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Also called: mixed lineage acute leukemia, hybrid leukemia, biphenotypic acute leukemia, bilineage acute leukemia
Mixed phenotype acute leukemia is a mixture of 2 forms of leukemia: acute lymphoblastic leukemia (ALL) and acute myeloid leukemia (AML). The term mixed phenotype” means “both types.”
Leukemia is a cancer of the blood and bone marrow. Bone marrow is a soft, sponge-like tissue in the center of many bones. It makes blood cells. In leukemia, the bone marrow makes too many white blood cells that do not work correctly. There is no room for healthy cells to develop. As a result, children and teens cannot fight infections well.
Mixed phenotype acute leukemia is rare. It is more common in adults than children. But it can occur at any age.
Symptoms of mixed phenotype acute leukemia include:
Tests and exams to diagnose mixed phenotype acute leukemia may include:
Treatment has 2 phases: induction and post-remission
Four types of treatment may be used during these phases:
Mixed phenotype acute leukemia can be hard to treat because grows quickly and has features of both acute lymphoblastic leukemia and acute myeloid leukemia.
The survival rate for mixed phenotype acute leukemia ranges from 60–85%.
St. Jude offers clinical trials and cancer research studies for children, teens, and young adults for mixed phenotype acute leukemia. Learn more about clinical research at St. Jude.
Study goal:
To find the best dose of SNDX-5613 to use along with chemotherapy for young patients with KMT2A-R leukemia
Age:
1 month to 5 years old
Patients accepted to St. Jude must have a disease we treat and must be referred by a physician or other qualified medical professional. We accept most patients based on their ability to enroll in an open clinical trial.
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