NORD is very grateful to Kenneth D. Aldape, MD, Professor of Pathology, University of Texas MD Anderson Cancer Center, for assistance in the preparation of this report.
Synonyms of Astrocytoma
- No synonyms found.
- grade I astrocytoma
- grade II astrocytoma
- grade III astrocytoma
- grade IV astrocytoma
An astrocytoma is a tumor that arises from the star-shaped cells (astrocytes) that form the supportive tissue of the brain. Other supportive cells of the brain include oligodendrocytes and ependymal cells. Collectively, these cells are known as glial cells and the tissue they form is known as glial tissue. Tumors that arise from the glial tissue, including astrocytomas, are collectively referred to as gliomas.
The World Health Organization (WHO) classifies astrocytomas into four grades depending on how fast they are growing and the likelihood that they will spread (infiltrate) to nearby brain tissue. Noninfiltrating astrocytomas usually grow more slowly than the infiltrating forms. Infiltrating, or diffuse astrocytomas are more common than noninfiltrating astrocytomas. They are generally more common in men and are most common in the cerebral hemispheres of adult patients. In children they occur both in the cerebral hemispheres as well as the brain stem. Tumors from oligodendrocytes (oligodendrodendrogliomas) are also in the category of infiltrating gliomas and can occasionally be difficult to distinguish from astrocytomas. Some infiltrating gliomas are categorized as mixed oligodendroglioma-astrocytoma (oligoastrocytoma).
Grade I astrocytoma is usually a noninfiltrating tumor. The most common type of grade I astrocytoma is pilocytic astrocytoma which is also known as juvenile pilocytic astrocytoma or JPA. This tumor grows slowly but can become very large. Pilocytic astrocytoma occurs most often in the cerebellum, cerebrum, optic nerve pathway and brainstem. This tumor occurs most often in children and teens and accounts for 2% of all brain tumors.
Grade II astrocytoma is also called low-grade astrocytoma or diffuse astrocytoma and is usually an infiltrating tumor. This tumor grows relatively slowly and usually does not have well-defined borders. It occurs most often in adults between the ages of 20 and 40.
Grade III astrocytoma is also called anaplastic (malignant) astrocytoma because this tumor grows more quickly than a grade II astrocytoma. Anaplastic astrocytoma occurs most often in adults between the ages of 30 and 50, and accounts for 4% of all brain tumors.
Grade IV astrocytoma is also called glioblastoma or GBM and is the most aggressive type of nervous system tumor. It is also referred to as glioblastoma multiforme because of its wide variety of appearances under the microscope. Rarely, non-glial tissue elements can exist in a glioblastoma. The most common variant of GBM showing these additional tissue elements is called a mixed glioblastoma-sarcoma, or gliosarcoma. GBM occurs most often in adults between the ages of 50 and 80, is more common in men, and accounts for 23% of all primary brain tumors.
Symptoms of grade I and grade II astrocytomas are subtle because the brain is able to temporarily adapt to the presence of a slow-growing tumor. Symptoms of grade III and grade IV astrocytomas may be sudden and debilitating. Symptoms can result from increased pressure within the brain and may include headaches, vision changes and nausea or vomiting. Symptoms may also occur based on the location of the tumor due to interference with normal brain function and include focal seizures, difficulty with speaking, loss of balance and weakness, paralysis or loss of sensation of one side of the body. Fatigue and depression are common in individuals with an astrocytoma.
Desmoplastic infantile astrocytoma (DIA) is a very rare grade I astrocytoma. This tumor tends to occur the cerebral hemispheres and is usually diagnosed in children less than two years of age. Symptoms may include an increased head size, bulging soft spots (fontanelles) in the skull, eyes that focus downward and seizures. A related tumor, desmoplastic infantile ganglioglioma, is a mixed astrocytic and neuronal tumor, but is otherwise similar to DIA.
Subependymal giant cell astrocytoma occurs in the ventricles of the brain and is almost always associated with a genetic condition called tuberous sclerosis. Other rare neuroepithelial tumors include pleomorphic xanthoastrocytoma (PXA) and ganglioglioma (a mixed glial-neuronal tumor).
The cause of most astrocytomas is not known. Researchers speculate that genetic and immunologic abnormalities, environmental factors (e.g., exposure to ultraviolet rays, certain chemicals, ionizing radiation), diet, stress, and/or other factors may play contributing roles in causing specific types of cancer. Investigators are conducting ongoing basic research to learn more about the many factors that may result in cancer.
Astrocytomas occur with greater frequency with certain genetic disorders including Turcot syndrome, neurofibromatosis type-I tuberous sclerosis, Ollier's disease and Li-Fraumeni syndrome.
Grade I astrocytoma occurs most often in children and teens and account for 2% of all brain tumors. Grade II astrocytoma occurs most often in adults between the ages of 20 and 60. Grade III astrocytoma occurs most often in adults between the ages of 30 and 60, is more common in men and accounts for 4% of all brain tumors. Grade IV astrocytoma occurs most often in adults between the ages of 50 and 80, is more common in men and accounts for 23% of all primary brain tumors.
