Abstract
Background: Emerging evidence suggests that STK11 mutations may influence clinical outcome and response to immunotherapy in cancer. Materials and methods: Next-generation targeted sequencing of STK11 mutation status in a large cohort of 188 meningiomas. Results: STK11 loss-of-function mutations were identified in 3.7% of meningiomas. STK11 mutations were found in both low- and high-grade lesions and samples from primary and recurrent disease. There was a 2.8-fold increased risk of death for patients whose meningioma harbored an STK11 mutation, after controlling for lesion grade and occurrence status. The median overall survival for patients with STK11-mutated meningiomas was 4.4 years compared with 16.8 years. Conclusion: These data identify recurrent STK11 mutations in a subset of meningiomas. Genotyping of STK11 is encouraged for meningioma patients undergoing immunotherapy-based therapy.
| Original language | English |
|---|---|
| Pages (from-to) | 2585-2589 |
| Number of pages | 5 |
| Journal | Neurological Sciences |
| Volume | 41 |
| Issue number | 9 |
| DOIs | |
| State | Published - 1 Sep 2020 |
Keywords
- Central nervous system
- Meningioma
- Neurooncology
- STK11
- Sequencing