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

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Drugs that treat it

Common Acute myeloid leukemia with isocitrate dehydrogenase-1 (IDH1) mutation therapies.

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TIBSOVO (ivosidenib)

ACUTE MYELOID LEUKEMIA WITH ISOCITRATE DEHYDROGENASE-1 (IDH1) MUTATION·+2
AGIOS PHARMACEU

TIBSOVO (ivosidenib)

ANTINEOPLASTIC - ISOCITRATE DEHYDROGENASE-1 INHIBITOR (IDH1)·ACUTE MYELOID LEUKEMIA WITH ISOCITRATE DEHYDROGENASE-1 (IDH1) MUTATION·+2
SERVIER PHARMAC

REZLIDHIA (olutasidenib)

ANTINEOPLASTIC - ISOCITRATE DEHYDROGENASE-1 INHIBITOR (IDH1)·ACUTE MYELOID LEUKEMIA WITH ISOCITRATE DEHYDROGENASE-1 (IDH1) MUTATION
RIGEL PHARMACEU
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About 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.

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.

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