FIELD: medicine; pharmaceutics.
SUBSTANCE: invention relates to medicine and pharmaceutics, namely to a method for determining whether a patient will respond to treatment of a haematological malignant growth, which is refractory to chemotherapy, using a molecule bispecific to CD123×CD3 molecules, wherein said method includes: (A) evaluating the expression of one or more target genes in a cell sample obtained from said patient relative to the expression of the set of target genes and/or one or more reference genes, and (B) identifying said patient as a patient who will respond to treatment with a therapeutically effective amount of the bispecific CD123×CD3 molecule, if it is found that expression of said one or more target genes, the expression of which is assessed, is increased compared to said expression of one or more target genes and/or reference genes, the expression of which is assessed.
EFFECT: identifying a subpopulation of patients with a refractory haematologic malignant neoplasm responding well to treatment with bispecific to CD123×CD3 binding molecules.
25 cl, 14 dwg, 12 tbl, 2 ex
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Authors
Dates
2025-04-02—Published
2019-10-29—Filed