This information has been written for parents and carers whose child is having radiotherapy treatment to the whole lungs. This 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 page answers some of your questions surrounding radiotherapy.
If you still have any questions or concerns, please ask. We are here 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 or proton beam therapy.
- 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.
- First treatment - Your child will start treatment 2-3 weeks after the planning scan. Each appointment will take approximately 30-40 minutes.
- 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.
- 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.
UCLH 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 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 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.
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.
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.
Sore throat
Your child may experience a mild discomfort when swallowing food as the radiotherapy irritates the gullet (oesophagus). In most cases, children are still able to eat and drink normally, but some may require oral medication to ease any discomfort.
Effects on the voice
Very rarely, your child’s voice may become sore and occasionally hoarse. Some children may require oral medication to ease any discomfort. When the treatment has finished it may be a few weeks before his/her voice starts to recover.
Eating and drinking
It is important that your child tries to eat a well-balanced diet and drink plenty of fluids during treatment. If your child has a sore throat due to treatment, they may lose their appetite or find swallowing food painful. They may require oral medication to assist with swallowing. 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.
Feeling sick
Occasionally, some children may feel sick and vomit because of the radiotherapy treatment. This can be well controlled with anti-sickness medication which will be prescribed if your child experiences such symptoms.
Hair Loss
There may be a loss of hair at the back of the neck if this is in the treatment area. Once treatment is over the hair will start to regrow in three to six months.
Cough
Occasionally, some children may experience a dry irritating cough. This is a short-term reaction to the radiotherapy and can be eased with a simple linctus.
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 whole lungs 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.
Lung function
It is possible for lung function to be affected by the radiotherapy treatment. This can take two forms: six to twelve weeks after radiotherapy your child may experience some shortness of breath and dry cough. This may be due to radiation pneumonitis, which may be treated with a short course of steroids and usually recovers completely. This occurs in a small proportion of children only. In some children symptoms may never occur. There may be some long-term effect on your child’s breathing. This is very unusual, but if it occurs it tends to be noticeable on moderate to severe exercise only.
After treatment your child will have regular lung function checks in a dedicated follow-up service. It is very important that any child who has received this treatment never smokes, especially if he/she has received chemotherapy as well.
Decreased thyroid function
Radiotherapy can affect your child’s thyroid gland if it is in the treated area. It may become underactive, overactive (very rarely), or tend to form lumps many years after treatment has finished. This reduces the level of thyroid hormone that regulates the body’s metabolism. Your child will be monitored through regular blood tests and if a dysfunction is detected, it can easily be treated.
Growth
Radiotherapy can 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), collar bones and ribs if they are included in the treatment field. There might be some underdevelopment of these bones, with some loss of height and a small chest.
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. The radiotherapy doctors will discuss this with you and your child.
Heart
The heart is also in the treatment field when the whole lungs are treated. Radiation to the heart can eventually cause later problems with function and/or rhythm disturbance, particularly if radiotherapy is given with chemotherapy. This will be monitored closely in a late effects clinic.
Some treated females have an increased risk of heart failure in later life, particularly under the stressful conditions of pregnancy and labour. Pre-pregnancy checks are essential, and, in the case of pregnancy, it is important that a full medical history is known by the obstetrician and that obstetric care is hospital-based.
Breast development
Radiotherapy to the whole lungs may cause a reduction in breast development in female patients. Both breasts will be underdeveloped, but this should occur symmetrically. Lactation (milk production in pregnancy) can also be reduced by radiotherapy which may prevent breast feeding. Any lumps in the breast should be reported to a doctor as they can be worrying.
Splenic dysfunction
If your child has received radiotherapy or proton beam therapy to the upper abdomen or lower chest there is the possibility that their spleen may have been irradiated. The spleen helps the body fight against bacterial infections. The spleen is very radiosensitive, and radiotherapy can have an impact on splenic function in the future. The higher the dose received, the higher the risk of splenic dysfunction. Patients with a dysfunctional spleen are at an increased risk of severe, life-threatening infections such as pneumonia, septicaemia (blood poisoning) and meningitis.
If your child is at risk of splenic dysfunction their consultant will discuss this with you and what this will mean for your child and the family. Your child may need to take lifelong antibiotics, may require prophylactic vaccinations, may have to carry a card to alert health professionals to the risk of infection and be educated as to the potential risks of overseas travel and the risk of infection.
For up-to-date patient information on splenic dysfunction and a health alert card please visit the following links:
- https://assets.publishing.service.gov.uk/government/uploads/system/uploads /attachment_data/file/1059549/UKHSA-12074-splenectomy-leaflet.pdf
- https://assets.publishing.service.gov.uk/government/uploads/system/uploads /attachment_data/file/1059548/UKHSA-12074-splenectomy-record-card.pdf
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.
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.
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
Children With Cancer UK
t: 0800 222 9000
e: info
w: www.
Children’s Cancer and Leukaemia Group (CCLG)
e: info
w: www.
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.
Page last updated: 02 August 2024
Review due: 30 June 2025