HODGKIN'S DISEASE & NON-HODGKIN'S LYMPHOMA

by Lymphoma Association

About lymphomas

Hodgkin's disease (HD) and non Hodgkin's lymphomas (NHL) - which together are called lymphomas - are types of cancer. Cancer is not one condition but a word applied to many different diseases, which have diverse causes and a wide range of treatments.

The cells which make up our bodies normally divide in a set and orderly fashion so they can repair our tissues. This process sometimes goes wrong and there is an uncontrolled growth of cells. A characteristic of all cancers is this disorderly formation of body cells, causing swellings or tumours.

A tumour is referred to as benign when it remains contained in a localised area of the body and, on removal by surgery, does not recur.

The term cancer is used when the tumours are malignant i.e. they spread and invade healthy tissue.

The lymphatic system & lymphomas

The lymphatic system is part of the body's natural defence against infection. It consists of a wide network of nodes or glands, which are found all around the body, and are linked by tiny vessels (or lymphatics).

A clear fluid called lymph circulates around the body and is drained, via the lymphatics, into the bloodstream. Lymph contains white blood cells known as lymphocytes. They play a part in protecting the body from infection. As the lymph circulates through the lymphatics it is interrupted by the lymph nodes which provide the opportunity to sieve the lymph and attack invaders.

When the natural division of cells in the tissues of the lymphatic system become disrupted, tumours called lymphomas occur. In common with other cancers, lymphomas are not infectious and cannot be passed on to other people.

The causes of lymphomas are uncertain but, in some types of lymphoma, research points to a connection with particular viruses.

There are about 8,000 new cases of lymphomas diagnosed in Britain each year. Less than a fifth are cases of Hodgkin's disease, the greater number being non Hodgkin's lymphomas.

Hodgkin's disease

Hodgkin's disease was first identified by Dr Thomas Hodgkin in 1832. It is characterised by the large 'Reed-Sternberg' cells that may be seen under a microscope when a biopsy of an affected lymph node, or gland, is studied. The incidence of HD peaks in the 15 - 30 age group and more men are affected than women.

Nowadays, Hodgkin's disease can be very successfully treated and many people are completely cured. As the improvement in treatment is relatively recent - since 1965 - some textbooks may be out-of-date and thus the information they contain can be misleading.

Non hodgkin's lymphoma

There are many different types of non Hodgkin's lymphomas. Some are so mild that they require little or no treatment; some are very active. Broadly, NHL is divided into Low Grade (slow growing) or High Grade (the faster growing lymphomas).

Some consultants refer to a third category, the Intermediate Grade, which is often considered similar to High Grade.

Intermediate/High Grade NHL is an aggressive disease which always needs treatment but it can now be cured in a fair number of cases.

With Low Grade NHL, although a cure is not usually possible, the disease can often be controlled for years and most patients can expect to lead a nearly normal life.

Some rarer forms of lymphomas are hard to classify as they seem to have some characteristics of both HD and NHL.

NHL is most common in people over 50 years old. It can also arise when the immune system has been suppressed because of other illnesses or conditions, including organ transplantation.

Symptoms & diagnosis

Often the first symptom is a painless swelling in one or more of the glands in your neck, armpit, groin or abdomen. Other symptoms may include:

• night sweats
• fevers
• loss of weight, poor appetite and tiredness
• a cough or breathlessness
• persistent itch all over
• pain from drinking even a small quantity of alcohol

On their own, each of these symptoms can be caused by less serious illnesses. You should consult your GP who will examine you and decide if further investigation is needed.

Your doctor will refer you to a local hospital where you will be examined again, before tests take place. These tests may include:

A biopsy which is the removal of a small sample of tissue, such as an enlarged lymph node, for examination under a microscope. This is usually performed under a general anaesthetic, when you are sent to sleep for about half an hour or so. Blood samples will show the state of your general health and how, for example, your kidneys and liver are functioning. Chest x-rays will be taken to examine your lungs and the lymph glands in your chest. A bone marrow examination will show if tissue in this area is affected. The samples will normally be taken from your hip and the procedure, which takes only a few minutes, is carried out using a local anaesthetic and it may cause discomfort. Sedation may be offered, depending on the samples required.

