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A trial looking at treatment for children and young adults with an ependymoma (SIOP Ependymoma Program II) Pathway 1
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This trial is looking at treating ependymoma with chemotherapy after surgery and radiotherapy. It is open to children and young adults whose ependymoma has been completely removed by surgery. Cancer Research UK supports this trial.
There are 2 parts to this trial. In the 1st part the trial committee looks at the results of your tests and scans. The 2nd part is looking at treatment pathways.
More about this trial
Ependymoma is a type of brain tumour that mostly affects children and young people. We use the term ‘you’ in this summary, but if you are a parent, we are referring to your child.
Doctors usually treat ependymoma by removing it with surgery. Afterwards they might give radiotherapy to where the tumour was. But there is still a risk the tumour could come back in the same place or in another part of the brain or spine.
Researchers think that giving chemotherapy after radiotherapy might help stop the tumour coming back.
To find this out half the children and young people will have radiotherapy only. The other half will have chemotherapy after radiotherapy.
The aims of this trial are to find out
- how well chemotherapy after surgery and radiotherapy works to stop ependymoma coming back
- about the side effects of having chemotherapy after surgery and radiotherapy
- how safe it is to give chemotherapy after surgery and radiotherapy
Who can enter
The following bullet points list the entry conditions for this trial. Talk to your doctor or the trial team if you are unsure about any of these. They will be able to advise you.
You may be able to join this trial if all of the following apply. You
- Have been newly diagnosed with an ependymoma in the brain that is grade 2 or grade 3
- Have had surgery to remove your tumour
- Have had an
MRI scanafter surgery and if there is any tumour left it measures less than 5mm
- Have had an MRI scan and a
lumbar puncturethat shows your tumour has not spread to the spine
- Are able to have radiotherapy and chemotherapy
- Have satisfactory blood test results
- Are willing to use reliable contraception during treatment and for 6 months afterwards if you are sexually active and you or your partner could become pregnant
- Are between 1 year and 22 years old
You cannot join this trial if any of these apply
- You have been diagnosed with an ependymoma called a subependymoma, ependymomablastoma or myoxopapillary ependymoma
- You have already had radiotherapy
- You have already had chemotherapy apart from steroids
- Your ependymoma started in the spine
- You are already having treatment with another anti tumour drug
- You are already taking part in another clinical trial looking at treatment for ependymoma
- You are unable to have any of the drugs used in the trial for any reason
- You have an infection
- There is a medical or another reason why you can’t have the amounts of fluids you need as part of the treatment in this trial
- You have any other medical condition or mental health problem that the trial team think could affect you taking part
- You are pregnant or breastfeeding
There are 2 parts to the SIOP Ependymoma Program II.
In part A you have all the tests and scans that are normally done to diagnose your tumour. A national committee looks at the results of the tests and scans. This is to confirm your diagnosis and consider the most appropriate pathway for you.
The team want to find out more about ependymoma and its treatment. With your permission you will be entered on to a national registry even if you aren’t offered a treatment pathway. They will look at your hospital records to find out what treatment you have.
The trial team need 480 children and young people from the UK and Europe to join part A.
This is an international phase 3 trial. The trial team need 320 children and young people from the UK and Europe to join.
It is a randomised trial. After surgery to remove your tumour you are put into 1 of 2 groups by a computer. Neither you nor your doctor will be able to decide which group you are in.
Half of those who join will have radiotherapy (
The other half will have radiotherapy followed by chemotherapy.
You have radiotherapy once a day (Monday to Friday) for 6 to 7 weeks.
Before starting chemotherapy you have a central line put in. You have all your treatment as a drip through the central line. All blood samples will be taken through the central line.
You start chemotherapy 4 weeks after finishing radiotherapy. The chemotherapy drugs are
You have a combination of these drugs at regular times over 16 weeks.
- week 1 - on the first day of treatment you have vincristine, cyclophosphamide and etoposide. You then have etoposide for the next 2 days
- weeks 2 and 3 – no treatment
- week 4 - you have vincristine and cisplatin on the same day
- week 5 – no treatment
These 5 weeks of treatment is repeated another 2 times. Then you have a final week of treatment. In this week you have vincristine, cyclophosphamide and etoposide on the 1st day. You then have etoposide only for the next 2 days.
Quality of life studies
The trial team will ask you to fill out a few questionnaires
- before you start treatment
- 2 years after your diagnosis
- 5 years after your diagnosis
The questionnaires ask about side effects and how you’ve been feeling. This is called a quality of life study.
For children and teenagers diagnosed under the age of 18 they will ask you to do the same questionnaires again when you are 18 years old.
Tissue and blood samples
With your permission the researchers will ask for a sample of your cancer that was removed when you had surgery. They will also ask to take extra blood and
You see the doctor to have some tests before taking part. These tests include
- A physical examination
- Blood tests
- Urine test
- Lumbar puncture
- MRI scan of the head and spine
- Hearing test
- Test to see how your brain works (neurological test)
You see the doctor once a week during radiotherapy for a blood test and physical examination.
You stay in hospital on the days you are having chemotherapy. During chemotherapy the doctor will see you regularly to see how you are.
After your treatment has finished you see the doctor
- every 3 months for a year
- every 4 months for the 2nd year
- every 6 months for the 3rd, 4th and 5th year
- then at least once a year until you are 18
At these visits you will have
- A physical examination
- Blood tests
- MRI scan
You have a hearing test every 6 months in the 1st year and at 5 years.
After you are 18 years old your doctor will tell you how often they want to see you.
The most common side effects of the chemotherapy drugs used in this trial are
- a drop in blood cells causing bruising, bleeding and an increased risk of infection
- feeling and being sick
- loss of appetite
- mouth ulcers
- hair loss
Vincristine can also cause
- tingling in the hands and feet
- changes to the way your kidneys work
- constipation with tummy (abdominal) pains
- nerve pain
- reduced sense of touch
Cisplatin can also cause changes to the way the kidneys work and changes to hearing.
We have more information about the side effects of
We have information about the side effects of radiotherapy to the brain.
How to join a clinical trial
Professor R Grundy
Cancer Research UK
Centre Léon Bérard
University of Birmingham
This is Cancer Research UK trial number CRUK/12/036.