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 Name | Sensitivity | Supported |
---|---|---|
Atezolizumab | Resitance or Non-Reponse | true |
Nivolumab | Resitance or Non-Reponse | true |
Pembrolizumab | Resitance or Non-Reponse | true |