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This section is for teenagers and young adults and is about treatment of a type of cancer called a soft tissue sarcoma. There are different types of soft tissue sarcoma, and the information in this section covers rhabdomyosarcomas, synovial sarcomas and fibrosarcomas, which are the most common types in teenagers.
If you have a different type and want to know more, please contact us|.
The three main types of treatment for soft tissue sarcomas are surgery, chemotherapy and radiotherapy.
Most people have a combination of treatments.
If the sarcoma is in a part of the body where it’s difficult to remove with surgery, then chemotherapy and radiotherapy are the main treatments.
Your doctors will plan your treatment based on:
If you have any questions about your treatment, ask your doctor or nurse. They’ll be happy to help you understand what's involved.
If you have a type of soft tissue sarcoma called a soft tissue Ewing's sarcoma, it's treated in the same way as a Ewing sarcoma in a bone. You can read more about this in our bone cancer| section.
Surgery to remove the cancer is one of the main treatments for soft tissue sarcomas. Your surgeon will aim to remove all of the cancer, and at the same time reduce any long-term effects for you as much as possible.
The operation you have will depend on the size of the sarcoma and where it is in your body. You might meet other people with the same type of sarcoma who have had a different operation. Everyone is different. Your cancer doctor and specialist nurse will talk to you about your operation and make sure you understand why you need to have it and what's involved. Below are some of the different types of operation you might have for a soft tissue sarcoma.
We also have more information about what will happen before and after the operation in our surgery| section.
You’ll have an operation called a wide local excision to remove the cancer and an area of tissue surrounding it (called the margin). This tissue is checked to make sure it doesn’t contain any cancer cells. If there are cancer cells in the margin, some people may need to have more surgery.
Sometimes the surgeon removes some of the lymph nodes (glands) near the cancer to find out if there are any cancer cells there. If there are cancer cells in the lymph nodes, some people may need to have more surgery.
If you need to have a large area of tissue removed, you may need to have a skin graft or soft tissue graft. This is when skin and sometimes muscle is taken from a different part of the body to place over the area where the sarcoma was removed from. This is called plastic surgery or reconstructive surgery, It’s done to give you as natural an appearance as possible and to make sure you can still do the things you did before your operation. Both operation sites will gradually heal over a few weeks after the operation.
If the sarcoma is in an arm or leg you’ll have limb-sparing surgery. This means the surgeon takes away the cancer without removing the arm or leg. You’ll have all of the tumour taken away from your limb, including any bone and muscle affected by the tumour.
The surgeon then replaces what they’ve taken away. This may involve using plastic surgery or reconstructive surgery (see skin graft or soft tissue graft) to replace the tissue that’s been removed, or it may involve surgery to replace any bone that’s been removed. If you need to have bone removed, the surgeon replaces it with a specially designed metal implant called an endoprosthesis.
If the cancer affects a bone in or near a joint, your joint can be replaced with an artificial one.
Your physiotherapist might give you exercises before your operation to strengthen your muscles.
If you've had chemo, you'll need two or three weeks to recover from the treatment before you can have your op. Doctors will check that your blood count has returned to normal. They'll also make sure that you're well enough to have the operation. If you’ve lost weight or been off your food, you might need to build yourself up a bit before the op. The hospital dietitian can help you do this. You’ll probably see a physiotherapist, who’ll give you exercises to do to strengthen your muscles.
If you want to have a look at the endoprosthesis that will be put in during your surgery, your keyworker or surgeon can usually arrange this.
You’ll have a bandage or splint on your limb to keep it still and let it heal.
You’ll probably have a tube, called a drain, coming out of your wound. This stops fluid building up in your wound. A nurse will take it out after about 3-4 days.
You won’t feel like eating or drinking much for a few hours after your op, so you’ll be given fluids into a vein. This is called a drip.
You’ll probably feel a bit sore to begin with, but you’ll be given strong painkillers to help. It’s important to tell the nurses if you need extra pain relief. The pain usually starts to get better within 2-3 days. As time goes on you'll need fewer painkillers and will start to feel a lot more comfortable.
Once you’re home you’ll probably feel a bit better and stronger every day. But if you do have any problems it’s important to get them treated right away, as a delay could mean they get much more serious.
If your new joint starts to stiffen up you may need some more physiotherapy, so tell your doctor so they can arrange this for you if necessary.
If you notice any new redness, soreness or swelling in the limb that’s been operated on, it’s especially important to get in touch with your doctor right away. You might have an infection that needs treatment, so you’ll need to see the surgeon who did your operation without delay.
There’s more information about the long-term effects of limb-sparing surgery in our section on living with and after a soft tissue sarcoma|.
Very occasionally the only way to get rid of the cancer is to remove the limb where the sarcoma is growing. This is called an amputation and it’s only ever done if there is no alternative.
