Indication
Acute myeloid leukemia with isocitrate dehydrogenase-1 (IDH1) mutation
Acute myeloid leukemia with isocitrate dehydrogenase-1 (IDH1) mutation is an aggressive hematologic malignancy characterized by the clonal proliferation and accumulation of immature myeloid precursors in the bone marrow and peripheral blood. Read more about Acute myeloid leukemia with isocitrate dehydrogenase-1 (IDH1) mutation
3 drugs 3 manufacturers
Drugs that treat it
Common Acute myeloid leukemia with isocitrate dehydrogenase-1 (IDH1) mutation therapies.
TIBSOVO (ivosidenib)
REZLIDHIA (olutasidenib)
News & literature
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Coming soonAcute myeloid leukemia with isocitrate dehydrogenase-1 (IDH1) mutation is an aggressive hematologic malignancy characterized by the clonal proliferation and accumulation of immature myeloid precursors in the bone marrow and peripheral blood.
This molecularly defined subtype, observed primarily in adult patients, is driven by neomorphic somatic mutations in the cytosolic enzyme IDH1, most commonly at residue R132.
Pathophysiologically, the mutated enzyme converts alpha-ketoglutarate into the oncometabolite D-2-hydroxyglutarate (2-HG), causing DNA and histone hypermethylation that arrests normal myeloid cell differentiation and promotes leukemogenesis.
Consequently, patients frequently present with severe cytopenias, manifesting as fatigue, infection, and hemorrhage due to bone marrow failure.
- aacr.org
Acute myeloid leukemia with isocitrate dehydrogenase-1 (IDH1) mutation is an aggressive hematologic malignancy characterized by the clonal proliferation and accumulation of immature myeloid precursors in the bone marrow and peripheral blood Pathophysiologically, the mutated enzyme converts alpha-ketoglutarate into the oncometabolite D-2-hydroxyglutarate (2-HG), causing DNA and histone hypermethylation that arrests normal myeloid cell differentiation and promotes leukemogenesis Consequently, pati...
- semanticscholar.org
Acute myeloid leukemia with isocitrate dehydrogenase-1 (IDH1) mutation is an aggressive hematologic malignancy characterized by the clonal proliferation and accumulation of immature myeloid precursors in the bone marrow and peripheral blood Pathophysiologically, the mutated enzyme converts alpha-ketoglutarate into the oncometabolite D-2-hydroxyglutarate (2-HG), causing DNA and histone hypermethylation that arrests normal myeloid cell differentiation and promotes leukemogenesis Consequently, pati...
- nih.gov
This molecularly defined subtype, observed primarily in adult patients, is driven by neomorphic somatic mutations in the cytosolic enzyme IDH1, most commonly at residue R132
- nih.gov
This molecularly defined subtype, observed primarily in adult patients, is driven by neomorphic somatic mutations in the cytosolic enzyme IDH1, most commonly at residue R132
- patsnap.com
Pathophysiologically, the mutated enzyme converts alpha-ketoglutarate into the oncometabolite D-2-hydroxyglutarate (2-HG), causing DNA and histone hypermethylation that arrests normal myeloid cell differentiation and promotes leukemogenesis
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