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Mutations of the epidermal growth factor receptor (EGFR) gene have been identified in specimens from patients with non-small-cell lung cancer who have a response to anilinoquinazoline EGFR inhibitors. Despite the dramatic responses to such inhibitors, most patients ultimately have a relapse. The mechanism of the drug resistance is unknown. Here we report the case of a patient with EGFR-mutant, gefitinib-responsive, advanced non-small-cell lung cancer who had a relapse after two years of complete remission during treatment with gefitinib. The DNA sequence of the EGFR gene in his tumor biopsy specimen at relapse revealed the presence of a second point mutation, resulting in threonine-to-methionine amino acid change at position 790 of EGFR. Structural modeling and biochemical studies showed that this second mutation led to gefitinib resistance.
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Susumu Kobayashi
Beth Israel Deaconess Medical Center
Titus J. Boggon
Yale Cancer Center
Tajhal Dayaram
Institute of Molecular and Cell Biology
New England Journal of Medicine
Harvard University
Brigham and Women's Hospital
Dana-Farber Cancer Institute
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Kobayashi et al. (Wed,) studied this question.
synapsesocial.com/papers/6a0cc8bc59b087b0dc6257ca — DOI: https://doi.org/10.1056/nejmoa044238
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