A trial looking at treatment for patients with Ewing's Sarcoma or peripheral Primitive Neuroectodermal Tumour (pPNET) (EURO-EWING 99)
This trial is looking at chemotherapy, surgery and radiotherapy for children, young people and adults with Ewing’s sarcoma or primitive neuroectodermal tumour (PNET).
This trial is for children and adults up to the age of 50. We use the term ‘you’, but of course if you are a parent, we are referring to your child.
Ewing's sarcoma and peripheral Primitive Neuroectodermal Tumour (PNET) are similar types of cancer mostly affecting teenagers, young adults and children. These cancers mainly develop in or near the bones.
Ewing's sarcoma and PNET are usually treated with chemotherapy first. This is usually followed by surgery, radiotherapy and further chemotherapy, or a combination of these. This trial will compare several different combinations of chemotherapy drugs to see if they are more effective or have fewer side effects than the standard treatments normally used.
Recruitment
Phase
Who can enter
This trial is open to children and adults up to the age of 50 years.
You can enter this trial if you
- Have been diagnosed with Ewing’s sarcoma or PNET
- Have satisfactory blood results
You cannot enter this trial if you
- Have any other medical condition or illness that means you cannot have the treatment given in this trial
- There is a delay of more than 45 days between a tissue sample being taken from the cancer and registration on to the trial or the start of chemotherapy
- Are over 50 years of age
Trial design
This is a phase 3 trial. if you take part you will have a central or long line put in. It makes it easier to give chemotherapy and take blood samples.
First, you will have a course of chemotherapy called ‘induction’ chemotherapy. The drugs are called vincristine, ifosfamide, doxorubicin and etoposide. This is usually given the shortened name of VIDE. These drugs are given through the central line over 3 days in 3-week cycles.
This treatment takes at least 18 weeks. Your treatment may take longer if your chemotherapy is delayed by side effects (see below). During this time you will have stem cells collected. Stem cells are very early blood cells, which are collected and stored in case you need them in the future to replace blood cells damaged by chemotherapy. This is called a stem cell transplant.
After the induction chemotherapy, you may have surgery to remove the cancer. Your oncologist, surgeon and radiotherapy specialist will decide what further treatment you should have and this will be discussed with you.
You will then be put into 1 of 4 treatment groups, depending on
- The size of the tumour
- How well the chemotherapy has worked
- Whether the cancer has spread or not and where it has spread to
Everybody will have one cycle of treatment with VAI (vincristine, actinomycin D and ifosfamide). Chemotherapy after that is different for each group.
If you are in group 1, the treatment given so far has worked well and your cancer has not spread. You will have 7 more cycles of VAI.
People in groups 2 and 3 will be randomised to have one of two different treatments. Neither you nor your doctor will be able to decide which treatment you have.
If you are in group 2, the treatment given so far has not worked as well and the doctors were not able to remove all of the cancer during your operation. You will have either
- 7 more cycles of VAI or
- 1 cycle of busulphan and melphalan chemotherapy followed by a stem cell transplant
If you are in group 3, your cancer has spread to your lungs. You will have either
- 7 cycles of VAI (vincristine, actinomycin D and ifosfamide) and radiotherapy treatment to the lungs or
- 1 cycle of high dose busulphan and melphalan chemotherapy, followed by a stem cell transplant and no radiotherapy
If you are having a stem cell transplant, you will have it the day after chemotherapy has finished. This means the stem cells collected from you at the beginning of treatment will be given back through a drip into your central line.
If you are in group 4, your cancer has spread to places other than the lungs. The commonest sites for spread are other bones and, or the bone marrow. After the initial chemotherapy, your treatment will be decided on an individual basis. You may be offered treatment as part of another trial.
Hospital visits
Before your treatment, you will have a biopsy of your cancer. The researchers may also ask your permission to keep samples of your cancer to use in future research into the causes and behaviour of this type of cancer. Before, during and after your treatment, you will have a number of tests. These include
- Blood tests
- X-rays
- MRI or CT scans
- Tests to check that your heart is healthy
- Bone scan
- Bone marrow biopsy.
The treatment given for Ewings and PNET is very intensive. Your will be in hospital on and off for some months. This will vary depending on the type of treatment you have.
When the treatment has finished, a doctor will see you
- Every month for 6 months, then
- Every 2 months for 6 months
- Every 3 months for a year
- Every 6 months for 3 years
- Every year after that
Side effects
All chemotherapy drugs have side effects. The most common side effects are
- A drop in blood cells causing an increased risk of infection, bleeding problems, tiredness and breathlessness
- Feeling or being sick
- Hair loss
- Sore mouth
There is more information about the particular side effects of ifosfamide, vincristine, doxorubicin, etoposide, actinomycin D, cyclophosphamide, busulphan and melphalan in the main cancer drugs section of CancerHelp UK.
There is information about the side effects of radiotherapy on CancerHelp UK. The most common side effects of radiotherapy to the lungs are
- Sore or dry skin
- Tiredness
- Sore throat or trouble swallowing
- Feeling sick
Location of trial
For more information
Cancer Research UK
Angel Building
407 St John Street
London
EC1V 4AD
Tel: 0808 800 4040
Email: cancer.info@cancer.org.uk
Please note: we cannot help you to join a specific trial. Unless we state otherwise in this trial summary, you must go through your own doctor.






