Learn about Waldenstrom macroglobulinemia, a rare blood cancer, including symptoms, causes, diagnosis, treatment, survival rates and outlook.
Update Date: 17.10.2026
Waldenstrom macroglobulinemia (mak-roe-glob-u-lih-NEE-me-uh) is a rare cancer of white blood cells. It may be shortened to WM. It is a type of non-Hodgkin lymphoma called lymphoplasmacytic lymphoma (LPL). About 1,000 to 1,500 people are diagnosed with Waldenstrom macroglobulinemia each year in the United States. It accounts for about 1% of non-Hodgkin lymphomas.
In Waldenstrom macroglobulinemia, some white blood cells change and become cancer cells. These cells can build up in bone marrow, the soft tissue inside bones where blood cells are made. They can crowd out healthy blood cells. Cancer cells also may build up in lymph nodes, the spleen and other parts of the body.
Waldenstrom macroglobulinemia cells make a protein called immunoglobulin M (IgM). IgM can build up in the blood. Too much IgM can make blood too thick and slow blood flow. This can harm organs.
Waldenstrom macroglobulinemia can be serious, but it often worsens slowly. Some people do not need treatment right away. When treatment is needed, it can control symptoms and complications.
Waldenstrom macroglobulinemia and multiple myeloma are different blood cancers that occur in the bone marrow. Waldenstrom macroglobulinemia is a lymphoplasmacytic lymphoma affecting B cells and makes IgM. Multiple myeloma is a cancer of plasma cells.
Symptomatic Waldenstrom macroglobulinemia causes symptoms or other health issues that call for treatment.
Smoldering Waldenstrom macroglobulinemia also is called asymptomatic Waldenstrom macroglobulinemia. It means Waldenstrom macroglobulinemia is present but is not causing symptoms or organ damage that calls for treatment. People with smoldering Waldenstrom macroglobulinemia are watched closely instead of treated right away.
Waldenstrom macroglobulinemia worsens slowly. It might not cause symptoms for years.
When symptoms appear, they may include:
Waldenstrom macroglobulinemia can make the blood too thick and slow its flow. This is called hyperviscosity syndrome. It can happen when too much IgM builds up in the blood. Symptoms may include:
Make an appointment with a healthcare professional if you have symptoms that worry you.
Get emergency care right away for symptoms of hyperviscosity syndrome. Also get emergency care for unusual bleeding or bleeding from the nose that does not stop with simple pressure or packing.
It's not clear what causes Waldenstrom macroglobulinemia. Cancer starts when cells have changes in their DNA. DNA gives cells instructions. Healthy cells grow and die in a controlled way. Cancer-related DNA changes can tell cells to grow too much and live too long. This can lead to a buildup of cancer cells.
In Waldenstrom macroglobulinemia, these changes happen in B cells. B cells, also called lymphoplasmacytic cells, are a type of white blood cell. The changed cells can build up in bone marrow and crowd out healthy blood cells. They also may build up in lymph nodes and the spleen.
Waldenstrom macroglobulinemia cells make a monoclonal protein called IgM. IgM can build up in the blood. This can make the blood too thick and slow its flow. This can affect organs and cause other issues.
Most gene changes in Waldenstrom macroglobulinemia cells happen randomly. They usually are not passed down from a parent. MYD88 is the most common gene change. CXCR4 is another common gene change. Family history can raise the risk of Waldenstrom macroglobulinemia. But there is no single inherited gene that explains most family cases.
Factors that can raise the risk of Waldenstrom macroglobulinemia include:
IgM MGUS is not cancer. It can raise the risk of some blood cancers, including Waldenstrom macroglobulinemia. However, most people with IgM MGUS do not develop Waldenstrom macroglobulinemia.
Complications of Waldenstrom macroglobulinemia may include:
Bing-Neel syndrome is rare. It affects about 1% of people with Waldenstrom macroglobulinemia. An MRI scan of the brain and spine and a test of spinal fluid can help diagnose Bing-Neel syndrome.
Diagnosis of Waldenstrom macroglobulinemia often starts with a physical exam. Your healthcare professional talks with you about your symptoms and checks for swollen lymph nodes and an enlarged liver or spleen. The diagnosis isn't made with a single blood test. Multiple tests and procedures are used to diagnose Waldenstrom macroglobulinemia. These may include blood tests, bone marrow biopsy and aspiration, imaging, and other procedures.
Tests can help make a diagnosis and also estimate risk and outlook. Blood tests can:
Bone marrow biopsy and aspiration are procedures that involve collecting cells from the bone marrow. The cells are sent for testing. A bone marrow biopsy and aspiration help confirm Waldenstrom macroglobulinemia and rule out other conditions that can produce monoclonal IgM.
The samples most often come from the hip bone. The samples go to a lab where they are tested for cancer cells. If there are cancer cells, more tests can give more information about the cells.
