Paediatric Series No.16 - Radiotherapy to the pelvis

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.

1. You and your child will see a clinical oncologist radiographer who will discuss treatment options with you. You will also meet the paediatric/TYA clinical nurse specialist, specialist paediatric/TYA radiographer and health play specialists
2. Your child will be consented for radiotherapy or proton beam therapy.
3. Radiotherapy/ Proton Beam treatment planning appointment - Your child will have a planning CT scan using intravenous contrast dye if required. Some children may also require an MRI scan.
4. First treatment - Your child will start treatment 2-3 weeks after the planning scan. Each appointment will take approximately 30-40 minutes.
5. Review clinics - Your child will be reviewed by their consultant once a week during treatment. All review clinics are in the radiotherapy and proton beam therapy department and are timed with your child’s treatment.
6. 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.

Proton Beam Therapy appointments: All take place in the Proton Beam Therapy Department, floors B3 and B4, Grafton Way 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 6 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 or proton beam therapy, your child’s treatment must be carefully planned. Their first visit will be to the radiotherapy or proton 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.

Radiotherapy for children is an individualised treatment, and any side effects will vary depending on which area of pelvis is being treated, the type of radiotherapy chosen for your child and the radiotherapy dose given. 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. Some children may experience peeling of the skin which can be sore. If your child’s skin peels and is sore, they will be referred to the radiotherapy review team for appropriate skin care advice.

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 blisters and peels, stop using the moisturiser. They will be referred to the radiotherapy review team for appropriate skin care.

Avoid exposing the skin in the treatment area to strong sunlight or extreme temperature changes during treatment. After radiotherapy, the skin in the treatment area is always going to be more sensitive to the sun, so it needs to be protected with clothing, and we recommend that you always use a high protection sun cream, Factor 50 or more, on your child’s skin in strong sunlight.

Feeling sick

Very rarely, some children may feel sick and vomit if radiotherapy is given to the pelvis. Your child will be prescribed regular anti-sickness medication to take during their treatment, which may cause constipation. However, if they are still feeling sick it is important to tell us so we can refer them for further medication.

Diarrhoea

Mild diarrhoea may occur but is unusual. This is due to the radiation irritating the bowel. Your child may also experience wind pains and/or cramping sensations. If the diarrhoea persists or becomes severe your child may be prescribed regular antidiarrhoeal medication. It is important that your child maintains a good fluid intake if they have diarrhoea.

Effects on the bladder

During pelvic radiotherapy it is possible that your child may experience a burning sensation on passing urine and an increase in the need to pass urine. This is due to the radiotherapy irritating the bladder and is called “radiation cystitis”. If your child experiences such symptoms, please inform a member of staff. Your child will be sent for a urine test to check that it is radiation cystitis and not an infection. It may help if your child increases their fluid intake.

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.

Blood and bone marrow system

Treating the pelvis may affect the bone marrow. Bone marrow makes blood cells and is found in the centre of bones such as the spinal bones. The white blood cells (which fight infection) and platelets (which are important for blood clotting) might be affected.

Your child’s blood count will be monitored regularly during radiotherapy. If your child requires a blood transfusion, this will be arranged with the paediatric/teenage oncology teams.

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.

Growth

Radiotherapy will affect the growth of bones and soft tissues in the treated area. In younger children this will mean that the treated area will be smaller, thinner, or less muscular than the untreated areas.

The radiation may affect the growth of the vertebrae (the bones of the spine) and the pelvic bones if they are included in the treatment field. There might be some underdevelopment of these bones, with some loss of height and a small waist. The loss of height is unlikely to be more than two inches and will probably be less, but this will depend on your child’s age at treatment.

Bowel problems

Any potential bowel problems depend on the dose of radiotherapy given. The symptoms may vary from mild diarrhoea to bleeding. However, sometimes after surgery and radiotherapy the tissue surrounding the bowel can stick together (adhesions), and this can sometimes require further surgery to correct. This is a rare problem, but please do speak to the doctors or your child’s GP if you are worried.

Bladder

The bladder may shrink in size and be slightly smaller after radiotherapy. This may mean your child passes urine more often. Rarely, some bleeding may occur in the urine. This is not usually serious, but if it occurs it is important to let your child’s doctor, specialist nurse or GP know. They may wish to arrange further tests. 

Female fertility

It is likely that radiotherapy to the pelvis may mean treating both ovaries and the uterus (womb). This will almost invariably cause pubertal arrest and infertility, in which case hormone replacement therapy will be necessary. Some young girls may apparently recover ovarian function and retain a small window of fertility as adults. The doctors will discuss this with you and your child.

Male fertility

It is often possible to avoid treating the testes, but sometimes it cannot be avoided. The doctors will be able to tell you if the dose to the testes is likely to cause infertility or 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.

Low bone density (osteopaenia)

Low bone density can occur for several reasons. These can include immobilisation, poor nutrition, low calcium, steroid therapy as well as radiotherapy to the skeleton. Weight bearing exercise, eating a healthy diet and timely hormone replacement therapy can all prevent osteopaenia occurring. Your child will be screened for osteopaenia in the endocrine clinic as he/she grows up.

Second malignancy

Very rarely, children who have received treatment for one 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 079599

Paediatric/TYA Specialist Therapeutic Radiographer
t: 07817 941313

Radiotherapy Health Play Specialists
t: 07929 834430/ 07929 834428
e: uclh.radiotherapyplayspecialists@nhs.net

Proton Beam Therapy reception
t: 020 3456 8000/8001

Proton Beam Therapy Review Team (via Proton Beam Therapy reception)
t: 020 3456 8000/8001

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.pals@nhs.net

Young Lives vs Cancer (formerly CLIC Sargent)
t: 0300 330 0803
w: www.younglivesvscancer.org.uk

Teenage Cancer Trust
t: 020 7612 0370
e: hello@teenagecancertrust.org
w: www.teenagecancertrust.org

Teens Unite
t: 01992 440091
e: info@teensunite.org
w: teensunite.org

Children’s Cancer and Leukaemia Group (CCLG)
e: info@cclg.org.uk
w: www.cclg.org.uk

Children With Cancer UK
t: 0800 222 9000
e: info@childrenwithcancer.org.uk
w: www.childrenwithcancer.org.uk

Macmillan Cancer Support
t: 0808 808 0000
e: cancerline@macmillan.org.uk
w: www.macmillan.org.uk

Cancer Research UK
t: 0808 800 4040
w: www.cancerresearchuk.org

Carers UK
t: 0808 808 7777
e: adviceline@carersuk.org
w: www.carersuk.org

NHS Choices
w: www.nhs.uk

UCLH cannot accept responsibility for information provided by other organisations.