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Glioblastoma is the most common and most aggressive malignant brain tumor in adults. It is a grade IV astrocytoma, meaning it arises from star‑shaped support cells in the brain and spinal cord called astrocytes. Glioblastoma cells grow and divide quickly and infiltrate (spread into) nearby healthy brain tissue, which makes the tumor not able to be removed completely with surgery.
Glioblastoma tumors often contain abnormal blood vessels and areas of dead tissue (necrosis). They can sometimes extend to the opposite side of the brain via the corpus callosum or involve the fluid-filled ventricular system, but it is exceedingly rare for glioblastoma to spread outside the brain and spinal cord.
While there is currently no accepted cure, treatment is aimed at slowing tumor growth, managing symptoms, and improving length and quality of life.
Glioblastoma is an aggressive brain cancer. The median survival after diagnosis is about 15–20 months, and the five‑year survival rate is under 10%. These numbers reflect the difficulty of treating a tumor that:
Despite these challenges, ongoing progress in surgery, radiation therapy, chemotherapy, supportive care, and clinical trials is helping improve both outcomes and quality of life for many patients.
At the University of Colorado Anschutz Cancer Center, patients with glioblastoma receive compassionate, expert care from a team experienced in the complexities of brain tumor diagnoses. As the only National Cancer Institute designated Comprehensive Cancer Center in Colorado and one of four in the Rocky Mountain region, we provide advanced care informed by the latest research and medical innovation.
Our Neuro‑Oncology multidisciplinary clinic in Aurora, Colorado, specializes in treating adults with glioblastoma and other brain tumors. Patients benefit from a coordinated team of specialists who collaborate to create personalized treatment plans. Your care team may include neuro‑oncologists, neurosurgeons, medical oncologists, radiation oncologists, radiologists, palliative care specialists, genetic counselors, and nurse navigators, all dedicated to supporting you throughout your care.
This team-based approach enables patients to see multiple specialists in one location, reducing stress and streamlining care. From diagnosis to follow-up, your care is managed by professionals who communicate closely with each other and with you, ensuring your questions are addressed and your goals are prioritized.
Many patients with glioblastoma may be eligible for clinical trials at CU Anschutz. These studies offer access to new therapies not available elsewhere and demonstrate our commitment to advancing treatment options and outcomes for people with brain cancer.
At CU Anschutz Cancer Center, we treat every patient as a whole person, not just a diagnosis. We are committed to providing expert care, clear communication, and ongoing support throughout your glioblastoma treatment.
Most glioblastomas occur sporadically, meaning they develop with no identifiable cause.
Primary glioblastoma: The most common form; it develops de novo—arising directly from normal glial cells.
Secondary glioblastoma: Forms when a lower‑grade astrocytoma progresses over time into a more aggressive tumor.
Having a risk factor does not mean you will develop glioblastoma. Many people with these factors never develop a brain tumor. For the most part, there are no strong risk factors associated with glioblastoma.
Inherited glioblastoma is extremely rare, and generally speaking these tumors are not hereditary. Most cases result from random genetic changes that develop in glial cells over a person’s lifetime—not from genes passed down in families.
Glioblastoma symptoms can vary widely depending on where the tumor develops in the brain, how large it is, and how quickly it grows. If you notice new or worsening neurologic symptoms, contact your health care provider right away.
Glioblastoma most often develops in the frontal lobe—which can help control speech, behavior, memory, or movement—or the temporal lobe, which supports language, hearing, and memory formation. However, these tumors can arise anywhere in the brain, leading to a wide range of possible symptoms.
To understand your condition and create the best treatment plan, your care team will begin by reviewing your medical history and performing a detailed neurologic exam. Based on these results, your team may order additional tests. Brain imaging such as MRI, and in some cases CT, helps visualize the brain and identify the size and location of the tumor. In many cases, a biopsy or surgical removal of tumor tissue is needed to make a definitive diagnosis, allowing specialists to examine the cells under a microscope.
