A cancer of middle to old age, characterized by the uncontrolled proliferation and disordered function of cells called plasma cells in the bone marrow. To understand multiple myeloma, it is useful to know the difference between normal blood cells and myeloma cells.
Normal blood cells
Stem cells mature into different types of blood cells. Each type has a special function:
Myeloma begins when a plasma cell becomes abnormal. The abnormal cell divides to make copies of itself. The new cells divide again and again, making more and more abnormal cells. The abnormal plasma cells are myeloma cells. Myeloma cells make antibodies called M proteins (also called monoclonal proteins).
In time, myeloma cells collect in the bone marrow. They may crowd out normal blood cells. Myeloma cells also collect in the solid part of the bone. The disease is called "multiple myeloma" because it affects many bones. (If myeloma cells collect in only one bone, the single mass is called a plasmacytoma.)
Multiple myeloma is the most common type of plasma cell tumor.
Risk factorsStudies have found the following risk factors for multiple myeloma:
Most people who have known risk factors (being older, being African American, or having MGUS) do not get multiple myeloma. On the other hand, most people who do get the disease have no known risk factors.
SymptomsCommon symptoms of multiple myeloma include:
DiagnosisDoctors sometimes find multiple myeloma after a routine blood test. More often, doctors suspect multiple myeloma after an X-ray for a broken bone. Usually though, patients go to the doctor because they are having other symptoms.
To find out whether such problems are from multiple myeloma or some other condition, your doctor may ask about your personal and family medical history and do a physical exam. In addition, your doctor may order some of the following tests and exams:
StagingIf the biopsy shows that you have multiple myeloma, your doctor needs to know the extent (stage) of the disease to plan the best treatment. Staging may involve having more tests. You may have blood tests (including beta-2-microglobulin), CT scans, or an MRI of your bones.
Doctors may describe the disease as Stage I, Stage II, or Stage III. Higher numbers mean that a larger number of myeloma cells are in the body. The stage also takes into account whether the cancer is causing problems with your bones or kidneys.
TreatmentMany people with multiple myeloma want to take an active part in making decisions about their medical care. It is natural to want to learn all you can about your disease and your treatment choices. However, shock and stress after the diagnosis can make it hard to think of everything you want to ask the doctor. It often helps to make a list of questions before an appointment.
To help remember what the doctor says, you may take notes or ask whether you may use a tape recorder. You may also want to have a family member or friend with you when you talk to the doctor – to take part in the discussion, to take notes, or just to listen.
You do not need to ask all your questions at once. You will have other chances to ask your doctor to explain things that are not clear and to ask for more information.
Your doctor may refer you to a specialist, or you may ask for a referral. Specialists who treat multiple myeloma include medical oncologists, radiation oncologists, and hematologists.
Methods of treatmentThe choice of treatment depends mainly on the stage and symptoms of your disease. If you have multiple myeloma without symptoms, you may not need treatment for the cancer. The doctor monitors your health closely so that treatment can start when you begin to have symptoms.
If you have symptoms, your treatment will probably involve anticancer drugs (including steroids). Sometimes stem cell transplantation or radiation therapy is part of the treatment plan. Your doctor can describe your treatment choices and the expected results of each. You and your doctor can work together to develop a treatment plan that meets your needs.
Because standard treatment may not control myeloma, you may want to talk to your doctor about taking part in a clinical trial. Clinical trials are research studies of new treatment methods.
At any stage of disease, you may receive supportive care to control health problems (such as infections) caused by multiple myeloma.
Anticancer drug therapyTreatment of myeloma usually involves anticancer drugs. This treatment is called systemic therapy because the drugs enter the bloodstream and can affect myeloma cells all over the body.
Many different types of drugs are used to treat myeloma. Each type kills cancer cells in a different way.
Types of chemotherapy in common use include melphalan, cyclophosphamide, vincristine, and doxorubicin. Prednisone is a steroid that is often used. In some cases, the doctor may suggest new options, such as thalidomide and bortezomib. People often receive a combination of drugs.
You may receive the drugs by mouth or through a vein. The treatment usually takes place in an outpatient part of the hospital, at your doctor's office, or at home. Patients rarely need to stay in the hospital during treatment.
Stem cell transplantationSome people with multiple myeloma have stem cell transplantation. A stem cell transplant allows a person to receive high doses of chemotherapy, radiation therapy, or both. The high doses destroy both myeloma cells and normal blood cells in the bone marrow. Later, the patient receives healthy stem cells through a flexible tube placed in a large vein in the neck or chest area. New blood cells develop from the transplanted stem cells.
Stem cell transplants take place in the hospital. Some patients have two or more transplants.
