This information is for patients who are going to receive EBRT (radiation given from a machine outside the body) for the treatment of prostate cancer.
This leaflet will explain:
- When radiotherapy is given
- Preparation for planning and treatment
- General information about the side effects of treatment
- Any side effects that may affect you
- Who to contact when you need advice
You may find it useful to read our booklet called ‘Radiotherapy’ which explains how radiotherapy works and what to expect when you attend.
When EBRT treatment is given
Radiotherapy to your prostate can be given to either cure or control prostate cancer. The reason for your radiotherapy will be discussed with you prior to starting treatment:
- To treat cancer that has not spread outside the prostate gland (localised) as an alternative to surgery.
- After surgery if the PSA levels start to rise targeting the prostate bed (the area where the prostate was).
- When the disease is, or likely to be, in other tissues in the pelvis, i.e. just outside the gland (locally advanced) or the pelvic lymph glands. (We often use the term 'whole pelvis' when we treat the prostate and lymph glands).
- You may be offered radiotherapy to your prostate even if prostate cancer has spread to other areas of the body; if your consultant feels this will be beneficial to you.
- You may be offered radiotherapy to your prostate to help with symptoms such as bleeding.
Your doctor will explain why radiotherapy is recommended for you.
Before starting radiotherapy, you will have a CT scan which is used to design your radiotherapy (called planning). We recommend starting 10 days before your planning appointment and during the course of treatment, if possible, you should aim to drink 1.5-2.0 litres (3-4 pints) of fluid each day. Try to avoid caffeine and alcohol and drink mainly water. If your fluid intake is normally more than this, continue as usual.
If you have an artificial hip(s) please alert the therapeutic radiographer when you attend.
If you have a pacemaker please alert the therapeutic radiographer when you attend.
Some preparation before the scan is required; this usually takes about 45 minutes, followed by the CT scan, which takes about 20 minutes.
The preparation involves the use of a small enema to empty the rectum; this helps make the rectum smaller and moves it away from the area to be treated (target area).
We also ask you to drink some water, which, once it has reached the bladder, will help to move the bowel away from the target area.
When you arrive, the staff will go through everything with you. If you are worried about the preparation process, please raise any concerns with the planning staff.
Why is the preparation important?
To ensure we hit the target area with each treatment
To achieve this, we need to replicate the position of the target area at every treatment so the x-ray beams hit the area. (The target area is later defined on the scan images. It includes the prostate area (and any structures identified as being involved by previous investigations) plus a small band of tissue next to the target used as a safety margin. The target area receives the highest dose of radiation and is individually designed according to your internal anatomy.
Note: The preparation procedure is an important first stage in ensuring the accuracy of treatment. In addition, 'high-tech’ procedures, using images generated from the planning scan and treatment unit, are also in place.
To help reduce short and long term side effects
When the preparation process is achieved, the structures around the target area (rectum, bladder, and small bowel) are moved away, helping to reduce the radiation dose to these areas.
You will need to repeat the preparation before every treatment, so you will be asked to arrive ahead of your appointment time. You may not be keen to use the mini enema each day, but research at the centre has shown that the use of an enema is beneficial and that patients tolerate this procedure well.
When you start your treatment, it is important that you understand and follow the instructions we have given you. Do not hesitate to talk to your treatment staff about the preparation instructions / routine which is required immediately before your treatment, not for the whole of the day.
If you are taking diuretics (water tablets)
Diuretics are used to treat a number of conditions and work by removing excess fluid from the body through increasing the production and flow of urine (wee). They are usually taken in the morning.
Consequently, some men who have a morning appointment may be concerned about the effect of the diuretic while travelling to the hospital. If so, it is OK to take the diuretic as soon as you can after your appointment. If you attend in the afternoon, take your diuretic as usual.
Do not reduce your intake of fluid immediately before attending as this affects the filling of your bladder. It is important for your general health to drink and eat normally.