Your doctors may also conduct molecular testing of the tumor, including markers such as IDH status and MGMT promoter methylation, to guide treatment decisions and determine eligibility for specific clinical trials. A lumbar puncture (spinal tap) is used less commonly and is reserved for situations where a tumor may have spread to the tissue surrounding the brain or into the spinal fluid.
Imaging plays a key role in diagnosing brain tumors. CT and MRI scans help your care team understand where a tumor is located and whether it is affecting other areas of the brain. While imaging can show suspicious areas, only a tissue sample can confirm the presence, type, and grade of a primary brain tumor. Tissue can be obtained through a needle biopsy or during surgery that removes part or all of the visible tumor. Your neurosurgeon will recommend the approach that is safest and most appropriate for your situation.
In certain cases, your team may perform a lumbar puncture to collect a small sample of cerebrospinal fluid. This sample is examined to see whether tumor cells have spread to the meninges—the protective layers surrounding the brain and spinal cord.
Molecular diagnosis is another important part of modern cancer care. Because cancers differ at the molecular level, identifying these unique features allows your doctors to tailor treatment more precisely to your tumor. Some patients may also benefit from genetic testing to understand whether inherited mutations could influence their cancer risk or treatment options.
Together, imaging and tissue testing provide the information needed to confirm whether a brain tumor is present and to accurately determine its type and grade, ensuring you receive the most appropriate care.
Glioblastoma is not staged like many other cancers. Instead, brain tumors are classified by grades, which describe both the appearance of the cells under a microscope and the presence of various molecular markers and are used to determine how aggressively the tumor is likely to grow. According to the World Health Organization (WHO) grading system, all glioblastomas are grade 4 tumors, the highest and most aggressive grade. This is because glioblastoma cells look highly abnormal, possess certain molecular profiles, reproduce quickly, and tend to invade nearby brain tissue. They also form new blood vessels to support their rapid growth and may contain areas of necrosis (dead tissue). These features are present at diagnosis, which is why glioblastoma is always treated as an advanced, fast‑growing cancer.
Together, imaging, tissue sampling, and molecular testing provide the comprehensive information needed to determine whether a brain tumor is present and to accurately define its type and grade. This ensures that each patient receives a treatment plan designed specifically for their tumor’s biology.
Treatment plans are individualized and may combine several approaches. At the University of Colorado Anschutz Cancer Center, patients are cared for by a multidisciplinary team of neurosurgeons, neuro‑oncologists, radiation oncologists, neuroradiologists, neuropathologists, rehabilitation specialists, and supportive‑care experts.
Goal: Safely remove as much tumor as possible while relieving pressure on the brain. Because glioblastoma infiltrates normal brain tissue, surgery alone cannot eliminate every tumor cell.
To maximize safety and precision, our neurosurgeons may use:
Radiation therapy uses high‑energy beams to kill cancer cells or slow tumor growth.
Most patients receive:
The standard chemotherapy for newly diagnosed glioblastoma is temozolomide, an oral medication given during radiation and then in additional monthly cycles.
For recurrent disease, other oral or IV chemotherapy options may be used, often within a clinical trial. Blood counts and side effects—such as fatigue, nausea, or infection risk—are monitored closely.
A small subset of tumors carry molecular changes that make them eligible for targeted treatments. These therapies focus on specific pathways that drive tumor growth. Side effects vary depending on the drug but are often manageable with supportive care.
TTF therapy uses low‑intensity, alternating electric fields delivered through adhesive scalp patches to disrupt cancer cell division. It is typically used after chemoradiation and worn for most hours of the day. It requires the head to be shaved. The most common side effect is scalp irritation and/or thinning.
Several clinical trials aimed at improving outcomes for patients with glioblastoma are available at the CU Anschutz Cancer Center. If you are interested in participating in a clinical trial, please speak with your doctor to discuss whether any current studies may be appropriate for your treatment.
Comprehensive supportive care is a core part of neuro‑oncology at CU Anschutz Cancer Center. Your team may recommend:
Because microscopic tumor cells remain after initial treatment, most glioblastomas eventually recur. Options may include:
Your care team will partner with you to align treatment decisions with your goals and priorities.