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Osteosarcoma is a cancerous (malignant) bone tumor that usually develops in teenagers. It occurs when a teen is growing rapidly.
Causes, incidence, and risk factors
Osteosarcoma is the most common bone cancer in children. Age at diagnosis is around 15. Boys and girls are just as likely to get this tumor until the late teen years, when it occurs more often in boys. Osteosarcoma is also common in people over age 60.
The cause is not known. In some cases, osteosarcoma runs in families. At least one gene has been linked to an increased risk. This gene is also associated with familial retinoblastoma. This is a cancer of the eye that occurs in children.
Osteosarcoma tends to occur in the bones of the:
Osteosarcoma can occur in any bone. It occurs most commonly in large bones and in the area of bone with the fastest growth rate.
Signs and tests
Treatment usually starts after a biopsy of the tumor is done.
Before major surgery to remove the tumor, chemotherapy is usually given. This can shrink the tumor and make surgery easier. It also may kill any cancer cells that have spread to other parts of the body.
Chemotherapy medicines include:
Surgery is used after chemotherapy to remove any remaining tumor. In most cases, surgery can remove the tumor while saving the affected limb. This is called limb-salvage surgery. In rare cases, more involved surgery (such as amputation) is necessary.
You can ease the stress of illness by joining a cancer support group. Sharing with others who have common experiences and problems can help you and your family not feel alone.
If the tumor has not spread to the lungs (pulmonary metastasis), long-term survival rates are better. If the cancer has spread to other parts of the body, the outlook is worse. However, there is still a chance of cure with effective treatment.
Calling your health care provider
Call your health care provider if you have persistent bone pain, tenderness, or swelling.
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Lerner A, Antman KH. Primary and metastatic malignant bone lesions. In: Goldman L, Schafer AI, eds. Goldman's Cecil Medicine. 24th ed. Philadelphia, PA: Elsevier Saunders; 2011:chap 208.
National Cancer Institute. PDQ Osteosarcoma and malignant fibrous histiocytoma or bone treatment. Bethesda, MD: National Cancer Institute. Date last modified 8/9/2012. Available at: http://www.cancer.gov/cancertopics/pdq/treatment/osteosarcoma/HealthProfessional. Accessed November 16, 2012.
National Comprehensive Cancer Network. NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines): Bone Cancer. Version 2.2012. Available at: http://www.nccn.org/professionals/physician_glspdf/bone.pdf. Accessed November 16, 2012.
Reviewed by:Yi-Bin Chen, MD, Leukemia/Bone Marrow Transplant Program, Massachusetts General Hospital. Also reviewed by A.D.A.M. Health Solutions, Ebix, Inc., Editorial Team: David Zieve, MD, MHA, David R. Eltz, Stephanie Slon, and Nissi Wang.
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