Acute Myeloid Leukemia (AML)
(Acute Myelogenous Leukemia; Acute Myeloblastic Leukemia; Acute Myelomonocytic Leukemia; Acute Myelocytic Leukemia)
People may be tired or pale, may be easily susceptible to infection and fever, and may bruise or bleed easily.
Blood tests and bone marrow examination are needed for diagnosis.
Treatment includes chemotherapy to achieve remission plus additional chemotherapy to avoid relapse and sometimes stem cell transplantation.
Acute myeloid leukemia (AML) is the most common type of leukemia among adults, although it affects people of all ages. AML sometimes is caused by chemotherapy or radiation therapy given to treat another cancer.
In AML, immature leukemia cells rapidly accumulate in the bone marrow, destroying and replacing cells that produce normal blood cells. The leukemia cells are released into the bloodstream and are transported to other organs, where they continue to grow and divide.
There are several subtypes of AML, which are identified based on characteristics of the leukemia cells.
Acute promyelocytic leukemia is an important subtype of AML. In this subtype, chromosomal changes in promyelocytes—cells that are at an early stage in the development into mature neutrophils—allow accumulation of these immature cells.
The first symptoms of AML are very similar to those of acute lymphoblastic leukemia. People may have fever and excessive sweating, indicating infection. A high risk of infection results from too few normal white blood cells. Weakness, fatigue, and paleness may indicate anemia, which results from too few red blood cells. Easy bruising and bleeding, sometimes in the form of nosebleeds, bleeding gums, or bleeding in the brain or abdomen, results from having too few platelets.
Leukemia cells can invade other organs. Leukemia cells in the bone marrow may cause bone and joint pain. A sense of fullness in the abdomen and sometimes pain can result when leukemia cells cause enlargement of the liver and spleen. Leukemia cells can form small masses throughout the body, including in or just under the skin (called leukemia cutis) or gums, or in the eyes.
AML cells can spread to the layers of tissue covering the brain and spinal cord (meninges), leading to headaches, vomiting, stroke, and disturbances of vision, hearing, and facial muscles (leukemic meningitis). Leukemic meningitis occurs more often in acute lymphocytic leukemia. In acute promyelocytic leukemia, bleeding or blood clotting problems often occur.
The diagnosis of AML is also similar to that of acute lymphoblastic leukemia. A complete blood count is done, including measurement of the numbers of each of the types of white blood cells. A bone marrow examination is almost always done to confirm the diagnosis and to distinguish AML from other types of leukemia. The immature white blood cells (blasts) are tested for chromosome abnormalities, which helps doctors determine the type of the leukemia and what drugs to use to treat it.
Imaging tests may also be needed. Computed tomography (CT) or magnetic resonance imaging (MRI) is done if the person has symptoms that suggest leukemia cells in the brain. CT of the chest may be done to check for leukemia cells in the area around the lungs. CT, MRI, or ultrasonography of the abdomen may be done to determine whether internal organs are enlarged. An echocardiogram (ultrasound of the heart) may be done before starting chemotherapy because chemotherapy drugs sometimes affect the heart.
Without treatment, most people with AML die within a few weeks to months of the diagnosis. With therapy, between 20% and 40% of people survive at least 5 years, without any relapse. With intensive treatment, 40 to 50% of younger people can survive at least 5 years. Because relapses almost always occur within the first 5 years after initial treatment, most people who remain leukemia-free after 5 years are considered cured.
The strongest predictor of survival is the type of genetic abnormality present in the leukemia cells. People who are older than 60, those with certain findings on blood testing, such as a high white blood cell count, those who develop AML after undergoing chemotherapy or radiation therapy for other cancers, and those with a preceding myelodysplastic syndrome have the poorest prognosis.
Acute promyelocytic leukemia was once considered the most malignant form of leukemia. Now, it is one of the most curable forms of AML. More than 70% of people with acute promyelocytic leukemia can be cured. Rapid diagnosis is essential.
Treatment of AML is aimed at bringing about prompt remission—the destruction of the vast majority of leukemia cells. However, treatment often makes people sicker before they get better.
Treatment suppresses bone marrow activity, resulting in very few white blood cells, particularly neutrophils. Having too few neutrophils makes infection likely. Treatment also disrupts the mucosae (such as the lining of the mouth), which makes it easier for bacteria to enter the body. Meticulous care is taken to prevent infections, and infections that occur must be promptly treated. Red blood cell and platelet transfusions are also needed.
Induction chemotherapy is the first phase of AML treatment. Chemotherapy drugs generally include cytarabine for 7 days given by a continuous infusion and daunorubicin (or idarubicin or mitoxantrone) given intravenously for 3 days. Other drugs that may be given include midostaurin or gemtuzumab oxogamicin, or decitabine, azacitidine, venetoclax, or glasdegib (especially in older people or people with certain subtypes of AML).
Consolidation chemotherapy is given once AML is in remission. People usually receive several courses of additional chemotherapy beginning a few weeks after the initial treatment to help ensure that as many leukemia cells as possible are destroyed.
Allogeneic stem cell transplantation ("allogeneic" means the stem cells are from another person) is done after induction and consolidation in some people at risk of relapse. But transplantation can be done only if stem cells can be obtained from a person who has a compatible tissue type (human leukocyte antigen [HLA]–matched). The donor is usually a sibling, but cells from matched, unrelated donors (or occasionally partially matched cells from family members or unrelated donors, as well as umbilical stem cells) are sometimes used.
Unlike in acute lymphocytic leukemia, preventive treatment to the brain usually is not needed for adults, and long-term lower-dose chemotherapy (maintenance therapy) has not been shown to improve survival.
People with acute promyelocytic leukemia can be treated with a type of vitamin A called all-trans-retinoic acid (tretinoin). Chemotherapy is frequently combined with the all-trans-retinoic acid, especially if the person has a high white blood cell count at the time of diagnosis or if the white blood cell count rises suddenly. Arsenic trioxide is also uniquely effective in this subtype of AML.
People who have not responded to treatment and younger people who are in remission but who are likely to have a high rate of relapse (generally identified by certain chromosomal abnormalities) may be given high doses of chemotherapy drugs followed by stem cell transplantation.
When relapse occurs, additional chemotherapy for people unable to undergo stem cell transplantation is less effective and often poorly tolerated. Another course of chemotherapy is most effective in younger people and in people whose initial remission lasted longer than 1 year. Doctors take many factors into consideration when determining the advisability of additional intensive chemotherapy for people with AML in relapse.
The following is an English-language resource that may be useful. Please note that the MANUAL is not responsible for the content of this resource.
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