Cancer treatment combinations
There are provided, inter alia, compositions and methods for treatment of cancer. The methods include administering to a subject in need a therapeutically effective amount of a Bruton's tyrosine kinase (BTK) antagonist and a ROR-1 antagonist. Further provided are pharmaceutical compositions including a BTK antagonist, ROR-1 antagonist and a pharmaceutically acceptable excipient. In embodiments, the BTK antagonist is ibrutinib and the ROR-1 antagonist is cirmtuzumab.
1. A method of treating an ROR-1 expressing cancer or a cancer susceptible to a BTK antagonist in a subject in need thereof, said method comprising administering to said subject a therapeutically effective amount of a Bruton's tyrosine kinase (BTK) antagonist and an anti-ROR-1 antibody, wherein said anti-ROR-1 antibody comprises a humanized heavy chain variable region and a humanized light chain variable region, wherein said humanized heavy chain variable region comprises the sequences set forth in SEQ ID NO:1, SEQ ID NO:2, and SEQ ID NO:3, and wherein said humanized light chain variable region comprises the sequences set forth in SEQ ID NO:4, SEQ ID NO:5, and SEQ ID NO:6.
2. The method of claim 1 , wherein said BTK antagonist is a small molecule.
3. The method of claim 1 , wherein said BTK antagonist comprises ibrutinib, acalabrutinib, ONO/GS-4059, BGB-3111, or CC-292 (AVL-292).
4. The method of claim 1 , wherein said BTK antagonist is ibrutinib.
5. The method of claim 1 , wherein said anti-ROR-1 antibody is cirmtuzumab.
6. The method of claim 1 , wherein said BTK antagonist and said anti-ROR-1 antibody are administered in a combined synergistic amount.
7. The method of claim 1 , wherein said BTK antagonist and said anti-ROR-1 antibody are administered simultaneously or sequentially.
8. The method of claim 1 , wherein said anti-ROR-1 antibody is administered at a first time point and said BTK antagonist is administered at a second time point, wherein said first time point precedes said second time point.
9. The method of claim 1 , wherein said BTK antagonist and said anti-ROR-1 antibody are admixed prior to administration.
10. The method of claim 1 , wherein said BTK antagonist is administered at an amount of about 1 mg/kg, 2 mg/kg, 5 mg/kg, 10 mg/kg or 15 mg/kg.
11. The method of claim 1 , wherein said BTK antagonist is administered at an amount of about 5 mg/kg.
12. The method of claim 1 , wherein said BTK antagonist is administered at an amount of about 420 mg.
13. The method of claim 1 , wherein said anti-ROR-1 antibody is administered at an amount of about 1 mg/kg, 2 mg/kg, 3 mg/kg, 5 mg/kg or 10 mg/kg.
14. The method of claim 1 , wherein said anti-ROR-1 antibody is administered at an amount of about 2 mg/kg.
15. The method of claim 1 , wherein said BTK antagonist is administered at an amount of about 5 mg/kg and said anti-ROR-1 antibody is administered at about 2 mg/kg.
16. The method of claim 1 , wherein said BTK antagonist is administered at an amount of about 5 mg/kg and said anti-ROR-1 antibody is administered at about 1 mg/kg.
17. The method of claim 1 , wherein said BTK antagonist is administered daily over the course of at least 14 days.
18. The method of claim 1 , wherein said BTK antagonist is administered daily over the course of about 28 days.
19. The method of claim 1 , wherein said anti-ROR-1 antibody is administered once over the course of about 28 days.
20. The method of claim 1 , wherein said BTK antagonist is administered intravenously.
21. The method of claim 1 , wherein said anti-ROR-1 antibody is administered intravenously.
22. The method of claim 1 , wherein said subject is a mammal.
23. The method of claim 1 , wherein said subject is a human.
24. The method of claim 1 , wherein said ROR-1 expressing cancer or said cancer susceptible to a BTK antagonist is lymphoma, leukemia, myeloma, AML, B-ALL, T-ALL, renal cell carcinoma, colon cancer, colorectal cancer, breast cancer, epithelial squamous cell cancer, melanoma, stomach cancer, brain cancer, lung cancer, pancreatic cancer, cervical cancer, ovarian cancer, liver cancer, bladder cancer, prostate cancer, testicular cancer, thyroid cancer, head and neck cancer, uterine cancer, adenocarcinoma, or adrenal cancer.
25. The method of claim 1 , wherein said ROR-1 expressing cancer or said cancer susceptible to a BTK antagonist is chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma, marginal cell B-Cell lymphoma, Burkitt's Lymphoma, or B cell leukemia.
26. The method of claim 1 , wherein said BTK antagonist and said anti-ROR-1 antibody are administered on different treatment schedules.
27. The method of claim 1 , wherein said BTK antagonist and said anti-ROR-1 antibody are administered on different days.
28. The method of claim 1 , wherein said BTK antagonist and said anti-ROR-1 antibody are administered separately.
29. A pharmaceutical composition comprising a BTK antagonist, an anti-ROR-1 antibody, and a pharmaceutically acceptable excipient, wherein said anti-ROR-1 antibody comprises a humanized heavy chain variable region and a humanized light chain variable region, wherein said humanized heavy chain variable region comprises the sequences set forth in SEQ ID NO:1, SEQ ID NO:2, and SEQ ID NO:3, and wherein said humanized light chain variable region comprises the sequences set forth in SEQ ID NO:4, SEQ ID NO:5, and SEQ ID NO:6.
30. The pharmaceutical composition of claim 29 , wherein said BTK antagonist and said anti-ROR-1 antibody are present in a combined synergistic amount, wherein said combined synergistic amount is effective to treat an ROR-1 expressing cancer or a cancer susceptible to a BTK antagonist in a subject in need thereof.
31. The pharmaceutical composition of claim 29 , wherein said BTK antagonist is a small molecule.
32. The pharmaceutical composition of claim 29 , wherein said BTK antagonist is ibrutinib, acalabrutinib, ONO/GS-4059, BGB-3111 or CC-292 (AVL-292).
33. The pharmaceutical composition of claim 29 , wherein said BTK antagonist is ibrutinib.
34. The pharmaceutical composition of claim 29 , wherein said anti-ROR-1 antibody is cirmtuzumab.