| CPC C07K 16/28 (2013.01) [A61K 31/704 (2013.01); A61K 31/706 (2013.01); A61K 31/7068 (2013.01); A61K 39/395 (2013.01); A61K 39/39558 (2013.01); A61K 45/06 (2013.01); A61N 5/1027 (2013.01); A61N 5/1045 (2013.01); A61N 5/1084 (2013.01); C07K 16/2896 (2013.01); A61K 39/001126 (2018.08); A61K 2039/505 (2013.01); C07K 2317/21 (2013.01); C07K 2317/56 (2013.01); C07K 2317/565 (2013.01); C07K 2317/73 (2013.01); C07K 2317/732 (2013.01); C07K 2317/734 (2013.01)] | 12 Claims |
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1. A method of treating relapsed or refractory acute myeloid leukemia (AML) in a subject in need thereof, comprising administering to the subject an anti-CD38 antibody:
b) for a time sufficient to treat the relapsed or refractory AML, wherein the anti-CD38 antibody consists of daratumumab, and wherein the AML is AML with at least one mutation in a gene selected from the group consisting of fms-related tyrosine kinase 3 (FLT3), nucleophosmin (NPM1), isocitrate dehydrogenase 2 (IDH2), DNA (cytosine-5) methyltransferase 3 (DNMT3A) and CCAAT/enhancer binding protein alpha (CEBPA).
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