Combination Therapies for Treating Cancer
Disclosed herein are methods and materials for treating cancer. The disclosure further provides methods and materials for using one or more antigen binding proteins (for example anti-B-cell maturation antigen (BCMA) antigen binding proteins) and one or more T cell engagers for treating a subject having cancer.
1 . A combination comprising:
a. an anti-BCMA antigen binding protein; and
b. a T cell engager that binds to CD3.
2 . The combination of claim 1 , wherein the anti-BCMA antigen binding protein comprises an antibody.
3 .- 4 . (canceled)
5 . The combination of claim 2 , wherein the antibody is afucosylated.
6 . (canceled)
7 . The combination of claim 1 , wherein the anti-BCMA antigen binding protein comprises a CDRH1 comprising the amino acid sequence set out in SEQ ID NO:1; a CDRH2 comprising the amino acid sequence set out in SEQ ID NO:2; a CDRH3 comprising the amino acid sequence set out in SEQ ID NO:3; a CDRL1 comprising the amino acid sequence set out in SEQ ID NO:4; a CDRL2 comprising the amino acid sequence set out in SEQ ID NO:5; and a CDRL3 comprising the amino acid sequence set out in SEQ ID NO:6.
8 . The combination of claim 1 , wherein the anti-BCMA antigen binding protein comprises a heavy chain variable region (V H ) comprising the amino acid sequence set out in SEQ ID NO:7; and a light chain variable region (V L ) comprising the amino acid sequence set out in SEQ ID NO:8.
9 . The combination of claim 1 , wherein the anti-BCMA antigen binding protein comprises a heavy chain (H) comprising the amino acid sequence set out in SEQ ID NO:9 and a light chain (L) comprising the amino acid sequence set out in SEQ ID NO:10.
10 . (canceled)
11 . The combination of claim 1 , wherein the anti-BCMA antigen binding protein is an immunoconjugate comprising an antibody conjugated to a cytotoxin, wherein the cytotoxin is MMAE or MMAF.
12 .- 13 . (canceled)
14 . The combination of claim 1 , wherein the anti-BCMA antigen binding protein is belantamab mafodotin.
15 . (canceled)
16 . The combination of claim 1 , wherein the T cell engager is a bispecific T cell engager.
17 . The combination of claim 23 , wherein the T cell engager is selected from the group consisting of Cevostamab, Talquetamab, Teclistimab, PF-3135, TNB-383B, REGN5458, Blinatumomab, Solitomab, CC-93269, AMG701, AMG420, JNJ-7957, and GBR 1342.
18 . The combination of claim 1 , wherein the T cell engager is an anti-FcRH5 T cell engager.
19 . The combination of claim 18 , wherein the T cell engager is Cevostamab.
20 . (canceled)
21 . The combination of any one of claims 1 - 16 , wherein the T cell engager is an anti-GPCR5D T cell engager.
22 . The combination of claim 21 , wherein the T cell engager is Talquetamab.
23 . The combination of claim 1 , wherein the T cell engager is an anti-BCMA T cell engager, an anti-FcRH5 T cell engager, or an anti-GPCR5D T cell engager.
24 .- 29 . (canceled)
30 . A method of treating cancer in a subject in need thereof comprising administering to the subject a therapeutically effective dose of the combination of claim 1 .
31 . (canceled)
32 . The method of claim 30 , wherein the cancer is selected from the group consisting of multiple myeloma, chronic lymphocytic leukemia, Waldenstrom macroglobulinemia, and non-Hodgkin's lymphoma.
33 . The method of claim 30 , wherein the cancer is multiple myeloma.
34 . The method of claim 30 , wherein the cancer is relapsed and/or refractory multiple myeloma.
35 .- 40 . (canceled)
41 . The method of claim 30 , wherein the anti-BCMA antigen binding protein is administered to the subject in a dose of at least about 0.5 mg/kg, 0.95 mg/kg, 1 mg/kg, 1.25 mg/kg, 1.4 mg/kg, 1.7 mg/kg, 1.9 mg/kg, 1.92 mg/kg, 2.5 mg/kg or 3.4 mg/kg.
42 .- 45 . (canceled)