<i>EGFR</i> Mutations in Lung Cancer: Correlation with Clinical Response to Gefitinib Therapy

J. Guillermo Paez(Broad Institute), Pasi A. Jänne(Broad Institute), Jeffrey C. Lee(Broad Institute), Sean Tracy(Broad Institute), Heidi Greulich(Broad Institute), Stacey Gabriel(Broad Institute), Paula Herman(Broad Institute), Frederic J. Kaye(Broad Institute), Neal I. Lindeman(Broad Institute), Titus J. Boggon(Broad Institute), Katsuhiko Naoki(Broad Institute), Hidefumi Sasaki(Broad Institute), Yoshitaka Fujii(Broad Institute), Michael J. Eck(Broad Institute), William R. Sellers(Broad Institute), Bruce E. Johnson(Broad Institute), Matthew Meyerson(Broad Institute)
Science
May 3, 2004
Cited by 9,408

Abstract

Receptor tyrosine kinase genes were sequenced in non-small cell lung cancer (NSCLC) and matched normal tissue. Somatic mutations of the epidermal growth factor receptor gene EGFR were found in 15of 58 unselected tumors from Japan and 1 of 61 from the United States. Treatment with the EGFR kinase inhibitor gefitinib (Iressa) causes tumor regression in some patients with NSCLC, more frequently in Japan. EGFR mutations were found in additional lung cancer samples from U.S. patients who responded to gefitinib therapy and in a lung adenocarcinoma cell line that was hypersensitive to growth inhibition by gefitinib, but not in gefitinib-insensitive tumors or cell lines. These results suggest that EGFR mutations may predict sensitivity to gefitinib.


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