This page has been written for parents and carers whose child is having radiotherapy treatment to the testes. The page explains the side effects your child may experience during and after treatment, and how best to cope with them.
We understand that this is a worrying time for children and their families. You may feel that you have been given lots of information about your child’s treatment. We hope this information answers some of your questions surrounding radiotherapy.
If you still have any questions or concerns, please ask. We are here for to help.
We want to involve you and your child in all the decisions about their care and treatment. If you decide to go ahead with treatment, by law, we must ask for your consent and will ask you to sign a consent form. This confirms that you agree to your child having the procedure and understand what it involves.
Staff will explain all the risks, benefits, and possible alternatives before they ask you to sign a consent form. If you are unsure about any aspect of your child’s proposed treatment, please do not hesitate to speak to the team looking after your child.
- You and your child will see a clinical oncologist who will discuss treatment options with you. You and your child may also meet the paediatric/TYA clinical nurse specialist, specialist paediatric/TYA radiographer and health play specialists.
- Your child will be consented for radiotherapy.
- Radiotherapy treatment planning appointment - Your child will have a radiotherapy planning appointment.
- First treatment - Your child will start treatment 1-2 weeks after the planning appointment. Each appointment will take approximately 20 minutes.
- Review clinics - Your child will be reviewed by their consultant once a week during treatment. All review clinics are in the radiotherapy department and are timed with your child’s treatment.
- Treatment complete - Your child will be reviewed by their clinical oncologist 2-3 weeks after treatment has ended. This will either be at Great Ormond Street Hospital, University College Hospital or your child’s referring hospital.
Radiotherapy appointments: All take place in the Radiotherapy Department, basement floor, main UCH hospital building.
Radiotherapy is the specialised treatment of cancer (and some other diseases) using high energy radiation beams. These can either be photons (also called x-rays), electrons or protons. Photons and electrons are delivered from a machine called a linear accelerator whilst protons are delivered from a machine called a cyclotron. University College Hospital Trust is one of two NHS proton beam therapy (PBT) centres in the UK, alongside The Christie in Manchester.
Proton beam therapy (PBT) is an advanced form of radiotherapy. However, it is not appropriate to treat all paediatric/TYA tumours with proton beam therapy. The most appropriate treatment for your child will be decided by their clinical oncologist and discussed with you.
Radiotherapy does not hurt, and it will not make your child radioactive. They are completely safe to be around siblings, friends, family, and pregnant women. Your child will feel nothing from the treatment and the machine will not touch them. The most important thing is for your child to lie very still for treatment.
Lying still can be very difficult for some children and we have health play specialists who will support your child throughout their treatment. However, some children, particularly very young children, will require a general anaesthetic for their treatment.
Treatment is given daily Monday to Friday, including Bank Holidays. A course of treatment can last up to 4 weeks. Your child’s treatment schedule will be decided by their clinical oncologist and confirmed on your first visit to the radiotherapy or proton beam therapy department.
Before beginning radiotherapy, your child’s treatment must be carefully planned. Their first visit will be to the radiotherapy planning pre-treatment department.
There will be plenty of opportunity to explore what radiotherapy involves for your family. You will meet the team members who will spend time getting to know your child’s needs and how best to support them, and the family, through treatment.
We have a series of short films and photo books that help to explain the different aspects of radiotherapy. This allows children and young people the opportunity to ask questions and to gain an understanding of what radiotherapy is all about. The radiotherapy paediatric team, which includes a specialist paediatric radiographer, a paediatric clinical nurse specialist and radiotherapy health play specialists, will go through step by step what to expect with treatment specific to your child.
Whenever possible, and especially with younger children, we plan separate visits to the mould room, CT scanner and treatment machine in advance of the actual treatment. This is a hands-on experience and questions are encouraged. This ensures your child is comfortable and familiar with what is going to happen.
For more information on preparing your child for radiotherapy treatment you may contact the health play specialists directly on 020 3447 3792.
The side effects that your child may experience are usually mild, as the dose of radiotherapy needed to treat the testes is relatively low. Your child’s clinical oncologist and specialist radiographer will discuss with you how the radiotherapy will affect your child in more detail. However, there will still be plenty of opportunity to talk about anything that you feel needs further discussion.
There are side effects that start during treatment. They gradually get worse during treatment and for a couple of weeks afterwards and then get better after several weeks. Late effects can develop months or years after treatment has ended.
We give radiotherapy treatment in addition to surgery and/or chemotherapy. Patients receiving chemotherapy in addition to radiotherapy may experience more severe or additional side effects to those listed here, depending on the drug regimen used. The main side effects that occur during radiotherapy treatment are:
Skin changes
The skin in the area being treated will gradually change colour. Your child’s skin will gradually become pink /red or darker, depending on their skin colour. Your child may get some dry peeling of the skin in the treatment area, which may become itchy. During treatment we advise that your child wash normally using warm water and the soap products they would normally use.
Gently pat the skin dry with a soft towel. Radiotherapy skin reactions cannot be prevented, but to minimise any skin irritation we recommend using a moisturiser of your choice. Use the moisturiser frequently and gently smooth it on to your child’s skin until it is absorbed. You do not need to wipe the moisturiser off before treatment, but please do not apply moisturiser immediately before their treatment. If your child does not use a moisturiser, speak to the radiographers and they will be able to suggest a few options.