On Treatment Review Radiographer (OTR)
During your treatment, you can raise any concerns with your treatment staff. Clinic appointments with the On Treatment Review Advanced Practitioner will also be booked to discuss how you are managing and any side effects etc. It is important to let us know when your side effects start; we will give you medicines and advice to help you cope.
General information about the side effects of radiotherapy treatment
Every patient is different and you may not have the same side effects as someone else. Your doctor will talk to you about the side effects that are likely to affect you.
Most are temporary but some may last for weeks or months after your treatment has finished (see later). Long term or permanent effects can occur but are fairly rare. Often, these effects can be easily managed and may not have a marked effect on your life.
During your treatment, a therapeutic radiographer or nurse will be able to answer any questions and deal with most of your problems. As you go through your treatment, how you feel and your ability to cope may change. It is important to let staff know how you feel so that we can give additional information, support and medicines etc if they are needed.
During your treatment you should try to continue with your normal daily activities to the best of your ability.
The usual pattern for the development of the short-term (acute) side effects is to gradually start about 5-10 days after the first treatment. They usually persist and worsen, the effects being most troublesome about 10 days after the last radiotherapy treatment. After this, the healing process begins. The side effects usually settle over the following 6-8 weeks but sometimes effects may persist for longer.
Your bladder
The bladder and prostate are next to each other so it is impossible to avoid giving the bladder some radiation dose, which results in some inflammation (soreness). Consequently, you may feel the need to pass urine (wee) more often, get a burning sensation, a slowing of the stream of urine and an urgent need to pass urine.
You can help yourself by:
- Drinking more fluid; about 1.5-2 litres (3-4 pints) of fluid each day until the symptoms settle. Avoid caffeine (tea, coffee, energy and cola-type drinks) and change to Decaffeinated options
- Avoid sugary and fizzy drinks as these will irritate your bladder
- If you wish, you may take alcohol in moderation, but stop if it causes irritation in your bladder
- Letting us know if you develop a burning sensation when you pass urine; if it is severe you may have an infection. If so, we will give you antibiotics and your treatment will carry on
Unable to empty your bladder during, or shortly after the course of radiotherapy?
This happens rarely. The urethra (see diagram in the section on 'Preparation for planning and treatment') passes through the prostate. Inflammation can cause it to be squeezed, making it difficult or impossible to pass urine.
If you can’t pass urine at all, get help quickly - otherwise this can make you very unwell. You may need a catheter for a short time. Please contact The Clatterbridge Cancer Centre Hotline 0800 169 5555 or attend A&E.
Your bowels
The treatment is likely to irritate your bowels.
You may have to open your bowels more often or occasionally they become stubborn. If your bowel habits change, advice on changing your diet may be appropriate as many people find this helpful.
Meanwhile, carry on with your normal diet.
You may also feel the urge to open your bowels, passing only small amounts or just mucus and wind. You may have discomfort and you may pass some blood.
You can help yourself by:
- Letting staff know about any symptoms so that they can give you advice and/or medicines
- Eating a good balanced diet
Tiredness (fatigue)
It is quite common to feel more tired and have less energy than usual during your course of radiotherapy and for several weeks after your treatment has finished. It may be useful to try to keep your normal routine but to reduce the amount of time that you spend on each task. It is important to rest when you feel the need to do so.
If you have family and friends nearby, consider asking for, or accepting, offers of help.
If you live alone, do only the tasks that are essential until you feel stronger.
It can also help to take a brisk walk or try some exercise as this can help with your tiredness / fatigue.
Your pelvic skin and hair
Your skin may slightly change colour, or become dry and itchy. If your skin becomes uncomfortable, ask the radiographer or nurse for advice.
You can help yourself by:
- Wearing loose fitting clothes made from natural fibres, such as cotton, to allow the air to circulate around the pelvic area
- Continue with your normal washing and skin care routine. If your skin becomes sore try mild / unscented moisturisers and soaps, avoid shaving and let your team know. You may be given a cream to help with your skin
Thinning or loss of pelvic / pubic hair can happen which can be temporary or permanent. The loss of pubic hair is most likely to be noticed.
