Medulloblastoma

Also called: cerebellar PNET

What is medulloblastoma?

Medulloblastoma is a cancerous tumor—also called cerebellar primitive neuroectodermal tumor (PNET)—that starts in the region of the brain at the base of the skull, called the posterior fossa.

  • These tumors tend to spread to other parts of the brain and to the spinal cord.

How common is medulloblastoma?

  • Medulloblastoma is the most common malignant brain tumor of childhood, and it accounts for about 20 percent of all childhood brain tumors.
  • Between 250 and 500 children are found to have medulloblastoma each year in the United States.
  • Most medulloblastoma tumors are found in children younger than age 16, but they can rarely occur in adults.
  • Medulloblastoma is slightly more common in boys than in girls.

What are the symptoms of medulloblastoma?

If your child has medulloblastoma, the following symptoms may occur:

  • Headaches
  • Morning nausea or vomiting that gradually gets worse
  • Clumsiness
  • Problems with handwriting
  • Visual problems (rare) at the time of diagnosis

If the tumor has spread to the spinal cord, symptoms may include:

  • Back pain
  • Trouble walking
  • Problems controlling bladder and bowel functions

How is medulloblastoma treated?

  • Surgery—is usually the first step in treating medulloblastoma:
    • The goal is to take out as much of the tumor as possible.
    • If the tumor has been completely removed, the patient is treated with reduced-dose radiation to the brain and spinal cord before receiving chemotherapy.
    • If some tumor remains after surgery, or if the cancer has spread, the patient is given higher-dose radiation therapy before chemotherapy.
  • Radiation therapy—uses high-energy X-rays or other types of radiation to kill cancer cells or stop them from growing.
  • Chemotherapy (“chemo”)—uses powerful medicines to kill cancer cells or stop them from growing (dividing) and making more cancer cells:
    • Chemo is injected or given orally, so that it can travel throughout the body.
    • Combination therapy uses more than one type of chemo at a time.

What are the survival rates for medulloblastoma?

Survival rates in children with medulloblastoma depend on the patient’s age and how much the tumor spreads.

  • If the disease has not spread, survival rates are around 70 to 80 percent.
  • If the disease has spread to the spinal cord, the survival rate is about 60 percent.
  • Children younger than age 3 often have lower survival rates because their disease tends to be more aggressive.

Why choose St. Jude for your child’s medulloblastoma treatment?

  • St. Jude is the only National Cancer Institute-designated Comprehensive Cancer Center devoted solely to children.
  • The hospital has one of the largest pediatric brain tumor programs in the United States.
  • St. Jude has created more clinical trials for cancer than any other children’s hospital in the United States.
  • The nurse-to-patient ratio at St. Jude is unmatched—averaging 1:3 in hematology and oncology, and 1:1 in the Intensive Care Unit.
  • The program offers a closely knit group of doctors, scientists, nurses and support staff providing the many types of treatment and support services crucial to the complete care of children with brain tumors.
  • Because St. Jude doctors and scientists work closely, they are always studying ways to better understand and treat the tumor. Through this partnership, they have discovered that not all medulloblastoma tumors are the same. The team members are now working to show that medulloblastoma can be better treated by focusing therapy on these differences.
  • The current St. Jude clinical trial for treatment of medulloblastoma is the first to treat differences in medulloblastoma. Tests determine which type of medulloblastoma each child has and how aggressive that cancer is. Therapy is then based on these results and targeted to each patient’s tumor.

Contact the Brain Tumor Team any time, 24 hours a day, 7 days a week.

Call our Brain Tumor Coordinator, Tabatha E. Doyle, RN:
(901) 595-2544 or
(901) 595-4599

Or email us at braintumors@stjude.org

Associated Clinical Trials

SJMB12: A Clinical and Molecular Risk-Directed Therapy for Newly Diagnosed Medulloblastoma/PNET

Clinical and Molecular Risk-Directed Craniospinal Irradiation and Combination Chemotherapy in Treating Younger Patients With Newly Diagnosed Medulloblastoma

Diseases Treated:

Medulloblastoma (includes all variants of medulloblastoma and posterior fossa PNET)

Eligibility:

  • Diagnosis of newly medulloblastoma
  • Must be least 3 but not more than 22 years of age
  • Has not received previous treatment with radiation therapy or chemotherapy
  • Must start treatment within 36 days of surgery to remove the tumor
View Trial

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