Annotation Detail

Information
Associated Genes
STK11
Associated Variants
STK11 MUTATION
STK11 MUTATION
Associated Disease
lung adenocarcinoma
Source Database
CIViC Evidence
Description
In a retrospective analysis in two separate datasets (Stand Up To Cancer 2 Cohort and Checkmate-057), patients with concomitant KRAS and STK11 mutations had significantly worse response rates, PFS and OS compares to KRAS only and KRAS-TP53 Mutant Patients. This work identifies STK11/LKB1 alterations as the most prevalent genomic driver of primary resistance to PD-1 axis inhibitors in KRAS-mutant lung adenocarcinoma. Genomic profiling may enhance the predictive utility of PD-L1 expression and tumor mutation burden and facilitate establishment of personalized combination immunotherapy approaches for genomically defined LUAC subsets.
Variant Origin
somatic
Variant Origin
Somatic
Evidence URL
https://civic.genome.wustl.edu/links/evidence_items/6441
Gene URL
https://civic.genome.wustl.edu/links/genes/5534
Variant URL
https://civic.genome.wustl.edu/links/variants/715
Rating
4
Evidence Type
Predictive
Disease
Lung Adenocarcinoma
Evidence Direction
Supports
Drug
Atezolizumab,Nivolumab,Pembrolizumab
Evidence Level
B
Clinical Significance
Resistance
Pubmed
29773717
Drugs
Drug NameSensitivitySupported
AtezolizumabResitance or Non-Reponsetrue
NivolumabResitance or Non-Reponsetrue
PembrolizumabResitance or Non-Reponsetrue