Symptoms of the following disorders can be similar to those of astrocytomas. Comparisons may be useful for a differential diagnosis:
Motor neuron disease is a group of neuromuscular disorders characterized by the progressive degeneration of motor neurons, the nerve cells that control movement and reflex. Symptoms of Motor Neuron Diseases may include muscle weakness, spasms and exaggerated reflexes.
Multiple sclerosis (MS) is a chronic disease of the brain and spinal cord. MS is characterized by small lesions called plaques that may form randomly throughout the brain and spinal cord. These lesions consist of areas of dissolved myelin, the fatty material that forms a sheath around nerve cells (neurons) and conducts nerve impulses. Large, star-shaped nerve cells (astrocytes) overgrow and harden in the lesions, forming scars in the brain and spinal cord called scleroses. Destruction of the myelin sheath creates a variety of neurological symptoms that may include visual difficulties, impairment of speech, abnormal skin sensations or numbness, walking disturbances and difficulties with bladder and bowel function.
There are many different types of brain tumors. The classification of brain tumors is based on the cells that the tumor originated from and the likelihood that it will spread to other tissues.
The diagnosis of astrocytoma is based on a thorough clinical evaluation, characteristic physical findings, a careful patient history, and specialized tests, such as blood tests, neuroimaging techniques, and/or other diagnostic studies. Neuroimaging techniques, such as computed tomography (CT) scanning and magnetic resonance imaging (MRI) of the brain assist in evaluating tumor size, location, and other factors. During CT scanning, a computer and x-rays are used to create cross-sectional images of certain tissue structures. MRI uses a magnetic field to create cross-sectional images of particular organs and bodily tissues. Examination of a sample of the tumor (biopsy) and microscopic examination of tumor cells is used to determine the tumor type and grade.
Grade I astrocytoma: Surgery is the standard treatment. Total surgical removal of accessible astrocytomas is often possible and successful. Accessible tumors are those that can be operated on without causing unacceptably severe damage to other parts of the brain. If surgery is performed, the surgeon will attempt to remove all identifiable parts of the astrocytoma when possible. When the astrocytoma involves a crucial part of the brain, partial removal of the growth usually reduces pressure, relieves symptoms and helps control seizures.
Full or partial removal of the astrocytoma is sometimes followed by radiation therapy to destroy any remaining tumor cells. With the use of CT (computed tomography) and MRI (magnetic resonance imaging), radiation sometimes may be deferred for several months or years while the patient is scanned at regular intervals. Radiation as primary therapy is occasionally used on grade I astrocytomas.
Chemotherapy may be administered after radiation in an attempt to destroy any cells that remain or may also be given during the course of radiation treatment. Chemotherapy may be used instead of radiation in very young children to avoid damage to the developing brain. The type of chemotherapeutic drug therapy selected is determined by a neuro-oncologist who examines the grade of tumor, previous treatment and current health status of the affected individual.
Grade I astrocytoma can sometimes progress to a higher grade so follow-up scans at regular intervals are necessary to check for re-growth.
Grade II astrocytoma: Treatment depends on the size and location of the tumor. Surgery may be used to remove accessible tumors. As with all infiltrating astrocytomas (grades II-IV) it cannot be completely removed with surgery because the tentacle-like projections of the tumor grow into the surrounding tissue. Radiation may be used if the tumor is not accessible or in addition to surgery. Grade II astrocytoma can also progress to a higher grade so follow-up is necessary to check for re-growth. A recurrent tumor may be treated with surgery, radiation or chemotherapy.
Grade III astrocytoma: Treatment depends on the size and location of the tumor, what it looks like under the microscope and how far it has spread. The standard treatment is surgery and radiation therapy, accompanied or followed by chemotherapy. If surgery is not possible, radiation and chemotherapy may be recommended. Several different types of radiation therapy are available including conventional external beam radiation, focused radiation, stereotactic radiosurgery implanted radiation or conformal radiation. A radiation oncologist determines the most appropriate form of radiation for a particular tumor. Chemotherapeutic agents that are commonly used to treat grade III astrocytoma include carmustine (BCNU), lomustine (CCNU), procarbazine, cisplatin and temozolomide. Biodegradable wafers (called Gliadel Wafers) containing BCNU is sometimes inserted in the cavity that remains after a tumor is removed. Grade III astrocytoma tend to recur and treatment depends on the grade of tumor that recurs.
The Food and Drug Administration (FDA) has approved temozolomide (Temodar) for the treatment of adults with anaplastic astrocytoma that has not responded to other forms of therapy (refractory anaplastic astrocytoma). For more information, contact:
2000 Galloping Hill Road
Kenilworth, N.J. 07033-0530
Grade IV astrocytoma: The three main forms of treatment for GBM are surgery and radiation or chemotherapy. These treatments may be used alone or in combination with one another. The initial treatment in most cases is surgical excision and removal of as much as the tumor as possible (resection). Often, only a portion of the tumor can be safely removed because malignant cells may have spread to surrounding brain tissue. Because surgery cannot completely remove a tumor, radiation therapy and chemotherapy are used following surgery to continue treatment.