Sex, fertility and contraception
Radiotherapy to the pelvic area is known to affect the reproductive organs. Retaining your fertility after completion of radiotherapy may or may not be important to you. If required, you will be referred to a local specialist centre for further advice and information. It is important to be referred before starting your radiotherapy.
It is not safe to presume that radiotherapy will make you infertile.
If you are sexually active and conception is a possibility, it is important to use contraception during, and after, your course of radiotherapy. If relevant, talk to your oncologist about when it is safe to stop the use of contraception.
You can continue with sexual activity while you are having radiotherapy. However, the side effects of radiotherapy can cause temporary discomfort in the pelvic area. You may find that intercourse is uncomfortable or you have no desire for sex. If so, try to talk to your partner and explain how you feel.
Men should also avoid receiving anal sex during and for two months afterwards, as it could make side effects worse, be painful, or result in long-term complications such as rectal bleeding or damage to the tissue in this area.
Inflammation may cause pain or discomfort when you ejaculate. This will likely settle in the weeks after treatment - please let your team know if this doesn’t.
You may also experience 'dry ejaculation' which means you may climax without producing any fluid (semen). This will not cause any harm and may be permanent.
Radiotherapy can cause long-term changes to the normal tissues in your pelvis (bladder and bowels) which are known as late effects. This will not affect all people who have radiotherapy to the prostate.
Late effects may occur months or years after your treatment and can include pain, discomfort or bleeding or difficulties when passing urine or opening your bowels. They may appear months or years after treatment and may not have a marked effect on your life.
If you develop any health problems that you suspect may be related to your radiotherapy, you should discuss this with your GP or prostate cancer team. If necessary, you will be referred you to specialist services, further investigations and/or an appointment with your oncology doctor.
The following may occur:
- The use of surgery or hormone therapy is frequently used in the treatment of prostate cancer. With these treatments, impotence (inability to achieve an erection) and loss of libido (sex drive) may occur. The addition of radiotherapy can affect your sex life further. Please speak with your team as we can suggest medications or devices that may be helpful. We may also refer you to a specialist clinic for support
- Following hormonal treatment (if given with your radiotherapy) changes to the sexual organs can occur, i.e. some loss of length and girth in penis size and the size and volume of the testis can be smaller
- Reduced volume or lack of ejaculate fluid (dry ejaculation) can develop though you should still have the sensation of ejaculation and orgasm
- There is a small long-term risk of damage to your bowels. This risk is slightly increased if you have the whole pelvis treated. You may have looser more frequent bowel movements, pass some mucus or small amounts of blood. These side effects can often be helped by adjusting your diet and the use of medicines. You should talk to your GP (or oncology staff at follow-up appointments) about any persistent changes in bowel habits as further assessment / investigations may be indicated. Very rarely, these effects may need surgery
- There is a small long-term risk of scarring to your bladder, which may mean that you need to empty your bladder more often and there may be a small amount of blood in your urine. If you develop these symptoms let your GP or team know
- Rarely, a narrowing (stricture) of the tube between the bladder and penis (urethra) can develop, causing urinary frequency (wanting to urinate more often) and a slow stream. This can be treated with a simple procedure
- Lymphoedema
- Treatment with radiotherapy carries a small increased risk of developing a new pelvic cancer. This risk is balanced against your current health needs
As you complete your radiotherapy, your care needs will be assessed.
In the first few weeks after finishing treatment, your side effects may get worse; however they should gradually settle over time. The oncology team will see the majority of patients within a couple of months after completion of their radiotherapy. This appointment is usually at your local hospital or cancer centre. Meanwhile, if you have any concerns you should contact our Hotline. This service is available for 6 weeks after finishing your treatment. After this time, you should contact your GP.
