| Literature DB >> 16043828 |
David A Eberhard1, Bruce E Johnson, Lukas C Amler, Audrey D Goddard, Sherry L Heldens, Roy S Herbst, William L Ince, Pasi A Jänne, Thomas Januario, David H Johnson, Pam Klein, Vincent A Miller, Michael A Ostland, David A Ramies, Dragan Sebisanovic, Jeremy A Stinson, Yu R Zhang, Somasekar Seshagiri, Kenneth J Hillan.
Abstract
PURPOSE: Epidermal growth factor receptor (EGFR) mutations have been associated with tumor response to treatment with single-agent EGFR inhibitors in patients with relapsed non-small-cell lung cancer (NSCLC). The implications of EGFR mutations in patients treated with EGFR inhibitors plus first-line chemotherapy are unknown. KRAS is frequently activated in NSCLC. The relationship of KRAS mutations to outcome after EGFR inhibitor treatment has not been described. PATIENTS AND METHODS: Previously untreated patients with advanced NSCLC in the phase III TRIBUTE study who were randomly assigned to carboplatin and paclitaxel with erlotinib or placebo were assessed for survival, response, and time to progression (TTP). EGFR exons 18 through 21 and KRAS exon 2 were sequenced in tumors from 274 patients. Outcomes were correlated with EGFR and KRAS mutations in retrospective subset analyses.Entities:
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Year: 2005 PMID: 16043828 DOI: 10.1200/JCO.2005.02.857
Source DB: PubMed Journal: J Clin Oncol ISSN: 0732-183X Impact factor: 44.544