Ewing sarcoma

Ewing sarcoma is a rare type of cancer that affects bones or the tissue around bones.

It mainly affects children and young people, with most cases diagnosed in people aged 10 to 20. It's more common in males than females.

Symptoms of Ewing sarcoma

The main areas affected by Ewing sarcoma are the:

  • legs (most often around the knee)
  • pelvis
  • arms
  • ribs
  • spine

Symptoms include:

  • bone pain – this may get worse over time and may be worse at night
  • a tender lump or swelling
  • a high temperature (fever) that doesn't go away
  • feeling tired all the time
  • weight loss

Affected bones may also be weaker and more likely to break. Some people are diagnosed after they have a fracture.

Tests for Ewing sarcoma

Ewing sarcoma can be difficult to diagnose because it's quite rare and the symptoms can be similar to lots of other conditions.

Several tests may be needed to diagnose the cancer and see where it is in the body.

These tests may include:

Treatments for Ewing sarcoma

Treatment for Ewing sarcoma often involves a combination of:

  • surgery to remove the cancer
  • chemotherapy – where medicine is used to kill cancer cells
  • radiotherapy – where radiation is used to kill cancer cells

Most people have chemotherapy to shrink the cancer, followed by surgery to remove as much of it as possible and then further chemotherapy to kill any leftover cancer cells.

Radiotherapy is often used before and after surgery, or it may be used instead of surgery if the cancer can't be removed safely.

Your care team will recommend a treatment plan they think is best. Talk to them about why they have suggested it and ask about the benefits and possible risks involved.

As Ewing sarcoma is rare and requires complicated treatment, you should be treated by a team specialising in the condition. If it affects your bones, surgery should be carried out at a specialist bone cancer centre.

Surgery

There are three main types of surgery for Ewing sarcoma:

  • removing the affected bone or tissue – this is called a resection
  • removing the bit of bone containing cancer and replacing it with a piece of metal or a piece of bone taken from another part of the body – this is called a limb-sparing surgery
  • removing all or part of an arm or leg – this is called an amputation 

The best option depends on where the cancer is in the body and how big it is.

Ask your care team which type of surgery they recommend and what care might be needed afterwards – for example, if you'll need a prosthetic limb and support to help you regain the use of the affected limb.

Outlook for Ewing sarcoma

Ewing sarcoma can spread to other parts of the body quite quickly. The earlier it's diagnosed, the better the chance there is of the treatment being successful.

It can be cured in some cases, but this might not be possible if the cancer has spread.

The cancer can also come back after treatment, so regular check-ups will be offered to look for any signs of this.

Overall, more than half of people with Ewing sarcoma live at least five years after being diagnosed, but this can vary quite a lot.

Speak to your care team if you would like to know the chances of treatment being successful for you or your child.

More information and support

Being told you or your child has cancer can be very upsetting and overwhelming.

As well as the support from your care team, you may find it useful to get information and advice from charities and support groups.

Two of the main organisations for people with Ewing sarcoma are:

Other good sources of information and support include:

There may be a clinical trial suitable for your or your child. You can ask your doctor for further information and can find out about trials for Ewing sarcoma at the Euro Ewing Consortium and the Cancer Research UK clinical trials page.

Information about you

If you or your child has Ewing sarcoma, your clinical team will pass the information on to the National Congenital Anomaly and Rare Diseases Registration Service (NCARDRS).

This helps scientists look for better ways to prevent and treat this condition. You can opt out of the register at any time.

Find out more about the NCARDRS register.

Page last reviewed: 28/07/2017
Next review due: 28/07/2020