Treatment for neuroendocrine cancer
TAE works by reducing the blood supply to the liver tumour. The blood supply brings oxygen and nutrients that cells need to survive and grow. Blocking the blood supply also stops the NET releasing its hormones into the bloodstream.
Doctors may only block the blood supply to the liver. Or they might also give a chemotherapy drug to the liver at the same time. This is called trans arterial chemoembolisation (TACE).
You might have TAE if the NET has spread to your liver and you have symptoms caused by high hormone levels. It might be an option for you if:
you can’t have surgery to remove the liver tumour
other treatments have not controlled your symptoms
TAE can help to reduce the size of the NET in the liver. It can also reduce the amount of hormones the tumour makes. This won’t get rid of the cancer but can control the symptoms and help you feel better.
In some cases, TAE might shrink a tumour so that surgery is possible. You might have TAE more than once.
You usually can’t eat for 4 to 6 hours before having treatment. This is because you might have a drug that makes you sleepy (sedation). You can usually drink water up to 2 hours beforehand.
You also have a drug called octreotide as a drip into a vein for 8 to 12 hours before the start of treatment. This is to prevent a carcinoid crisis which can happen when people with NETs have sedation.
Find out about carcinoid crisis
You usually have the treatment in the x-ray (radiology) department. It takes up to an hour and a half.
A specialist doctor called an interventional radiologist does the treatment. A nurse will also be with you in the room.
First you get changed into a hospital gown. You lie on your back on the x-ray table. Your doctor or nurse puts a small tube (cannula) into your arm or back of your hand. They use this to give you sedation and other drugs you might need, such as anti sickness. Your nurse regularly checks your heart rate and blood pressure. They may give you some oxygen to breathe as well.
Your doctor cleans the area at the top of your leg (groin) or wrist. They inject a local anaesthetic to numb the area. They make a small cut and put a long tube called a catheter into one of the blood vessels. They then thread the catheter along the artery until it reaches the hepatic artery that supplies blood to the liver.
They inject a type of dye that shows up on x-rays (contrast medium). You might have a warm sensation through your body for a few seconds. This is normal.
Your doctor takes a series of x-rays which show the blood vessels that feed the tumour in the liver. They inject the substance they use to block the blood vessels.
Your radiologist removes the catheter and puts a pressure dressing onto the site. You need to stay lying down for about 4 to 6 hours afterwards. Your nurse checks the site for bleeding before you get up.
You can usually eat and drink as normal after the test. Drink plenty afterwards to help flush the dye out of your body.
You usually stay in hospital for a night or two.
TAE can cause side effects. These include:
feeling or being sick
pain in your tummy (abdomen)
high temperature
These side effects are called post embolisation syndrome and are common. They usually last for 2 to 3 days. Your doctor will give you painkillers and anti sickness drugs to help with this.
Tiredness is also a common side effect of TAE and can last for a couple of weeks.
Other side effects include:
a small bruise where the catheter was put in
infection – you might need antibiotics through a drip
damage to the blood vessel by the catheter – this is very rare
leakage of the contrast medium out of the blood vessels
an allergic reaction to the contrast medium
Rarely, TAE can cause liver failure. Because of this you usually won’t be able to have TAE if you have moderate or severe liver damage (cirrhosis).
Contact the hospital if you have an increase in pain and get a temperature when you are at home.
Treatment for neuroendocrine cancer can be difficult to cope with for some people. Your nurse will give you phone numbers to call if you have any problems at home.
Find out more about coping with a neuroendocrine cancer and how to get support
Last reviewed: 07 Feb 2025
Next review due: 07 Feb 2028
Neuroendocrine cancers are also called neuroendocrine neoplasms (NENs). There are 2 key groups - neuroendocrine tumours (NETs) and neuroendocrine carcinomas (NECs).
You usually start by seeing your GP. They might refer you to a specialist doctor and organise tests.
There are many different types of neuroendocrine cancer. They are usually named after the part of the body where they develop.
Treatment depends on the type of neuroendocrine cancer you have, where it is, its size and whether it has spread (the stage).
Practical and emotional support is available to help you cope with neuroendocrine cancer.
Neuroendocrine cancers develop in cells of the neuroendocrine system. They can develop in different parts of the body including the lungs, stomach, pancreas and bowel.

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