Does chemo cure amyloidosis?

Primary amyloidosis (AL) is usually treated with a chemotherapy-based regimen (similar to that used for multiple myeloma) to destroy the abnormal plasma cells that give rise to the amyloid proteins or plaque. Chemotherapy is “systemic” medicine—it interferes with all fast-dividing cells in your body.
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How long is chemo for amyloidosis?

Our AL amyloidosis patients typically undergo treatment for six months to two years. In some cases, treatment can be curative.
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Can you recover from amyloidosis?

There is not currently a cure for amyloidosis. The amyloid deposits cannot be directly removed. But there are treatments to stop more of the abnormal proteins being produced and treat your symptoms. These treatments can give your body time to gradually clear the deposits before they build up again.
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What type of chemo is used for amyloidosis?

Some of the common types of chemotherapy used to treat amyloidosis are cyclophosphamide (Cytoxan, Neosar) and melphalan (Alkeran) combined with the steroids dexamethasone (multiple brand names) and prednisone (multiple brand names).
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What is the latest treatment for amyloidosis?

For hereditary ATTR amyloidosis, the treatment has been liver transplantation. Since the transthyretin protein which causes hereditary amyloidosis is made in the liver, replacing this organ removes the source of mutant protein production. A new liver will make only normal transthyretin.
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Chemotherapy Treatment 34 Cardiac Amyloidosis



Does amyloidosis ever go away?

There's no cure for amyloidosis and severe amyloidosis can lead to life-threatening organ failure. But treatments can help you manage your symptoms and limit the production of amyloid protein. Diagnosis as early as possible can help prevent further organ damage caused by the protein buildup.
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Does amyloidosis go into remission?

Treatment. There is no cure for patients with AL amyloidosis but more frequently patients can go into remission with drug therapy. In our experience, the majority of patients surviving the first six months can often start recovering thereafter and can typically live normal or near normal lives for years to come.
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How long can you live with amyloidosis with treatment?

Overall, people with AA amyloidosis who undergo proper treatment can have a good outlook. The average life expectancy after diagnosis is 11 years.
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Where is the best treatment for amyloidosis?

Mayo Clinic transplant centers are leaders in the use of blood stem cell transplants to treat amyloidosis. Mayo Clinic specialists are also researching new ways to diagnose and treat amyloidosis.
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How do you get rid of amyloid protein?

Alzheimer's Amyloid Plaque Removal May Be Aided By Vitamin D And Omega 3. In a small pilot study, a team of US researchers has discovered how vitamin D3, a form of vitamin D, and omega 3 fatty acids may help the immune system clear the brain of amyloid plaques, one of the physical hallmarks of Alzheimer's disease.
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How long can you live after amyloidosis diagnosis?

Average life expectancy varies based on the type of cardiac amyloid (protein), how much the organs are involved and the stage at diagnosis. Based on these factors, the worst case scenario could be six months, while in some cases, life expectancy can be eight to 10 years after diagnosis.
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How fast does amyloidosis progress?

How long that takes depends on the patient and the affected organ. Typically, 12 to 18 months will pass before amyloid buildup in the heart becomes fatal, while a patient with an affected kidney could live for 5 to 10 years, according to Gertz.
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What triggers amyloidosis?

The cause of AL amyloidosis is usually a plasma cell dyscrasia, an acquired abnormality of the plasma cell in the bone marrow with production of an abnormal light chain protein (part of an antibody).
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What does chemo do to amyloidosis?

Primary amyloidosis (AL) is usually treated with a chemotherapy-based regimen (similar to that used for multiple myeloma) to destroy the abnormal plasma cells that give rise to the amyloid proteins or plaque. Chemotherapy is “systemic” medicine—it interferes with all fast-dividing cells in your body.
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Can stem cell transplant cure amyloidosis?

Stem Cell Transplantation for AL Amyloidosis Leads to Long-term Survival and Possible Cure in Selected Patients. AL amyloidosis is a life-threatening disease related to bone marrow cancer, multiple myeloma.
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What is the most common cause of death in amyloidosis?

Heart complications are the most common cause of death in patients with amyloidosis. The degree to which amyloidosis affects the heart is important in determining your prognosis. These amyloid deposits are in the kidneys.
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Is amyloidosis always terminal?

If diagnosed and treated early on, AL amyloidosis may become a chronic disease. But left untreated, it leads to life-threatening conditions that may be fatal.
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When is amyloidosis fatal?

If left untreated, AL amyloidosis can be fatal in six months. Hereditary or familial amyloidosis can be fatal in 2.5 to 3.5 years on average, if untreated.
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What cancers cause amyloidosis?

Amyloidosis is a rare disease affecting about 3,000 patients in the United States each year. Although amyloidosis may be associated with blood cancers such as multiple myeloma, it is not a cancer itself. Amyloidosis results from the buildup of an abnormal protein called amyloid.
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What foods should I avoid with amyloidosis?

In some cases, avoiding certain foods can help a person with amyloidosis stay healthy. Diet can play a role in preventing or worsening certain symptoms.
...
Healthy Diets for Digestive Problems
  • Processed foods.
  • Fast food.
  • Fatty meat and dairy products.
  • Tomatoes.
  • Citrus fruits.
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How do you feel with amyloidosis?

Signs and symptoms of amyloidosis may include:
  1. Severe fatigue and weakness.
  2. Shortness of breath.
  3. Numbness, tingling, or pain in the hands or feet.
  4. Swelling of the ankles and legs.
  5. Diarrhea, possibly with blood, or constipation.
  6. An enlarged tongue, which sometimes looks rippled around its edge.
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Where does amyloidosis start?

Types of Amyloidosis

AL starts in plasma cells within the bone marrow. Plasma cells create antibodies with both heavy chain and light chain proteins. If the plasma cells undergo abnormal changes, they produce excess light chain proteins that can end up in the bloodstream.
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Are there stages of amyloidosis?

The Mayo 2004 staging system uses a TnT cutoff level of 0.035 mcg/L and NT-proBNP level of 332 ng/L to place AL amyloidosis patients into three groups: (1) stage I, normal levels of both, (2) stage II, an elevated level of either but not both, and (3) stage III, elevated levels of both.
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