WHO grade 3 anaplastic meningioma represents the most aggressive end of the meningioma spectrum. This subtype is associated with rapid growth, a high likelihood of early recurrence, and a risk of systemic metastasis — alongside distinct molecular features at the genetic and epigenetic level.
This protocol applies to patients with cerebral meningioma classified at WHO grade 3 (anaplastic). These tumors are characterized by rapid growth, early recurrence, risk of systemic metastasis, and particular molecular features on genetic and epigenetic levels, making management substantially more complex than lower-grade disease.
When no further local treatment option remains available, systemic salvage pharmacotherapy may be considered. The approach involves targeted antiangiogenic or multikinase inhibitor strategies — the specific selection, sequencing, and application criteria are detailed in the full protocol.
DOI: 10.1093/neuonc/noab150
These tumors are characterized by rapid growth, early recurrence, risk of systemic metastasis, and particular molecular features on genetic and epigenetic levels.
Pharmacotherapy using bevacizumab or multikinase inhibitors targeting VEGF receptors should only be considered if no further local treatment option exists.
View source ↗