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A visual guide

Understanding Meningioma,
from diagnosis to care

Meningiomas arise from the meninges — the protective layers around the brain and spinal cord. Most are benign and slow-growing, and the WHO 2021 system classifies them by grade and molecular features.

Plain-language explanations Evidence-based Updated continuously
Epidemiology
~35,000

New meningioma cases per year (U.S. est.)

Classification
WHO Grades 1–3

Diagnosis combines imaging, pathology, and molecular features to guide care.

Treatment model
Team-based care

Most plans combine surgery, radiation, systemic therapy, and ongoing supportive care.

Understanding Meningioma

What is meningioma, and how is it classified?

The subtypes below summarise how this condition is classified in modern neuro-oncology — each behaves differently and is treated differently.

Grade 1 — Benign

~80% of cases. Slow-growing. Often curable with complete resection. 5-year survival >90%.

Grade 2 — Atypical

~15-18% of cases. Higher recurrence rate. May require adjuvant radiation. 5-year survival ~80%.

Grade 3 — Anaplastic / Malignant

~2-3% of cases. Aggressive. High recurrence. 5-year survival ~55-65%.

Molecular markers

The biomarkers that define your tumor

Modern classification depends on specific molecular markers — each revealing something different about the tumor and its likely behaviour.

Diagnostic
NF2
Chromosome 22q Loss

Most common genetic alteration in meningioma. Loss of NF2/merlin function is associated with all grades and is foundational to meningioma biology.

~60% of meningiomas
Diagnostic
AKT1
E17K Mutation

Found predominantly in Grade 1 meningothelial meningiomas with skull base predilection. Potential therapeutic target.

~10% of meningiomas
Diagnostic
TRAF7
TRAF7 Mutation

Often co-occurs with KLF4 or AKT1 mutations. Plays a key role in non-NF2 meningioma pathogenesis.

~25% of meningiomas
Diagnostic
SMO
Hedgehog Pathway Mutation

Activating mutations in the Hedgehog signaling pathway. Preferentially found in olfactory groove meningiomas.

~5% of meningiomas
Diagnostic
KLF4
K409Q Mutation

Co-occurs with TRAF7 mutations. Strongly associated with secretory meningioma subtype.

~10% of meningiomas
Diagnostic
PIK3CA
PI3K Pathway Mutation

Activating mutations in the PI3K signaling pathway. Found in skull base meningiomas. Potential therapeutic target.

~5% of meningiomas
Prognostic
TERT
TERT Promoter Mutation

Associated with higher grade and increased recurrence risk. Considered a poor prognostic marker across meningioma subtypes.

Poor prognostic marker
Prognostic
CDKN2A/B
Homozygous Deletion

Associated with Grade 3 meningioma. WHO 2021 allows grading upgrade to anaplastic based on this deletion alone. More aggressive course.

Key grading criterion
Predictive
SMARCE1
SMARCE1 Mutation

Defines clear cell meningioma subtype. Associated with familial clear cell meningioma predisposition.

Clear cell subtype
Predictive
BAP1
BAP1 Loss

Associated with rhabdoid morphological features. Part of the BAP1 tumor predisposition syndrome affecting multiple organ systems.

BAP1 syndrome marker
Treatment

Treatment options for Meningioma

Treatment depends on tumor type, grade, location, and overall health. Most plans combine several approaches.

Surgery

Primary treatment. Simpson grading scale (I-V) for extent of resection. Skull base approaches for complex locations.

Radiation Therapy

Post-operative for incompletely resected or higher-grade tumors. IMRT and proton therapy options available.

Stereotactic Radiosurgery

Gamma Knife, CyberKnife for small tumors (<3cm), residual, or recurrent meningiomas. Single fraction delivery.

Observation

For small, asymptomatic tumors. Serial MRI monitoring at regular intervals to track growth rate.

Systemic Therapy

Limited role currently. Hydroxyurea, bevacizumab for refractory cases. Emerging: SMO inhibitors, CDK4/6 inhibitors, FAK inhibitors.

Clinical Trials

Access cutting-edge experimental treatments and emerging targeted therapies

Care team

Your multidisciplinary care team

Care is delivered by a team — specialists who diagnose and treat, and those who protect day-to-day quality of life.

Core specialist

Neurosurgeon

Performs brain or spine surgery for tumor removal or biopsy.

Best for: resection strategy, biopsy decisions, and surgery-related risk.

Core specialist

Neuro-oncologist

Brain-tumor specialist who leads treatment planning.

Best for: integrating pathology, imaging, medication, and trial options into one plan.

Core specialist

Radiation oncologist

Plans and delivers precision radiation therapy.

Best for: dose planning, side effects, and timing around surgery or systemic therapy.

Support role

Nurse navigator

Guides you through appointments, insurance, and logistics.

Best for: referrals, scheduling, records, and getting the right people in the room.

Support role

Oncology nurse

Day-to-day care coordination and symptom management.

Best for: new symptoms, medication questions, and urgent care coordination.

Support role

Mental health

Psychological support for patients and caregivers.

Best for: coping with uncertainty, caregiver strain, and adjustment after diagnosis.

Resources

You are not alone

These organisations provide information, community, and support for brain & spine tumor patients and caregivers.

Ready to explore clinical trials?

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