The FDA has approved temozolomide (Temodar) for the treatment of adults with GBM. Temozolomide is used concurrently with radiation therapy. For more information, contact:
2000 Galloping Hill Road
Kenilworth, N.J. 07033-0530
Gliadel Wafers have been approved by the FDA for the treatment of individuals with newly-diagnosed GBM as an adjunct to surgery and radiation. It has also been approved for individuals with recurrent GBM. Several of the wafers are placed in the cavity created by the surgical removal of a GBM. The wafers release the drugs into the surrounding tissue over a period of two or three weeks. For more information, contact:
MGI Pharma, Inc.
5775 West Old Shakopee Road
Bloomington, MN 55437
Phone: (952) 346-4700
Fax: (352) 346-4800
Information on current clinical trials is posted on the Internet at www.clinicaltrials.gov. All studies receiving U.S. government funding, and some supported by private industry, are posted on this government website.
For information about clinical trials being conducted at the National Institutes of Health (NIH) in Bethesda, MD, contact the NIH Patient Recruitment Office:
Tollfree: (800) 411-1222
TTY: (866) 411-1010
For information about clinical trials sponsored by private sources, contact:
Contact for additional information about astrocytoma:
Kenneth D. Aldape, MD
Professor of Pathology
University of Texas MD Anderson Cancer Center
1515 Holcombe Blvd.
Houston, TX 77030
NORD Member Organizations:
(To become a member of NORD, an organization must meet established criteria and be approved by the NORD Board of Directors. If you're interested in becoming a member, please contact Susan Olivo, Membership Manager, at email@example.com.)
Vassall E. Essential Guide to Brain Tumors. Darby, PA: Diane Publishing Company; 2005.
Asher A, Burger PC, et al. A Primer of Brain Tumors: A Patient's Reference Manual, 8th Edition. Des Plains, Il: The American Brain Tumor Association; 2004.
Reardon DA, Rich JN, Friedman HS, Bigner DD. Recent advances in the treatment of malignant astrocytoma. J Clin Oncol. 2006;24(8):1253-65.
Jennings MT, Ivengar S. Pharmacotherapy of malignant astrocytomas of children and adults: current strategies and future trends. CNS Drugs. 2001;15(9):719-43.
Davis FG, McCarthy BJ. Epidemiology of brain tumors. Curr Opin Neurol. 2000;13(6):635-640.
MacDonald T, Packer RJ. Pediatric astrocytoma. Emedicine. http://emedicine.medscape.com/article/985927-overview. Updated February 29, 2012. Accessed March 14, 2012.
Bruce JN, Kennedy B. Glioblastoma Multiforme. Emedicine. http://emedicine.medscape.com/article/283252-overview. Updated December 6, 2011. Accessed March 14, 2012.
Lo SS, Kish KK. Imaging in juvenile pilocytic astrocytoma. Emedicine. http://emedicine.medscape.com/article/341293-overview. Updated May 27, 2011. Accessed March 14, 2012.
The Essential Guide to Brain Tumors. Edythe Vassall, ed. National Brain Tumor Society. Copyright 2010. http://www.braintumor.org/assets/docs/essentialguide.pdf. Accessed March 20, 2012
Schiff D. Low Grade Astrocytomas. American Brain Tumor Association. http://hope.abta.org/site/DocServer/LowGradeAsx.pdf?docID=301. February 2007. Accessed March 14, 2012.
Children's Hospital Boston. Glioblastoma multiforme and anaplastic astrocytoma. Copyright 2010. http://www.childrenshospital.org/az/Site962/mainpageS962P0.html. Accessed March 14, 2012.
Children's Hospital Boston. Cerebellar pilocytic astrocytoma. Copyright 2005-2011. http://www.childrenshospital.org/az/Site684/mainpageS684P0.html. Accessed March 14, 2012.
Children's Hospital Boston. Low-grade gliomas. Copyright 2010. http://www.childrenshospital.org/az/Site1249/mainpageS1249P0.html. Accessed March 14, 2012.
The information in NORD’s Rare Disease Database is for educational purposes only. It should never be used for diagnostic or treatment purposes. If you have questions regarding a medical condition, always seek the advice of your physician or other qualified health professional. NORD’s reports provide a brief overview of rare diseases. For more specific information, we encourage you to contact your personal physician or the agencies listed as “Resources” on this report.
The National Organization for Rare Disorders (NORD) web site, its databases, and the contents thereof are copyrighted by NORD. No part of the NORD web site, databases, or the contents may be copied in any way, including but not limited to the following: electronically downloading, storing in a retrieval system, or redistributing for any commercial purposes without the express written permission of NORD. Permission is hereby granted to print one hard copy of the information on an individual disease for your personal use, provided that such content is in no way modified, and the credit for the source (NORD) and NORD’s copyright notice are included on the printed copy. Any other electronic reproduction or other printed versions is strictly prohibited.
Copyright ©1990, 1995, 2005, 2007, 2012
Report last updated: 2012/03/20 00:00:00 GMT+0
NORD's Rare Disease Information Database is copyrighted and may not be published without the written consent of NORD.