Committee . Toronto. Ontario: Canadian Cancer Society; 2009. Canadian Cancer Statistics 2009.
    1. Venook AP. Epidermal growth factor receptor-targeted treatment for advanced colorectal carcinoma. Cancer. 2005;103(12):2435–46. - PubMed
    1. Sanoff HK, Sargent DJ, Campbell ME, et al. Five-year data and prognostic factor analysis of oxaliplatin and irinotecan combinations for advanced colorectal cancer: N9741. J Clin Oncol. 2008;26(35):5721–27. - PMC - PubMed
    1. André T, Louvet C, Maindrault-Goebel F, et al. CPT-11 (irinotecan) addition to bimonthly, high-dose leucovorin and bolus and continuous-infusion 5-fluorouracil (FOLFIRI) for pretreated metastatic colorectal cancer. GERCOR. Eur J Cancer. 1999;35(9):1343–47. - PubMed
    1. Cunningham D, Pyrhönen S, James RD, et al. Randomised trial of irinotecan plus supportive care versus supportive care alone after fluorouracil failure for patients with metastatic colorectal cancer. Lancet. 1998;352(9138):1413–18. - PubMed

LinkOut - more resources