Anti-EGFR Therapy: Mechanism and Advances in Clinical Efficacy in Breast Cancer
Author(s) -
John F. Flynn,
Christina S.F. Wong,
Joseph Wu
Publication year - 2009
Publication title -
journal of oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.228
H-Index - 54
eISSN - 1687-8469
pISSN - 1687-8450
DOI - 10.1155/2009/526963
Subject(s) - lapatinib , medicine , mechanism (biology) , breast cancer , tyrosine kinase inhibitor , erbb , cancer , trastuzumab , epidermal growth factor receptor , receptor tyrosine kinase , oncology , receptor , philosophy , epistemology
This review will focus on recent advances in the application of antiepidermal growth factor receptor (anti-EGFR) for the treatment of breast cancer. The choice of EGFR, a member of the ErbB tyrosine kinase receptor family, stems from evidence pinpointing its role in various anti-EGFR therapies. Therefore, an increase in our understanding of EGFR mechanism and signaling might reveal novel targets amenable to intervention in the clinic. This knowledge base might also improve existing medical treatment options and identify research gaps in the design of new therapeutic agents. While the approved use of drugs like the dual kinase inhibitor Lapatinib represents significant advances in the clinical management of breast cancer, confirmatory studies must be considered to foster the use of anti-EGFR therapies including safety, pharmacokinetics, and clinical efficacy.
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