Stem cells may come from the patient or from a donor:
Radiation therapyRadiation therapy (also called radiotherapy) uses high-energy rays to kill myeloma cells and to help control pain. People receive radiation therapy at a hospital or clinic.
Radiation therapy is given two ways for people with myeloma:
Side effects of treatmentBecause cancer treatment often damages healthy cells and tissues, unwanted side effects are common. Side effects depend mainly on the type and extent of the treatment. Side effects may not be the same for each person, and they may change from one treatment session to the next. Before treatment starts, your health care team will explain possible side effects and suggest ways to help you manage them.
Anticancer drug therapyThe side effects of anticancer drugs depend mainly on the specific drugs and the dose. The drugs affect cancer cells and other cells that divide rapidly:
Stem cell transplantationPeople who have stem cell transplantation face an increased risk of infection, bleeding, and other side effects because of the large doses of chemotherapy or radiation they receive. In addition, graft-versus-host disease (GVHD) may occur in people who receive stem cells from a donor. In GVHD, the donated stem cells react against the patient's tissues. Most often, GVHD affects the liver, skin, or digestive tract. GVHD can be serious. It can occur any time after the transplant, even years later. Steroids or other drugs may help treat or control GVHD.
Radiation therapyThe side effects of radiation therapy depend mainly on the dose of radiation and the part of the body that is treated. For example, your skin in the treated area may become red, dry, and tender. You also may lose your hair in the treated area.
You are likely to become very tired during radiation therapy, especially in the later weeks of treatment. Resting is important, but doctors usually advise patients to try to stay as active as they can.
Supportive careMultiple myeloma and its treatment can lead to other health problems. You probably will receive supportive care to prevent or control these problems and to improve your comfort and quality of life.
InfectionPeople with multiple myeloma get infections very easily. You may receive antibiotics and other drugs to help protect you. Your health care team may advise you to stay away from crowds and from people with colds or other contagious diseases. If an infection develops, it can be serious and should be treated promptly. Some people need to stay in the hospital for treatment.
AnemiaMyeloma and its treatment can lead to anemia, which may make you feel very tired. Drugs or blood transfusions can help with this problem.
PainMultiple myeloma often causes bone pain. Your health care provider can suggest ways to relieve or reduce pain. For example, drugs and local radiation therapy can help control bone pain. A brace may relieve pain in the neck or back. Some people get pain relief from massage or acupuncture when used along with other approaches. Also, the patient may learn relaxation techniques such as listening to slow music or breathing slowly and comfortably. Sometimes surgery is needed if the spinal cord is compressed (squeezed).
Thinning bonesMyeloma cells keep new bone cells from forming, and bones become thin wherever there are myeloma cells. Your doctor may give you drugs to prevent bone thinning and help reduce the risk of fractures. Physical activity, such as walking, also helps keep bones strong.
Too much calcium in the bloodMultiple myeloma may cause calcium to leave the bones and enter the bloodstream. If you have a very high level of calcium in your blood, you may lose your appetite. You also may feel nauseated, restless, or confused. A high calcium level can also make you very tired, weak, dehydrated, and thirsty. Drinking a lot of fluids and taking drugs that lower the calcium in the blood can be helpful.
Kidney problemsSome patients with multiple myeloma have kidney problems. If the problems are severe, they may need dialysis. Dialysis removes wastes from the blood. In some cases, people with serious kidney problems may need a kidney transplant.
AmyloidosisSome people with myeloma develop amyloidosis. Abnormal protein collects in tissues of the body. The build-up of protein can cause many problems, some of them severe. For example, protein can build up in the heart, causing chest pain and swollen feet. Drugs are used to treat amyloidosis.
Complementary and alternative medicineSome people with cancer use complementary and alternative medicine (CAM) to ease stress or to reduce side effects and symptoms:
However, some types of CAM may interfere with standard treatment. Combining CAM with standard treatment may even be harmful. Before trying any type of CAM, you should discuss its possible benefits and risks with your doctor.
NutritionIt is important for people with multiple myeloma to eat well and to drink plenty of fluids. Eating well means getting enough calories to maintain a good weight and enough protein to keep up your strength. Good nutrition often helps people with cancer feel better and have more energy.
But eating well can be difficult. You may not feel like eating if you are uncomfortable or tired. Also, the side effects of treatment (such as poor appetite, nausea, vomiting, or mouth sores) can be a problem. Some people find that foods do not taste as good during cancer therapy.
Follow-up careFollow-up care after treatment for multiple myeloma is important. Your doctor will monitor your health and check for recurrence or changes in the cancer. Checkups help ensure that any changes in your health are noted and treated as needed. Checkups may include a physical exam, lab tests, bone marrow aspiration, and X-rays. Between scheduled visits, you should contact the doctor right away if you have any health problems.
Related category HEALTH AND DISEASE
Source: National Cancer Institute
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