| Literature DB >> 34114474 |
Alexander P Davis1, Wendy A Cooper2,3,4, Michael Boyer1,5, Jenny H Lee1,6, Nick Pavlakis5,7,8, Steven C Kao1,5,9.
Abstract
KRAS-mutant non-small-cell lung cancer is the most common molecular driver of lung adenocarcinoma in western populations. No KRAS specific therapy has been approved by the US FDA until 2021. Despite significant heterogeneity in comutations, patients typically receive single-agent immunotherapy or chemoimmunotherapy as standard first-line therapy. It is unclear whether KRAS mutations predict outcomes with immunotherapy; however, there is emerging data suggesting improved outcomes in patients with a TP53 comutation and worse outcomes in patients with a STK11/LKB1 or KEAP1 comutation.Entities:
Keywords: KEAP1; KRAS; LKB1; NSCLC; STK11; TP53; comutations; immune checkpoint inhibitors
Mesh:
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Year: 2021 PMID: 34114474 DOI: 10.2217/imt-2021-0090
Source DB: PubMed Journal: Immunotherapy ISSN: 1750-743X Impact factor: 4.196