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Diagnosis and what to expect

See how doctors diagnose MM.

Multiple myeloma is a blood cancer that affects plasma cells made in the bone marrow. These cells are part of the immune system.

At first, there may be no symptoms. If symptoms do occur, they include, but aren’t limited to, bone pain or weakness, infections, tiredness, dizziness, or shortness of breath.

Doctors diagnose MM through biopsy and imaging tests and possibly biomarker testing.

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Biopsy

For blood cancers like MM, a biopsy usually involves surgically collecting small pieces of marrow from inside your bone, then examining them in a lab. Blood and urine samples are also used to spot cell count, gene, and protein markers.

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Biomarker testing

Biomarkers are signals in cancer cells that can show how cancer may change, grow or respond to treatment. Biomarker testing may be done at the same time as a biopsy.

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Have you asked about biomarker testing?

Biomarker testing can help your care team design a treatment plan tailored to you. We’ll help you build a discussion guide you can take to your next visit.

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Take a deeper look at biomarkers

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The “CRAB” signs of MM

Doctors look at blood and imaging test results for signs of MM. These signs can be described using the acronym CRAB. If someone has one or more CRAB signs, and at least 10% of their bone marrow contains cancer cells, that’s usually a signal of active myeloma. CRAB stands for:

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Calcium elevation

High levels of calcium in the blood

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Renal insufficiency

Poor kidney function

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Anemia

Low levels of red blood cells

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Bone abnormalities

Such as lesions

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Not all MM types are the same.

Different tests may be used to identify the type of MM you have. Biomarker testing may also be used to further determine type.

Knowing your type helps you understand your cancer and your treatment plan.

Here are some, but not all, of the types you may hear about.

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Active myeloma

White blood cells in your bone marrow make antibodies called immunoglobulins to help fight infection. When you have MM, your plasma cells make too many of these antibodies and they become abnormal.

Testing for these antibodies helps show the type of active MM you have.

  • IgG myeloma: Approximately 65% of patients have IgG myeloma
  • IgA myeloma: This is the second-most common type. Patients sometimes have tumors outside of the bone
  • IgD, IgE, and IgM myelomas: These types are very rare. IgD myeloma can be accompanied by plasma cell leukemia (PCL)
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Light chain myeloma

Light chain myeloma is the third most common type, making up about 15% of cases. In this type, cancerous cells produce incomplete antibodies.

Normally, antibodies have two kinds of chains, light and heavy. In light chain myeloma, only light chains are produced.

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Nonsecretory myeloma

This rare form makes up 3%-5% of cases. Nonsecretory myeloma cells don’t make or release (secrete) any extra antibodies making them harder to detect with standard blood or urine tests.
Instead, doctors may use a serum free light chain test to accurately test a blood sample before making a diagnosis.

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MM stages

Staging defines how far the cancer has grown or spread, from early-stage to more advanced. Staging MM can be challenging for two reasons:

  • Symptoms may not be felt before MM reaches an advanced stage
  • Doctors may use one of two different staging systems

Your doctor will measure your stage based on the amount of certain proteins in the blood and on specific gene changes in the cancer cells.

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Explore treatment types

There’s more than one way to treat MM.

Your doctor will recommend systemic or local therapies, sometimes in combination, depending on your cancer type, age, overall health, and kidney function.

  • Systemic treatments: These include drug therapies that target cancer cells throughout the body. A systemic treatment plan could include up to four different types of medication
  • Local treatments: These include surgery and radiation therapy that target a specific part of the body. Typically used if your cancer is not too advanced

Treating MM is challenging because it’s difficult to successfully destroy all the myeloma cells. There is a chance that some will remain and will start growing again.

Remember to ask about the side effects, risks, and benefits of any cancer treatment.

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Targeted therapy

Targeted therapy is designed to act on specific features of cancer cells, such as proteins or gene changes identified through biomarker testing, although it can also affect some normal cells. It’s also called personalized or individualized therapy and is used alone or with chemo.

Targeted therapy can be given as a pill, infusion (IV), or injection. Here are some of the kinds you may hear about.

  • Proteasome inhibitors: These therapies help stop cell division in tumor cells
  • Antibody drug conjugates: These target specific parts of cancer cells with a medication that enters the cell and binds to its protein (or receptor), thereby killing it
  • Nuclear export inhibitors: These therapies target specific proteins in cancer cells and keep them from leaving the cell which causes the cancer cell to die
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Immunotherapy

A therapy that boosts your body’s own immune system to fight cancer or helps train the immune system to attack certain cancer cells. Here are some of the kinds you may hear about.

  • Monoclonal antibodies: These are man-made cancer fighting cells that attach to a specific target on MM cells. They may be used alone or with otYher treatments and are given as an IV or injection
  • Bispecific antibodies (BsAbs): These are also man-made cancer fighting cells. Unlike monoclonal antibodies, BsAbs are able to attach to 2 specific targets. For example, one type of BsAbs medication attaches to immune system cells and myeloma cells. This brings both types together and helps the immune system cells destroy the myeloma cells
  • CAR T-cell therapy (chimeric antigen receptor): A sample of your blood is taken and put through a lab process to separate out T cells. The cells are then changed in a way that allows them to attach to cancer cells before being put back into your body. The T cells then boost the immune system and help it destroy cancer cells
  • Immunomodulatory medicines (IMiDs): These medicines are taken as pills that directly affect the immune system. They are taken daily with regular breaks each month. Doctors may also prescribe blood thinners or aspirin with IMiDs because they may increase the risk of blood clots
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Chemotherapy

Chemotherapy, or chemo, uses a combination of two or three powerful medications to attack and stop cancer cells from growing. It can also kill some healthy cells, which is why people may experience side effects, like hair loss.

