Glioblastoma (GBM)

Glioblastoma (GBM)

Glioblastomas (also called GBM) is a malignant grade 4 tumor, where a large portion of tumor cells are reproducing and dividing at any given time. They are nourished by an ample and abnormal tumor vessel blood supply. The tumor is predominantly made up of abnormal astrocytic cells, but also contain a mix of different cell types (including blood vessels) and areas of dead cells (necrosis). Glioblastomas are infiltrative and invade into nearby regions of the brain. They can also sometimes spread to the opposite side of the brain through connection fibers (corpus callosum). It is exceedingly rare for glioblastomas to spread outside of the brain.

Glioblastomas may arise de novo, meaning they begin as a grade 4 tumor with no evidence of a lower grade precursor. De novo tumors are the most common form of glioblastoma. They tend to be more aggressive and are more common in patients 60 years of age or older, though younger patients may also be affected. Alternatively, secondary glioblastomas may progress from a lower-grade astrocytic tumors (grade 2 or 3) and evolve into grade 4 tumors over time. In general, these tumors tend to be slower growing initially, but can progressively become aggressive.

Glioblastomas are usually diagnosed as either IDH-wildtype or IDH-mutant (please see the Genetic Profile section below for more information). IDH-wildtype glioblastomas are more common, tend to be more aggressive, and have worse prognosis than IDH-mutant glioblastomas.

In 2021 the World Health Organization (WHO) updated CNS tumor classifications, incorporating new knowledge gained from additional molecular markers and new diagnostic techniques. What used to be classified as Glioblastoma, IDH mutant is now classified as Astrocytoma, IDH mutant, grade 4. For information on Astrocytoma, IDH mutant, grade 4, please see our web page on Astrocytoma (Adult type).


Glioblastoma is most commonly found in the frontal lobe, followed by the temporal, parietal, and occipital lobes.


Patients with glioblastomas develop symptoms rapidly due to mass effect from the tumor itself or from the fluid surrounding the tumor that causes further brain swelling (edema). Common presenting symptoms at diagnosis include:

  • Seizures
  • Severe headaches
  • Memory and language problems
  • Changes in personality and behavior
  • Muscle weakness or paralysis
  • Fatigue
  • Issues with coordination
  • Speech, hearing, and vision problems

Other symptoms may occur depending on the size and location of the tumor.


Glioblastomas can be difficult to treat for the following reasons:

  • They are fast-growing and invade nearby brain tissue, making 100% removal nearly impossible.
  • The blood brain barrier prevents certain treatments from being able to reach the tumor.
  • They have many different types of tumor cells (heterogeneous) and can change over time, which makes them difficult to treat.

Because of this, the treatment plan for glioblastoma may combine several approaches, including surgery, radiation therapy, chemotherapy, clinical trials, Tumor Treating Fields (TTFields), and targeted therapies.

Surgery is often the first step in treating glioblastoma. Surgery allows the medical team to get a biopsy and make a diagnosis, relieve pressure on the brain, and safely remove as much tumor as possible. Glioblastomas are diffuse and have finger-like tentacles that infiltrate the brain, which make them very difficult to remove completely. This is particularly true when the tumors are growing near important regions of the brain that control functions such as language and movement/coordination.

Radiation and chemotherapy are used to slow down the growth of residual tumor after surgery and for tumors that cannot be removed with surgery. Tumor Treating Fields (TTFields) may also be offered in combination with chemotherapy.

Standard of care treatment for newly diagnosed GBM depends on a variety of factors, including molecular biomarkers (MGMT status & IDH mutation) and age. Recurrent GBM is treated based on the patient’s response to initial treatments and assessment of disease progression. Some patients may also be eligible for clinical trials. In a disease like glioblastoma, clinical trial participation is highly encouraged both in the newly diagnosed setting and in recurrence. To learn more, download the ABTA’s Clinical Trials brochure.


Prognosis means a prediction of outcome. This information is usually based on information gathered from groups of people with the same disease. It is important to remember these statistics are not individualized. How well a person responds to treatment is affected by the grading of malignancy of the tumor cells, the amount of tumor removed and their general health. Age also plays a key role in outcome. Younger adults and children tend to have a better prognosis. IDH-mutant glioblastoma tends to have a more favorable prognosis than IDH-wildtype.

The 5-year relative survival rates for glioblastoma by age group are as follows:

Children (0-14): 19.4%*

Adolescents & Young Adults (15-39): 26.0%*

Adults (40+): 5.6%*

*These percentages represent the prior classification of Glioblastoma which included what is now considered Astrocytoma, IDH mutant, grade 4.


Glioblastomas represent about 14% of all primary brain tumors. On average, more than 12,000 Glioblastoma cases are diagnosed each year in the U.S. Glioblastomas are slightly more common in men than in women.

Age Distribution

Glioblastomas can occur at any age but are more common in older patients between the ages of 65 and 74. The median age of a glioblastoma diagnosis is 65.

Risk Factors

The exact cause of glioblastoma is unknown. The majority of glioblastoma patients have no family history or identifiable risk factors. Patients with Li-Fraumeni syndrome, neurofibromatosis, Turcot syndrome Lynch syndrome, or constitutional mismatch repair deficiency syndrome, however, may be at higher risk of developing high grade gliomas like glioblastoma. Exposure to ionizing radiation as a result of radiation therapy for childhood brain tumors or leukemia is also a risk factor for high grade gliomas1.

Molecular Profile

Glioblastomas can have the presence of IDH1 and IDH2 mutations. Some tumors may also have methylated MGMT (inactive gene). Tumors that are methylated have been found to predict a longer length of survival and tend to respond better to chemotherapy like temozolomide (Temodar). In about 40% of all glioblastomas, amplification of the EGFR gene (epidermal growth factor receptor) is found. Other molecular markers include CDK4/6, TERT, and TP53.

Content last reviewed:

April 2022


Call the ABTA CareLine to receive personalized support and resources.

& Side Effects

Learn more about treatment options and common side effects.


The ABTA YouTube Channel provides educational videos about tumor types, treatments, and support strategies for newly diagnosed, survivors and caregivers.