Adult Acute Myeloid Leukemia (AML): Types and Treatment

Autor: Christina Bach, MBE, LCSW, OSW-C
Contribuidor de contenido: Allyson Van Horn, MPH
Fecha de la última revisión: July 19, 2024

This article gives you detailed information about Adult Acute Myeloid Leukemia (AML). You may want to read  Leukemia: The Basics first, so you have a basic understanding of leukemia.

AML is a blood cancer that affects white blood cells, red blood cells, and/or platelets. AML may also be called acute myelocytic leukemia, acute granulocytic leukemia, or acute non-lymphocytic leukemia.

If your provider thinks you have AML, you will have tests done to find out which subtype (classification) of AML you may have. These tests may include:

  • A bone marrow biopsy and aspiration.
  • Cytogenetic tests, immunophenotyping, and molecular testing which tell your provider the type of AML you have.
  • CT scan/MRI.
  • A lumbar puncture (spinal tap) to see if there are any leukemia cells in your spinal fluid.
  • MUGA scan.
  • HLA testing for possible future bone marrow transplant.

Staging

AML is not staged like most other cancers. It is classified based on genetic abnormalities (changes) in the cancer cells. The classification also helps your provider decide what kind of treatment you will need for your AML.

AML is classified using the World Health Organization (WHO) system. These are the different classifications (types) of AML:

Acute Myeloid Leukemia (AML) and Related Neoplasms (cancers)

  • AML with recurrent genetic abnormalities.
    • AML with t(8;21)(q22;q22.1);RUNX1-RUNX1T1.
    • AML with inv(16)(p13.1q22) or t(16;16)(p13.1;q22);CBFB-MYH11.
    • APL with PML-RARA.
      AML with t(9;11)(p21.3;q23.3);MLLT3-KMT2A.
      AML with t(6;9)(p23;q34.1);DEK-NUP214.
      AML with inv(3)(q21.3q26.2) or t(3;3)(q21.3;q26.2); GATA2, MECOM.
    • AML (megakaryoblastic) with t(1;22)(p13.3;q13.3);RBM15-MKL1.
    • Provisional entity: AML with BCR-ABL1.
    • AML with mutated NPM1.
    • AML with biallelic mutations of CEBPA.
    • Provisional entity: AML with mutated RUNX1.
  • AML with myelodysplasia-related changes.
  • Therapy-related myeloid neoplasms.
    • AML, NOS.
    • AML with minimal differentiation.
    • AML without maturation.
    • AML with maturation.
    • Acute myelomonocytic leukemia.
    • Acute monoblastic/monocytic leukemia.
    • Pure erythroid leukemia.
    • Acute megakaryoblastic leukemia.
    • Acute basophilic leukemia.
    • Acute panmyelosis with myelofibrosis.
  • Myeloid sarcoma.
  • Myeloid proliferations related to Down syndrome.
    • Transient abnormal myelopoiesis (TAM).
    • Myeloid leukemia associated with Down syndrome.
  • Blastic plasmacytoid dendritic cell neoplasm.

Acute Leukemias of Ambiguous Lineage

  • Acute undifferentiated leukemia.
  • Mixed phenotype acute leukemia (MPAL) with t(9;22)(q34.1;q11.2); BCR-ABL1.
  • MPAL with t(v;11q23.3); KMT2A rearranged.
  • MPAL, B/myeloid, NOS.
  • MPAL, T/myeloid, NOS.

Myeloid Neoplasms with Germline Predisposition without a Preexisting Disorder or Organ Dysfunction

  • AML with germline CEBPA mutation.
  • Myeloid neoplasms with germline DDX41 mutation.

Myeloid Neoplasms with Germline Predisposition and Preexisting Platelet Disorders

Myeloid Neoplasms with Germline Predisposition and Other Organ Dysfunction

How is AML treated?

Treatment for AML is based on things like your age, AML subtype, if you have had treatment for other cancers in the past, your overall health, and testing results. Your treatment may include some or all of the following:

Chemotherapy, Targeted Therapy, and Immunotherapy

Chemotherapy for AML has these three phases: 

  • Induction: The goal of induction is remission. Remission is when there are less than 5% blast cells in your bone marrow.
  • Consolidation: After a remission, you will enter this second phase of treatment. The goal of consolidation is to keep you in remission.
  • Maintenance: Some patients will need ongoing maintenance treatment depending on how much consolidation treatment you have received, as well as if you had a stem cell transplant. The goal of maintenance is to prevent relapse (the cancer coming back) and to keep you in remission.

These treatments are made to kill the abnormally functioning leukemia cells. However, this treatment also kills many healthy cells. This puts you at risk for bleeding and infection, which can be life-threatening. Chemotherapy medications can also cause side effects such as mouth sores (mucositis), diarrhea, nausea/vomiting, and hair loss (alopecia).

If you are less than 60 years old, induction chemotherapy for AML is often a combination of medications: cytarabine with daunorubicin, idarubicin, fludarabine, or cladribine. The goal of this therapy is to put you in remission. If you do not go into remission after having chemotherapy, you may need chemotherapy again.

