In most hospitals, a team of specialists will discuss the treatment that is best for you. This multidisciplinary team (MDT) will include a surgeon who specialises in bowel cancers, one or more oncologists (doctors who specialise in cancer treatments such as radiotherapy or chemotherapy) and a number of other health professionals.
How treatment is planned
Together, the MDT will be able to advise you on the best course of action and plan of treatment. They will take into account a number of factors, including your general health, age, the size of the cancer, where it is in the colon, and whether it has begun to spread.
The stage is very important in determining treatment:
Your doctors will have carried out various tests and investigations to help them plan your treatment. Although they will have a good idea about which treatments you need, they may not be able to tell you exactly until after an operation.
You will be asked to give your permission (consent) for the hospital staff to give you the treatment. It‘s important that you discuss with your doctors the treatments they are recommending and that you understand why a particular type of treatment has been suggested for you.
Treatment according to stage
Often, the cancer can be completely removed with surgery, and for most people it will never come back. People who have stage 1 colon cancer don‘t usually need to have any further treatment after their surgery.
People with stage 2 colon cancer are also usually treated with surgery. There may be a risk that the cancer could come back in the future, especially if cancer cells are found in the blood vessels or lymph vessels around the cancer. So, treatment with chemotherapy is sometimes given after surgery to help reduce the risks of the cancer coming back.
In people with stage 3 colon cancer, there is a greater risk that the cancer will come back after surgery, so chemotherapy is usually recommended. Research trials are trying to find out whether giving drugs known as monocolonal antibodies, as well as chemotherapy, after surgery can further reduce the chance of the cancer coming back. Other types of treatment that are in the very early stages of research are being tested in clinical trials.
Stage 4 colon cancer means that the cancer has spread from where it started in the bowel. It is also called advanced colon cancer. It can spread into the area around the bowel, such as the abdomen, and this is known as local spread. If the cancer has spread to other parts of the body such as the liver or lungs, this is known as secondary or metastatic cancer.
It‘s not usually possible to cure stage 4 colon cancer, but treatment may be able to control it for some time. Treatment may also be used to reduce symptoms and give a good quality of life. However, for some people in this situation, treatment will have little effect upon the cancer and they will have the side effects with little benefit.
The treatment that is most appropriate for you will depend on:
Chemotherapy is the most commonly used treatment for stage 4 colon cancer. It may be given into a vein by injection or drip, or may be taken as tablets or capsules.
Surgery may sometimes be used – to remove a cancer that is blocking the bowel, for example, or sometimes to remove secondary bowel cancers from the liver or lungs.
Radiotherapy may be used to shrink a cancer that is causing pain. This is known as palliative radiotherapy.
Monoclonal antibodies such as bevacizumab (Avastin®), cetuximab (Erbitux®) and panitumumab (Vectibix®) may be used to control advanced colon cancer for a time.
The benefits and disadvantages of treatment
Many people are frightened at the thought of having cancer treatments, because of the side effects that may occur. Some people ask what will happen if they don‘t have any treatment.
Although the treatments can cause side effects, these can often be well controlled with medicines.
Treatment can be given for different reasons and the potential benefits will vary depending upon your particular situation.
If you have early-stage colon cancer (stages 1, 2 and 3) and have been offered treatment that is intended to cure it, it may be easy to decide whether to accept the treatment. Your doctor will talk through your treatment and any other options with you.
However, if a cure is not possible and the treatment is being given to control the cancer for a period of time, it may be more difficult to decide whether to go ahead. Making decisions about treatment in these circumstances is always difficult. You may need to discuss in detail with your doctor whether you wish to have treatment. If you choose not to, you can still be given supportive (palliative) care, which often involves medicines to control any symptoms.
You can ask for a second opinion if you feel it would be helpful.
For more on planning your treatment, you may find it helpful to read our information on:
Surgery for colon cancer
Surgery is the most common type of treatment for colon cancer and should be carried out by a surgeon who specialises in bowel surgery.
There are different types of colon cancer surgery. Your doctor will discuss with you the most appropriate type of surgery, depending on the stage of your cancer and where it is in your bowel.
Before your operation
Before your surgery the doctor and specialist nurses will explain the operation to you. They will tell you what to expect immediately after the surgery and in the few days
following. This is a good opportunity to ask any questions you may have about the operation.
You‘ll probably be admitted to the ward the day before your operation, so that the doctors and nurses can do any further tests. To make sure that your bowel is completely empty, you‘ll be asked to follow a strict diet and take a medicine (laxative) to help your bowels to empty the day before surgery. Your nurse or the doctor will explain this to you.
