Journal article
MET amplification identifies a small and aggressive subgroup of esophagogastric adenocarcinoma with evidence of responsiveness to crizotinib
JK Lennerz, EL Kwak, A Ackerman, M Michael, SB Fox, K Bergethon, GY Lauwers, JG Christensen, KD Wilner, DA Haber, R Salgia, YJ Bang, JW Clark, BJ Solomon, AJ Iafrate
Journal of Clinical Oncology | Published : 2011
Abstract
Purpose: Amplification of the MET proto-oncogene in gastroesophageal cancer (GEC) may constitute a molecular marker for targeted therapy. We examined a GEC cohort with follow-up and reported the clinical response of four additional patients with MET-amplified tumors to the small molecule inhibitor crizotinib as part of an expanded phase I cohort study. Patients and Methods: From 2007 to 2009, patients with GEC were genetically screened as a consecutive series of 489 tumors (stages 0, I, and II, 39%; III, 25%; IV, 36%; n = 222 esophageal, including n = 21 squamous carcinomas). MET, EGFR, and HER2 amplification status was assessed by using fluorescence in situ hybridization. Results: Ten (2%) ..
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Awarded by National Cancer Institute
Funding Acknowledgements
Supported by Pfizer and by National Cancer Institute Grant No. 5R01CA125541-05 (R.S).