Childhood Rhabdomyosarcoma Treatment
Treatment Options for Childhood Rhabdomyosarcoma
Key Points for this Section
A link to a list of current clinical trials is included for each treatment section. For some types or stages of cancer, there may not be any trials listed. Check with your doctor for clinical trials that are not listed here but may be right for you.
Previously Untreated Childhood Rhabdomyosarcoma
Surgery options
Childhood rhabdomyosarcoma may be treated with chemotherapy and/or radiation therapy before or after surgery. Treatment with surgery may include the following:
Rhabdomyosarcoma of the head and neck
- For tumors of the head and neck that are not near the brain and spinal cord and not in or near the eye: Treatment may include surgery (wide local excision). Some lymph nodes may be removed from the same side of the neck as the tumor. Surgery will be followed by chemotherapy with or without radiation therapy.
- For tumors of the head and neck that are in or near the eye: A biopsy of the tumor is done, followed by chemotherapy and radiation therapy. If the tumor remains or comes back after treatment with chemotherapy and radiation therapy, surgery to remove the eye and some tissues around the eye may be needed.
- For tumors of the head and neck that cannot be removed by surgery: Chemotherapy and radiation therapy are given.
Rhabdomyosarcoma of the arms or legs
Rhabdomyosarcoma of the chest or abdomen
Rhabdomyosarcoma of the area near the testicles
Rhabdomyosarcoma of the bladder and prostate
Rhabdomyosarcoma of the vagina, vulva, or uterus
Rhabdomyosarcoma in unusual areas
- For tumors of the brain: Surgery to remove the tumor followed by radiation therapy and chemotherapy.
- For tumors of the larynx (voice box): A biopsy of the tumor is followed by chemotherapy and radiation therapy. Surgery is usually not done, so that the voice is not harmed.
- For tumors of the diaphragm: A biopsy of the tumor is followed by chemotherapy to shrink the tumor. Surgery may be done later to remove any remaining cancer cells.
- For tumors of the kidney: Surgery is done to remove as much of the tumor as is safely possible.
- For tumors of the ovary: Combination chemotherapy may be followed by surgery to remove the remaining tumor.
Metastatic rhabdomyosarcoma
Chemotherapy options
Every child treated for rhabdomyosarcoma should receive chemotherapy. The dose of the chemotherapy and the number of treatments given depend on the child's risk group, as follows:
Low-risk patients
Intermediate-risk patients
High-risk patients
Radiation therapy options
Radiation therapy may be used if childhood rhabdomyosarcoma tumor cells remain after surgery, after chemotherapy, or if the tumor is of the alveolar type.
Treatment may include certain kinds of radiation therapy that cause less damage to normal tissue and lessen late effects of treatment. These include:
Check for U.S. clinical trials from NCI's list of cancer clinical trials that are now accepting patients with previously untreated childhood rhabdomyosarcoma. For more specific results, refine the search by using other search features, such as the location of the trial, the type of treatment, or the name of the drug. General information about clinical trials is available from the NCI Web site.
Recurrent Childhood Rhabdomyosarcoma
Treatment options for recurrent childhood rhabdomyosarcoma are based on many factors, including where in the body the cancer has come back, what type of treatment the patient had before, and the needs of the individual child. Treatment may include one or more of the following:
Check for U.S. clinical trials from NCI's list of cancer clinical trials that are now accepting patients with recurrent childhood rhabdomyosarcoma. For more specific results, refine the search by using other search features, such as the location of the trial, the type of treatment, or the name of the drug. General information about clinical trials is available from the NCI Web site.