You‘ll be given antibiotics as an injection into a vein (intravenously) just before and after surgery to prevent infections.
Types of colon cancer surgery
Removal of all or part of the colon
Removal of the whole colon is called a total colectomy.
If only half of the colon needs to be removed, this is known as a hemi-colectomy . Either the left side or the right side may be removed, depending on the location of cancer.
Some people have a sigmoid-colectomy , (removal of the sigmoid colon), or a transverse colectomy (removal of the transverse colon ). The sigmoid colon and transverse colon are shown in the diagram in our section on the large bowel.
During the surgery, the piece of bowel that contains the cancer is removed and the two open ends are then joined together. The join is known as an anastomosis. The lymph nodes near to the colon are also removed, because this is usually the first place the cancer spreads to.
After surgery to remove a cancer in the colon, you will usually have a wound that goes in a straight line from just below your breast bone (sternum) to just above your pelvis.
This operation uses four or five small cuts in the abdomen rather than one bigger incision. A laparoscope (a thin, flexible tube containing a light and camera) is passed into the abdomen through one of the cuts and the cancer is removed. Recovery from this operation is usually quicker. However, this is a new operation that is currently being researched to find out its risks and benefits.
Very early-stage colon cancers can sometimes be removed using an operation called local resection. Using an endoscope, similar to the one used to take a biopsy, the surgeon will remove the cancer from the lining of the bowel. A pathologist will examine the cancer that has been removed. If it‘s found to be high-grade your surgeon may recommend that you have a second operation. This is done to remove more of the colon to make sure that no cancer cells have been left behind.
If the ends of the bowel can‘t be rejoined, the upper end can be brought out onto the skin of the abdominal wall. This is known as a colostomy, and the opening of the bowel is known as a stoma. A bag is worn over the stoma to collect the stool (bowel motions). Sometimes a colostomy is only temporary and another operation to rejoin the bowel can be done a few months later.
The operation to rejoin the bowel is known as stoma reversal. If it isn‘t possible to reverse the colostomy, the stoma is permanent. However, only a small number of people with cancer of the colon will need a permanent colostomy.
Some people need to have an operation called an ileostomy. Here, the end of the small bowel (ileum), or a loop of ileum, is brought out onto the right side of the abdominal wall. As with a colostomy, stools are then collected in a bag worn over the stoma.
For people with cancer of the colon, this is generally a temporary operation. If it‘s likely that at a later date the bowel will be rejoined and the stoma removed (reversed), your specialist nurse will discuss this with you.
Surgery for advanced colon cancer
If the cancer is too large to be removed and is pressing on the bowel causing it to narrow, it may be possible to insert a thin metal tube (a stent) into the bowel to keep it open. The stent is inserted using a colonoscope. You will be given a mild sedative to help you relax and may have a short stay in hospital.
Surgery may sometimes be used to remove the cancer when it has spread to another part of the body, such as the liver or lungs. Sometimes chemotherapy may be given before or after the surgery.
You may find our JASCAP booklets on Secondary Liver Cancer and Secondary Lung Cancer helpful.
After your operation for colon cancer
How quickly you recover from your operation will depend on your age and health, and the type of surgery you‘ve had. Your doctor and specialist nurse can give you an idea about what to expect.
In the hospital
After your operation you‘ll be encouraged to start moving around as soon as possible. This is an essential part of your recovery. Even if you have to stay in bed, it‘s important to do regular leg movements and deep-breathing exercises.
A physiotherapist or nurse will explain the exercises to you.
As you won‘t be moving around as much as usual, you may be at risk of blood clots forming. To prevent this you will be asked to wear special stockings, and may be given an anti-clotting drug called heparin.
Drips and diet
When you go back to the ward, you will have a drip (infusion) which gives you fluids through a thin tube (cannula) inserted into a vein in your hand or arm. This will be taken out once you are able to eat and drink normally again.
You may also have a thin tube that passes down your nose into your stomach (nasogastric or NG tube). This allows any fluids to be removed from your stomach so that you don‘t feel sick. It‘s normally taken out within a few days.
As an anaesthetic slows down the movement of the bowel, it‘s important that you don‘t start drinking until the bowel is working normally again. You will probably be ready to start taking sips of water within a few days. This will be increased gradually over a couple of days until you are able to eat a light diet.
Often, a small tube (catheter) is put into your bladder, and your urine is drained through this into a collecting bag. This is usually taken out after a couple of days.
