Synovial sarcoma can be cured if detected in the early stages. Learn about treatment and survival rates for this rare type of cancer
Synovial sarcoma can be cured if detected in the early stages. However, this cancer rarely causes any signs and symptoms during early stages. It is an aggressive type of sarcoma that may have already spread in the body by the time it is diagnosed.
Whether synovial sarcoma can be cured depends on:
- Stage of cancer (how early it is diagnosed and treated) including how far it has spread in the body
- Extent to which sarcoma can be removed by surgery
- Site of synovial sarcoma in the body
How is synovial sarcoma treated?
Doctors decide on a treatment plan based on factors such as the site of synovial sarcoma, its stage, the patient’s age, preferences, and whether there are any underlying health conditions.
Primary treatment for synovial sarcoma involves surgical removal of the entire tumor along with a margin of surrounding healthy tissue. This ensures that all the cancerous tissue has been removed from the site. Surgical removal gives better outcomes when the tumor has not spread to other sites in the body (metastasized). Moreover, surgical removal depends on the site where the tumor is present. If the tumor is at an inoperable site, it may not be removed by surgery.
Doctors may also consider other therapy options with or without surgery:
- Radiation therapy before or after the surgery to kill the sarcoma cells
- Chemotherapy if the sarcoma has spread in the body or cannot be completely removed by surgery
Studies have suggested that about 36% to 76% of patients with synovial sarcoma live for at least 5 years after their first diagnosis. They may need to follow up with their doctors to detect and treat recurrence at an early stage.
What is synovial sarcoma?
The term synovial sarcoma is a misnomer because this cancer does not arise from synovial tissue (tissue lining the cavities of joints, tendon sheaths, and bursae) as was previously thought. Instead, synovial sarcoma or synovial cell sarcoma is a type of cancer arising from soft tissues (such as the muscles, tendons, and ligaments).
It is one of the rarest types of cancer that affects about 1-2 individuals out of every million people in the United States.
Synovial sarcoma often occurs within the first 30 years of life and affects men more than women. It is typically not inherited, and the affected patient may not have family members with a history of the cancer.
What are the symptoms of synovial sarcoma?
Synovial sarcoma generally does not cause symptoms during the initial stages. Usually, the patient reports:
- A small lump, often painless, that has rapidly increased in size
- As the tumor increases in size, it may cause symptoms such as pain, numbness, and reduced range of motion
Synovial sarcoma can occur in any part of the body, but it is most commonly located around the:
Synovial sarcoma may also occur in the hands, lungs, or abdomen.
How is synovial sarcoma diagnosed?
Synovial sarcoma may be diagnosed by:
- Taking a detailed medical history and performing a physical examination
- Performing imaging tests including X-ray, computed tomography (CT) scan, ultrasonography, and magnetic resonance imaging (MRI) scan
- Performing tumor biopsy (collecting a small sample of the tumor tissue and examining it under a microscope)
- Conducting cytogenetic analysis that involves detecting specific chromosomal abnormalities (such as chromosomal translocation between the X chromosome and chromosome 18)
Timely diagnosis is the key to proper treatment. A painless lump anywhere in the body must be investigated as soon as possible.