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

Science · 2004 · Vol. 304(5676) · pp. 1497–1500
J. Guillermo PaezPasi A. JänneJeffrey C. LeeSean TracyHeidi GreulichStacey GabrielPaula HermanFrederic J. KayeNeal I. LindemanTitus J. BoggonKatsuhiko NaokiHidefumi SasakiYoshitaka FujiiMichael J. EckWilliam R. SellersBruce E. JohnsonMatthew Meyerson

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.

Lung Cancer Treatments and MutationsHER2/EGFR in Cancer ResearchColorectal Cancer Treatments and StudiesGefitinibLung cancerEpidermal growth factor receptorAdenocarcinomaCancer researchSomatic cellMedicineOncologyTyrosine kinaseInternal medicine

MeSH terms

GefitinibAdenocarcinomaAmino Acid SequenceAntineoplastic AgentsCarcinoma, Non-Small-Cell LungEnzyme InhibitorsFemaleHumansJapanLung NeoplasmsMaleMolecular Sequence DataMutationPhosphorylationProtein Conformation
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