You may also have a drainage tube in your wound, to drain any extra fluid and make sure that the wound heals properly. A drain isn‘t always needed.
After your operation, you‘ll probably have some pain or discomfort for a few days.
There are several different types of painkillers that can be given to you at regular intervals or when you need them. You may be given painkillers into a vein in your arm through a pump. The pump can be set to give you a controlled amount of painkiller, or you may be able to control this yourself by pressing a button. This is called patient controlled analgesia (PCA).
Always let your doctor or nurse know if you have any pain or discomfort. The painkillers or their dose can be changed to suit your needs. Some people may continue to have some pain after they go home. Let your doctor or nurse know if you think you might need painkillers to take home with you.
Depending on the type of operation you‘ve had, you‘ll probably be ready to go home between 3–10 days after surgery. If you think that you might have problems when you go home (for example, if you live alone or have several flights of stairs to climb), let your nurse or the social worker know when you are admitted to the ward. They can then arrange help before you leave hospital.
You‘ll be given an appointment to attend an outpatient clinic for your post-operative check-up. At the appointment your doctor will be able to discuss with you whether you need to have any further treatment, such as chemotherapy.
Some people take longer than others to recover from their operation. If you have any problems, you may find it helpful to talk to someone who is not directly involved with your illness. See our useful organisations section for more information about who can help.
Our cancer support specialists can talk to you, and tell you how to contact a counsellor or local cancer support group.
Enhanced Recovery Programmes (ERP)
Some hospitals follow an Enhanced Recovery Programme that can help to reduce complications following surgery and speed up your recovery. The programme involves careful planning before your operation so that you are properly prepared and any arrangements that are needed for you to go home are already in place. You‘ll also be encouraged to take high-protein and high-calorie supplements before and after your surgery, and to start moving around as soon as possible, sometimes on the day of the operation. After you have gone home you‘ll be regularly reviewed to make sure that you are recovering well.
Diet after bowel surgery
After any bowel operation, you may notice that certain foods upset the normal working of your bowel, or your colostomy if you have one. High-fibre foods, such as fruit and vegetables, may give you loose stools and make you pass them more often than normal. Depending on the type of surgery you‘ve had, you may have diarrhoea.
Tell your doctor or nurse if this happens, as they can give you medicine to help.
It‘s important to drink plenty of fluids if you have diarrhoea. This is often a temporary reaction, and after a while you may find that the same foods don‘t have any effect.
There are no set rules about the types of food to avoid and each person needs to experiment for themselves. Some foods that disagree with one person may be fine for another.
You may also find that your bowel produces more wind than before, and this can sometimes build up in the abdomen and cause pain. Drinking peppermint water or taking charcoal tablets can help to reduce this. Your doctor can prescribe these for you, or you can get them from your chemist.
It can sometimes take months for your bowel movements to get back to normal after surgery, and you‘ll probably need to find out which foods are right for you by trial and error. Some people may find that their bowel is always more active than before their surgery, and that they have to eat carefully to control their bowel movements.
If you continue to have problems, it‘s important to talk to a dietitian at the hospital, as they can give you specialist advice for your individual situation.
You may find JASCAP booklet on Diet and Cancer helpful.
Sex life after bowel surgery
Once you have recovered from the operation, there is usually no medical reason why you shouldn‘t have a normal sex life again. However, you may find that you feel self-
conscious about the change in your body‘s appearance, especially if you now have a colostomy. This may stop you from wanting to make love.
Talking about your feelings may help lessen your anxieties. Try not to feel embarrassed talking to your nurse or doctor about what is troubling you. They can refer you for specialist counselling if you think that would be helpful.
Sometimes the operation can cause damage to the nerves that go to the sexual organs. If this occurs, a man may not be able to have or maintain an erection, and may have problems with orgasm and ejaculation. Women may also find that their sexual function or response is affected. This may improve over time, but sometimes it is permanent. There are treatments available, such as sildenafil (Viagra®) that can help men achieve erections. It‘s important to discuss this with your doctor as soon as you notice a problem, as treatment can often be more effective if started sooner.
We may find JASCAP booklet on Sexuality and Cancer helpful.
If you have any problems, your doctor or specialist nurse will be able to discuss them with you in more detail.
Living with a stoma
Some people with cancer of the colon will need to have a colostomy or ileostomy. In these operations, the colon is brought to the outside of the body through the abdominal wall. The opening is called a stoma.
This can be daunting at first. Learning to look after a stoma takes time and patience and no-one expects you to be able to cope straight away. Like anything new, it will get easier with time and practice.
