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Published bySølvi Kristoffersen Modified over 5 years ago
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Identifying the Appropriate FISH Criteria for Defining MET Copy Number–Driven Lung Adenocarcinoma through Oncogene Overlap Analysis Sinéad A. Noonan, MD, MSc, Lynne Berry, PhD, Xian Lu, MS, Dexiang Gao, PhD, Anna E. Barón, PhD, Patrick Chesnut, MS, Jamie Sheren, PhD, Dara L. Aisner, MD, PhD, Dan Merrick, MD, Robert C. Doebele, MD, PhD, Marileila Varella-Garcia, PhD, D. Ross Camidge, MD, PhD Journal of Thoracic Oncology Volume 11, Issue 8, Pages (August 2016) DOI: /j.jtho Copyright © 2016 International Association for the Study of Lung Cancer Terms and Conditions
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Figure 1 Patient disposition. CMOCO, Colorado Molecular Correlates Laboratory; LCMC, Lung Cancer Mutation Consortium; MET, Mesenchymal-epithelial transition factor gene; MET/CEP7, mean MET–to–chromosome 7 centromere ratio. Journal of Thoracic Oncology , DOI: ( /j.jtho ) Copyright © 2016 International Association for the Study of Lung Cancer Terms and Conditions
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Figure 2 Rate of oncogenic drivers according to low, intermediate, and high mean mesenchymal-epithelial transition factor gene (MET) per cell value and mean MET–to–chromosome 7 centromere ratio (MET/CEP7). Journal of Thoracic Oncology , DOI: ( /j.jtho ) Copyright © 2016 International Association for the Study of Lung Cancer Terms and Conditions
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Figure 3 Complete response to first-line crizotinib in a patient with a high mean mesenchymal-epithelial transition factor gene (MET)–to–chromosome 7 centromere ratio. (A) Baseline scan demonstrating splenic metastases. (B) Complete metabolic and anatomic response on scan after 8 weeks of treatment. (C) Corresponding carcinoembryonic antigen (CEA) at baseline, after one cycle, and after two cycles. C2D1, cycle 2 day 1; C3D1, cycle 3 day 1. Journal of Thoracic Oncology , DOI: ( /j.jtho ) Copyright © 2016 International Association for the Study of Lung Cancer Terms and Conditions
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