When refering to evidence in academic writing, you should always try to reference the primary (original) source. That is usually the journal article where the information was first stated. In most cases Physiopedia articles are a secondary source and so should not be used as references. Physiopedia articles are best used to find the original sources of information (see the references list at the bottom of the article).
If you believe that this Physiopedia article is the primary source for the information you are refering to, you can use the button below to access a related citation statement.
Acute myeloid leukemia (AML) is the most common leukemia among the adult population and accounts for about 80% of all cases.
AML is a type of cancer involving the blood and bone marrow.
The main cell involved in this disorder is myeloid stem cells which can become either red blood cells, white blood cells, or platelets.
In this disorder: Myeloid stem cells become a type of immature white blood cell called myeloblasts. These myeloblasts never become healthy white blood cells; Abnormal red blood cells, white blood cells, or platelets begin to crowd in the bone marrow to prevent healthy cells from forming.
With recent advancements in the management guidelines, the cure rates have increased up to 15% in patients older than 60 years and about 40% in patients below 60 years of age[1].
Despite advancements in therapeutic regimens, the prognosis remains very poor in the elderly population[2][1]
Epidemiology
The number of new cases among men and women per year is about 4.2 per 100,000 population.
The incidence is over 20,000 cases per year in the United States.
The average age at the time of diagnosis is about 65 years.
It is more prevalent among non-Hispanic whites.
Males have more predominance compared to females with a ratio of 5:3[1]
Acute Myeloid Leukemia is the most common leukemia in adults, comprising 80% of adult acute leukemias.
The other 20% of AML patients are children.
People over the age of 70 are 12 times more likely to develop AML.[3]
Characteristics/Clinical Presentation
Due to ineffective erythropoiesis and bone marrow failure, patients experience a variety of symptoms including
Rheumatoid Arthritis- Chronic inflammatory autoimmune disease that targets the joint synovium.[4]
Diagnostic Tests/Lab Tests/Lab Values
Diagnostic tests for AML include:
History and Physical Examination
Blood Test: Tests of patients with AML will commonly reveal increased leukocyte count initially with excessive immature cells as well as low red blood cell and platelet counts.
Bone marrow biopsy and aspiration: The removal of bone marrow, blood, and bone will be looked at by the pathologist under a microscope for signs of cancer.
Immunophenotyping: It is the process used to determine the subtype of AML by comparing the cancer cells to normal cells in the immune system. [2][3]
Etiology/Causes
Although the exact causes of AML are unknown, there are many risk factors associated with AML including:
Patients with AML can develop a variety of systemic complications including:
Headache/disorientation- due to abnormal white blood cells infiltrating the CNS.
Anaemia is accompanied by pallor, fatigue, malaise, hypoxia, and bleeding- Caused by rapidly proliferating leukocytes inhibiting formation of erythrocytes and thrombocytes.
Infections (pneumonia) and mouth/throat ulcerations- Caused by increased numbers of immature or abnormal leukocytes which are unable to fight off infections.
Increased metabolic rate with weakness, pallor, and weight loss- Caused by increased leukocyte production which requires increased nutrient production; destruction of cells also increases metabolic waste.
Hyperuricemia which may lead to renal pain, obstruction, and infection; later development includes renal insufficiency with uremia- Caused by a great number of leukocytes being destroyed which releases large amounts of uric acid; in late stages, leukocytes infiltrate the kidneys.
Enlarged organs (spleen, liver)- Caused by increased number of white blood cells accumulating within liver and spleen causing tissue distension.
Lymphadenopathy and bone pain- Caused by an excessive number of white blood cells accumulating in lymph nodes and bone marrow.[3]
Medical Management
The primary treatment of Acute Myeloid Leukemia is chemotherapy. The treatment of AML can be divided into three phases which include:
Induction: This is the first phase that clears the blood of leukemia cells and reduces the number of blasts in the bone marrow. The goal is to return blood counts to a normal level over time. This should rid the body of signs of the disease for an extended period.
Consolidation: This is administered after a rest period where the patient recovers from the induction phase. This phase is meant to kill the small number of leukemia cells that are still present. These cells cannot be seen because there are so few left after the induction phase.
Maintenance: This phase is necessary for only certain types of leukemia and includes giving low doses of a chemo drug for months or years after the consolidation phase.