Stoma care nurses
In most hospitals there are specially trained nurses called stoma care nurses (or colorectal nurses) who you will usually meet before your operation. They will show you how to look after your stoma and help you cope with any problems.
Before your operation, the nurse or doctor will carefully plan the position of your stoma so that your bag stays in place, whether you are sitting, standing or moving around.
For the first few days after your operation, the nurse will look after your colostomy or ileostomy for you and make sure that the bag is emptied and changed as often as necessary. At first your stoma will be slightly swollen and it can take several weeks before it settles down to its normal size. As soon as you are feeling well enough, the nurse will show you how to clean your stoma and change the bags. There are several different types of bag or appliance available and the nurse will help you choose a suitable one.
Talking to people who have a stoma
You may find it helpful to talk to someone who has a colostomy or ileostomy. Your nurse or doctor can often arrange for a volunteer to visit you and talk to you about the more practical and personal aspects, or you can contact the Colostomy Association
or the Ileostomy and Internal Pouch Support Group. This advice, coming from personal experience, can be invaluable, particularly in the first few months after your operation. The Healthtalkonline website has information about colostomies and ileostomies. It also has video and audio clips of people who have stomas talking about their experiences.
Looking after a stoma
When the nurse is showing you how to look after your stoma, it may help for a close relative or partner to be with you, in case you have any difficulties when you get home.
Before you leave hospital, your nurse will make sure that you have a good supply of stoma bags.
Make sure that you have plenty of bags and cleaning materials to hand before you start to change or empty your bag. It‘s a good idea to keep everything you need in one place, so that you don‘t have to start searching for things at the last minute.
Make sure that you allow yourself plenty of time and privacy, so that you can work at your own pace without any interruptions.
Some people with a colostomy avoid wearing a bag by flushing out (or irrigating) their colostomy about once a day, although this method doesn‘t suit everyone. Your stoma nurse will be able to discuss this with you in more detail.
There are different ways of getting stoma supplies when you are at home. You can get all your supplies from your chemist. Sometimes it‘s better to get them direct from a specialised supply company. These may also offer a cutting and delivery service. The Colostomy Association has details of companies. The supplies are free, but you‘ll need a prescription from your GP. If you are aged between 16 and 60, make sure that your doctor signs the form saying that you‘re entitled to free prescriptions.
Once you are at home you can phone the stoma nurse if you have any problems. Your GP may also arrange for a district nurse to visit you for a few days when you first leave hospital. They can make sure that you are coping at home, and sort out any problems you may have with your stoma.
Having a colostomy or ileostomy is a big change in your life. Many people find that they are embarrassed by the stoma, and that it affects the way that they feel about their body. Embarrassment about a stoma can also affect relationships and some people are uncomfortable about their partner seeing it. These feelings are a natural part of coming to terms with the changes that a stoma causes, and usually decrease gradually over time.
You can contact our cancer support specialists if you want to chat about any concerns you have. Details of other helpful organisations can be found in the further resources section.
Chemotherapy for colon cancer
Chemotherapy is the use of special anti-cancer (cytotoxic) drugs to destroy
cancer cells. In colon cancer, it's mainly used after surgery. Its aim is to get rid of any remaining cancer cells and reduce the chance of the cancer coming back in the future. This is called adjuvant chemotherapy.
If the cancer is advanced (stage 4), chemotherapy may be used to reduce symptoms.
Chemotherapy for early-stage colon cancer (stages 1, 2 and 3)
Chemotherapy usually isn‘t needed for stage 1 colon cancers that haven‘t begun to grow through the muscle wall and aren‘t affecting the lymph nodes (Dukes A).
In the treatment of stage 2 colon cancer (Dukes B), the risk of the cancer coming back is low, so chemotherapy may not be needed. However, after surgery the cancer will be examined carefully under the microscope, and your doctor may recommend that you have chemotherapy if cancer cells are found in the blood or lymph vessels very close to the cancer. You may also be offered chemotherapy as part of a clinical trial. Your cancer specialist will discuss whether chemotherapy will be of any benefit to you if you have stage 2 colon cancer.
People with stage 3 colon cancer (Dukes C) are usually offered chemotherapy. They may also be offered chemotherapy as part of a clinical trial.
Drugs used to treat early-stage colon cancer
The main drugs used are:
Your specialist will discuss your particular course of treatment with you.
There are several research trials in the UK looking at different chemotherapy drugs, or combinations of drugs, to treat colon cancer. Some of these may be given as tablets. You may be asked if you‘d like to take part in a clinical trial to test one of these treatments.