You will probably be asked to undergo a scan. This can be a CT scan (also known as CAT or body scan) or an MRI scan or an ultrasound scan of the abdomen. These scans are painless and take only about an hour, although preparation may be necessary in advance.

Occasionally a lymphangiogram is used. This is a special X-ray of the lymphatic system, taken after a dye has been injected into your foot. The dye highlights the lymphatic channels and lymph glands. An overnight stay in hospital may be required for this test. A dye is also used for anintravenous urogram (sometimes called an IVU or IVP) but this time it is injected into a vein in your arm and passes through the bloodstream to show doctors, via an X-ray, any abnormalities in your kidneys or urinary system. This test takes place in the X-ray department and lasts about an hour.

Such tests are necessary because many lymph nodes (or glands) in the body cannot be seen or felt, and other organs must be checked to see if they are affected.

The assessment of what treatment is required will be based on these tests. You will probably have the results within 10 - 14 days.

Staging is a system of assessing the spread of the lymphoma and is one of the factors considered in deciding your treatment. The stages refer to the parts of the body affected and also to 'significant symptoms' - namely, the amount of weight loss, fever and drenching night sweats.

A simplified version of staging is:
Stage 1: one group of lymph nodes (or glands) affected, on one side of the diaphragm
Stage 2: two or more groups affected, on one side of the diaphragm
Stage 3: lymph nodes (or glands) affected on both sides of the diaphragm
Stage 4: lymphoma has spread beyond the lymph nodes (or glands) to other organs such as liver, lungs, bone marrow etc.

The lymphoma is classified as 'B' where significant symptoms are present and 'A' where there are no significant symptoms. Therefore, you may hear your doctor refer to your condition as Stage 1A or Stage 2B and so on.

Even when a lymphoma is suspected, treatment will usually be delayed until all the tests and staging are complete. This may be frustrating for you, but a delay of a few weeks normally has no adverse effects medically and is far better than giving an inappropriate treatment too early.

Treatment

Your doctor will explain your treatment timetable. The length of treatment will depend on how well the disease responds to the drugs but will usually last for several months.

The treatment of each person varies considerably. The results of your tests, the staging assessment, your age and general health are all takeninto consideration. If the first course of treatment is not completely successful, there are other possible treatments.

Hodgkin's disease is treated with radiotherapy or chemotherapy, or a combination of both.

Intermediate/High Grade NHL is treated with chemotherapy or a combination of chemotherapy and radiotherapy. If it is localised it may be treated with radiotherapy alone or, occasionally surgery.

Low Grade NHL may require no treatment initially. It may develop slowly and need only mild treatment with chemotherapy tablets which give few side effects. Sometimes, radiotherapy and/or intravenous chemotherapy are necessary.

The object of treatment is to cure you, if this is possible. Where this is not, the aim is to keep the disease under control and minimise the side effects of treatment. Your quality of life is very important. However, you may need to accept that the treatment is sometimes unpleasant but essential in order for you to achieve a normal life in due course. It is important that you understand what your doctor is trying to do and that there is confidence between you.

Treatment for other conditions

You should advise your specialist of any treatment you are having for other conditions, existing or new. Do not even have a minor operation or dental treatment without telling the doctor or dentist that you are undergoing treatment for a lymphoma.

Treatment of children

The care and treatment of children varies from that of adults and is usually undertaken in one of the specialist children's cancer units. These units have excellent information and support services for both young patients and their families. The Lymphoma Association has two booklets available Hodgkin's Disease in Children and Non Hodgkin's Lymphoma in Children - phone the Helpline for more details. Radiotherapy Radiotherapy uses powerful X-rays which are directed onto the cancerous cells to destroy them, while causing minimal damage to healthy tissue. Before treatment starts, you will be asked to meet the radiotherapists who will be supervising your treatment. The area to be treated will be measured precisely and outlined on your skin using a marker pen.

The machines used to give radiotherapy vary but some are not dissimilar in appearance to X-ray machines. Treatment is usually daily, on weekdays, in an outpatient clinic and a course can last from between 2 - 6 weeks. Your radiographer will position you on a couch and will protect areas of your body which do not need treatment. The actual process is painless and lasts only a few minutes. You will be told how to look after the skin of the treated area and this is very important. Always ask if you are unsure about any aspect of your treatment.

