Abstract
A 37-year-old female never smoker with metastatic large cell carcinoma of the lung had a partial response to a second line palliative therapy with the EGF-R tyrosine kinase inhibitor erlotinib after platinum based first line therapy failed. Molecular analysis of the primary and a liver metastasis did neither find any EGF-R mutation nor an EGF-R amplification. However, both the primary and the metastasis showed an increased gene expression of vascular-endothelial growth factor-A in contrast to normal tissue, which was confirmed by immunohistochemistry. To our knowledge, this is the first report about a high vascular-endothelial growth factor-A expression in the tumor of a patient responding to an EGF-R inhibitor postulating that there might be a link between both tyrosine kinase pathways.
Publication types
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Case Reports
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Research Support, Non-U.S. Gov't
MeSH terms
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Adult
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Carcinoma, Non-Small-Cell Lung / drug therapy
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Carcinoma, Non-Small-Cell Lung / metabolism*
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Carcinoma, Non-Small-Cell Lung / secondary
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DNA, Neoplasm / genetics*
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ErbB Receptors / antagonists & inhibitors*
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ErbB Receptors / biosynthesis
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ErbB Receptors / genetics
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Erlotinib Hydrochloride
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Fatal Outcome
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Female
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Follow-Up Studies
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Gene Expression Regulation, Neoplastic / drug effects*
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Humans
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Liver Neoplasms / diagnosis
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Liver Neoplasms / metabolism
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Liver Neoplasms / secondary
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Lung Neoplasms / diagnosis
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Lung Neoplasms / drug therapy
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Lung Neoplasms / metabolism*
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Mutation
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Protein Kinase Inhibitors / therapeutic use
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Quinazolines / therapeutic use*
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Retrospective Studies
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Vascular Endothelial Growth Factor A / biosynthesis
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Vascular Endothelial Growth Factor A / genetics*
Substances
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DNA, Neoplasm
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Protein Kinase Inhibitors
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Quinazolines
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Vascular Endothelial Growth Factor A
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Erlotinib Hydrochloride
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ErbB Receptors