Pros and cons of chemotherapy for early-stage colon cancer
There are various benefits and risks of having chemotherapy and your doctor can discuss these with you.
Chemotherapy can reduce the chance of the cancer coming back, but doesn‘t guarantee this. It can also sometimes cause side effects that may be unpleasant. To help decide whether adjuvant chemotherapy may be appropriate in your case, your specialist will take into account the risk of any cancer cells being left behind, the
likelihood that the chemotherapy will get rid of them, and the possible side effects of the treatment.
If the chance of the cancer coming back is low, the chemotherapy may only slightly reduce the chance of the cancer returning. However, if the risk of the cancer coming back is high, the benefit of chemotherapy may be greater. It‘s important to discuss with your doctor the possible risks and benefits of chemotherapy in your particular situation.
Chemotherapy for advanced (secondary) cancer of the colon
Chemotherapy may also be given when the cancer has spread to another part of the body. Many people have no further problems after their original treatment for colon cancer, but unfortunately, in some people the cancer comes back or spreads to other parts of the body. This is called secondary, advanced or metastatic cancer.
Sometimes, when the cancer is first diagnosed, it may already have spread beyond the bowel. The most common place for it to spread to is the liver. JASCAP has a booklet about Secondary Cancer in the Liver. The next most common place is the lungs.
Although secondary cancer of the colon can‘t usually be cured, treatment with chemotherapy may be recommended by your doctor. The aim of the chemotherapy is to shrink the cancers and reduce symptoms. This can sometimes help to prolong life. Chemotherapy may also be given to shrink cancers before they are removed from the liver or, more rarely, the lungs. Sometimes drugs called monoclonal antibodies are given in combination with chemotherapy.
Improvements in surgical techniques combined with drug treatment have meant that some people who have had liver secondaries removed, often combined with drug treatment, appear to be cured as a result of their treatment. Your doctor or specialist nurse can discuss this with you further.
JASCAP has booklets about Secondary Cancer in the Liver and Secondary Cancer in the Lungs.
Drugs used to treat advanced colon cancer
The most commonly used chemotherapy drugs for advanced colon cancer are:
Several research trials are being carried out to test new drugs for advanced colon cancer, and to help find the best way of using the current drugs. You may be asked if
you‘d like to take part in a research trial using new chemotherapy drugs or new types of treatments.
If the cancer starts to grow again, during or after the chemotherapy, you may be given a different type of chemotherapy (this is known as second-line treatment). Sometimes a third course of chemotherapy (third-line treatment) may also be given.
Benefits and disadvantages of chemotherapy for advanced colon cancer
There are various benefits and disadvantages of chemotherapy for advanced colon cancer, and it‘s important to discuss these with your cancer specialist.
It isn‘t possible to predict whether chemotherapy will work for a particular person, but if they are fairly fit the treatment is more likely to be effective. It‘s also less likely to have side effects than in someone who is unwell when they start the treatment.
You don‘t have to have chemotherapy unless you want to. If you choose not to, you‘ll still be given treatment to help control any symptoms caused by the cancer. This is known as supportive, or palliative, care. Palliative care can also be given alongside chemotherapy if needed.
Your doctor will consider a number of things before asking you to make a decision about particular treatments. This will include the position of the secondary cancer, your general health and any chemotherapy treatment you‘ve had in the past.
If you have advanced cancer, there are many difficult issues to deal with. You may find it helpful to read our JASCAP booklet on Coping with advanced cancer.
Our JASCAP booklets on Controlling Cancer Pain and Controlling Cancer Symptoms explain ways that pain and symptoms can be treated. They also give information on the support that is available from health professionals and other sources.
How chemotherapy is given
Many people having chemotherapy for colon cancer are given capsules or tablets, which are swallowed with water.
Some people with colon cancer will have their chemotherapy drugs given by injection into a vein (intravenously). The drugs may be given through a vein in the back of your hand; a plastic line called a central line, in your chest; or a thin tube inserted into a vein in the crook of your arm (a PICC line).
Position of a central line
The PICC line is threaded through the vein until the end is near your heart
Sometimes chemotherapy can be given to you continuously through a small portable pump which is attached to your central or PICC line. A controlled amount of the drug can be given into the bloodstream over a period of time. This means that you can go home with the pump, and spend less time in hospital. Some people whose cancer has spread to the liver may be given chemotherapy into an artery that goes directly into the liver.
