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associated with microsatellite instability, BRAF mutation, medullary morphology and cytotoxic tumor-infiltrating lymphocytes . Mod Pathol 2016 ; 29 : 1104 – 1112 . 11. Llosa NJ Cruise M Tam A . The vigorous immune microenvironment of
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papillary thyroid cancer who have ALK gene fusions; however, these ALK gene fusions are rarely reported in patients with ATC. 97 – 100 BRAF mutations have been reported in patients with ATC. 35 , 101 – 103 Individual Disclosures of the NCCN
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NCCN Guidelines Insights: Non–Small Cell Lung Cancer, Version 2.2021
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David S. Ettinger, Douglas E. Wood, Dara L. Aisner, Wallace Akerley, Jessica R. Bauman, Ankit Bharat, Debora S. Bruno, Joe Y. Chang, Lucian R. Chirieac, Thomas A. D’Amico, Thomas J. Dilling, Jonathan Dowell, Scott Gettinger, Matthew A. Gubens, Aparna Hegde, Mark Hennon, Rudy P. Lackner, Michael Lanuti, Ticiana A. Leal, Jules Lin, Billy W. Loo Jr, Christine M. Lovly, Renato G. Martins, Erminia Massarelli, Daniel Morgensztern, Thomas Ng, Gregory A. Otterson, Sandip P. Patel, Gregory J. Riely, Steven E. Schild, Theresa A. Shapiro, Aditi P. Singh, James Stevenson, Alda Tam, Jane Yanagawa, Stephen C. Yang, Kristina M. Gregory, and Miranda Hughes
testing using a validated test(s) that assesses a minimum of the following potential genetic variants: ALK rearrangements (category 1), BRAF mutations, EGFR mutations (category 1), METex14 skipping mutation s , NTRK1/2/3 gene fusions, RET
Rajmohan Murali, Deborah F. Delair, Sarah M. Bean, Nadeem R. Abu-Rustum, and Robert A. Soslow
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without BRAF mutation . N Engl J Med 2015 ; 372 : 320 – 330 . 7. Brahmer J Reckamp KL Baas P . Nivolumab versus docetaxel in advanced squamous-cell non-small-cell lung cancer . N Engl J Med 2015 ; 373 : 123 – 135 . 8. Perou CM
Jessica S.W. Borgers, Richard P. Tobin, Robert J. Torphy, Victoria M. Vorwald, Robert J. Van Gulick, Carol M. Amato, Dasha T. Cogswell, Tugs-Saikhan Chimed, Kasey L. Couts, Adrie Van Bokhoven, Christopher D. Raeburn, Karl D. Lewis, Joshua Wisell, Martin D. McCarter, Rao R. Mushtaq, and William A. Robinson
mutations in patients with AGM (n=1; 5%) compared with those without (n=13; 24%) ( P =.095) ( Table 1 ). BRAF mutations were present in 45% and c-KIT mutations in 2% of the patients with AGM compared with 39% and 6%, respectively, in those without