Abstract
For breast cancer patients, treatment decisions based on the molecular profile of the primary tumor have been used for many years. In Her2-overexpressing tumors, trastuzumab is a key component of therapy. However, despite persistent expression of Her2, most tumors eventually become resistant to trastuzumab. When this happens, the patients benefit from a regime containing lapatinib, a dual EGFR and Her2 tyrosine kinase inhibitor. We report on a patient affected by chemo-refractory metastatic Her2-positive breast cancer enrolled in a translational research program for the detection and characterization of circulating tumor cells (CTCs). Depletion of the EGFR-positive CTC pool in the blood was associated with tumor response, whereas disease progression was related to a recurrence in CTCs, which were both EGFR and Her2 negative. Although a proof for the clinical significance of EGFR-positive circulating tumor cells is currently lacking, expression of EGFR may predict response to lapatinib-based treatments as in the case presented.
MeSH terms
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Antibodies, Monoclonal / therapeutic use
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Antibodies, Monoclonal, Humanized
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Antineoplastic Agents / adverse effects
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Antineoplastic Agents / therapeutic use
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Antineoplastic Combined Chemotherapy Protocols / adverse effects
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Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
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Breast Neoplasms / drug therapy*
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Breast Neoplasms / pathology
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Capecitabine
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Deoxycytidine / analogs & derivatives
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Deoxycytidine / therapeutic use
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Disease Progression
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Drug Resistance, Neoplasm
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ErbB Receptors / antagonists & inhibitors
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ErbB Receptors / metabolism*
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Female
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Flow Cytometry
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Fluorouracil / analogs & derivatives
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Fluorouracil / therapeutic use
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Gene Expression Profiling
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Genetic Markers
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Humans
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Lapatinib
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Middle Aged
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Neoplasm Metastasis
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Neoplastic Cells, Circulating / metabolism*
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Neoplastic Cells, Circulating / pathology
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Protein Kinase Inhibitors / pharmacology
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Protein Kinase Inhibitors / therapeutic use
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Quinazolines / therapeutic use*
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Receptor, ErbB-2 / antagonists & inhibitors
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Receptor, ErbB-2 / genetics
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Receptor, ErbB-2 / metabolism
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Trastuzumab
Substances
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Antibodies, Monoclonal
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Antibodies, Monoclonal, Humanized
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Antineoplastic Agents
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Genetic Markers
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Protein Kinase Inhibitors
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Quinazolines
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Lapatinib
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Deoxycytidine
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Capecitabine
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ErbB Receptors
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Receptor, ErbB-2
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Trastuzumab
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Fluorouracil