The prognosis and treatment strategies for atypical meningiomas have been a focal point in recent research, highlighting the need for effective prognostic markers and timely surgical intervention. A study by Zanconato explored the significance of chromosome 1p deletion in a cohort of 98 primary atypical meningiomas, utilizing fluorescent in situ hybridization (FISH) to validate findings against next-generation sequencing (NGS) results, thereby refining prognostic stratification (ref: Zanconato doi.org/10.1186/s40478-025-01973-6/). Additionally, Tang's analysis of the National Cancer Database revealed that a shorter time to surgery significantly improved overall survival rates for patients with atypical intracranial meningiomas, with a hazard ratio of 1.03 for each additional month of delay (ref: Tang doi.org/10.3171/2024.11.JNS241896/). This underscores the critical role of timely surgical intervention in enhancing patient outcomes. Furthermore, Isidor's multicenter study compared various embolic agents used in preoperative embolization, finding that the choice of embolic material influenced surgical outcomes, including estimated blood loss and gross total resection rates (ref: Isidor doi.org/10.1136/jnis-2025-023062/). Liao's integration of genome-wide association studies and transcriptomics identified four novel drug targets for meningioma, emphasizing the potential for targeted therapies (ref: Liao doi.org/10.1093/braincomms/). Lastly, the introduction of SYHA1813, a novel compound that activates the p53 pathway, presents a promising avenue for treating malignant meningiomas (ref: Lan doi.org/10.3389/fonc.2025.1522249/).