These medications can be combined with targeted therapies. Targeted therapies target specific mutations (changes) in cancer cells. Oral midostaurin and gilteritinib target a mutation on the FLT3 gene. Another mutation is in the IDH1 or IDH2 gene. IDH inhibitors including ivosidenib and enasidenib can be used in patients with AML with this mutation. Gemtuzumab ozogamicin is a monoclonal antibody that attaches to CD33, a protein found in most AML cells.

In the consolidation phase, chemotherapy is continued for 4-5 more cycles (4-6 months). The types of medications you take during this phase depend on your cytogenetic test results and if you are at risk for relapse. The medications used during consolidation are the same but given in different doses.

If you are over 60 years old and your provider thinks you can handle standard induction chemotherapy, you will get the same therapies listed above. Your provider will consider your overall health and cytogenetic test results. The doses of the medications may be different than if you were younger.

If you are over 60 years old and can’t have intensive induction, other medications are used to treat your AML. The goal is always for you to go into remission. Two targeted therapies used to treat older patients with AML are venetoclax and glasdegib. Other medications used in those over 60 include idarubicin, daunarubicin, mitoxantrone, gemtuzumab ozsogamicin, ivosidenib, enasidenib, decitabine,azacitidine, midostaurin and clofarabine. The medications you get are based on the results of your cytogenetic tests. If you are over 60, consolidation treatment is also given. Medications used in consolidation are like those used in induction but may be given in lower doses and over different time periods.

Medications used in the maintenance phase include oral azacytidine or sorafenib.

Acute Promyelocytic Leukemia (APL or APML)

APML is a type of AML and treatment for this subtype has changed a lot in the past 20 years. A medication called all-trans retinoic acid (ATRA) is used only in this subtype of AML. ATRA is given with arsenic trioxide in the induction phase. Gemtuzumab ozogamicin is also used in combination with ATRA and arsenic trioxide to treat APML. In patients with pre-existing heart problems, daunorubicin and cytarabine at lower doses may also be used. These medications are used through the induction and consolidation phases.

One serious side effect of APML is called DIC (disseminated intravascular coagulation). In DIC, the body makes blood clots where it should not and quickly uses up the parts that are needed for blood clotting. This leads to bleeding at the same time as these clots are being formed. If you get DIC, you will need treatment for it as soon as possible. This includes blood product transfusions and emergent treatment of the leukemia. 

Supportive Care

Some people cannot get treatment for AML based on their health conditions. In these cases, supportive care is given. The goal of supportive care is to help your quality of life by treating your side effects. It does not put you in remission from AML. Supportive care includes treatment with blood and platelet transfusions, as well as hydroxyurea. Hydroxyurea is used to lower the white blood cell count, which can help relieve symptoms caused by a high count, such as pain.

Measurable/Minimal Residual Disease (MRD) Testing

Measurable or minimal residual disease (MRD) testing is used to see if the cancer treatment is working and to guide further treatment plans. MRD tests use highly sensitive methods to look for any remaining cancer cells that cannot be seen in routine tests. Currently, MRD testing is being studied so treatment teams can better understand how to use it.

Bone Marrow Transplant

After consolidation, your team may recommend an allogeneic bone marrow transplant from a matched sibling or unrelated donor. Your decision to have a bone marrow transplant is based on your subtype of AML, as well as cytogenetic factors of your AML, donor availability, your age, and your health. Transplant is used more often in those under 60 years old but is being studied in those over 60 who have lower risk cytogenetics and are in good overall health.

Complications & Concerns of Leukemia and Treatment

Some people with AML will have a very high white blood cell count at diagnosis. This is called leukocytosis and it can cause symptoms like headache, shortness of breath, and pain. In some cases, chemotherapy will be started right away to lower the white blood cell count. In some people, pre-treatment testing to confirm the diagnosis and your ability to tolerate the treatment may take some time. In these cases, you may need leukopheresis, which removes white blood cells from the blood. Hydroxyurea may also be used to lower the white blood cell count

Leukemia puts you at a higher risk of infection (because your functioning white blood cell count is low) and bleeding (because your platelet count is low). Treatment of leukemia should help your abnormal blood counts, but your counts may get worse before they get better. You will likely get blood and platelet transfusions, antibiotics, and will need to be extra careful to avoid infection or bleeding.

Hand washing is the best way to prevent infection. You and your visitors should wash your hands often. You may not be able to eat some types of fresh fruit and vegetables or get fresh flowers or plants while in the hospital. (See the gift guide for ideas on what to send a patient with these restrictions). This may sound odd, but these items can bring in bacteria and may put you at higher risk of infection. Ask any sick family members to hold off on visiting until they feel better.

You may get an infection or fever. If this happens, you will have some tests done to look for where the infection is in your body. These tests can include blood, urine, and stool cultures, and a chest x-ray. Antibiotics may be started or adjusted if they are already being given.