Chemotherapy

Chemotherapy means the use of one or more cytotoxic (anti-cancer) drugs which destroy malignant cells. Often a combination of four or more drugs is given, normally at intervals of between one and four weeks.

The drugs are either injected or given via an intravenous infusion (drip) into a vein, so that they circulate in the bloodstream throughout the body. Certain drugs may be given as tablets. Another method is to fit you with a central line (for example a Portacath or Hickman line). This is a tube which is inserted, after anaesthetic, into a vein just above your collar bone. It tunnels beneath your skin and exits through your chest wall. It is used to administer your drugs and to collect your blood samples.

The effectiveness of the treatment will be assessed throughout. In most instances, you should be able to have most of your treatment as an outpatient, but occasionally a night in hospital may be necessary. Some of the treatment regimens you may hear mentioned are; CHOP, LOPP, EVAP, Mini BEAM, BEAM, PACEBOM, Ch1Vpp, PABLOE (the initials refer to the combination of drugs).

Steroids

These are part of your treatment and have a direct effect on your tumour. They can also help to boost appetite and energy levels. The downside is that in the short term they may cause some sleepiness and, if taken over a long time, can give the face a moon-like appearance and cause weight-gain and sometimes insomnia. Discuss any problems with your doctor, both when taking steroids and afterwards.

Steroids can make you irritable when you first take them and depressed for a few days on stopping. Short courses have very few side effects. Never stop taking steroids suddenly; your doctor will advise you on reducing them gradually. They are not the same as anabolic steroids which are banned in sport. Always carry a card stating that you are taking steroids, in case of emergencies.

Intensive treatment

A small number of people may be treated with high dose chemotherapy. While 'blitzing' the cancer cells, this treatment severely suppresses the bone marrow where blood cells are formed, so patients are also given Autologous Bone Marrow Transplant (ABMT) or a Peripheral Blood Stem Cell Transplant (PBSCT).

If you have an ABMT, bone marrow is drawn off under anaesthetic, and stored before chemotherapy starts. After the intensive treatment, the bone marrow is returned using an intravenous infusion or drip, rather like a blood transfusion. It will take your bone marrow some weeks to recover and resume its full role of fighting infection. For this reason you will have to stay in hospital for 3-6 weeks until your immune system begins to work again.

With PBSCT, the procedure may start with a 'priming' dose of chemotherapy plus a growth factor drug to mobilize the production of stem cells, the primitive cells from which most blood cells develop. Blood will be taken from you using a machine called a cell separator. This collects the stem cells, and returns the rest of your blood to you. This does not involve anaesthetic but does take 3-4 hours. The collected stem cells are then stored while the main treatment takes place, and returned via a drip to help the bone marrow recover. Your recovery time afterwards should, generally, be shorter than for an ABMT.

Non response or recurrence

Occasionally the disease does not respond to the first treatment used or recurs afterwards. There will be a number of options. Another treatment will be devised, taking into account the response to the first, for example, if radiotherapy was used alone, chemotherapy may be a good second treatment. A different combination of drugs may be required if chemotherapy has not been successful the first time, or intensive treatment may be considered.

Infections

Throughout your treatment and during the period immediately afterwards, you will be very susceptible to infection. If your spleen has been removed, you are especially vulnerable to certain infections and should see your doctor immediately at the first sign of illness. Ask TheLymphoma Association for further information on splenectomies.

Most infections arise from bacteria in your body and cannot be avoided, so tell your specialist if you develop a sore throat, fevers, unexplained sweats or shivers.

Avoid people with infectious diseases, particularly chickenpox or measles, but don't become a hermit - fresh air does no harm!

Side effects

Your doctor will be able to tell you if you are likely to have any side effects from your chemotherapy or radiotherapy. Such side effects are usually temporary and there are ways of mitigating them. Chemotherapy drugs affect not only lymphoma cells but also normal cells, especially the ones which multiply fast such as those in your intestine, hair and bone marrow.

The following table lists the common side effects and suggests some ways in which they can be minimised.

Research & clinical trials

There is a great deal of research under way into both the causes and the treatment of lymphomas. The aims of these studies are to improve the cure rate of lymphomas and reduce the side effects of treatments.

