Brain tumour radiotherapy

What you need to know about

Brain tumour radiotherapy

We understand that facing the prospect of brain tumour radiotherapy for your child can be daunting. In this section, we aim to provide you with the knowledge and assurance you need.

You’re not on this journey alone, OSCAR’s are here to give you support and keep you informed.

If we can help support you in any other way, please get in touch here.

What is radiotherapy?

Brain tumour radiotherapy aims powerful high-energy X-ray beams at the tumour to target and destroy cancer cells. It is commonly used after surgery to shrink any tumour cells that weren’t removed. If your child’s tumour isn’t suitable to be operated upon, radiotherapy may be their main treatment. It may also be given in conjunction with chemotherapy.

Radiotherapy takes advantage of the fact healthy tissue repairs itself quicker than diseased tissue, so short blasts of radiation will kill off cancer cells reducing the size of the tumour or stopping further growth.

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What happens?

To begin, your child will undergo a ‘radiotherapy planning scan,’ typically a CT or MRI scan. This scan creates a detailed 3D image of your child’s tumour, to precisely determine its size and location within the brain. This information is crucial for planning the treatment. The goal is to avoid exposing critical areas of the brain to radiation..

During the actual treatment, your child will need to remain perfectly still to ensure the radiation is accurately targeted. To help with this, a custom treatment mask is created specifically for your child’s face and head. This mask is designed to fit comfortably and securely, and it keeps your child’s head in the same position for each treatment session. Various types of masks are available, and they are crafted in conjunction with your child’s wishes with openings for the eyes, nose, and mouth to ensure your child can breathe easily.

We understand that wearing the mask may be intimidating for your child, and there are dedicated play therapists who can work with them to make the experience less frightening. Additionally, staff can arrange for your child to see the radiotherapy machine before the treatment begins, which can help ease anxieties they may have.

It’s important to emphasise that each treatment plan is tailored to your child’s unique needs, so their experience may differ from that of other children. If your child is very young or feeling extremely anxious and has difficulty staying still, measures can be put in place to ensure their comfort and cooperation.

During the treatment session, your child will lie on the radiotherapy bed with the machine positioned above them. Medical staff will gently place the mask on your child’s head and secure it to the bed, taking all the time necessary to ensure accurate alignment. Before the radiation machine is activated, staff will leave the room but remain close by, ensuring they can see, hear, and communicate with your child if needed.

It’s important to note that your child won’t see or feel the radiation beams, and they won’t experience any heat from the machine. They will, however, hear the machine, which is entirely normal.

After each treatment session, the medical team return to the room, remove the mask, and assist your child off the bed, safely storing the mask for their next session.

The duration of treatment will vary depending on your child’s individual plan, but please know that each treatment session is relatively short, usually lasting only a few minutes. The overall appointment may be longer due to the careful positioning required or if other treatments are needed alongside.

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How often will my child have it?

If your child is receiving radiotherapy as part of their treatment plan, they will usually have one session per weekday. This is usually for 4-6 weeks, depending on their treatment plan.
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What happens after treatment?

Side effects of radiotherapy vary – and some children may not have any. The most common side effects are tiredness, nausea, headaches, dry mouth, and skin soreness where the beam is focused. Sometimes children can lose some hair in this area too. Radiotherapy can sometimes cause pressure inside the skull. This can be caused by inflammation to the tissues being targeted by the radiotherapy. If there are any signs of this, doctors will prescribe steroids to reduce inflammation. Your child will likely have some follow-up scans after their radiotherapy to check how much the tumour has shrunk. Cell destruction is a slow process, and often requires up to six months for doctors to be able to see the treatment’s impact. This is why follow-up scans are done a few months after treatment is finished.
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Proton beam therapy

Proton beam therapy is a type of radiotherapy that uses high-energy protons to precisely target and treat the tumour. This is instead of the X-rays used in traditional radiotherapy.

It is even more targeted and precise than traditional radiotherapy,. This reduces harm to nearby brain tissues. However, it doesn’t always offer a better option than traditional radiotherapy. That all depends on your child’s type of tumour and location.

Currently there are only two hospitals in the UK that have proton beam therapy facilities. They are The Christie Hospital in Manchester and University College Hospital in London. This means that to receive the treatment families need to be away at one of these locations for 6-8 weeks, which provides its own challenges.

Your child’s clinical oncologist will discuss with you whether proton therapy is the best option for your child and will talk you through the pros and cons of both types of radiotherapy.

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Larsen’s Pride is a charity that does great work in improving children’s experiences of radiotherapy.

