Treating KRAS-mutant NSCLC: latest evidence and clinical consequences

KRAS mutations represent one of the most prevalent oncogenic driver mutations in non-small cell lung cancer (NSCLC). For many years we have unsuccessfully addressed KRAS mutation as a unique disease. The recent widespread use of comprehensive genomic profiling has identified different subgroups with...

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Bibliographic Details
Published in:Therapeutic Advances in Medical Oncology Vol. 9; no. 9; pp. 589 - 597
Main Authors: Garrido, Pilar, Olmedo, María Eugenia, Gómez, Ana, Paz Ares, Luis, López-Ríos, Fernando, Rosa-Rosa, Juan Manuel, Palacios, José
Format: Book Review Journal Article
Language:English
Published: London, England SAGE Publications 01-09-2017
Sage Publications Ltd
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Summary:KRAS mutations represent one of the most prevalent oncogenic driver mutations in non-small cell lung cancer (NSCLC). For many years we have unsuccessfully addressed KRAS mutation as a unique disease. The recent widespread use of comprehensive genomic profiling has identified different subgroups with prognostic implications. Moreover, recent data recognizing the distinct biology and therapeutic vulnerabilities of different KRAS subgroups have allowed us to explore different treatment approaches. Small molecules that selectively inhibit KRAS G12C or use of immune checkpoint inhibitors based on co-mutation status are some examples which anticipate that personalized treatment for this challenging disease is finally on the horizon.
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ISSN:1758-8359
1758-8340
1758-8359
DOI:10.1177/1758834017719829