Intravenous chemotherapy (see above) is usually given as a session of treatment. A session may last from a few hours to several days. If you have treatment for a few hours, this may be repeated each week for several months. This chemotherapy is usually given as an outpatient.
If your treatment lasts a few days you‘ll usually have a rest period of a few weeks before the next session. This allows your body to recover from the side effects of the treatment. The chemotherapy session and the rest period make up a cycle of treatment. You may need to stay in hospital for your treatment, but it can also often be given to you as an outpatient. Your specialist will discuss this with you.
The number of cycles you have will depend on the stage of the cancer and how well it‘s responding to the drugs.
Contraception during chemotherapy
It is not advisable to become pregnant or father a child while taking any of the chemotherapy drugs used to treat colon cancer, as they may harm the developing baby. It‘s important to use effective contraception during your treatment and for a year afterwards. You can discuss this with your doctor or specialist nurse.
Condoms should be used during sex within the first 48 hours after chemotherapy to protect your partner from any of the drug that may be present in semen or vaginal fluid.
Our JASCAP Chemotherapy booklet describes the treatment in more detail.
Side effects of chemotherapy for colon cancer
Chemotherapy can sometimes cause unpleasant side effects. These will vary depending on which chemotherapy drugs you are given. Your doctor or nurse will tell you what problems to expect from your treatment. Common side effects include:
Although side effects may be hard to bear at the time, they will gradually disappear once your treatment is over. For some people this can take some months.
Most people have some side effects from chemotherapy. But if your cancer is causing symptoms it can also make you feel better by relieving them.
There are many things that can be done to help reduce and control side effects so let the staff looking after you know if you are having problems.
Lowered resistance to infection (neutropenia)
While the drugs are acting on the cancer cells in your body, they may also temporarily reduce the number of normal white blood cells. This is called neutropenia. When these cells are reduced you are more likely to get an infection.
While your level of white blood cells is low, it‘s important to avoid crowded places, where you may come into contact with infection, and to avoid anyone who already has an infection, such as a cold or flu.
Contact your doctor or the hospital straight away if you have any signs of infection, such as a high temperature (above 38°C or 100.5°F), or if you suddenly feel unwell (even with a normal temperature). During chemotherapy your blood will be tested regularly and, if necessary, you will be given antibiotics to treat any infection.
Bruising or bleeding
Chemotherapy can reduce the production of platelets (which help the blood to clot). Let your doctor know if you have any unexplained bruising or bleeding, such as nosebleeds, blood spots or rashes on the skin, or bleeding gums.
Anaemia (low number of red blood cells)
While having treatment with chemotherapy you may become anaemic. This may make you feel tired and breathless.
You‘re likely to find that you become very tired and have to take things much more slowly. Just do as much as you feel like and try not to overdo it. We have a section on coping with fatigue, which you may find helpful.
Some of the drugs may make you feel sick (nauseated) and possibly be sick (vomit). There are anti-sickness drugs (anti-emetics) to prevent or reduce nausea and vomiting. Your doctor will prescribe these for you. Let your doctor or nurse know if your anti-sickness drugs are not helping, as there are several different types you can take. Our section on controlling nausea and vomiting has further information about this.
Some of the chemotherapy drugs used to treat bowel cancer can cause diarrhoea.
This often starts several days after the treatment. If you‘re taking chemotherapy tablets or capsules at home, it‘s important that you let your doctor or nurse know if you have diarrhoea. Your treatment may need to be stopped.
If you have diarrhoea your doctor can give you medicine to reduce this and slow down the bowel. You may also be able to help control it by eating a low-fibre diet. Our section on diet and cancer has useful advice on this.
If you‘ve had a colostomy or ileostomy, it may be more difficult to cope with diarrhoea caused by the chemotherapy. Your stoma nurse or cancer specialist can give you advice and support. Some people find that they need to make sure they are close to a toilet during the course of their treatment and for a while afterwards. This can be frustrating, but usually improves gradually a few weeks after the treatment has ended. If the diarrhoea continues after this time it‘s important to talk to your cancer specialist or stoma nurse, so that they can help you find ways of overcoming the diarrhoea.
You may find that you get a sore mouth and mouth ulcers while having chemotherapy. Keeping your mouth clean with regular mouthwashes is important. Your nurse will show you how to use these properly. If a sore mouth makes eating difficult, you can try replacing meals with nutritious drinks — our section on mouth care during chemotherapy has some useful tips on coping with a sore mouth.