Your doctor will talk things through with you so that you fully understand what’s involved. Losing a limb can feel very scary and you might want to talk to a specialist nurse or a counsellor about your feelings. It might also help to talk to someone who has had an amputation - your nurse or doctor can arrange this. It's really important to get support at this tough time.
You’ll have bandages or a plaster cast on the area that’s been operated on. There’ll be a tube (called a drain) coming from the wound to remove any excess fluid that builds up. The drain is usually taken out by a nurse on the ward after 3-4 days. You’ll also have a drip to give you fluid into a vein in your arm until you feel like eating and drinking again.
You’ll probably feel a bit sore after your op, especially for the first 2-4 days, but you'll be given strong painkillers to help with this. It’s important to tell the nurses if you need extra pain relief. You may have pain that feels as if it’s coming from the part of the limb that’s been removed. This is known as ‘phantom pain’. Let your doctor or nurse know if you have this - there are medicines that can help ease it or take it away. It usually gets better and goes away in time.
A physiotherapist will visit you a day or so after your operation. They’ll show you exercises to keep your muscles strong and flexible.
If you’ve had an arm removed, you’ll be able to get up and move around once you’ve recovered from the anaesthetic and don’t feel too sore. If you’ve had a leg removed, the physiotherapist will show you how to move around in bed and get from your bed to a chair. You'll probably be moving around with crutches or in a wheelchair within a few days.
Once you’re up and around you’ll go to the hospital gym for physiotherapy. This is a big part of your recovery. Your physiotherapist will give you more exercises to do as your wound heals and you get stronger.
It’ll take a few months for your limb to heal to its final shape after the operation, so you won’t be fitted with your permanent prosthesis until this happens. In the meantime, you’ll be given a temporary prosthesis and you’ll start learning how to use it in physiotherapy. A specialist team will help you recover from the operation and get you used to the artificial limb that you’re fitted with.
You'll be able to go home about two weeks after your operation.
You can read more about recovering after the operation in our information about living with and after a soft tissue sarcoma|.
Radiotherapy treats cancer by using high-energy x-rays to destroy cancer cells while doing as little harm as possible to normal cells. There’s more information about it in the radiotherapy| section.
For soft tissue sarcomas radiotherapy can be given in a number of situations:
Radiotherapy is generally given every weekday (Monday-Friday). Each treatment takes a few minutes.
Radiotherapy isn't painful, but it can cause some side effects. After a few treatments you may begin to feel tired, and your skin may go red or get darker and feel sore or itchy around the area that’s being treated. This gets better once your radiotherapy treatment is over.
Other side effects depend on which part of your body is being treated. Having radiotherapy around a joint can make it feel stiff, but physiotherapy can help.
This is when you're given anti-cancer drugs to destroy the cancer cells. For soft tissue sarcomas, chemo can be given in a number of situations:
For soft tissue sarcomas chemo is given into a vein, usually through a central line, a port or a PICC line. You can find out more about chemo| and how it's given..
You’ll have chemo over a few days, then you’ll have a few weeks off so that your body can recover from any side effects. The days you have the chemo and the rest period afterwards is called a cycle. Most people have several cycles of chemo.
You'll probably need to stay in hospital for some of the time during chemo, but it’s often possible to have part of your treatment as an outpatient.
Different chemo drugs are used for soft tissue sarcomas, and you’ll usually have two or three drugs in combination. This is sometimes called a regimen or treatment plan. You may be given chemotherapy treatment as part of a clinical research trial.
Some of the main chemotherapy drugs for soft tissue sarcomas are:
If you have a rhabdomyosarcoma, you may be given ifosfamide, vincristine and actinomycin. Giving these drugs together is called IVA.
You might also be given ifosfamide, vincristine actinomycin and doxorubicin. Giving these drugs together is called IVADO.
We have more information about chemotherapy|, including information about individual drugs| and combinations of drugs|. IVA and IVADO chemotherapy. This info is written for anyone who's looking for information about chemotherapy, not just for young adults.
Other types of soft tissue sarcoma can be treated with different combinations of drugs, such as ifosphamide and doxorubicin, or vinorelbine and cyclophosphamide. Your cancer doctor and specialist nurse will explain more about the type of chemotherapy you’re going to have and how many cycles you’ll need.
Different chemo drugs cause different side effects. Some people have just a few side effects and others have more. It's hard to know how it's going to be for you, as everyone’s different. The most common are hair loss, tiredness, sickness and being more at risk of getting an infection.
Side effects can often be controlled, so always let your doctor or nurse know about the side effects you’re having. They can usually do something to improve them. Most side effects are short-term (temporary) and gradually disappear once treatment stops.
If you want to know more about the type of chemo you’re having and its side effects, there’s lots more information in the chemotherapy section.
We also have more info about:
|If you're looking for information about soft tissue sarcomas in people of all ages, please see our general soft tissue sarcoma| section.
Content last reviewed: 1 June 2012
Next planned review: 2014
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