Browser does not support script.
Skip to main content
Find out how we produce our information|
This information is about liver tumours in children. Liver cancer can be either primary or secondary. Primary liver cancers| start in the liver, and secondary liver cancers| have spread into the liver from a different part of the body. This information is about primary liver cancer in children.
More children than ever are surviving childhood cancer. There are new and better drugs and treatments. But it remains devastating to hear that your child has cancer, and at times it can feel overwhelming. There are many healthcare professionals and support organisations to help you through this difficult time.
Understanding more about the cancer your child has and the treatments that may be used can often help parents to cope. We hope you find the information here helpful. Your child's specialist will give you more detailed information. If you have any questions it’s important to ask the specialist doctor or nurse who knows your child’s individual situation.
We hope this information answers your questions. If you have any further questions, you can ask a nurse or doctor involved in your child's treatment.
Approximately 10 children in the UK develop liver tumours each year. Boys are affected more commonly than girls. Liver tumours can be non-cancerous (benign) or cancerous (malignant). This section is about malignant liver tumours.
The liver is the largest organ in the body. It's surrounded by a fibrous capsule and is divided into sections called lobes. It lies across the upper part of the abdomen and is larger on the right hand side of the body than on the left. It's surrounded, and protected from injury, by the lower ribs.
The liver is an extremely important organ that has many functions. One of these functions is to produce proteins that circulate in the blood. Some of the proteins help the blood to clot and prevent excessive bleeding. Others are essential for maintaining the balance of fluid in the body. The liver also destroys harmful substances. It breaks down waste products not used by the body so that they can be passed out in the urine or stools (bowel motions).
Position of the liver
View a large copy of the position of the liver image|
The liver is responsible for breaking down food containing carbohydrates (sugars) and fats, so they can be used by the body for energy. It stores substances such as glucose and vitamins so that they can be used by the body when needed.
The liver also produces bile, a substance that breaks down the fats in food so that they can be absorbed from the bowel (intestine).
The liver is connected to the small intestine (duodenum) by a tube called the bile duct. This duct takes the bile produced by the liver to the intestine.
The liver has an amazing ability to repair itself. It can function normally even if only a small part of it is working.
There are two main types of primary liver cancer:
This usually occurs in children under five years of age. About eight children in the UK are diagnosed with hepatoblastoma each year.
This is rarer and usually occurs in older children. About two children in the UK are diagnosed with hepatocellular carcinoma each year.
The cause of most primary liver tumours in the western world is unknown. However, in other parts of the world, hepatocellular cancer (HCC) is commonly related to the presence of liver infection. This happens in countries where mothers commonly have hepatitis B and vaccination is not readily available at birth for their children.
Children who are infected with hepatitis B have a higher risk of developing HCC in late childhood than uninfected children.
The most common symptom is a lump or swelling in the abdomen, which can be painful. Other possible symptoms include weight loss, a loss of appetite, feeling sick (nausea) and being sick (vomiting).
A variety of tests| and investigations may be needed to diagnose a liver tumour.
An ultrasound scan and x-rays will be taken, which can show if there's a tumour in the liver. Further tests, including CT (computerised tomography) scans or MRI (magnetic resonance imaging) scans, will be done to find out the extent of the disease, both inside and outside the liver. Blood tests will also be carried out.
Most hepatoblastomas and hepatocellular carcinomas produce a protein that's released into the bloodstream. This protein is known as alpha-fetoprotein (AFP). It's possible to measure levels of AFP in the blood, which can be a useful indicator of whether the liver tumour is responding to treatment or whether it may have come back after treatment. AFP is also known as a tumour marker.
Any tests and investigations that your child needs will be explained to you. Our section on children’s cancers| gives more detailed information on what the tests and scans involve.
To assess the extent of the cancer, a grouping system called PRETEXT (pre-treatment extent of disease) is used. It uses an MRI scan to measure the amount of cancer in the liver at diagnosis. It's also used to help establish the best treatment for each child.
This grouping system is unique to liver tumours and is increasingly used all over the world.
This grouping process is essential because liver tumours need to be removed surgically. Grouping divides the liver into four surgical areas (sectors) and gives an indication of the kind of surgery that is needed to remove the tumour. Grouping also helps doctors decide whether a liver transplant surgeon needs to be involved from the start or not.
One liver sector is affected and the tumour can be removed by straightforward surgery.
Two adjoining sectors are affected and the tumour can be removed with more extensive surgery.
Two or three sectors are affected with no two adjoining sectors free of disease, and the tumour can be removed with major surgery.
All four sectors of the liver are affected, and the tumour cannot be removed without replacing the liver with a donor liver transplant.
Doctors also look at the extent of the spread of cancer beyond the liver:
Sometimes the tumour gets into the blood vessels that are entering or leaving the liver. This may affect the type of surgery needed to remove the tumour.
Sometimes the tumour spreads outside the liver and into the abdomen (tummy). This makes it impossible to remove the tumour completely.
If the tumour spreads outside the liver through the bloodstream (metastatic disease), it usually goes to the lungs. About 1 in 5 children are found to have affected lungs when they are diagnosed. Doctors use x-rays and CT or MRI scans to assess whether the lungs are affected.
The diagnosis is made by taking a sample of cells from the tumour (biopsy). This is done under a general anaesthetic. Once the diagnosis and staging have been confirmed, plans for treatment will be made.
For hepatoblastoma the type of treatment will depend on the PRETEXT staging and whether the cancer has spread to other parts of the body (metastatic disease).
