What is cyproterone acetate?

Cyproterone acetate is a hormonal therapy drug. It is used to treat prostate cancer. It may sometimes be used to treat other cancers.

It is best to read this information with our general information about hormonal therapy and the type of cancer you have.

Your cancer team will talk to you about this treatment and its possible side effects before you agree (consent) to have treatment.

More information about this treatment

This information is correct at time of publishing. But sometimes the types of cancer this treatment is used for, or treatment side effects, may change between revision dates.

You can talk to your cancer team if you want more detailed information about this treatment. Or visit the electronic Medicines Compendium (eMC) website, which has patient information leaflets (PIL) for individual drugs.

How cyproterone acetate works

Hormones are chemicals that our bodies make. They act as messengers and help control how cells and organs work. Hormonal therapy drugs change how hormones are made or work in the body.

Most prostate cancers need the hormone testosterone to grow. Testosterone is mainly made by the testicles. A small amount is also made in the adrenal glands. Cyproterone acetate stops the testicles from making testosterone. This reduces testosterone levels and may shrink the prostate cancer or stop it growing.

Cyproterone acetate may be given for a few weeks when you start taking hormonal drugs called LHRH agonists. This is to prevent a temporary rise in testosterone making symptoms worse (called tumour flare).

How cyproterone acetate is given

You have cyproterone acetate as tablets you can take at home. You may have cyproterone acetate on its own or with other cancer drugs.

During your treatment, you will meet someone from your cancer team, such as a: 

  • cancer doctor
  • specialist nurse
  • specialist pharmacist.

This is who we mean when we mention doctor, nurse or pharmacist in this information.

Taking cyproterone acetate tablets

Your cancer team will discuss your treatment plan with you.

Always take the tablets exactly as they tell you to. This is important to make sure they work as well as possible for you. Make sure you:

  • take the tablets after a meal
  • swallow them whole with a glass of water
  • do not chew, open, break or crush them
  • take them at the same time every day.

If you forget to take the tablets, take the missed dose as soon as possible within the same day. If a full day has passed, do not take a double dose.

Other things to remember about your tablets:

  • Keep them in the original package and at room temperature, away from moisture, heat and direct sunlight.
  • Keep them safe, where children cannot see or reach them.
  • If you are sick (vomit) just after taking them, do not take an extra dose. Take your next dose at the usual time.
  • Get a new prescription before you run out, and make sure you have plenty for holidays.
  • Do not throw away unused tablets. Return them to a pharmacy.

Your cancer team may also give you other medicines to take home. Take all your medicines exactly as they tell you to. Do not stop taking any of your medicines unless your doctor tells you to.

About side effects

We explain the most common side effects of this treatment here. We also include some that are less common.

You may get some of the side effects we mention, but you are unlikely to get all of them. And you may have some side effects, including rarer ones, that we have not listed here. 

Other cancer treatments may cause different side effects. If you are also having other cancer treatment, you may have other side effects.

When you have this treatment, you will have regular appointments with a doctor, nurse or pharmacist. Always tell them about any side effects you have. They can give you: 

  • drugs to help control most side effects 
  • advice about managing side effects. 

Most side effects can be managed. But sometimes side effects are harder to control. It is important not to stop taking hormonal therapy without telling your doctor. If side effects cannot be managed, your doctor may suggest a different type of hormonal therapy.

Serious and life-threatening side effects

Some cancer treatments can cause serious side effects. Sometimes, these may be life-threatening. Your doctor, nurse or pharmacist can explain the risk of these side effects to you.

Contact the hospital

Your doctor, nurse or pharmacist will give you 24-hour contact numbers for the hospital. If you feel unwell or need advice, you can call at any time of the day or night. Save these numbers in your phone or keep them somewhere safe.

Very common side effects

These side effects happen to 10 or more people in every 100 people (10% or more) who have this treatment.

Sexual effects

It is common to lose your sex drive and have erection difficulties with hormonal therapy. Hormonal therapy may also make your penis shorter and your testicles smaller. 

