Methods for treating melanoma
Methods of inhibiting melanoma tumor growth, methods of treating melanoma and metastatic melanoma, and methods of reducing the frequency of tumor initiating cells (or cancer stem cells) in melanoma tumors are described. The methods described comprise administering a DLL4 antagonist (e.g., an antibody that specifically binds the extracellular domain of human DLL4) to a subject. Related polypeptides and polynucleotides, compositions comprising the DLL4 antagonists, and methods of making the DLL4 antagonists are also described.
1. A method of inhibiting growth of a melanoma tumor comprising administering a therapeutically effective amount of a delta like ligand-4 (DLL4) antagonist to a human subject in need thereof, wherein the DLL4 antagonist is an antibody comprising:
(a) a heavy chain CDR1 comprising TAYYIH (SEQ ID NO:1), a heavy chain CDR2 comprising YISCYNGATNYNQKFKG (SEQ ID NO:2), YISSYNGATNYNQKFKG (SEQ ID NO:3), or YISVYNGATNYNQKFKG (SEQ ID NO:4), and a heavy chain CDR3 comprising RDYDYDVGMDY (SEQ ID NO:5); and
(b) a light chain CDR1 comprising RASESVDNYGISFMK (SEQ ID NO:9), a light chain CDR2 comprising AASNQGS (SEQ ID NO:10), and a light chain CDR3 comprising QQSKEVPWTFGG (SEQ ID NO:11).
2. The method of claim 1 , wherein the DLL4 antagonist is an antibody comprising:
(a) a heavy chain variable region having at least about 90% sequence identity to SEQ ID NO:6, SEQ ID NO:7 or SEQ ID NO:8; and/or
(b) a light chain variable region having at least about 90% sequence identity to SEQ ID NO:12.
3. The method of claim 1 , wherein the antibody is a recombinant antibody, a monoclonal antibody, a chimeric antibody, a humanized antibody, a human antibody, a bispecific antibody, an IgG1 antibody, an IgG2 antibody, or an antibody fragment.
4. The method of claim 1 , wherein the antibody is administered as part of a pharmaceutical composition.
5. The method of claim 1 , wherein the melanoma tumor has metastasized.
6. The method of claim 1 , wherein the melanoma comprises a wild type B-raf or a B-raf mutation.
7. The method of claim 6 , wherein the wild-type B-raf or the B-raf mutation is detected in a sample by a PCR-based assay or nucleotide sequencing.
8. The method of claim 7 , wherein the sample is a fresh sample, a frozen sample, or a formalin-fixed paraffin-embedded sample.
9. The method of claim 1 , wherein the melanoma is substantially non-responsive to at least one B-raf kinase inhibitor.
10. The method of claim 1 , further comprising administering to the subject a therapeutically effective amount of at least one additional therapeutic agent.
11. The method of claim 10 , wherein the at least one additional therapeutic agent is a chemotherapeutic agent.
12. The method of claim 10 , wherein the at least one additional therapeutic agent is a B-raf inhibitor.
13. The method of claim 12 , wherein the B-raf inhibitor is selected from the group consisting of PLX4032, PLX4720, and GDC-0879.
14. A method of treating melanoma in a human subject, comprising:
(a) determining if the melanoma comprises a mutation in the MAPK pathway, and
(b) administering to the subject a therapeutically effective amount of a DLL4 antagonist, wherein the DLL4 antagonist is an antibody comprising:
(i) a heavy chain CDR1 comprising TAYYIH (SEQ ID NO: 1), a heavy chain CDR2 comprising YISCYNGATNYNQKFKG (SEQ ID NO:2), YISSYNGATNYNQKFKG (SEQ ID NO:3), or YISVYNGATNYNQKFKG (SEQ ID NO:4), and a heavy chain CDR3 comprising RDYDYDVGMDY (SEQ ID NO:5); and
(ii) a light chain CDR1 comprising RASESVDNYGISFMK (SEQ ID NO:9), a light chain CDR2 comprising AASNQGS (SEQ ID NO: 10), and a light chain CDR3 comprising QQSKEVPWTFGG (SEQ ID NO:11).
