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.
Keywords: Central nervous system; Meningioma; Neurooncology; STK11; Sequencing.