Soft tissue sarcomasOverview
Soft tissue sarcomas are a group of rare cancers affecting the tissues that connect, support and surround other body structures and organs.
Tissues that can be affected by soft tissue sarcomas include fat, muscle, blood vessels, deep skin tissues, tendons and ligaments. Bone sarcomas are covered separately.
Soft tissue sarcomas can develop in almost any part of the body, including the legs, arms and trunk (torso).
Symptoms of soft tissue sarcomas
Soft tissue sarcomas often have no obvious symptoms in the early stages.
They can cause symptoms as they get bigger or spread. The symptoms depend on where the cancer develops.
- cancer in the tissue under the skin may cause a soft, painless lump that can't easily be moved around and gets bigger over time
- cancer near the stomach may cause tummy (abdominal) pain, a persistent feeling of fullness and constipation
- cancer near the lungs may cause a cough or breathlessness
You should see your GP if you have a worrying lump – particularly one that's getting bigger over time or is the size of a golf ball or larger – or any other troublesome symptoms.
Although it's much more likely you have a non-cancerous condition, such as a cyst (fluid under the skin) or lipoma (fatty lump), it's important to get your symptoms checked out.
Types of soft tissue sarcoma
There are many different types of soft tissue sarcoma, depending on where in the body it develops.
- leiomyosarcoma – develops in muscle tissue
- liposarcoma – develops in fat tissue
- angiosarcoma – develops in the cells of the blood or lymph glands
- gastrointestinal stromal tumours (GISTs) – develop in the connective tissues that support the organs of the digestive system (a charity called GIST UK provides information and advice for people with GISTs)
Causes of soft tissue sarcomas
Cancer occurs when cells multiply uncontrollably, forming growths called tumours.
In the vast majority of soft tissue sarcomas it's unclear what causes this to happen, but there are a number of things known to increase the risk, including:
- age – soft tissue sarcomas can occur at any age, including in children, but are more common in middle-aged or elderly people and your risk increases as you get older
- certain genetic conditions – some genetic conditions, such as neurofibromatosis type 1 and retinoblastoma, are associated with an increased risk of soft tissue sarcomas
- previous radiotherapy – some people who have previously had radiotherapy for another type of cancer go on to develop a soft tissue sarcoma, often many years later
- exposure to certain chemicals – exposure to some chemicals, including vinyl chloride, dioxins and phenoxyacetic herbicides, has been associated with increased rates of soft tissue sarcomas
Diagnosing soft tissue sarcomas
If your GP feels there's a possibility you have cancer, they'll refer you for a number of hospital tests.
A diagnosis of a soft tissue sarcoma will usually be made by a hospital specialist and will be based on your symptoms, a physical examination, and the results of:
- scans – an ultrasound scan is usually the first test performed and is fairly simple and quick; further scans such as magnetic resonance imaging (MRI) scan may be performed later
- a biopsy – where a sample of suspected cancerous tissue is removed using a needle or during an operation so it can be tested and analysed in a laboratory
If a diagnosis of a soft tissue sarcoma is confirmed, these and further tests will also help determine how likely the cancer is to spread (known as the "grade"), and whether or how far the cancer has spread (known as the "stage").
Treatments for soft tissue sarcomas
People with a soft tissue sarcoma are cared for by a team of doctors and nurses at specialist centres, who will help decide on the most appropriate treatment.
The best treatment depends on things such as where the cancer developed, the type of sarcoma it is, how far it has spread, your age and your general health.
The main treatments are:
- surgery to remove any tumour
- radiotherapy – where high-energy radiation is used to kill cancer cells
- chemotherapy and other medications to kill cancer cells
Surgery is the main treatment for soft tissue sarcomas that are diagnosed at an early stage.
It usually involves removing the tumour along with a section of surrounding healthy tissue. This will help ensure no cancer cells are left behind.
Every effort will be made to reduce the impact of surgery on the appearance and function of the affected body part. But there is a chance you'll have some difficulty using the affected body part after surgery and sometimes further surgery may be needed to repair it.
In a very small number of cases, there may be no option but to amputate the part of the body where the cancer is located, such as part of the leg.
In some sarcomas, radiotherapy is used before or after surgery to improve the chance of cure. This is carried out using a machine that directs beams of radiation at a small treatment area.
Radiotherapy alone may also sometimes be used when surgery is not possible, to reduce symptoms caused by the sarcoma or slow its progression.
Chemotherapy is very occasionally used before surgery to shrink a tumour and make it easier to remove. This involves being given anti-cancer medication directly into a vein (intravenously).
Chemotherapy may also be used alone or alongside radiotherapy for soft tissue sarcomas that can't be surgically removed.
Common side effects of chemotherapy include feeling tired and weak all the time, feeling and being sick, and hair loss. These can be unpleasant but are usually temporary.
There are also other types of anti-cancer medications used to treat sarcoma that may be given as injections or tablets.
Outlook for soft tissue sarcomas
The outlook for a soft tissue sarcoma mostly depends on the type of sarcoma it is, how likely it is to spread (the grade) and how far it has already spread (the stage) by the time it's diagnosed.
If it's detected at an early stage or is a low grade tumour and it can be removed during surgery, a cure is usually possible. However larger, higher grade tumours have a greater risk of coming back or spreading.
After initial treatment, you'll need regular check-ups to look for any signs the cancer has come back. You may also need physiotherapy and occupational therapy to help you manage any physical difficulties resulting from surgery.
A cure isn't usually possible if a soft tissue sarcoma is only detected when it has already spread to other parts of the body, although treatment can help slow the spread of the cancer and control your symptoms.
Want to know more?
- Cancer Research UK: soft tissue sarcomas
- Macmillan: soft tissue sarcomas
- Sarcoma UK: soft tissue sarcoma
Page last reviewed: 10/09/2016
Next review due: 10/09/2019