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Macmillan and Cancerbackup merged in 2008. Together we provide free, high quality information for people affected by cancer through our publications, website and phone service. Find out more| .
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This information is about 90Y-Ibritumomab tiuxetan, which is also known as Zevalin®. It is used to treat people with a type of non‑Hodgkin lymphoma called follicular lymphoma| . Zevalin may also be used to treat other types of cancer as part of a research trial| .
Zevalin is used to treat follicular lymphoma , which is a type of non-Hodgkin lymphoma (NHL) . NHL is a cancer of the lymphatic system (the network of glands in our bodies that defend against infection). valin is a type of drug called a radiolabelled monoclonal antibody. This means that it is a monoclonal antibody that has been combined with a radioactive substance. It's currently given to people who have been treated with another monoclonal antibody, rituximab| , but whose lymphoma either did not respond or came back.
Because Zevalin requires special facilities and specially trained staff, it can only be given safely in a small number of hospitals. As a result you may need to travel a long way to another hospital to receive it.
Monoclonal antibodies are used to try to destroy some types of cancer cells while causing as little harm as possible to normal cells. They work by recognising certain proteins that are found on the surface of particular cancer cells and ‘locking’ onto them (like a key in a lock). This may trigger the body’s immune system to attack the cancer cells and can sometimes cause the cells to destroy themselves.
Zevalin is used with rituximab| . Together they lock onto a protein called CD20, which is found on the surface of one of the main types of normal white blood cells (B-cell lymphocytes). CD20 is also present on the surface of most of the abnormal B-cell lymphocytes, which occur in many types of non-Hodgkin's lymphoma. The monoclonal antibodies attack both normal and abnormal (malignant) B-cell lymphocytes. We have separate information about rituximab.
Radioisotopes are chemicals that give off energy in the form of radiation. Zevalin is a monoclonal antibody that is combined with the radioisotope Yttrium-90 (90Y). Yttrium-90 produces radiation that is strong enough to destroy cancer cells. It can also affect normal cells.
As Zevalin enters the bloodstream, the monoclonal antibody portion recognises and attaches to the CD20 protein (as described). Radiation is then released from the yttrium radioisotope, damaging or killing the B-cell. Zevalin attacks both normal and abnormal (malignant) B-cell lymphocytes. However, the body quickly replaces any normal white blood cells that are damaged, so the risk of side effects from this is very small.
Zevalin is given as a single 'one-off'treatment and not as repeated courses of treatment. It consists of two parts, given approximately one week apart:
Rituximab is given on the first day of treatment to reduce the number of normal healthy B-cells. This prevents the Zevalin from attaching to and destroying healthy, non-cancerous cells. Rituximab is given as a drip into a vein (intravenous infusion). It is given slowly over a few hours. You will be given some steroids and antihistamines beforehand to reduce the risk of an allergic reaction.
You will receive a second infusion of rituximab about one week after your first dose. Within four hours of this infusion you will go to the nuclear medicine or radiotherapy department to have the Zevalin treatment. This is given by drip and takes about 10 minutes.
Each person’s reaction to treatment is different. Some people have very few side effects, while others may experience more. The side effects described here will not affect everyone.
We have outlined the most common side effects and rarer ones, so that you can be aware of them if they occur. However, we have not included those which are very rare and therefore extremely unlikely to affect you. If you do notice any effects which you think may be due to the drugs, but which are not listed here, please discuss them with your doctor or nurse.
While receiving the drugs, people have experienced some of the following: shortness of breath| ; facial flushing; cough; chills; irritation of the throat; fever; headache; nausea, vomiting| ; abdominal pain; back pain; dizziness; and a rash.
If you have any symptoms during the infusions, it is important to tell the nurse or doctor immediately. These can be signs of an allergic reaction and need prompt treatment.
Lowered resistance to infection Zevalin can reduce the number of white blood cells in your blood, making you more prone to infection. This effect can occur up to two months after the end of treatment. You may have low numbers of white blood cells for a few weeks.
Contact your doctor or the hospital straight away if:
Your doctors will check your blood levels during treatment and as part of your follow-up.
Precautions are needed after treatment with Zevalin® because the radiation effects of the drug can stay in the body and bodily fluids for a short time afterwards. This includes the blood, stools, urine and saliva. Therefore, for seven days after therapy, you should avoid transfer of body fluids to other people. It is important to wash your hands thoroughly after going to the toilet and clear up any spillages. You should also use a condom during sexual intercourse. All of this will help to minimise exposure to radiation for those close to you.
Pregnancy should be avoided for one year after treatment.
Some medicines should only be used under the supervision of your doctor while you have Zevalin treatment. This includes blood thinners (anticoagulants) and drugs such as aspirin and ibuprofen.
This information has been compiled using information from a number of reliable sources including:
For further references, please see the general bibliography| .
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