PRETEXT 1, 2 and 3 tumours are called 'standard risk'. PRETEXT 4 is called 'high risk' and includes tumours that have spread to other parts of the body.
Treatment is broadly similar for all PRETEXT stages. Chemotherapy| (anti-cancer drugs) is given first. The aim of chemotherapy is to shrink the tumour in the liver and hopefully get rid of any metastatic tumours. Surgery| to remove any remaining tumour will take place after a few weeks of chemotherapy. Further chemotherapy is usually given after surgery. Your child's doctor will give you more detailed information about the chemotherapy drugs and their side effects.
For hepatocellular carcinoma, treatment is a little different. The role of chemotherapy is less certain and surgery is the main treatment. Doctors usually recommend removing the tumour (if it's small enough) at diagnosis. Chemotherapy may be given afterwards. However, in many situations the tumour is too large to remove at first and so chemotherapy is given to shrink the tumour so that surgery can be done later.
Hepatocellular tumours don't always respond to chemotherapy as well as hepatoblastomas. For this reason, other treatments, such as chemoembolisation and
targeted treatments (see below), may be used.
This refers to the giving of drugs directly into the artery going into the liver. Very occasionally, this may be used for hepatocellular cancer.
Targeted drugs are a group of treatments that work in a different way to conventional chemotherapy. Some drugs may cause cancer cells to die directly. Others act to cut off the blood supply to the tumour cells (antiangiogenesis drugs). Some drugs, called multi-targeted agents, work in both ways.
Research is looking into how useful targeted treatments are on their own and in combination with chemotherapy. Your child's doctor may talk to you more about this research.
All children, if they are able to, will have surgery following chemotherapy. If there's cancer in the lungs, which hasn't completely disappeared with the chemotherapy, the lungs will be operated on first. If the liver tumour can be surgically removed, the operation to do so will follow, usually a week or two later.
If the tumour involves all four sectors of the liver (PRETEXT 4), a liver transplant will be necessary. This is recommended for hepatoblastoma but only in particular circumstances for hepatocellular carcinoma. In a transplant, the whole liver is removed and replaced with a liver from another person.
This will be discussed with you from the beginning, and you will be given the opportunity to think about donating half of your liver, or for your child to have a liver from a donor. The transplant team will be there to answer all of your questions. A liver transplant is only possible if all the cancer outside the liver has gone.
Treatment often causes side effects, and your child's doctor will discuss these with you before treatment starts. Side effects can include:
The chemotherapy used to treat liver cancer can cause late side effects. These may include hearing problems, kidney problems and possibly heart problems. There will be a slightly increased risk of your child developing another type of cancer later in life. Most children will develop some late effects and need to have some follow-up tests. Your child's doctor or nurse will tell you more about any possible late side effects|.
If the cancer comes back after initial treatment, this is known as a recurrence. It can come back in the liver or in other parts of the body. If the cancer comes back, often (before anything is seen on scans) the levels of alpha-fetoprotein (AFP) in the child's blood will start to rise again and reaches levels of over 100. Small rises in AFP can occur in the weeks after surgery, as the liver regenerates as much as it can.
Many children have their treatment as part of a clinical research trial|. Trials aim to improve our understanding of the best way to treat an illness, usually by comparing the standard treatment with a new or modified version. Specialist doctors carry out trials for children's cancer. If appropriate, your child's medical team will talk to you about taking part in a clinical trial and will answer any questions you have. Written information is often provided to help explain things.
Taking part in a research trial is completely voluntary, and you'll be given plenty of time to decide if it's right for your child.
When the treatment ends, your child will have regular blood tests to measure the level of AFP in the blood (if appropriate), as well as scans and chest x-rays. More than three quarters of children with hepatoblastoma are cured, and for children with small tumours that are confined to the liver, the outlook is even better. The outcome for hepatocellular carcinoma is not quite as good. The staff at the hospital can give you information about the likely outcome for your child. Our cancer support specialists| can also offer support.
If you have specific concerns about your child’s condition and treatment, it's best to discuss them with your child’s doctor, who knows the situation in detail.
As a parent, the fact that your child has cancer is one of the worst situations you can be faced with. You may have many different emotions, such as fear, guilt, sadness, anger and uncertainty. These are all normal reactions| and are part of the process that many parents go through at such a difficult time.
It's not possible to address all of the feelings you may have in this section. However, the children’s cancers| section talks about the emotional impact of caring for a child with cancer and suggests sources of help and support.
CCLG| coordinates research and care for children and their parents. There are 21 CCLG specialist centres for the treatment of childhood cancer and leukaemia, covering all areas of the UK and Ireland (there's a map of the centres| on the website). Has information about the CCLG, childhood cancer and leukaemia.
CLIC Sargent| offers practical support to children and young people with cancer or leukaemia, and to their families.
This section has been compiled using information from a number of reliable sources, including:
With thanks to Dr Bruce Morland, Clinical Director, and the people affected by cancer who reviewed this information. Reviewing information is just one of the ways you could help when you join our Cancer Voices| network.
We worked with the Children's Cancer and Leukaemia Group (CCLG) to write our information about children's cancer.
Content last reviewed: 1 January 2013
Next planned review: 2015
For answers, support or just a chat, call the Macmillan Support Line free (Monday to Friday, 9am-8pm)
If you have any questions about cancer, need support or just want someone to talk to, ask Macmillan.
If you have any questions about Macmillan we would love to hear from you| .
You can also follow us| on Facebook, Twitter, Flickr or YouTube.
© Macmillan Cancer Support 2013
what are these?|