If your child’s skin becomes irritated or peels, stop using the moisturiser. They will be referred to the radiotherapy review team for appropriate skin care. We recommend your child wears loose cotton boxer shorts during treatment, and to avoid elasticated pants as these may rub and irritate their skin.
Pubic hair loss
In many cases the pubic hair in post-pubertal boys has been lost due to chemotherapy. If not, it will start to fall out about two weeks after the start of treatment. It usually begins to grow back about three months after radiotherapy has finished.
Passing urine
During treatment your child’s penis will be moved out of the treatment field as much as possible using tape. However, it is possible for your child to experience some mild discomfort on passing urine. This is a normal reaction as the radiation can irritate the urethra (the tube running through the penis). If your child experiences any discomfort, we advise drinking plenty of fluids.
Eating and drinking
It is important that your child tries to eat a well-balanced diet and drink plenty of fluids during treatment. Some children may lose their appetite during treatment. Your child will be weighed weekly by the team and if there is any significant weight loss your child will be referred to the dietitian for helpful advice about nutrition.
It is important that your child drinks plenty of fluids, between one to two litres a day. This can include water, squash, or hot drinks. This will vary depending upon their individual needs. You will be advised accordingly by the team members.
Tiredness
Tiredness is a very common side effect of treatment. Your child may feel more tired and have less energy than usual, both during and after treatment. Do not worry, this is normal. The tiredness is usually at its worst near the end of treatment and for several weeks afterwards. Allow your child to do as much as they feel they can and rest when they need to. However, gentle exercise has been found to improve energy levels in patients.
Some children do not have a problem with tiredness and should be encouraged to lead a normal life as much as possible. Please tell us if your child is struggling with tiredness. They can be referred to physiotherapy and occupational therapy for practical tips and advice.
Late side effects incurred during treatment can appear to develop months or years after radiotherapy has finished. They are the hardest to accurately predict and, unfortunately, when they do occur, they are usually permanent.
Fertility
Radiotherapy affects the production of sperm from the testes, and this will lead to infertility and can affect the production of the male sex hormone testosterone. Your child will be referred to an endocrinologist to discuss the implications on growth and sexual maturation.
Second malignancy
Very rarely, children who have received treatment for one particular tumour may develop another type of tumour some years later. The radiotherapy doctors will discuss this with you if it is relevant to your child.
Other factors, such as smoking and excess sun exposure may also lead to an increased cancer risk in later life. It is therefore very important that any child who has received this treatment never smokes and always takes precautions against excess sun exposure.
This page deals with the physical aspects of your child’s treatment, but their emotional wellbeing and that of the family is just as important.
Having treatment can be deeply distressing for your child and family. Within the radiotherapy department there will be access and support from the paediatric clinical nurse specialist, the specialist paediatric radiographer, health play specialists, treatment radiographers and the radiotherapy review team.
However, if your child requires further medical or emotional support, they can be referred to a variety of health professionals specialising in children’s and young people’s needs.
Once your child has finished radiotherapy treatment you will be given a follow-up appointment to see the radiotherapy doctors in two to three weeks’ time. This will either be at Great Ormond Street Hospital, University College Hospital, or your child’s local referring hospital.
Any side effects your child is experiencing will continue for some weeks after treatment has finished.
The side effects may become worse before they start to improve. This can be very worrying for families. We expect the side effects to worsen, but please be assured they will gradually settle.
Please continue to follow the skin care advice you have been given by the radiotherapy team until your child’s skin returns to normal.
If you are worried about your child’s skin or any other side effects after their radiotherapy treatment, please call the paediatric clinical nurse specialist or paediatric specialist radiographer for advice. Please see the contact numbers at the bottom of this page.
My child’s keyworker is:
Paediatric/TYA Clinical Nurse Specialist
t: 07929 079599Paediatric/TYA Specialist Therapeutic Radiographer
t: 07817 941313
Radiotherapy Health Play Specialists
t: 07929 834430/ 07929 834428
e: uclh.
Radiotherapy Reception
t: 020 3447 3700/3701
Radiotherapy Review Team (via Radiotherapy Reception)
t: 020 3447 3700/3701
T11 North Ward
t: 020 3447 1102
T11 North Nurse In Charge (available 24 hours)
t: 07939 788096
T12 North Ward
t: 020 3447 1202
T12 North Nurse In Charge (available 24 hours)
t: 07908 468555
TYA Ambulatory Care (Monday to Friday, 8am to 6.30pm)
t: 020 3447 1837
TYA Ambulatory Care (available 24 hours)
t: 020 3456 7111
If you have any concerns that you would like to discuss in confidence, please contact our PALS (Patient Advice and Liaison Service) for information and advice.
t: 020 3447 3042
e: uclh.
Young Lives vs Cancer (formerly CLIC Sargent)
t: 0300 330 0803
w: www.
Teenage Cancer Trust
t: 020 7612 0370
e: hello
w: www.
Teens Unite
t: 01992 440091
e: info
w: teensunite.org
Childrens Cancer and Leukaemia Group (CCLG)
e: info
w: www.
Children With Cancer UK
t: 0800 222 9000
e: info
w: www.childrenwithcancer.org.uk
Macmillan Cancer Support
t: 0808 808 0000
e: cancerline
w: www.
Cancer Research UK
t: 0808 800 4040
w: www.
Carers UK
t: 0808 808 7777
e: adviceline
w: www.
NHS Choices
w: www.
UCLH cannot accept responsibility for information provided by other organisations.
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Page last updated: 29 July 2024
Review due: 30 June 2025