St. Jude Children's Research Hospital
Memphis, United States
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Childhood cancers are cancers found in children; the most common are leukaemias, brain and spinal cord tumours, and lymphomas.
Childhood cancers are cancers diagnosed in children. In children up to the age of 14, the most common types are leukaemias, tumours of the brain and spinal cord, and lymphomas. As in adults, they are thought to begin with changes in genes that make cells grow out of control. For most childhood cancers the cause is not known. About 8 to 10 in every 100 are caused by gene changes passed on from a parent.
Treatment depends on the type of cancer and how advanced it is. Common options are surgery, chemotherapy, radiotherapy, immunotherapy and stem cell transplant. Children are not always treated in the same way as adults: a growing body reacts differently to treatment, and children may receive more intensive treatment. Many children are cared for at children's cancer centres, where specialist teams work together and clinical trials are often available.
Effective treatments now exist for many childhood cancers. In the US, the cancer death rate in children up to the age of 14 fell by 70 percent between 1970 and 2020. Most of the progress towards treatments that cure has come from clinical trials. Even so, cancer is still the leading disease-related cause of death in children.
Machine summary of published research · sources and dates below · 2026-11-06
Written from: NCI: Childhood Cancers (2025-04-24) · read on 2026-11-06
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Here you will find questions you can ask, help with difficult talks, organisations for carers and your relative's rights.
Questions for your relative's doctor
You do not need the right words. Ask what your relative wants to know, and let them set the pace. These pages can help.
Looking after someone is work too. These organisations help carers, and the list further down this page shows helplines by country.
A doctor can share information and a relative can act only with the patient's consent or a legal authority. It is easier to arrange this early.
Children are often treated differently from adults, in specialist centres. Here is where to start.
These European networks connect paediatric cancer centres and families.
Parents often receive offers of paid treatment. Please go through this list before you pay for anything.
You can share or print these pages for your members. They are free and need no account.
The trial team decides who can take part; your doctor can help you ask.
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Results, new trials and publications, newest first. Every item links to its source.
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PubMed · PMID 42996412Pick up to 5 questions for your situation, then print them or take them on your phone.
Choose questionsIf the treatment has stopped working, or you were told there are no more options, here is what you can ask and where you can look next.
Do not stop or put off treatment without talking to your doctor.
Many trials look specifically for people who have already had treatment. Registries mark these with words like "previously treated", "refractory" or "relapsed". The trial team decides who can take part.
A phase 1 trial mainly tests whether a new medicine is safe and which dose can be given. It is not built to show that the medicine works.
In cancer, older figures show that fewer than 1 in 20 people in a phase 1 trial respond. Many people expect far more, so ask openly: what can I expect, and what will it mean for my daily life?
Some medicines not yet approved can be given outside a trial when there is no other option. This does not exist for every medicine or in every country. Your doctor makes the request, and the authority or the manufacturer decides.
Asking for a second opinion is normal and does not mean you distrust your doctor. Take your results and a list of your treatments with you. For rare diseases, your doctor can also ask a European Reference Network.
This is care for symptoms and quality of life, and you can have it alongside cancer treatment. It does not mean anyone has given up on you. In a randomised trial in advanced lung cancer, palliative care from early on improved quality of life.
In this situation many people receive offers of paid treatment. Go through this list before you pay for anything.
You can talk to someone. In Hungary and in the UK, 116 123 is a free line for emotional support, day and night. The list on this page shows helplines in other countries.
Not medical advice. Talk to your care team before you change anything in your treatment.
Helplines, patient groups and support services for you and your family.
Select your country to see the organisations there, starting with the ones closest to you.
Global network of parent and survivor organisations: member directory to find a national group, survivor network and knowledge portal.
Visit site: Childhood Cancer International (CCI)Network of parent and survivor organisations in 38 countries, with a map to find your national group.
Visit site: Childhood Cancer International Europe (CCI Europe)European network of paediatric cancer centres with virtual tumour boards and a section for patients and families.
Visit site: ERN PaedCan – ERN for paediatric oncologyUmbrella of European cancer patient groups, with a patient toolbox and a legal network for cancer patients.
Visit site: European Cancer Patient Coalition (ECPC)The European Commission's 24 expert networks for rare and complex diseases; your doctor can contact them.
Visit site: European Reference Networks (European Commission)Alliance of over 1,000 rare disease patient organisations, with a list of rare disease helplines by country.
Visit site: EURORDIS – Rare Diseases EuropePatient-led network of young people (adolescents and young adults) affected by cancer: peer community, help finding local support, and advocacy.
Visit site: Youth Cancer Europe (YCE)For anyone who is ill, whatever the disease: patients' rights and legal aid, crisis lines, hospice and palliative care, care in another EU country, and patient organisations' umbrella bodies.
Umbrella of European patient organisations and national patient coalitions.
Visit site: European Patients' Forum (EPF)Global alliance of patient organisations of all diseases, promoting patient-centred healthcare.
Visit site: International Alliance of Patients' OrganizationsFrontlight is not affiliated with these organisations; we list them because they help.
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Memphis, United States
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Toronto, Canada
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Philadelphia, United States
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Atlanta, United States
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Toronto, Canada
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Boston, United States
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Seattle, United States
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Stanford, United States
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Houston, United States
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