Myeloma (also known as multiple myeloma) and amyloid light-chain (AL) amyloidosis are serious conditions caused by abnormal antibody-producing plasma cells found in the bone marrow where all blood cells are made. While myeloma (a blood cancer) and AL amyloidosis (a blood disease) can develop independently of one another, they’re sometimes diagnosed together.
Understanding myeloma and AL amyloidosis
Myeloma and AL amyloidosis are both caused by plasma cells in the bone marrow. The key difference is how the plasma cells cause disease and make patients sick.
Imagine white blood cells as security guards in your bloodstream that are constantly on patrol for disease and infection. When they’re alerted to potential harm, they spring into action by changing into plasma cells that ultimately produce proteins known as antibodies (also called immunoglobulins). These antibodies bind to the harmful substances, remove them from your body and leave your bloodstream once their job is done.
Myeloma occurs when plasma cells multiply and produce atypical antibodies. The malignant plasma cells grow out of control to the point that there’s not enough space in the bone marrow for healthy cells to fight infection or disease. Meanwhile, in amyloidosis, abnormal proteins called amyloids mutate into twisted clumps that build up on your organs and tissues.
Conditions
Plasma cell diseases change your body’s healthy rhythm. When you feel or suspect that something is off, know that our team of experts is well-versed in treating the following plasma cell conditions:
Myeloma with AL amyloidosis
Myeloma is sometimes diagnosed in association with the light-chain (AL) amyloidosis. The damage in AL amyloidosis happens when the light chains misfold, multiply and clump together as amyloid deposits in organs such as:
- Kidneys (in 70% of people)
- Heart (in 70% of people)
- Liver (in 25% of people)
- Gastrointestinal tract (in 25% of people)
- Peripheral nervous system (in 20% of people)
50% of patients with AL amyloidosis have involvement of 2 or more organ systems. The National Institutes of Health published a 2021 study revealing an estimated 10–15% of people with myeloma develop AL amyloidosis, and about 10% of people with AL amyloidosis have symptomatic myeloma at the time of diagnosis.
Testing
We turn to the following 3 tests to diagnose myeloma and amyloidosis:
- Protein immunofixation electrophoresis: This test measures certain proteins in your blood.
- Bone marrow biopsy and aspiration: This is a standard test we perform during your initial consultation. In bone marrow aspiration, your doctor will take a sample of the liquid part of your bone marrow called stem cells. For a biopsy, your doctor will take a solid sample to examine. We can also perform this test if you’re not responding to treatment or when you’re pre- or post-transplant.
- Cytogenetic evaluation: Part of your bone marrow aspiration sample may be examined for chromosomal abnormalities (cytogenetic evaluation). The lab may examine dividing cells or may perform a fluorescence in situ hybridization (FISH) analysis to look for chromosomal changes.
Tracking your body’s response to treatment
The hallmark of plasma cell diseases is the production of antibody proteins called immunoglobulins. Plasma cells produce an identifiable immunoglobulin signature with a heavy chain and a light chain and frequently, only a free light chain.
We follow these signatures during therapy because as the number of malignant cells decreases, these proteins also decrease. This is a clear sign that the person is responding to treatment.
One of the most rewarding moments in a person’s health journey is learning that they have achieved a positive response to treatment. We’re able to share that momentous news when we can no longer identify signature proteins. An even better result is becoming PET/CT and MRD negative.
It’s important to know that myeloma and amyloidosis will require lifelong care because relapsing is common. Relapse occurs because a very small amount of the disease remains in the body even after we cannot find signature proteins in the blood or urine or evidence of residual disease.
Treatments
A principle that applies to all plasma cell diseases is that early diagnosis and treatment offer the best outlook for your overall wellness. The sooner we can control the plasma cell disease and reverse potential organ damage, the sooner we can offer you the comfort and quality you look forward to in life.
Our top goal for treating plasma cell diseases like myeloma and amyloidosis is to target the cancerous plasma cells with approaches like:
- Stem cell transplantation
- Bone marrow transplantation
- Affected organ or tissue transplantation (like the heart)
- Chemotherapy
- Radiation therapy
For newly diagnosed myeloma patients, treatment decisions are based on whether or not you are eligible for a stem cell transplant. Usually, this means your age will determine the best treatment options for you.
We’re always pursuing what’s next in healthcare and what’s next for your health. We welcome people living with plasma cell diseases to ask us about our latest research and how to participate in available clinical trials.
Treating myeloma with AL amyloidosis
Treating multiple myeloma with AL amyloidosis involves targeting the cancerous plasma cells. We can approach this with an autologous stem cell transplant, where stem cells are collected from your blood and transplanted back into your body following chemotherapy.
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