Your doctor can prescribe drugs and treatments to help with erection difficulties. These will not increase your sex drive. But they might work, even with a low sex drive. 

Things can improve a few months after you stop taking the drug. But it depends on how long you take hormonal therapy, and what other treatments you have had. Some people continue to have problems after treatment ends.

Fertility

This treatment reduces the number of sperm and the amount of ejaculate you produce. This can affect whether you can make someone pregnant. If you are worried about this, it is important to talk with your doctor before you start treatment.

Other side effects

These side effects happen to less than 10 in 100 people (less than 10%) who have this treatment. Some of them are much rarer than this but they are still important to know about. Rare means a side effect that happens to less than 1 in 1,000 people (less than 0.1%).

Feeling tired (fatigue)

Feeling tired is a common side effect. Try to pace yourself and plan your day so you have time to rest between activities.

Being physically active can help to manage tiredness and give you more energy. It also:

  • helps you sleep better
  • reduces stress
  • improves your bone health.

If you feel sleepy, do not drive or operate machinery.

Feeling breathless

You may feel slightly short of breath while you are taking this treatment. If this happens, tell your doctor, nurse or pharmacist. This should stop when the treatment ends.

Mood changes

You may feel low or depressed, or have mood swings, during this treatment. Talking to family and friends about how you feel might help. If mood changes last for more than a few weeks, tell your doctor, nurse or pharmacist. They can talk to you about different ways to manage low mood or depression.

Weight gain

You may gain weight when you are having this treatment. Eating healthily and being active can help you keep to a healthy weight.

Sometimes weight gain can be caused by a build-up of fluid in the body. Your doctor, nurse, pharmacist or dietitian can give you more advice and treatment to help.

Breast swelling or tenderness

This treatment may cause swelling and tenderness of your breast tissue. This is called gynaecomastia. To prevent this, some people have 1 or more low-dose radiotherapy treatments to the chest before treatment starts. Another type of hormonal drug might be used to treat the breast swelling. Your doctor can give you more advice.

Hot flushes and sweats

Hot flushes are a common side effect of this treatment. During a flush, your neck and face may feel warm. If you have white skin, your skin may look red. If you have black or brown skin, your skin colour may deepen. Flushes may last up to 5 minutes. You might also have sweats or feel anxious or irritable during a hot flush.

Here are some things you can do to reduce the effects of hot flushes:

  • Wear natural fabrics, such as cotton.
  • Wear layers so you can remove clothes as needed.
  • Use cotton sheets and layers of bedding you can remove.
  • Try cooling pads or pillows to keep you cool.
  • Keep rooms cool or use a fan.
  • Have cold drinks and avoid caffeine and alcohol. 

You might have fewer hot flushes as your body adjusts to this treatment. You could try therapies to help you cope with hot flushes, such as:

  • talking therapies like cognitive behaviour therapy (CBT)
  • controlled breathing exercises
  • yoga 
  • acupuncture. 

If they do not improve, talk to your doctor. Certain drugs can help to improve hot flushes. 

Flushes usually stop a few months after treatment ends. But some people continue to have them.

Effects on the liver

This treatment can affect how the liver works. You will have regular blood tests to check this. Sometimes liver changes can be serious. Contact the hospital straight away on the 24-hour number if you have any of these symptoms:

  • yellow skin or eyes
  • feeling very sleepy
  • dark urine (pee)
  • unexplained bleeding or bruising
  • pain in the right side of your tummy (abdomen).

Skin changes

This treatment can affect your skin. It may cause a rash, which may be itchy. Your doctor or nurse can tell you what to expect. If your skin feels dry, try using soap-free cleansers and unperfumed moisturising cream every day. 

Always tell your doctor or nurse about any skin changes. They can give you advice and may prescribe creams or medicines to help. Changes to your skin usually improve when treatment ends.

Hair thinning

While you are having this treatment, there may be changes to how your hair grows. For example, the hair on your head might become thicker or thinner, or you may lose some body hair. Your hair may also be drier, more brittle than usual, or change colour.

