HEALTH & DISEASE A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z                    HOME ABOUT CATEGORIES SITE MAP COPYRIGHT ADVERTISE CONTACT entire Web this site multiple myeloma 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 Normal plasma cells help protect the body from germs and other harmful substances. Most blood cells develop from cells in the bone marrow called stem cells. Bone marrow is the soft material in the center of most bones. Stem cells mature into different types of blood cells. Each type has a special function: White blood cells, also called leukocytes help fight infection. There are several types of white blood cells. Red blood cells, also called erythrocytes carry oxygen to tissues throughout the body. Platelets help form blood clots that control bleeding. Plasma cells are white blood cells that make antibodies. Antibodies are part of the immune system. They work with other parts of the immune system to help protect the body from germs and other harmful substances. Each type of plasma cell makes a different antibody. Myeloma cells Myeloma cell (abnormal plasma cell) making M proteins. Myeloma, like other cancers, begins in cells. Normally, cells grow and divide to form new cells as the body needs them. When cells grow old, they die, and new cells take their place (see cell division. In cancer, this orderly process goes wrong. New cells form when the body does not need them, and old cells do not die when they should. These extra cells can form a mass of tissue called a growth or tumor. 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 factors Studies have found the following risk factors for multiple myeloma: Age: Growing older increases the chance of developing multiple myeloma. Most people with myeloma are diagnosed after age 65. This disease is rare in people younger than 40. Race: The risk of multiple myeloma is highest among African Americans and lowest among Asian Americans. The reason for the difference between racial groups is not known. Personal history of monoclonal gammopathy of undetermined significance (MGUS): MGUS is a condition in which abnormal plasma cells make a low level of M proteins. MGUS is a benign condition, but it increases the risk of certain cancers, including multiple myeloma. Scientists are studying other possible risk factors for multiple myeloma. Radiation, pesticides, hair dye, certain viruses, obesity, and diet are under study. But it is not clear that these factors are involved in the development of the disease. Researchers also are studying families in which more than one person has multiple myeloma. However, such families are extremely rare. 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. Symptoms Common symptoms of multiple myeloma include: Bone pain, usually in the back Broken bones, usually in the spine Feeling weak and very tired Feeling very thirsty Frequent infections and fevers Weight loss Nausea or constipation Frequent urination Most often, these symptoms are not due to cancer. Other health problems can cause the same symptoms. Diagnosis Doctors 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: Blood tests: The lab checks the level of blood cells and other substances. Myeloma causes a high level of plasma cells and calcium. Most people with myeloma have anemia. Myeloma also causes high levels of certain proteins. The lab checks for M protein, beta-2-microglobulin, and other proteins. Urine tests: The lab checks for Bence Jones protein, a type of M protein, in urine. The lab measures the amount of Bence Jones protein in urine collected over a 24-hour period. If the lab finds a high level of Bence Jones protein in your urine sample, doctors will monitor your kidneys. Bence Jones protein can clog the kidneys and damage them. X-rays: You may have X-rays to check for broken or thinning bones. Biopsy: The doctor removes tissue to look for cancer cells. A biopsy is the only sure way to know whether myeloma cells are in the bone marrow. The doctor removes some bone marrow from your hipbone or another large bone. Local anesthesia helps reduce the discomfort. A pathologist uses a microscope to check the tissue for cancer cells. There are two ways the doctor can obtain bone marrow: Bone marrow aspiration: The doctor uses a thin needle to remove samples of bone marrow. Bone marrow biopsy: The doctor uses a thick needle to remove a small piece of bone and bone marrow. Staging If 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. Treatment Many 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 treatment The 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 therapy Treatment 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 transplantation Some 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: Autologous stem cell transplantation: This type of transplant uses the patient's own stem cells. The stem cells are removed from the patient, and the cells may be treated to kill myeloma cells that may be present. The stem cells are frozen and stored. After the patient receives high-dose treatment, the stored stem cells are thawed and returned to the patient. Allogeneic stem cell transplantation: Sometimes healthy stem cells from a donor are available. The patient's brother, sister, or parent may be the donor. Or the stem cells may come from an unrelated donor. Doctors use blood tests to be sure the donor's cells match the patient's cells. Syngeneic stem cell transplantation: This type of transplant uses stem cells from the patient's healthy identical twin. Radiation therapy Radiation 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: Local radiation: A large machine aims radiation at the bone or the part of the body where myeloma cells have collected. It is local therapy because it affects cells only in the treated area. This is the main treatment for people with a single plasmacytoma. People receive radiation for 4 to 5 weeks. A shorter course of radiation therapy can be used to control the growth of tumors in bones and help relieve pain. Total-body irradiation: Some patients receive radiation to their whole body before stem cell transplantation. The radiation treatments may be given 2 to 3 times a day for several days. Side effects of treatment Because 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 therapy The 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: Blood cells: When drugs affect your healthy blood cells, you are more likely to get infections, bruise or bleed easily, and feel very weak and tired. Cells in hair roots: Anticancer drugs can cause you to lose your hair. The hair will grow back, but it may be somewhat different in color and texture. Cells that line the digestive tract: Anticancer drugs can cause poor appetite, nausea and vomiting, diarrhea, or mouth and lip sores. The drugs used for myeloma also may cause skin rash, blisters, cramps, blurred vision, lung problems, headache, dizziness, drowsiness, numbness or tingling in hands or feet, and blood clots. Stem cell transplantation People 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 therapy The 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 care Multiple 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. Infection People 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. Anemia Myeloma and its treatment can lead to anemia, which may make you feel very tired. Drugs or blood transfusions can help with this problem. Pain Multiple 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 bones Myeloma 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 blood Multiple 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 problems Some 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. Amyloidosis Some 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 medicine Some people with cancer use complementary and alternative medicine (CAM) to ease stress or to reduce side effects and symptoms: An approach is generally called complementary medicine when it is used along with standard treatment. An approach is called alternative medicine when it is used instead of standard treatment. Acupuncture, massage therapy, herbal products, vitamins or special diets, visualization, meditation, and spiritual healing are types of CAM. Many people say that such approaches help them feel better. 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. Nutrition It 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 care Follow-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 Also on this site: Encyclopedia of Alternative Energy & Sustainable Living Encyclopedia of History Transport Concepts & Designs (partner site) BACK TO TOP