Ask your doctor if the drugs you are taking are likely to make your hair fall out. Most drugs used to treat colon cancer do not, but some may make your hair thin. If your hair does fall out, it will start to grow back again once your treatment is over.
JASCAP has a booklet about Coping with Hair Loss.
Soreness of hands and feet
If 5FU or capecitabine are given over a long period of time or are given continuously through a pump, soreness and redness of your palms and the soles of your feet can occur. This is known as hand/foot syndrome or palmar-plantar syndrome. Vitamin B6 may be prescribed to help reduce this side effect and non-perfumed moisturising creams can often help to relieve the symptoms. If the symptoms are severe your doctor may reduce the dose of the chemotherapy or give you a short break from it.
Numbness or tingling
Oxaliplatin can affect the nerve endings and cause numbness, burning or tingling in the hands, feet, neck or throat (known as peripheral neuropathy). You may also find it hard to do up buttons etc. The numbness or tingling may not happen with the first treatment. If it occurs, it should gradually disappear once the treatment has finished.
Sometimes in the first few days after oxaliplatin is given, these side effects can be triggered by anything cold, such as cold drinks or washing water, but often they only last a few minutes.
Our Chemotherapy booklet discusses the treatment in more detail and has tips for coping with the side effects.
Biological therapies (targeted therapies) for colon cancer
Biological therapies use substances that occur naturally in the body to destroy cancer cells. There are several different types of biological therapies. The main ones used to treat colon cancer are monoclonal antibodies and include bevacizumab
(Avastin®), cetuximab (Erbitux®) and panitumumab (Vectibix®).
They can be used to treat some cases of colon cancer that have spread outside the bowel (stage 4, advanced or metastatic cancer).
Research trials are trying to find out whether, for stage 3 colon cancer, giving monoclonal antibodies, as well as chemotherapy, after surgery can further reduce the chance of the cancer coming back.
How monoclonal antibodies work
Monoclonal antibodies are drugs that recognise and lock onto specific proteins (receptors) that are present in particular cancer cells. Because of this they are often called targeted therapies, because they =target‘ the cancer cells.
Some cancer cells have proteins known as epidermal growth factor receptors (EGFRs). When other proteins in the body, known as growth factors, attach to these receptors, the cancer cell is stimulated to grow and divide. The monoclonal antibodies cetuximab (Erbitux®) and panitumumab (Vectibix®) lock onto the EGFR, stopping growth factors from attaching, and so may prevent the cancer cell from growing and dividing.
Not all colon cancers respond to cetuximab or panitumumab. Before having either drug your doctors will test the cancer cells for a gene called KRAS. Knowing if the KRAS gene is normal or changed (mutated) can help the doctors to decide whether cetuximab or panitumumab will be appropriate for you.
Bevacizumab (Avastin®) works by preventing the cancer from developing a new blood supply, and so starves the cancer of oxygen and nutrients. Drugs that interfere with blood vessel growth in this way are called angiogenesis inhibitors or anti- angiogenics.
How the drugs are given
Cetuximab is usually given in combination with chemotherapy, although it can be used on its own. It‘s given as a drip (infusion) into a vein. Panitumumab is usually given on its own as an infusion into a vein.
Bevacizumab is given as an infusion through a small tube (cannula) inserted into a vein. It may be given in combination with chemotherapy drugs.
The National Institute for Health and Clinical Excellence (NICE), which advises doctors about treatment, have recommended the use of cetuximab in combination with chemotherapy for some people who have advanced (metastatic) colon cancer that has spread to the liver. Treatment with the combination of cetuximab and chemotherapy may make it possible to remove the secondary cancers in the liver using surgery. The NICE guidance doesn‘t recommend cetuximab for everyone in
this situation. Your cancer specialist can discuss with you whether cetuximab is recommended for you. Currently, panitumumab is not recommended by NICE.
Bevacizumab can also be used to treat advanced cancers of the colon that have not been controlled by other chemotherapy combinations. Bevacizumab is currently not recommended by NICE and as a result it may not be possible to get it on the NHS.
Some people can have an allergic reaction to monoclonal antibodies. This can make you have a flu-like reaction, a drop in blood pressure or feel sick.
Other possible side effects include skin rashes and tiredness. With some monoclonal antibodies, the first dose is given slowly, over a number of hours. You may be given some other drugs first to make a reaction less likely.
Radiotherapy for colon cancer
Radiotherapy treats cancer by using high-energy rays to destroy the cancer cells, while doing as little harm as possible to normal cells.
Radiotherapy is rarely used to treat colon cancer except occasionally to shrink the cancer and relieve symptoms such as pain. This is called palliative radiotherapy.
