The University of Texas MD Anderson Cancer Center
Houston, United States
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Acute myeloid leukaemia (AML) is a fast-growing cancer of the blood and bone marrow, in which the marrow makes too many abnormal immature blood cells.
In AML, the bone marrow makes large numbers of abnormal, immature blood cells that crowd out healthy ones. It is the most common type of acute leukaemia in adults. ‘Acute’ means it usually gets worse quickly if it is not treated, so treatment needs to start straight away. The risk is higher with older age, being male, smoking, past chemotherapy or radiotherapy, contact with benzene, and some earlier blood disorders.
Early signs can feel like flu. They include:
Treatment usually comes in two phases. The first aims to clear leukaemia cells from the blood and bone marrow (remission). The second aims to destroy any cells that are left, so the leukaemia does not come back. Options include chemotherapy, targeted drugs chosen by gene tests, and a stem cell transplant. People who cannot have intensive chemotherapy may be offered other drugs. A subtype called acute promyelocytic leukaemia is treated with its own specific medicines.
The outlook depends on things such as age, the AML subtype, a very high white blood cell count, infection at diagnosis, spread to the brain or spinal cord, and whether the leukaemia followed an earlier blood disorder or cancer treatment. Older age may mean a lower chance of remission. Remission means normal blood counts and no signs of leukaemia, but leukaemia cells can still come back, which is why treatment continues after remission.
Machine summary of published research · sources and dates below · 2026-11-06
Written from: NCI PDQ: Acute Myeloid Leukemia Treatment (PDQ®)–Patient Version (2025-05-16) · MedlinePlus: Acute Myeloid Leukemia (2023-11-27) · read on 2026-11-06
For family members and people at higher risk: free checks can find some cancers early, before there are symptoms.
There is no routine screening for this cancer. If you have symptoms or a family history, talk to your doctor.
If several people in your family had cancer, ask your GP whether genetic counselling makes sense for you.
Four steps, from proven to unproven.
Usual treatment: Intensive chemo, often a stem cell transplant. ESMO
We do not have the list of medicines approved in Austria yet. Your doctor knows what is available here.
13 open trials in Austria, 621 worldwide. See the trials
Phase 1 – first tests in people, mainly for safety · Phase 2 – does it help? · Phase 3 – compared with the usual treatment.
Trials taking new patients now. Each trial counts once; one in two phases counts as the higher one.
Not counted yet for this disease.
Animal worm medicines (ivermectin, fenbendazole) for cancer: not approved, and not enough research in people to know if they help. American Cancer Society: What to Know About Ivermectin (21 May 2026) · American Cancer Society: What to Know About Fenbendazole (21 Oct 2025)
The five newest articles. The label comes from the PubMed index: whether it was tested in people, in animals or only in the lab.
Not labelled yet: PubMed has not indexed the article yet, so we do not guess.
All articles further down this pagePatient groups and help in Austria.
All supportOrganisations that can help, further down this page
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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 42997612Pick 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 69 acute leukaemia patient organisations (hosted by the Swiss Leukemia Patient Advocates Foundation); member list helps patients find a national group.
Visit site: Acute Leukemia Advocates Network (ALAN)Umbrella 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 EuropeNetwork of pan-European cancer patient umbrella groups (including the blood cancer networks): joint advocacy, WECAN Academy training for patient advocates, patient experience data courses.
Visit site: Workgroup of European Cancer Patient Advocacy NetworksFor 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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