There are 4 types of standard treatments for AML which include:
Chemotherapy
Uses drugs to stop the growth of cancer cells either by killing the cells or stopping them from dividing. Chemo can be administered by mouth or injected into a vein or muscle to enter the bloodstream to reach the cancer cells throughout the body (systemic chemotherapy). Chemo can also be administered directly into the Cerebrospinal fluid (intrathecal chemotherapy). This technique can be utilized when adult AML has spread or may spread to the brain or spinal cord. Chemotherapy can also be administered into a body cavity such as the abdomen or organ affecting only the specified region (regional chemotherapy). The way the chemotherapy is administered depends on the subtype of AML.
2. Radiation Therapy
Uses high energy X-rays or other types of radiation to kill cancer cells or keep them from growing. There are 2 types of radiation therapy, external and internal radiation. External radiation utilizes a machine outside the body to direct radiation towards cancer. Internal radiation uses radioactive material encapsulated in needles, seeds, wires, or catheters placed directly into the affected region. The type of radiation therapy depends on the subtype of AML.
3. Stem Cell Transplant
Method of administering chemo and replacing blood-forming cells that are affected or destroyed by the cancer treatment. Stem cells are removed from the patients (or donors) blood or bone marrow. These cells are then frozen and stored. After chemotherapy has completed, the cells are thawed and reinfused into the patient's bloodstream. These reinfused stem cells restore the body's blood cells.
Targeted Therapy: Uses drugs or other substances to destroy specific cancer cells without harming the patients' normal cells. Monoclonal antibody therapy is a type of targeted therapy being studied for adult AML treatment. This therapy uses antibodies made in a laboratory from a single type of immune cell. These antibodies identify structures on cancer cells or normal substances that help cancer cells grow. The antibodies destroy, block, or prevent the cancer cells from spreading. These antibodies are administered via an infusion. They may be used alone or with other types of drugs.[3][2]
Physical Therapy Management
Physical Therapy and exercise are indicated for patients with Acute Myeloid Leukemia undergoing cancer treatments. These interventions are aimed at symptom management, preservation of muscle function, pain control, and increased quality of life. Physical Therapy interventions for the patient with AML include:
Aerobic Training:Studies have shown that 12 minutes of walking 5x per week can reduce fatigue, symptom distress, anxiety, and depressive status while maintaining cardiovascular health. This also can help reduce secondary effects of bedrest including contractures, bedsores, GI dysfunction, pulmonary hygiene, etc.[6]
Strength Training: Studies have shown that strength training combined with aerobic exercises 3x per week, twice daily, for 30 minutes improves cardiorespiratory endurance, reduces total fatigue and depression, maintains the quality of life, and may reduce inflammatory markers. Strength training can include UE and LE resistive activities with a theraband, active range of motion against gravity, gripping activities, etc.[7]
Pain Management: Modalities including TENS, hot packs, cold packs, massage, and positioning can be utilized in order to manage pain associated with AML treatments.
Stretching: Daily stretching routines including sustained stretch, active and passive ROM, splinting, or orthotics may help offset the adverse affects of bedrest, especially contractures due to prolonged immobilization and fatigue. Stretching should be done at least 5x per week and repeated 4x for 12-15 seconds per muscle group.
All of the above interventions can be done throughout the cancer treatments; however, the following precautions should be taken:
No exercise if patient is extremely fatigued, has low red cell counts (anemia), or has become ataxic.
Avoid public areas if white blood cell counts are below 3,500 due to increased risk for infection.
If patient is experiencing neuropathy be aware of increased risk of falls due to impaired sensation and pain.
Be aware of adverse affects of medications.
Practice universal precautions due to the patient being immunocompromised.[8]
Conclusion
AML is a common hematological malignancy in adults.
Despite many advances, the malignancy still carries a poor prognosis. Hence, it is best managed by a Multidisciplinary Team (MDT) that includes a hematologist, oncologist. internist, pathologist, and an intensivist.
The key is to prevent more harm to the patient and hence a universal treatment plan must be developed and carried out.[1]
↑Chang PH, Lai YH, Shun SC, et al. Effects of a walking intervention on fatigue-related experiences of hospitalized acute myelogenous leukemia patients undergoing chemotherapy: a randomized controlled trial. J Pain Symptom Manage. 2008;35(5):524-34.
↑Battaglini CL, Hackney AC, Garcia R, Groff D, Evans E, Shea T. The effects of an exercise program in leukemia patients. Integr Cancer Ther. 2009;8(2):130-8.