You may be invited to take part in a research study or clinical trial, in order that different treatments can be properly compared. The advantages of taking part in a clinical trial are that you will be provided with full information, including the potential benefits, effects and outcomes of the treatment, before coming to your decision. If you agree to take part in a study, you have the right to withdraw at any stage and still be treated.

Follow up

After your treatment is complete, you will be asked to attend follow-up visits at your clinic. You may be given further tests, similar to those you had at diagnosis. Initially, your visits will probably be monthly but, if there are no difficulties, the intervals will gradually lengthen. If any problems arise between check-ups, let your specialist know as soon as possible.

Coping

Everyone reacts differently to being told they have cancer. For most it is very traumatic, but there are no 'right' or 'wrong' reactions. One of the reasons Lymphoma Association was formed was so that people could share their feelings and many are relieved to know that others have experienced similar emotions. Your feelings may change from day to day; it is not unusual to have up days and down days and this may last over a period of many months.

Shock or a feeling of numbness and the inability to take in information is usually the first reaction as too is denial, refusing to believe that anything is wrong. Sometimes family and friends react this way too. A very normal reaction is anger about why me? and why now? often coupled with feelings of fear and sadness. This can make you irritable and impatient with the people around you, which is particularly hard on those closest to you. Try to see that it is the illness you are angry with. Your family and friends may also be resentful about the changes your illness is making to family life. Both you and your family may like to seek the help of a counsellor at the hospital or contact The Lymphoma Association.

Sometimes there may be withdrawal, of wanting to be alone and not wanting anyone to help you or even know about your illness. This can be very difficult for relatives and friends.

Guilt is not uncommon, blaming yourself or other people for your illness. Current research shows that it is unlikely that anything you have or have not done is the cause of your illness. Fear and uncertainty may come in many forms: of the cancer - and all the myths surrounding it - of whether the treatment will work, of recurrence.

Fear of the unknown is usually far worse than reality. Worrying is natural and you may find that family and friends feel awkward about discussing your illness. It will help them as well as you to talk openly and honestly.

Another frequent reaction is depression. Sometimes, just talking it over with friends or relations or making the effort to do enjoyable things will ease the situation. Talking to a counsellor or nurse may help. Some people may benefit from mild anti-depressant medication, prescribed by their doctor.

Feeling positive?

It is all too easy to get into the why bother? syndrome which leads to depression. It is more constructive to try to develop a positive attitude which can make you feel better in every way. Sometimes this is easier said than done, you simply cannot or do not want to do this. Do what feels right to you.

Try to do things which give you pleasure and a sense of achievement. Give yourself credit for your successes rather than dwell on what, for the moment, you cannot manage. Some people find it helpful and enjoyable to work while others do not. Do whatever feels comfortable.

It is pointless to compare how you feel today with yesterday. Your illness has its own timescale. Even if you are living with an illness which cannot be cured, you should aim to live life to the full. If you have any problems, however trivial they may seem, do not be afraid to ask your medical team. Bottling things up never helps.

Knowing

Knowledge helps to solve problems and conquer fear. You may like to leave everything to your doctor or you may want to know about every aspect of your illness and treatment. If so, ask. Your doctor will not know you want information unless you ask.

At first you may not take in what your doctor or medical team say. Never be afraid to go back and ask again, even if you feel the doctor is too busy. If he or she is very busy, you could make an appointment when there will be time to talk at greater length.

Write your questions down when you think of them. Keep a running list to take to your appointment. If you are worried about going on your own, or fear you may forget what you are told, take a family member or friend with you. Take notes while you are there.

You will want to know how successful your treatment is going to be and what the long term outlook is but, as every patient is different and reactions to treatment are highly individual, your doctor may be unable to give a precise answer.

Family & friends

Some relatives and friends feel that the patient should not be told they have cancer because of worries that they may not cope with the news. Many patients suspect the true diagnosis even when they are not told and experience shows that confirmation is often a relief.

People are better able to fight their illness when they know what it is. Sometimes relatives wish to conceal facts from other people and occasionally, patients may decide to keep the information to themselves. Both attitudes cause problems, not least stress. The patient or relatives can become very isolated. It may be better to introduce the subject gradually. Always be sensitive to the needs of the patient. Their requirements should come first, that of relatives and friends second. Do not rush patients into talking about their illness. Often it is enough just to listen and let the patient talk when ready.