Typically a fluid delivered into a vein (IV), it may also be given as an injection or pills.

Chemo is used before stem cell transplants but is otherwise used infrequently for MM.

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Stem cell transplant

This common MM treatment uses high-dose chemotherapy to first kill cancer cells in the bone marrow. Then new, healthy, blood-forming stem cells are given through an IV infusion.

The transplant may use either a patient’s own healthy stem cells removed before chemo (autologous) or less commonly, someone else’s stem cells (allogenic).

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Surgery

Surgery for MM is used to:

  • Remove plasma cell tumors from the body if present
  • Correct spinal cord compression; may be used with radiation therapy
  • To attach plates or rods to support bones or to prevent breaks
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Radiation therapy

Radiation therapy uses high-energy rays to destroy cancer cells. It may be used if medication or other treatments haven’t worked or to treat certain tumors.

In most cases, external beam therapy is used. Doctors use a machine outside the body to beam radiation directly to affected areas.

Radiation can also be used to treat bones that cause pain, are at risk of breaking, or have been damaged by MM.

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Clinical trials

If available treatments aren’t a fit for your particular cancer, participating in a clinical trial may be right for your situation. Clinical trials study the safety and efficacy of potential new medicines, including cancer treatments. Your doctor can tell you about the benefits and risks, and whether taking part in a clinical trial is right for you.

Explore clinical trials

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Ways to work with your care team

From questions to clarity, your doctor can help.

Diagnosis, testing, and treatment types can bring lots of questions. We can help prepare you to get the most out of your conversations.

Get ready

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Get answers about your diagnosis.

  • What type of cancer do I have?
  • Has it spread or grown?
  • What stage is my cancer?

Get more diagnosis questions

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Talk about your treatment plan.

  • What types of treatment are used for my cancer?
  • If biomarker testing was done, how do the results impact my treatment plan?
  • What are the goals of my treatment plan?

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Ask about support and resources.

  • What support services are available?
  • Who can help me navigate care and next steps?
  • Who on my care team can I reach out to when I have questions?

Get more support questions

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We’re committed to helping you afford your Pfizer prescriptions.

From co-pay cards to help navigating insurance approvals, we’ll guide you to the right support. And if you’re eligible for our programs, we’ll help you get the Pfizer medicines you need.

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You could help advance a breakthrough.

Clinical trials study the safety and efficacy of potential new medicines, including cancer treatments.

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Living with cancer

Get a little inspiration.

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The biggest myth about cancer is that it consumes your whole life. Just live your life around it, and keep doing the things you want to do.”

Jordan

Actual patient with cancer

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To me, living is not waiting for the next thing to happen, it’s making the next thing happen.”

Erin

Actual patient with cancer

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Still have questions?

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What are targeted therapies?

Targeted therapies are treatments that target the ways cancer cells grow, divide, and spread. One of the ways doctors determine if targeted therapies make sense in a treatment plan is through biomarker testing.

Find out more about biomarker testing

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What can I do if I’m having trouble affording my medicine?

Managing treatment costs and paying for your medicine can be overwhelming. We’ve got resources on how to help manage costs and information on where you may be able to find financial support for Pfizer medications.

Get help navigating costs

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Can I still go to work if I’m getting cancer treatment?

About half of people living with cancer are at an age where they’re still working. If you’re one of them, you may be wondering about how to talk to your co-workers about what you’re going through, what you need, and your ability to do your job. We’ve got you covered.

Communicating what you need at work

Getting back to work after treatment

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Are there communities and advocacy groups I can join?

There are many patient advocacy and support groups in the bladder cancer community. Here are a couple to get you started with connecting to other patients and caregivers, as well as resources to support you during your journey:

themmrf.org

myeloma.org

bloodcancerunited.org

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How do race and ethnicity affect my outlook for MM?

The outlook for a MM diagnosis is different for some racial and ethnic groups. For example, MM is twice as common, and has poorer outcomes, for Black patients than for White patients.

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What is the difference between leukemia, lymphoma, and multiple myeloma?

All 3 are blood cancers, but each starts in and affects different parts of the body. Leukemia causes bone marrow to produce large amounts of abnormal blood cells. Lymphoma starts in cells that are part of the immune system. Multiple myeloma affects cells made in the bone marrow called plasma cells.

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When should I seek a second opinion?

Getting a second opinion is a common process that can give you peace of mind. You may want or need a second opinion because:

  • You have a rare type of cancer and want to be sure of your diagnosis
  • Your doctor gives you limited treatment options, and you think other treatments might be available at a different medical center
  • Your doctor is not a specialist in your type of cancer
  • Your doctor tells you there is uncertainty about your type or stage of cancer
  • You’re having trouble understanding and communicating with your doctor, or you want your options explained by someone else
  • You feel uncomfortable with your doctor and their ability to answer your questions or give you the time you need
  • Your insurance company asks you to get another opinion before you start treatment
  • You want to feel confident in your treatment plan