Acute Myeloid Leukemia (AML)

What is Acute Myeloid Leukemia or AML?

Acute myeloid leukemia: (uh-KYOOT my-uh-LOYD loo-KEE-mee-uh) A cancer of the blood cells. It happens when very young white blood cells (blasts) in the bone marrow fail to mature. The blast cells stay in the bone marrow and become to numerous. This slows production of red blood cells and platelets. Some cases of MDS become… (AML) is a blood cancer. It happens when young abnormal white blood cells called blasts: See Blast Cells. (leukemia cells), begin to fill up the bone marrow: The soft, spongy tissue inside most bones. Blood cells are formed in the bone marrow. , preventing normal blood production. Doctors diagnose AML when 20 out of every 100 white blood cells in the bone marrow is a blast cell: A young white blood cell. The number of blast cells in the bone marrow helps define how severe MDS is in a person. When 20 out of 100 cells in the bone marrow are blasts, this is considered acute myeloid leukemia. . AML is the most common acute leukemia affecting adults, with about 20,000 new cases diagnosed each year.

When people have AML, blasts make copies of themselves quickly. This slows the production of red blood cells and platelets, causing tiredness from anemia: (uh-NEE-mee-uh) A condition in which there is a shortage of red blood cells in the bloodstream. This causes a low red blood cell count. Symptoms of anemia are fatigue and tiredness. and a risk of bleeding from a low platelet: The smallest type of blood cell. Platelets help the blood to clot and stop bleeding. Also called a thrombocyte. count. There is also an increased risk of infection, since infection-fighting white blood cells are not maturing and cannot fight off infection.

AML is also known as acute myelogenous leukemia: (uh-KYOOT my-uh-LAH-juh-nuss loo-KEE-mee-uh) A cancer of the blood cells. It happens when very young white blood cells (blasts) in the bone marrow fail to mature. The blast cells stay in the bone marrow and become to numerous. This slows production of red blood cells and platelets. Some cases of… , acute myeloblastic leukemia and acute nonlymphocytic leukemia.

Relation to bone marrow failure diseases:

Over time, about one-third of all MDS cases evolve to become AML. The risk of developing AML depends largely on which MDS subtype you have at the time of diagnosis.

  • A patient with lower-risk MDS has up to a 2 in 10 chance of developing AML.
  • A patient with higher-risk MDS has more than a 4 in 10 chance of developing AML.

A smaller number of people with aplastic anemia: (ay-PLASS-tik uh-NEE_mee-uh) A rare and serious condition in which the bone marrow fails to make enough blood cells - red blood cells, white blood cells, and platelets. The term aplastic is a Greek word meaning not to form. Anemia is a condition that happens when red blood cell count is low. Most… and PNH go on to develop AML.

What Causes AML?

AML can occur at any age but is most common in older people. For most people with AML, there is no easily identifiable cause. There are, however, a few known risk factors that can increase the chances of getting AML. They include:

  • Repeated exposure to the chemical benzene: A chemical that is widely used by the chemical industry in the United States to make plastics, resins, nylon and synthetic fibers. Benzene is found in tobacco smoke, vehicle emissions, and gasoline fumes. Exposure to benzene may increase the risk of developing a bone marrow failure disease. Benzene… , as well as other chemicals like it called fluorocarbons, which are found in cigarette smoke, petroleum products and in certain industrial settings
  • Certain uncommon genetic conditions such as Down syndrome, Fanconi anemia: A rare inherited disorder that happens when the bone marrow does not make enough blood cells (red cells, white cells, and platelets). Fanconi anemia is diagnosed early in life. People with Fanconi anemia have a high likelihood of developing cancer. Genetic testing is used to diagnose Fanconi anemia. , dyskeratosis congenita: An inherited disease that may lead to bone marrow failure. , MonoMAC syndrome, Bloom syndrome, Shwachman syndrome and Diamond-Blackfan syndrome
  • Having other blood cancers or disorders like polycythemia vera, primary myelofibrosis, essential thrombocythemia and myelodysplastic syndromes: (my-eh-lo-diss-PLASS-tik SIN-dromez) A group of disorders where the bone marrow does not work well, and the bone marrow cells fail to make enough healthy blood cells. Myelo refers to the bone marrow. Dysplastic means abnormal growth or development. People with MDS have low blood cell count for at… (MDS)
  • Previous chemotherapy: (kee-moe-THER-uh-pee) The use of medicines that kill cells (cytotoxic agents). People with high-risk or intermediate-2 risk myelodysplastic syndrome (MDS) may be given chemotherapy to kill bone marrow cells that have an abnormal size, shape, or look. Chemotherapy hurts healthy cells along with… or radiation treatments for other cancers

What are the symptoms of AML?