The diagnosis of cancer, together with the impact of treatment and any side effects, can have a major impact on how you feel, which then affects how you behave. Sometimes, your relationship(s), including sexual intimacy, are affected. If you are able, talking to staff about how you feel can be a great help.
Sometimes, more help is required to help you cope and overcome any negative feelings. Often, these feelings become more apparent once you have completed all your treatments and you are beginning to recover. You should discuss these issues with your GP or your oncologist, specialist nurse or radiographer at your follow up appointments. Referrals to specialist staff (e.g. a psychologist or sexual health) can be beneficial and may also be offered to you.
If you are feeling low or experience mood swings, it may be useful to talk about how you feel and your recent experiences. Some find it useful to have the support of others who have experience of cancer by attending a local support group. Contact the Cancer Information and Support Centre for more details.
Maggie's
Maggie's is a charity providing free cancer support and information to anybody who been affected by cancer. Our cancer nurse specialists, psychologists and benefits advisors are here to support you during treatment or after your treatment has finished.
The Maggie's Centres allow you to share experiences with others in a similar situation around our kitchen table. We provide courses on survivorship, bereavement, stress management, mindfulness, tai chi, yoga, relaxation or cancer support groups. You do not need an appointment or a referral to access any support from Maggie's - you can just drop in. Our telephone number is 0151 334 4301.
Alternatively, if you are familiar with using the internet, the major cancer charity websites have online communities.
If you are gay or bisexual, a trans-female or non-binary, you may wish to contact the Out with Prostate Cancer support group.
If you find that you have long or frequent periods of low mood, you should seek help from your GP. There are many ways to be helped, including, but not always, a short course of antidepressant tablets.
Prostate Cancer UK and Macmillan Cancer Support have lots of free information on coping and living with cancer that are available free of charge and at our Cancer Information and Support Centres at Clatterbridge Cancer Centre - Liverpool, Wirral and Aintree.
Diet and prostate cancer
Research is emerging which suggests that a balanced healthy diet may slow down the growth of prostate cancer in individuals who already have the disease or reduce the chance of prostate cancer returning after treatment. Please contact Prostate Cancer UK for more information (see contact details).
Clatterbridge Cancer Centre - Liverpool
65 Pembroke Place, Liverpool, L7 8YA
Tel: 0151 556 5000
www.
Clatterbridge Cancer Centre - Wirral
Clatterbridge Road, Bebington, Wirral, CH63 4JY
Tel: 0151 556 5000
www.
Clatterbridge Cancer Centre - Aintree
Lower Lane, Fazakerley, Liverpool, L9 7AL
Tel: 0151 556 5959
www.
Prostate Cancer UK
www.
Tel: 0800 074 8383
Out with Prostate Cancer
Support group for gay and bisexual men and trans-female and non binary people with prostate cancer
www.
Macmillan Cancer Support
89 Albert Embankment, London, SE1 7UQ
www.
Tel: 0808 808 0000
Cancer Information and Support Centres
Macmillan information available in our centres at:
- Clatterbridge Cancer Centre – Liverpool. Tel: 0151 318 8805
- Clatterbridge Cancer Centre - Wirral
- Clatterbridge Cancer Centre - Aintree
It is also available at Nobles Hospital, Isle of Man. Tel: 01624 650 735
Toilet cards
Toilet cards are available at all Clatterbridge Cancer Centre information centres or by accessing the Macmillan website page about using public toilets. A toilet card is a card that you can show quickly and easily to staff in shops, pubs and other places. It explains that you have a medical condition and need urgent access to a toilet. Sometimes it is also called a bladder and bowel card or a ‘no waiting’ toilet card.
Disability Rights UK (RADAR key scheme; access to locked public toilets)
Disability Rights UK produce a key which gives access to over 9,000 locked public toilets found in UK shopping centres, bus and train stations, department stores etc. Cost (March 2024) is £5.00 plus postage.
Find out how to get a RADAR key.
Maggie’s Centre - Wirral
Tel: 0151 334 4301