Imaging tests make pictures of the body. They can show if lymph nodes and the spleen are larger than usual and show if other areas of the body are affected by Waldenstrom macroglobulinemia. Tests may include a CT scan or a positron emission tomography (PET) scan. If Bing-Neel syndrome is suspected, an MRI of the brain and spine may be done.
A lumbar puncture may be done if you have symptoms of Bing-Neel syndrome. A lumbar puncture, also called a spinal tap, collects fluid from around the brain and spinal cord. This fluid is called cerebrospinal fluid. A healthcare professional places a needle between bones in the lower back and removes a small amount of fluid. A lab checks it for cancer cells and signs of other conditions.
If your healthcare professional suspects Bing-Neel syndrome, you may have a biopsy of tissue from the central nervous system. This involves taking a tiny sample of tissue from the brain or spinal cord for testing in a lab.
Cells collected during testing can help your care team decide if you have Waldenstrom macroglobulinemia. Healthcare professionals in the lab look for:
These changes can affect how the disease behaves and how well treatment with BTK inhibitors works. Testing for MYD88 and CXCR4 gene changes may help guide treatment with a BTK inhibitor.
Waldenstrom macroglobulinemia is not curable with current treatments. Treatment is based mainly on symptoms and complications. The goals of treatment are to ease symptoms, prevent or limit organ damage, and control the condition.
Even though the condition is not curable, many people live with it for years. Some people do not need treatment right away. When treatment is needed, it can control symptoms and complications.
Waldenstrom macroglobulinemia treatment may include watchful waiting, plasma exchange, immunotherapy, targeted therapy and chemotherapy. A bone marrow transplant, also called a stem cell transplant, may be right for some people. Your plan depends on your symptoms, test results and how fast the condition is changing. Your healthcare professional also considers your overall health and your choices.
If you have smoldering Waldenstrom macroglobulinemia without symptoms or organ damage that calls for treatment, you may not need treatment right away. Instead, you might have regular blood tests to monitor your condition. Healthcare professionals sometimes call this watchful waiting. Treatment may not be needed for years. Some people with smoldering Waldenstrom macroglobulinemia never need treatment.
Watchful waiting also is called active surveillance. Follow-up often includes a review of symptoms, blood counts and IgM levels. How often you're checked depends on your risk and how quickly the condition is changing.
Treatment usually starts when Waldenstrom macroglobulinemia causes symptoms or health issues. The IgM level alone usually is not a reason to start treatment. Your healthcare team looks at your symptoms and test results to decide when and what treatment is right for you.
Treatment may begin for symptoms or health issues such as:
Plasma exchange, also called plasmapheresis, removes IgM from the blood and replaces plasma with healthy plasma. It may be used if you have hyperviscosity syndrome.
Plasma exchange can lower IgM quickly and ease symptoms from thick blood. But the effect does not last. Other treatments are then used to control the cells that make IgM.
Possible side effects from plasma exchange include discomfort from IV lines and a drop in calcium that can cause tingling or muscle spasms.
Immunotherapy uses medicine to help the immune system attack cancer cells. The immune system typically finds and attacks germs and changed cells. Cancer cells can hide from the immune cells. Immunotherapy can help immune cells find and kill cancer cells.
Rituximab (Rituxan) is an immunotherapy used often for Waldenstrom macroglobulinemia. It may be combined with chemotherapy or targeted therapy. It also may be used if Waldenstrom macroglobulinemia comes back or earlier treatment does not work.
Rituximab can cause reactions during an infusion, such as chills, fever, nausea, rash, fatigue or headache.
Targeted therapy uses medicines that attack specific parts of cancer cells. Blocking these targets can cause cancer cells to die. It may be combined with immunotherapy. It also may be used if Waldenstrom macroglobulinemia doesn't respond to treatment or comes back after treatment.
Bruton tyrosine kinase (BTK) inhibitors are targeted medicines used for Waldenstrom macroglobulinemia. BTK inhibitors include ibrutinib (Imbruvica) and zanubrutinib (Brukinsa).
Pirtobrutinib (Jaypirca) is another BTK inhibitor that has shown promise in treating Waldenstrom macroglobulinemia that has come back, including after some prior BTK inhibitor treatments.
Ibrutinib can cross the blood-brain barrier, a protective layer around the brain and spinal cord, and is used to treat Bing-Neel syndrome. Zanubrutinib also is an effective treatment for Bing-Neel syndrome.
BTK inhibitors can cause diarrhea, bruising, low blood counts, bleeding, infections and heart rhythm issues. Your healthcare team can tell you whether targeted therapy is an option for you.
Chemotherapy treats cancer with strong medicines. There are many chemotherapy medicines. Most chemotherapy medicines are given through a vein. Some are taken by mouth.
Chemotherapy may be used for Waldenstrom macroglobulinemia. It often is combined with immunotherapy. It also may be used if Waldenstrom macroglobulinemia comes back or treatment doesn't work.
Chemotherapy side effects can include nausea, hair loss, mouth sores, diarrhea or constipation, and low blood counts. Some chemotherapy medicines also can damage nerves or the heart.
