Genetics In Acute Myeloid Leukemia (AML) Prognosis
- You should ask your doctor about your AML subgroup because it helps determine your treatment
- Studying genetics in DNA structure (cytogenetics) helps to determine subgroups of AML
- Cytogenic tests look for changes in leukemia cells that have developed over time. Examples of cytogenic tests include: karotype and FISH testing.
There are many types of AML. Genetic and biomarker testing can help identify your AML “subtype.”
Read More- Karotype – This is a picture of chromosomes to see if 46 (the number contained in normal human cells) are present.
- FISH (florescence in situ hybridization) testing involves the use of special dyes to detect chromosonal abnormalities.
Studying cytogenetics is key in acute myeloid leukemia (AML) research and treatment. In AML diagnoses, patients often have normal chromosomes within AML cells, but according to Dr. Roboz, that isn’t as positive as it sounds.
“In AML, although the majority of patients have normal chromosomes, that is associated with what is termed as an ‘Intermediate prognosis,’ which means that the treatment pathway is going to be different from what we would use for these so-called ‘good prognosis AML subgroups,'” Dr. Roboz says.
Cancer Patients As Their Own Advocates
Pushing for more answers and options is key for cancer patients after diagnosis and during treatment. Additionally, every patient to learn as much as possible about their diagnosis.
“It’s important to educate yourself and be your own healthcare advocate, and that’s something I think is very important,” Dr. Zuri Murrell, the Director of the Cedars-Sinai Colorectal Cancer Center, tells SurvivorNet. “You should leave each doctor’s appointment with a plan.”
By speaking up, cancer patients can learn about multiple options for care, which is something Dr. Steven Rosenberg, Chief of Surgery at the National Cancer Institute and pioneer of genetics and immunotherapy, encourages every patient to do.
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