CPC A61K 51/1033 (2013.01) [A61K 31/10 (2013.01); A61K 31/198 (2013.01); A61K 31/675 (2013.01); A61K 31/7076 (2013.01); A61K 51/1069 (2013.01); A61P 35/00 (2018.01); A61P 35/02 (2018.01); C07K 16/2803 (2013.01); C12Q 1/6886 (2013.01); A61K 2039/505 (2013.01); C07K 2317/24 (2013.01); C12Q 2600/156 (2013.01)] | 18 Claims |
1. A method of treating a hematologic malignancy in a subject comprising administering to the subject an effective amount of an anti-CD33 targeting agent, wherein the subject has a complex karyotype or a p53 mutation,
wherein the anti-CD33 targeting agent comprises a radiolabel selected from the group consisting of 131I, 125I, 123I, 90Y, 177Lu, 186Re, 188Re, 89Sr, 153Sm, 32p, 225Ac, 213Bi, 213Po, 211At, 212Bi, 213Bi, 223Ra, 227Th, 149Tb, 137Cs, 212Pb, and 103Pd, and
wherein the hematologic malignancy comprises myelodysplastic syndrome (MDS), multiple myeloma (MM), acute myeloid leukemia (AML), myeloproliferative neoplasm, or a combination thereof, and
wherein the anti-CD33 targeting agent comprises lintuzumab, gemtuzumab, or vadastuximab;
and wherein the effective amount of the anti-CD33 targeting agent is an amount sufficient to induce myeloconditioning, or an amount sufficient to induce myeloabation.
|