A bone marrow transplant, also called a stem cell transplant, may be an option for some people if treatment doesn't work or Waldenstrom macroglobulinemia comes back.
A bone marrow transplant puts healthy blood-forming stem cells into the body after treatment. The cells can come from your own body. This is called an autologous stem cell transplant. They also can come from a donor. This is called an allogeneic stem cell transplant.
Chemotherapy usually is given before the transplant. The high-dose treatment used with a stem cell transplant can cause serious, sometimes life-threatening side effects.
After treatment, you'll likely have regular follow-up visits to check for signs that Waldenstrom macroglobulinemia has come back. This is called a relapse. Blood tests can help check for relapse.
Follow-up may include a complete blood count, an IgM test and serum protein electrophoresis. You may have kidney and liver tests. Your healthcare team also checks for new or returning symptoms. The schedule depends on your condition and the treatment you had.
With time, you'll likely find what helps you cope with the uncertainty and worry of a cancer diagnosis. Until then, these ideas may help you decide what to do next.
Other sources of help include the International Waldenstrom's Macroglobulinemia Foundation, the National Cancer Institute, the American Cancer Society, Blood Cancer United and the Lymphoma Research Foundation. Mayo Clinic Connect also lets you talk with others for support and practical tips.
Make an appointment with a healthcare professional if you have any symptoms that worry you. If your healthcare team thinks that you may have Waldenstrom macroglobulinemia, you'll likely see a doctor who treats blood and bone marrow conditions, called a hematologist.
Here's some information to help you get ready for your appointment.
Ask if you need to do anything before the appointment. For example, you may need to change what you eat or drink before a test.
Bring a person you trust, such as a family member or friend, if you can. It can be hard to remember everything you hear during an appointment. Another person may help you remember key details.
Before your appointment, make a list of:
Basic questions may include:
Feel free to ask other questions during your appointment.
Your healthcare professional may ask you questions, such as:
Be ready to answer questions so that you have time to talk about what's most important to you.
Waldenstrom macroglobulinemia does not use numbered stages. Many cancers use stages 1 through 4 to show how far the cancer has spread. Waldenstrom macroglobulinemia does not use the amount of disease in the body to assign numbered stages. Instead, healthcare professionals use risk groups to estimate outlook. Treatment decisions are based mainly on symptoms, complications and test results.
For people with symptomatic Waldenstrom macroglobulinemia, healthcare professionals may use the Modified Staging System for Waldenstrom Macroglobulinemia (MSS-WM). These risk groups estimate outlook, but outlook also depends on age, overall health, complications and response to treatment.
The risk groups include:
To decide on the risk group, healthcare professionals use:
Waldenstrom macroglobulinemia does not use numbered stages, so there is no numbered "final stage." It often worsens slowly. As it progresses, it may cause anemia or other low blood counts, enlarged lymph nodes or spleen, hyperviscosity syndrome, nerve problems, or amyloidosis. In some people, the condition can relapse after treatment or change into a faster growing lymphoma.
Survival rates show how many people in a group are alive after a set number of years. For example, a five-year survival rate is the percentage of people alive five years after diagnosis. Survival statistics describe groups. They cannot tell exactly how long one person will live.
The estimated five-year overall survival rates based on the MSS-WM for a test group were:
The estimated 10-year overall survival rates in the same group were:
Severe Waldenstrom macroglobulinemia or its complications can be life-threatening. The exact cause of death varies from person to person. In people older than 65, the most common cause of death is not cancer related.
For active or symptomatic Waldenstrom macroglobulinemia, the Modified Staging System for Waldenstrom Macroglobulinemia (MSS-WM) uses age and two blood tests, albumin and lactate dehydrogenase (LDH), to estimate risk group and outlook. People in lower risk groups usually live longer than people in higher risk groups.
MSS-WM groups help healthcare professionals talk about outlook. A risk group cannot predict exactly how long you will live. Survival with Waldenstrom macroglobulinemia has improved over time, but each person's outlook is different.
Life expectancy with Waldenstrom macroglobulinemia varies widely. One recent review found a median survival of more than 10 years for people diagnosed before age 70. Median survival was about seven years for people ages 70 to 79 and about four years for people age 80 or older. Median survival is the length of time at which half of the people in a group are still living.
These numbers describe groups, not what will happen to one person. Age has a strong effect on survival.
Some people with Waldenstrom macroglobulinemia live for many years after diagnosis. Long-term survival depends on age, how the condition is affecting you, complications and how well the cancer responds to treatment.
Group statistics cannot predict whether one person will live 20 years or longer. Some people do live for many years after diagnosis, but individual outlook varies.
Survival statistics take years to collect. The latest numbers include people who were treated more than five years ago. Some of them did not have access to today's newer treatments. But survival rates are improving.
Ask your healthcare team what the survival numbers mean for you. Keep follow-up visits and report new or changing symptoms so your healthcare team can watch your condition and decide when treatment may be needed.
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