Literature DB >> 30758123

Unique mutation patterns in anaplastic thyroid cancer identified by comprehensive genomic profiling.

Saad A Khan1, Bo Ci2, Yang Xie2, David E Gerber1,2, Muhammad S Beg1, Steven I Sherman3, Maria E Cabanillas3, Naifa L Busaidy3, Barbara A Burtness4, Andreas M Heilmann5, Mark Bailey5, Jeffrey S Ross5, David J Sher6, Siraj M Ali5.   

Abstract

INTRODUCTION: Anaplastic thyroid cancer (ATC) is a highly aggressive thyroid cancer. Those ATC with genomic alterations (GAs) in TSC2, ALK, and BRAF may respond to targeted therapies.
METHODS: Comprehensive genomic profiling on 90 ATC specimens identified base substitutions, short insertions and deletions, amplifications, copy number alterations, and genomic rearrangements in up to 315 cancer-related genes and 28 genes commonly rearranged in cancer.
RESULTS: Median patient age was 65 (range, 33-86) years, 50 patients were male. There was a mean of 4.2 GA per case, range 1-11. The most common GA were TP53 (66%), BRAF (34%), TERT (32%), CDKN2A (32%), and NRAS (26%). BRAF V600E and NRAS/HRAS/KRAS alteration were mutually exclusive. BRAF, CDKN2A, PIK3CA, and JAK2 were more frequent in patients >70 years of age; while myc, PTEN, and NRAS were more common in those ≤50 years.
CONCLUSION: ATC shows many GA with potential therapeutic significance and suggesting different molecular pathways can lead to ATC.
© 2019 Wiley Periodicals, Inc.

Entities:  

Keywords:  anaplastic; neoplasms; thyroid

Year:  2019        PMID: 30758123      PMCID: PMC6542589          DOI: 10.1002/hed.25634

Source DB:  PubMed          Journal:  Head Neck        ISSN: 1043-3074            Impact factor:   3.147


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