Radiotherapy doesn‘t make you radioactive and it‘s perfectly safe for you to be with other people, including children, throughout your treatment.
How radiotherapy is given
Radiotherapy is usually given at a hospital outpatient clinic as a series of short daily treatments. The treatments are usually given each weekday with a rest at the weekend. How the treatment is given can vary, depending on what is considered to be most effective for your cancer and best for you. The course may last for just one week or a few weeks. Your doctor will discuss your treatment with you beforehand, including how it will be given and how long it will last.
Planning your treatment
To make sure that your radiotherapy is as effective as possible, it has to be carefully planned. Planning ensures the radiotherapy rays are aimed precisely at the cancer and cause the least possible damage to the surrounding healthy tissues. The treatment is planned by a specialist doctor known as a clinical oncologist. Planning is important and may take a few visits.
Marks may be drawn on your skin to help the radiographer, who gives you your treatment, to position you accurately and to show where the rays are to be directed. These marks must stay visible throughout your treatment, but they can be washed off once your course is over. At the beginning of your radiotherapy you will be told how to look after the skin in the area to be treated.
What happens in the treatment sessions
Before each session of radiotherapy, you‘ll be carefully positioned on the couch, either sitting or lying. The radiographer will make sure that you are comfortable.
During your treatment, which only takes a few minutes, you‘ll be left alone in the room, but you are able to talk to the radiographer who will be watching you carefully. Radiotherapy is not painful, but you do have to be still for a few minutes during your treatment.
Positioning the radiotherapy machine
Side effects of radiotherapy for colon cancer
Radiotherapy to the bowel area can cause side effects such as diarrhea, feeling sick (nausea) and tiredness. It can also cause more specific side effects, such as inflammation of the bowel or bladder lining. These side effects can be mild or more troublesome, depending on the strength of the radiotherapy dose and the length of your treatment. Some radiotherapy side effects can be permanent. Your clinical oncologist will tell you what to expect, and you can ask your radiographer for advice if side effects are becoming a problem for you.
Our Radiotherapy booklet discusses the treatment and its side effects in more detail.
Research - clinical trials for colon cancer
Cancer research trials are carried out to try to find new and better treatments for cancer. Trials that are carried out on patients are known as clinical trials.
Clinical trials may be carried out to:
Trials are the only reliable way to find out if a different operation, type of chemotherapy, radiotherapy, or other treatment is better than what is already available.
Taking part in a trial
There can be many benefits from taking part in a trial. Trials help improve knowledge about cancer and develop new treatments. You will be carefully monitored during and after the study. Usually, several hospitals around the country take part in trials. It=s important to bear in mind that some treatments that look promising at first are often later found to be not as good as existing treatments, or to have side effects that outweigh the benefits.
If you decide not to take part in a trial your decision will be respected and you do not have to give a reason. If you do decide to take part, you are allowed to withdraw from the trial at any time. In either case, there will be no change in the way that you are treated by the hospital staff and you will be offered the standard treatment for your situation.
Blood and tumour samples
Blood and tumour samples may be taken to help make the right diagnosis. You may be asked for your permission to use some of your samples for research into cancer. If you are taking part in a trial you may also be asked to give other samples which can be frozen and stored for future use, when new research techniques become available. These samples will have your name removed from them so you can‘t be identified.
The research may be carried out at the hospital where you are treated, or it may be at another hospital. This type of research takes a long time, and it may be many years before the results are known. The samples will be used to increase knowledge about the causes of cancer and its treatment. This research will hopefully improve the outlook for future patients.
Our booklet on Clinical Trials describes the process in more detail. It includes details of databases you can search to look at trials for colon cancer.
Follow-up after treatment for colon cancer
After your treatment has finished, you will have regular check-ups and blood tests, and possibly scans (CT, MRI or ultrasound), x-rays and sometimes colonoscopies. These may continue for several years, but will become less and less frequent.
If you have any problems or notice any new symptoms between your appointments, let your doctor know as soon as possible.
At the present time a lot of research is being carried out to find the best way of following up people who have had colon cancer. The pattern of timing of hospital visits and tests and the amount of follow-up done by GPs varies considerably.
Many people find that they get anxious for a while before their appointments. This is natural and it may help to get support from family, friends or one of the organisations listed during this time.
For people whose treatment is over apart from regular check-ups, JASCAP booklet on Recovery and Life after Cancer treatment gives useful advice on how to keep healthy and adjust to life after cancer.