The signs and symptoms of AML are mainly the result of low blood cell counts. Early in the disease, symptoms can mimic other common illnesses, like the flu. This may include fever, tiredness, loss of appetite and shortness of breath. As AML gets worse and more leukemia cells fill the bone marrow, symptoms may include:

  • A pale complexion from anemia caused by a low red cell count
  • Prolonged bleeding and easy bruising caused by a very low platelet count called thrombocytopenia: (throm-buh-sie-tuh-PEE-nee-uh) A condition in which there is a shortage of platelets in the bloodstream. This results in a low platelet count. Bleeding and bruising often occur with thrombocytopenia. , which may also include the appearance of pinhead-size red spots on the skin called petechiae: (puh-TEE-kee-ie) Small, flat red or purplish spots on the skin, caused by bleeding. It is often a symptom of a low platelet count.
  • Frequent infections caused by too few white cells called neutrophils
  • Swollen gums
  • Weight loss
  • Discomfort in bones or joints
  • Enlarged spleen
  • Enlarged liver

More serious symptoms can include:

  • Bleeding in the brain or lung
  • Serious infections caused by too few white cells called neutrophils
  • Myeloid sarcoma, a mass of AML cells that form a tumor in certain sites, such as the brain or spinal cord which can lead to neurological problems

How do you diagnose AML?

An accurate diagnosis is important to guide treatment. Doctors use a number of tests to confirm an AML diagnosis and identify the patient’s AML subtype. These include:

  • Physical exam and history
  • Blood tests that include:
    • A complete blood count with a differential that looks at the total number and type of blood cells in the blood
    • A blood smear that allows a doctor to look at the blood under a microscope
  • Bone marrow aspiration: A medical procedure to remove of a small amount of liquid bone marrow through a needle inserted into the back of the hip. The liquid bone marrow is examined for abnormalities in cell size, shape, or look. Tests may also be run on the bone marrow cells to look for any genetic abnormalities. and biopsy are used to see how the bone marrow looks under a microscope and how many blast cells are present.
  • Cytogenetic testing and molecular genetic testing that looks at abnormalities in the leukemia cell DNA.

How do you treat AML?

Most patients with AML need treatment soon after diagnosis because the disease often progresses fast. The initial goal is to put the patient into remission. The long-term goal is to cure the disease, although this is not always possible.

Doctors use several types of therapy for adults with AML:

  • Chemotherapy or other drug therapies are the first line of treatment. People with AML usually start chemotherapy right away. Some of the drugs most commonly used include cytarabine (also called cytosine arabinoside or ara-C.) and an anthracycline (such as daunorubicin: Daunorubicin is in a class of medications called anthracyclines. It works by slowing or stopping the growth of cancer cells in your body. It is used in combination with other chemotherapy drugs to treat a certain type of acute myeloid leukemia (AML).  or idarubicin).
  • Stem cell transplantation may be used after chemotherapy as a second phase of treatment and may provide an opportunity for a cure.
  • Clinical trials: Clinical research is at the heart of all medical advances, identifying new ways to prevent, detect or treat disease. If you have a bone marrow failure disease, you may want to consider taking part in a clinical trial, also called a research study. Understanding Clinical Trials Clinical… can involve therapy with new drugs and new drug combinations to increase the chance of first remission or new approaches to stem cell transplantation.

Other considerations that may impact treatment include:

  • If the person is older than 70 or has other serious health issues (like a bad heart, lungs or kidneys): Some people in this category may not be as able to tolerate toxic chemotherapy drugs. Drugs such as decitabine: It works by reducing the amount of methylation in the body. Methylation is a process that acts like a switch to turn off or “silence” genes in certain cells. When these genes (called tumor suppressor genes) are turned off, MDS cells and cancer cells can grow freely. Decitabine is approved by the U… or azacitidine: It works by reducing the amount of methylation in the body. Methylation is a process that acts like a switch to turn off or “silence” genes in certain cells. When these genes (called tumor suppressor genes) are turned off, MDS cells and cancer cells can grow freely. Azacitidine is approved by the U… or hydroxyurea: Hydroxyurea is in a class of medications called antimetabolites. Hydroxyurea treats cancer by slowing or stopping the growth of cancer cells in your body. It can be used alone or with other medications to treat a certain types of leukemias.  may be better tolerated by older patients.
  • If a child is being treated for AML:  Therapy may differ slightly from that of the average adult.
  • If the cancer has returned (relapsed) or is still present after the patient finishes standard therapy (refractory leukemia):  There may be a different approach to treatment than the first time around.

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