During treatment, you may need blood (for low hemoglobin levels) or platelet (for low platelet counts) transfusions. If you have a low hemoglobin count (also called anemia), you may feel fatigued, short of breath, and can look pale. A low platelet count (also called thrombocytopenia) can cause bleeding. This can be as small as gums bleeding when brushing the teeth or a nosebleed, or dangerous bleeding, such as a stroke. Be careful and try to avoid bumping into things. Don’t shave with a razor (an electric razor is okay to use with caution) and avoid any activities that increase the risk of bleeding or bruising. You should always tell your healthcare team if you have symptoms of anemia or thrombocytopenia.

Clinical Trials

You may be offered a clinical trial as part of your treatment plan. To find out more about current clinical trials, visit the OncoLink Clinical Trials Matching Service.

Making Treatment Decisions

Your care team will make sure you are a part of choosing your treatment plan. This can be overwhelming as you may be given a few options to choose from. Friends and family can help you talk through the options and the pros and cons of each, but they cannot make the decision for you. You need to be comfortable with your decision – this will help you move on to the next steps. If you ever have any questions or concerns, be sure to call your team.

SEER Statistics: AML http://seer.cancer.gov/statfacts/html/amyl.html

American Cancer Society, Acute Myeloid Leukemia.

NCCN Guidelines, Acute Myeloid Leukemia, (registration required), retrieved from https://www.nccn.org/professionals/physician_gls/pdf/aml.pdf

Arbor, D.A., Orazi, A., Hasserjian, R., Thiele J. et.al. (2016). The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia. Blood, 127(20), 2391-2405.

Breen, K. A., Grimwade, D., & Hunt, B. J. (2012). The pathogenesis and management of the coagulopathy of acute promyelocytic leukaemia. British Journal of Haematology, 156(1), 24-36.

Burnett, A. K., Goldstone, A., Hills, R. K., Milligan, D., Prentice, A., Yin, J., ... & Russell, N. (2013). Curability of patients with acute myeloid leukemia who did not undergo transplantation in first remission. Journal of Clinical Oncology, 31(10), 1293-1301.

Cancer Genome Atlas Research Network. (2013). Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia. The New England Journal of Medicine, 368(22), 2059.

Estey, E. H. (2013). Acute myeloid leukemia: 2013 update on risk stratification and management. American Journal of Hematology, 88(4), 317-327.

Godley, L. A. (2014, October). Inherited predisposition to acute myeloid leukemia. In Seminars in Hematology (Vol. 51, No. 4, pp. 306-321). WB Saunders.

Grimwade, D., Knapper, S., & Mrózek, K. (2016). Acute Myeloid Leukemia. In Molecular Pathology in Clinical Practice(pp. 527-559). Springer International Publishing.

Hourigan, C. S., Gale, R. P., Gormley, N. J., Ossenkoppele, G. J., & Walter, R. B. (2017). Measurable residual disease testing in acute myeloid leukaemia. Leukemia, 31(7), 1482.

Hourigan, C. S., & Karp, J. E. (2013). Minimal residual disease in acute myeloid leukaemia. Nature reviews Clinical oncology, 10(8), 460.

Khwaja, A., Bjorkholm, M., Gale, R. E., Levine, R. L., Jordan, C. T., Ehninger, G., ... & Scheinberg, D. A. (2016). Acute myeloid leukaemia. Nature Reviews. Disease Primers, 2, 16010-16010.

Lo-Coco, F., Avvisati, G., Vignetti, M., Thiede, C., Orlando, S. M., Iacobelli, S., ... & Specchia, G. (2013). Retinoic acid and arsenic trioxide for acute promyelocytic leukemia. New England Journal of Medicine, 369(2), 111-121.

Morton, L. M., Dores, G. M., Tucker, M. A., Kim, C. J., Onel, K., Gilbert, E. S., ... & Curtis, R. E. (2013). Evolving risk of therapy-related acute myeloid leukemia following cancer chemotherapy among adults in the United States, 1975-2008. Blood, 121(15), 2996-3004.

O'Donnell, M. R., Abboud, C. N., Altman, J., Appelbaum, F. R., Arber, D. A., Attar, E., ... & Lancet, J. (2012). Acute myeloid leukemia. Journal of the National Comprehensive Cancer Network, 10(8), 984-1021.

Patel, J. P., Gönen, M., Figueroa, M. E., Fernandez, H., Sun, Z., Racevskis, J., ... & Huberman, K. (2012). Prognostic relevance of integrated genetic profiling in acute myeloid leukemia. New England Journal of Medicine, 366(12), 1079-1089.

Rashidi, A., Ebadi, M., Colditz, G. A., & DiPersio, J. F. (2015). Outcomes of allogeneic stem cell transplantation in elderly patients with acute myeloid leukemia: a systematic review and meta-analysis. Biology of Blood and Marrow Transplantation.

Schlenk, R. F., Taskesen, E., van Norden, Y., Krauter, J., Ganser, A., Bullinger, L., ... & Kündgen, A. (2013). The value of allogeneic and autologous hematopoietic stem cell transplantation in prognostically favorable acute myeloid leukemia with double mutant CEBPA. Blood, 122(9), 1576-1582.

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