Clinical Efficacy and Toxicity of Anti-EGFR Therapy in Common Cancers
Author(s) -
Amir Harandi,
Aisha Zaidi,
Abigail Stocker,
Damian A. Laber
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 - 10.1155/2009/567486
Subject(s) - medicine , epidermal growth factor receptor , clinical trial , tyrosine kinase , toxicity , receptor tyrosine kinase , monoclonal antibody , clinical efficacy , egfr inhibitors , erbb , tyrosine kinase inhibitor , cancer research , pharmacology , oncology , receptor , cancer , immunology , antibody
Epidermal growth factor receptor (EGFR) is a cell surface molecule and member of the ErbB family of receptor tyrosine kinases. Its activation leads to proliferation, antiapoptosis, and metastatic spread, making inhibition of this pathway a compelling target. In recent years, an increasing number of clinical trials in the management of solid malignancies have become available indicating the clinical efficacy of anti-EGFR monoclonal antibodies and oral small molecule tyrosine kinase inhibitors (TKIs). This review addresses frequently used EGFR inhibitors, summarizes clinical efficacy data of these new therapeutic agents, and discusses their associated toxicity and management.
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