Indication

Acute myelomonocytic leukemia

Acute myelomonocytic leukemia is an aggressive subtype of acute myeloid leukemia characterized by the neoplastic proliferation of both granulocytic and monocytic precursor cells in the bone marrow and peripheral blood. Read more about Acute myelomonocytic leukemia

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Drugs that treat it

Common Acute myelomonocytic leukemia therapies.

Showing 1–9 of 17 drugs

ARSENIC TRIOXIDE

ANTINEOPLASTICS - ARSENIC COMPOUNDS·ACUTE PROMYELOCYTIC LEUKEMIA·+1
NEXUS PHARMACEU

ARSENIC TRIOXIDE

ANTINEOPLASTICS - ARSENIC COMPOUNDS·ACUTE PROMYELOCYTIC LEUKEMIA·+1
INGENUS PHARMAC

ARSENIC TRIOXIDE

ANTINEOPLASTICS - ARSENIC COMPOUNDS·ACUTE PROMYELOCYTIC LEUKEMIA·+1
ZYDUS PHARMACEU

ARSENIC TRIOXIDE

ANTINEOPLASTICS - ARSENIC COMPOUNDS·ACUTE PROMYELOCYTIC LEUKEMIA·+1
AMRING PHARMACE

ARSENIC TRIOXIDE

ANTINEOPLASTICS - ARSENIC COMPOUNDS·ACUTE PROMYELOCYTIC LEUKEMIA·+1
FRESENIUS KABI

ARSENIC TRIOXIDE

ANTINEOPLASTICS - ARSENIC COMPOUNDS·ACUTE PROMYELOCYTIC LEUKEMIA·+1
NORTHSTAR RX LL

ARSENIC TRIOXIDE

ANTINEOPLASTICS - ARSENIC COMPOUNDS·ACUTE PROMYELOCYTIC LEUKEMIA·+1
SAGENT PHARMACE

ARSENIC TRIOXIDE

ANTINEOPLASTICS - ARSENIC COMPOUNDS·ACUTE PROMYELOCYTIC LEUKEMIA·+1
STI PHARMA, LLC
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About Acute myelomonocytic leukemia.

Acute myelomonocytic leukemia is an aggressive subtype of acute myeloid leukemia characterized by the neoplastic proliferation of both granulocytic and monocytic precursor cells in the bone marrow and peripheral blood.

Primarily affecting adults, this hematologic malignancy disrupts normal hematopoiesis, leading to severe cytopenias that clinically manifest as fatigue, susceptibility to recurrent infections, and bleeding diatheses.

Pathophysiologically, the condition is defined by elevated blast counts with significant dual differentiation, where both neutrophilic lineage cells and monocytic lineage cells each comprise at least 20% of bone marrow leukocytes.

Patients frequently demonstrate extramedullary tissue infiltration—including gingival hyperplasia, hepatosplenomegaly, and skin involvement—driven by the intrinsic tissue-migratory properties of the leukemic monocytic lineage.

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