If you are worried about this, talk to your nurse about hair care.

Allergic reaction

This treatment might cause an allergic reaction. But this is not common. Signs of a reaction can include:

  • a skin rash or itching
  • feeling breathless or wheezy
  • swelling of your face, mouth or throat.

If you feel unwell or have any of these signs, contact the hospital straight away on the 24-hour number. Do not take any more of this treatment until you have checked with them.

Always call 999 if swelling happens suddenly or you are struggling to breathe.

Meningioma risk

When this treatment is taken for a long time, there is a very rare risk of developing a type of brain tumour called a meningioma. Your cancer doctor or specialist nurse can give you more information.

Raised blood sugar levels

If you have diabetes, this treatment may make your blood sugars higher than usual.

Signs of raised blood sugar include:

  • feeling thirsty
  • needing to pass urine (pee) more often than usual
  • feeling more tired than usual.

You may need to check your blood sugar level more often, or make changes to your diabetic treatment. Your diabetic doctor or nurse will talk to you about how to manage this.

Anaemia (low number of red blood cells)

This treatment can reduce the number of red blood cells in your blood. Red blood cells carry oxygen around the body. If the number of red blood cells is low, this is called anaemia. You may feel:

  • very low in energy
  • breathless 
  • dizzy and light-headed. 

If you have these symptoms, contact the hospital straight away on the 24-hour number. You may need treatment for anaemia. If you are very anaemic, you may need a drip to give you extra red blood cells. This is called a blood transfusion.

Bone thinning (osteoporosis)

Taking this treatment for several months or more can increase the risk of bone thinning. This is called osteoporosis. It can make you more likely to get a broken bone (fracture). 

You may have bone density scans to check your bone health before and during treatment. These scans can diagnose osteoporosis or osteopenia (low bone density) so that it can be monitored. If your scan shows osteoporosis, your doctor usually prescribes:

  • drugs to protect your bones called bisphosphonates
  • calcium and vitamin D supplements. 

Regular exercise where you support your body weight, like walking, running and dancing, can help look after your bones. This is called weight-bearing exercise. Other types of strength exercises are also helpful. If you have any bone thinning or the cancer is affecting your bones, get advice from your cancer team first. 

Eating a healthy diet and not smoking also helps take care of your bones.

Other important information

Lactose

This treatment may contain lactose. If you have a lactose allergy or intolerance, ask your doctor, nurse or pharmacist for more information.

Blood clot risk

This treatment might increase the risk of a blood clot in people who have had a previous blood clot or other circulation problems. Contact the hospital straight away on the 24-hour number if you have any of these symptoms during or after treatment:

  • throbbing pain or swelling in a leg or arm
  • reddening of the skin in the area – if you have black or brown skin, this can be harder to notice, but the skin might become darker
  • suddenly feeling breathless or coughing.

Always call 999 if you have:

  • chest pain
  • difficulty breathing.

A blood clot is serious, but it can be treated with drugs called anticoagulants. These thin the blood. Your doctor, nurse or pharmacist can give you more information about preventing and treating blood clots.

Other medicines

Some medicines can affect how this treatment works or be harmful while you are having it. Always tell your cancer doctor, nurse or pharmacist about any drugs you are taking or planning to take, such as: 

Medical and dental treatment

If you need medical treatment for any reason other than cancer, always tell the healthcare professional that you are having cancer treatment. Give them the contact details for your cancer doctor or cancer team so they can ask for advice.

If you have appointments with a dentist, always tell them you are having cancer treatment. Talk to your cancer team before you have any dental treatment.

About our information

This information has been written, revised and edited by Macmillan Cancer Support’s Cancer Information Development team. It has been reviewed by expert medical and health professionals and people living with cancer.

Date reviewed

Reviewed: 01 August 2024
|
Next review: 01 February 2027
Trusted Information Creator - Patient Information Forum
Trusted Information Creator - Patient Information Forum

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