15. The method of claim 14 , wherein the melanoma comprises a wild-type B-raf or a B-raf mutation.
16. The method of claim 15 , wherein the wild-type B-raf or the B-raf mutation is detected in a sample by a PCR-based assay or nucleotide sequencing.
17. The method of claim 16 , wherein the sample is a fresh sample, a frozen sample, or a formalin-fixed paraffin-embedded sample.
18. The method of claim 14 , wherein the melanoma is substantially non-responsive to at least one B-raf inhibitor.
19. A method of reducing tumor initiating cell frequency in a melanoma tumor, comprising contacting the melanoma tumor with an effective amount of a DLL4 antagonist, wherein the DLL4 antagonist is an antibody comprising:
(a) a heavy chain CDR1 comprising TAYYIH (SEQ ID NO:1), a heavy chain CDR2 comprising YISCYNGATNYNQKFKG (SEQ ID NO:2), YISSYNGATNYNQKFKG (SEQ ID NO:3), or YISVYNGATNYNQKFKG (SEQ ID NO:4), and a heavy chain CDR3 comprising RDYDYDVGMDY (SEQ ID NO:5); and
(b) a light chain CDR1 comprising RASESVDNYGISFMK (SEQ ID NO:9), a light chain CDR2 comprising AASNQGS (SEQ ID NO: 10), and a light chain CDR3 comprising QQSKEVPWTFGG (SEQ ID NO:11).
20. A method of inhibiting metastases in a human subject who has melanoma, comprising administering to the subject a therapeutically effective amount of a DLL4 antagonist, wherein the DLL4 antagonist is an antibody comprising:
(a) a heavy chain CDR1 comprising TAYYIH (SEQ ID NO:1), a heavy chain CDR2 comprising YISCYNGATNYNQKFKG (SEQ ID NO:2), YISSYNGATNYNQKFKG (SEQ ID NO:3), or YISVYNGATNYNQKFKG (SEQ ID NO:4), and a heavy chain CDR3 comprising RDYDYDVGMDY (SEQ ID NO:5); and
(b) a light chain CDR1 comprising RASESVDNYGISFMK (SEQ ID NO:9), a light chain CDR2 comprising AASNQGS (SEQ ID NO: 10), and a light chain CDR3 comprising QQSKEVPWTFGG (SEQ ID NO:11).
21. A method of inhibiting growth of a melanoma tumor comprising administering a therapeutically effective amount of a DLL4 antagonist to a human subject in need thereof, wherein the DLL4 antagonist is an antibody that specifically binds an epitope within amino acids 27-217 of the extracellular domain of human DLL4 (SEQ ID NO:14).
22. The method of claim 21 , wherein the antibody binds an epitope comprising amino acids 66-73 (QAVVSPGP, SEQ ID NO:17) of human DLL4.
23. The method of claim 21 , wherein the antibody binds an epitope comprising amino acids 139-146 (LISKIAIQ, SEQ ID NO:18) of human DLL4.
24. The method of claim 22 , wherein the antibody binds an epitope comprising amino acids 66-73 (QAVVSPGP, S EQ ID NO:17) and 139-146 (LISKIAIQ, SEQ ID NO:18) of human DLL4.
25. A method of treating a human subject who has melanoma which is substantially non-responsive to at least one B-raf inhibitor, comprising administering to the subject a therapeutically effective amount of a DLL4 antagonist, wherein the DLL4 antagonist is an antibody comprising:
(a) a heavy chain CDR1 comprising TAYYIH (SEQ ID NO:1), a heavy chain CDR2 comprising YISCYNGATNYNQKFKG (SEQ ID NO:2), YISSYNGATNYNQKFKG (SEQ ID NO:3), or YISCYNGATNYNQKFKG (SEQ ID NO:4), and a heavy chain CDR3 comprising RDYDYDVGMDY (SEQ ID NO:5); and
(b) a light chain CDR1 comprising RASESVDNYGISFMK (SEQ ID NO:9), a light chain CDR2 comprising AASNQGS (SEQ ID NO:10), and a light chain CDR3 comprising QQSKEVPWTFGG (SEQ ID NO:11).