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Molecular Testing of Lung Cancers

Cited 22 time in Web of Science Cited 27 time in Scopus
Authors

Shim, Hyo Sup; Choi, Yoon-La; Kim, Lucia; Chang, Sunhee; Kim, Wan-Seop; Roh, Mee Sook; Kim, Tae-Jung; Ha, Seung Yeon; Chung, Jin-Haeng; Jang, Se Jin; Lee, Geon Kook

Issue Date
2017-05
Publisher
대한병리학회
Citation
Journal of Pathology and Translational Medicine, Vol.51 No.3, pp.242-254
Abstract
Targeted therapies guided by molecular diagnostics have become a standard treatment of lung cancer. Epidermal growth factor receptor (EGFR) mutations and anaplastic lymphoma kinase (ALK) rearrangements are currently used as the best predictive biomarkers for EGFR tyrosine kinase inhibitors and ALK inhibitors, respectively. Besides EGFR and ALK, the list of druggable genetic alterations has been growing, including ROS1 rearrangements, RET rearrangements, and MET alterations. In this situation, pathologists should carefully manage clinical samples for molecular testing and should do their best to quickly and accurately identify patients who will benefit from precision therapeutics. Here, we grouped molecular biomarkers of lung cancers into three categories-mutations, gene rearrangements, and amplifications-and propose expanded guidelines on molecular testing of lung cancers.
ISSN
2383-7837
URI
https://hdl.handle.net/10371/191315
DOI
https://doi.org/10.4132/jptm.2017.04.10
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