In addition to genetic factors, the clinical implications of these findings are significant. A prospective phase II trial evaluating the dual mTORC1/2 inhibitor vistusertib in patients with NF2-associated meningiomas showed limited efficacy, with only 6% of tumors exhibiting a partial response (ref: Jordan doi.org/10.1093/noajnl/). This highlights the need for more effective treatment options for patients with meningiomas, particularly those associated with genetic syndromes. Moreover, a large retrospective cohort study analyzed the impact of postoperative radiotherapy on non-malignant meningiomas, revealing that while surgery remains the primary treatment, the addition of radiotherapy may improve outcomes in specific patient populations (ref: Jiang doi.org/10.1002/cam4.6177/). Overall, the integration of genetic insights and treatment outcomes is crucial for advancing the management of meningiomas.