You can download their guides above

Female doctor analyzing digital brain scan results on computer monitor in the hospital. brain tumour radiotherapy brain tumour chemotherapy

Do you need any help or assistance?

Rachel James

Community Fundraising Assistant
Rachel will join our team on September 1st and will be doing a wide range of tasks including promoting the charity in the local community, developing relationships with different people and organisations, and finding new fundraising opportunities. She comes from a caring background having been a teaching assistant and emotional literacy support assistant in York for many years, and previously leading a community care team. She has also done many years of work in the voluntary sector.

Matthew Taylor

Trustee

Matthew Taylor is Director of the York Health Economics Consortium at the University of York. He has been a supporter of OSCAR’s since its inception and, through his twenty years of research into the measurement of health-related quality of life, Matthew is keenly aware of the huge benefits that new treatments can bring to people living with brain tumours.

Matthew is actively involved in national-level healthcare decision making, having had former roles as the Scientific Director of the National Institute for Health and Care Excellence (NICE)’s Economic and Methodological Unit and as a committee member for NICE’s Public Health Advisory Group. He has over fifty peer-reviewed scientific publications, including a chapter in the textbook ‘The Business, Policy and Economics of Neurosurgery’.

Ryan Mathew

Clinical Trustee

Ryan Mathew is an Associate Professor at the University of Leeds and an Honorary Consultant Neurosurgeon at Leeds Teaching Hospitals.

The Hughes Family story had a big impact on Ryan. He first learnt of the charity when he became surgeon to Oscar’s dad, Ian. After a successful surgery, he continued to show great care and concern for the family when Ian became ill again and when Milo, Oscar’s brother, was diagnosed with a brain tumour. Ryan is driven to make life outcomes better for brain tumour patients and their families. His extensive work in both research and surgery is testament to that commitment.

His clinical practice covers the full spectrum of general neurosurgery with a subspecialty in brain tumours. His research focuses on advanced brain tumour models, residual therapy-resistant glioma cell populations, local therapeutic treatments and surgical technologies and devices. He peer-reviews for several journals and grant award committees and has published numerous papers.

More information on Ryan’s work

Lisa Dawson

Trustee

Lisa has been a friend of the Hughes family since 2016 and was honoured to be asked in 2022 to represent OSCAR’s PBTC as Social & Digital Trustee.  Both Lisa and her family have taken part in numerous fundraising events and are dedicated to raising awareness of paediatric brain tumours.  Lisa is a social media content creator, blogger and writer and lives in York with her husband Joe and three children, Ella, Max and Leo.

Alice Beckwith

Trustee

Alice has been involved with OSCAR’s PBTC since 2020. She passionately supports the aims of the charity and believes that if the charity can change one life for the better, then it is a success. Working in the public sector for 18 years, Alice has helped transform Adult and Children’s Social Care Services by ensuring heavy investment in preventative services. This is why the impact OSCAR’s work will have on families is at the forefront of Alice’s motivation to be involved.

As partnerships trustee, Alice is keen to involve businesses, trusts and individuals in the work OSCAR’s does and show them the role they can have in providing the base for the charity to continue to expand its projects to help children with brain tumours.

Sarah Jane Gray

Trustee/Secretary

Sarah has over 20 years of experience in the pharmaceutical and surgical sales sector and is very familiar with the importance of medical advancements for better patient outcomes. She believes research is essential for improving diagnosis, treatment and prognosis for all children with brain tumours and hopes OSCAR’s PBTC can offer much needed funding to help push the boundaries in finding better ways of curing this devastating disease. Sarah’s focus as a treasurer will ensure record-keeping and accounts meet the conditions of the statutory bodies and compliance with regulatory organisations.

Holly Dixon

Trustee

Holly is mother to George, diagnosed with an ATRT brain tumour in 2022, and works as a primary school teacher. She believes that action to support others -however small- can make a massive difference.


She brings real-life experience of what it is like for a parent navigating everyday life, the NHS, the education system, questions from people and a lively young child with different needs.

meet the oscar's team

Sam Marino

Trustee

Marie Hughes

ChAIR OF THE BOARD OF TRUSTEES

Marie founded the charity with her husband Ian, who passed away in 2020. She is the mother of four boys. Two of Marie’s sons have died from different types of brain tumours – Oscar who was 9 and Milo who was 5 years old. She is determined to help find better treatments for brain tumours so other children won’t have to go through what her own sons and her family have.

Marie is Chair of the Board of Trustees, working closely withe the team on strategy and vision. Marie lives in Copenhagen with her two other sons, Sebastian and Lucas, and works as a Risk Manager on the Danish railway.