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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Published in: | Therapeutic Advances in Medical Oncology Vol. 9; no. 9; pp. 589 - 597 |
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Main Authors: | , , , , , , |
Format: | Book Review Journal Article |
Language: | English |
Published: |
London, England
SAGE Publications
01-09-2017
Sage Publications Ltd |
Subjects: | |
Online Access: | Get full text |
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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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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 |
ISSN: | 1758-8359 1758-8340 1758-8359 |
DOI: | 10.1177/1758834017719829 |