ConditionCancer
Glioma
A glioma is a tumor that grows from glial cells, the support cells of the brain and spinal cord. Gliomas are the most common type of primary brain tumor. They range from slow-growing, low-grade tumors that people may live with for many years to glioblastoma, a fast-growing grade 4 cancer. Symptoms include headaches, seizures, personality changes, and weakness or speech problems depending on location. Treatment combines surgery, radiation and chemotherapy, guided by the tumor's genetic markers.
Also called: Glial tumor, glial cell tumor, diffuse glioma, brain glioma
At a glance
- What it is
- A primary brain or spinal cord tumor arising from glial cells.
- Main adult types
- Glioblastoma, astrocytoma (IDH-mutant), and oligodendroglioma.
- Grades
- 1 to 4, from slow-growing to aggressive.
- Symptoms
- Headaches, seizures, personality or memory changes, weakness, speech or vision problems.
- Treatment
- Surgery, radiation, chemotherapy (temozolomide), targeted therapy, tumor treating fields.
When to get help
Call 911 or go to the ER
- A first seizure, or a seizure lasting more than 5 minutes
- Sudden severe headache, sudden weakness, loss of speech, or vision loss
- Headache with vomiting, drowsiness or confusion that is getting worse
See a doctor within a day or two
- New, persistent headaches that are worse in the morning or when lying down, especially with nausea
- Progressive weakness, numbness, clumsiness or speech difficulty over days to weeks
- Personality change, confusion or memory loss developing over weeks
Book a routine appointment
- Headaches that are different from your usual pattern and persist for several weeks
- Gradual changes in vision, hearing, or balance
What glial cells are
Glial cells surround and support nerve cells. The main types are astrocytes, oligodendrocytes (which make the myelin insulation around nerves) and ependymal cells (which line the brain's fluid spaces). Gliomas are named after the cell type they most resemble.
Types and grades of glioma
Since 2021, the World Health Organization classifies gliomas using both their appearance under the microscope and their molecular markers, which predict behavior and response to treatment.
| Type | Key markers | Grade | Typical age | Notes |
|---|---|---|---|---|
| Glioblastoma | IDH-wildtype | 4 | Over 50 | Most common and most aggressive. See glioblastoma |
| Astrocytoma | IDH-mutant | 2, 3 or 4 | 20s to 40s | Slower-growing than glioblastoma at the same grade. See astrocytoma |
| Oligodendroglioma | IDH-mutant, 1p/19q codeleted | 2 or 3 | 30s to 50s | Best outlook of diffuse gliomas, sensitive to chemotherapy. See oligodendroglioma |
| Pilocytic astrocytoma | Often BRAF changes | 1 | Children and young adults | Usually curable with surgery |
| Ependymoma | Various | 1 to 3 | Children and adults | Near fluid spaces or spinal cord. See ependymoma |
| Diffuse midline glioma | H3 K27-altered | 4 | Mostly children | Brainstem, very serious |
"Low-grade" usually refers to grades 1 and 2, and "high-grade" to grades 3 and 4.
Symptoms
Symptoms depend on the tumor's location, size and speed of growth.
- Seizures: the first symptom in many low-grade gliomas
- Headaches: often worse in the morning or with coughing or bending, sometimes with nausea and vomiting, from raised pressure inside the skull
- Personality, mood or behavior changes, especially frontal lobe tumors
- Memory, concentration and thinking problems
- Weakness or numbness on one side of the body
- Speech and language difficulties
- Vision changes, including loss of part of the visual field
- Balance and coordination problems, with tumors in the cerebellum
- Fatigue and drowsiness
Causes and risk factors
The cause of most gliomas is unknown. Known risk factors include:
- previous radiation to the head, such as childhood radiotherapy
- inherited syndromes: neurofibromatosis type 1, Li-Fraumeni syndrome, Lynch syndrome, tuberous sclerosis
- age: glioblastoma becomes more common with age
- sex: slightly more common in men
There is no consistent evidence that mobile phones, head injury or diet cause gliomas.
