With technological advancements in the field of precision medicine through broad-based
genomic sequencing (BGS), the interrogation of an individual's tumor genome sequence
is now possible in the course of routine clinical care. BGS allows for assessments
of clinical trial eligibility and potential matching with emerging targeted treatments
[
[1]
,
[2]
]. For this reason, the National Comprehensive Cancer Network (NCCN) guidelines strongly
advises BGS in patients with advanced non-small cell lung cancer (aNSCLC) [
[2]
].Keywords
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Article info
Publication history
Published online: February 02, 2019
Accepted:
January 22,
2019
Received in revised form:
January 11,
2019
Received:
November 4,
2018
Identification
Copyright
© 2019 Elsevier Ltd. All rights reserved.