Response to second-line erlotinib in an EGFR mutation-negative patient with non-small-cell lung cancer: make no assumptions |
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Authors: | Karam I Melosky B |
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Affiliation: | Department of Radiation Oncology, BC Cancer Agency, Vancouver, BC. |
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Abstract: | Erlotinib-an oral tyrosine kinase inhibitor (tki) of the epidermal growth factor receptor (egfr)-has commonly been used as a therapeutic option in metastatic non-small-cell lung cancer (nsclc) patients in the second- or third-line treatment setting. A mutation in the EGFR gene (EGFR M+) confers an increased response to this class of drugs. In the first-line setting, use of tkis is restricted to patients having a mutation. The importance of this biomarker has been questioned in subsequent treatment lines.Here, we report a case showing a positive response to erlotinib treatment in the second-line setting. The patient, an elderly male smoker with stage iv nsclc, had a tumour that was EGFR mutation-negative (wild-type EGFR). Based on this clinical case, we discuss the controversy concerning the need for, and impact of, testing for EGFR mutation after first-line treatment. |
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Keywords: | Non-small-cell lung cancer gefitinib erlotinib EGFR mutation |
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