Diagnosis
- Neurological examination
- MRI of the brain with contrast, the main imaging test. Advanced MRI (perfusion, spectroscopy) helps assess grade and plan surgery
- Biopsy or surgical removal to confirm the diagnosis, grade and molecular markers: IDH mutation, 1p/19q codeletion, MGMT promoter methylation (which predicts response to temozolomide), and others
- Functional MRI and mapping before surgery near speech or movement areas
Treatment
Treatment is planned by a specialist neuro-oncology team and tailored to the tumor type, grade, markers, location and the person's health.
Surgery
The goal is maximal safe resection: removing as much tumor as possible without causing new deficits. Surgeons may use awake surgery and brain mapping for tumors near critical areas. Surgery also relieves pressure and provides tissue for diagnosis.
Radiation therapy
Usually given over several weeks after surgery for high-grade gliomas, and for many grade 2 tumors, sometimes delayed while the tumor is monitored.
Chemotherapy
- Temozolomide with and after radiation is standard for glioblastoma.
- PCV (procarbazine, lomustine, vincristine) or temozolomide for oligodendroglioma and IDH-mutant astrocytoma.
Targeted and other therapies
- Vorasidenib, an IDH inhibitor, for grade 2 IDH-mutant astrocytoma or oligodendroglioma after surgery, which can delay the need for radiation and chemotherapy
- BRAF and MEK inhibitors for tumors with BRAF changes
- Tumor treating fields: a wearable device delivering electric fields to the scalp, used with temozolomide for glioblastoma
- Bevacizumab for recurrent glioblastoma, mainly to reduce swelling
- Clinical trials of new drugs, vaccines and immunotherapies
Supportive care
- steroids such as dexamethasone to reduce brain swelling
- anti-seizure medicines
- rehabilitation, palliative care and psychological support from diagnosis onward
Outlook
Outlook varies greatly by type and grade:
- Pilocytic astrocytoma (grade 1): often cured by surgery.
- Oligodendroglioma: many people live 10 to 15 years or longer.
- IDH-mutant astrocytoma: median survival is often many years for grade 2 and less for grade 4.
- Glioblastoma: median survival is about 15 to 18 months with standard treatment, though some people live much longer, especially those with MGMT-methylated tumors.
Regular MRI scans monitor for recurrence. Many people continue working and living independently for long periods with low-grade gliomas.
Frequently asked questions
What is a glioma?
A glioma is a tumor that begins in the glial cells that support nerve cells in the brain or spinal cord. It is the most common type of primary brain tumor and ranges from slow-growing low-grade tumors to aggressive glioblastoma.
Is a glioma always cancer?
Gliomas are considered brain tumors that can be benign-behaving or malignant. Grade 1 tumors such as pilocytic astrocytoma are often curable. Most diffuse gliomas in adults, even low-grade ones, infiltrate the brain and eventually progress, so they are treated as cancers.
What are the first signs of a glioma?
Common early signs include a first seizure, new persistent headaches (often worse in the morning), personality or memory changes, weakness or numbness on one side, and speech or vision problems. Symptoms depend on where the tumor is.
What is the survival rate for glioma?
It depends on the type and grade. Grade 1 gliomas are often cured. People with oligodendroglioma frequently live more than 10 years. Glioblastoma has a median survival of about 15 to 18 months with treatment, though some people live much longer.
What causes gliomas?
Most have no known cause. Risk factors include previous radiation to the head and inherited conditions such as neurofibromatosis type 1 and Li-Fraumeni syndrome. Gliomas are not caused by head injuries, and evidence does not link them to mobile phone use.
Sources
This guide was written from current patient and clinical guidance, including:
- National Cancer Institute: Adult central nervous system tumors treatment (PDQ); Glioma
- World Health Organization: Classification of Tumours of the Central Nervous System, 5th edition (2021)
- National Comprehensive Cancer Network (NCCN): Guidelines for patients, brain cancer gliomas
- American Brain Tumor Association: Glioma
- MedlinePlus (US National Library of Medicine): Brain tumor, primary, adults