Methods for treating cancer using HSP90 inhibitors
The disclosure also provides compositions and methods related to combination therapy with HSP90 inhibitors and BCL-2 pathway inhibitors for treating cancer. The disclosure also provides compositions and methods related to the use of ‘low dose’ HSP90 inhibitors in the treatment of cancer, alone and in combination with other therapeutic agents.
1. A method for treating a hematopoietic or lymphoid cancer selected from a leukemia, a lymphoma and a multiple myeloma in a subject in need thereof, the method comprising administering to the subject an amount of an HSP90 inhibitor and a BCL-2 inhibitor, wherein the BCL-2 inhibitor is venetoclax and the HSP90 inhibitor is selected from MPC-0767, AT-13387, tanespimycin, TAS-116, SNX-5422, and XL-888, and pharmaceutically acceptable salts thereof.
2. The method of claim 1 , wherein the cancer is characterized as positive for BCL-2 expression based on the expression of BCL-2 in a biological sample of the cancer.
3. The method of claim 2 , wherein the cancer characterized as positive for BCL-2 expression is a cancer in which a biological sample from the cancer expresses BCL-2 at a level that is at least two-fold higher compared to the BCL-2 expression in a reference sample of non-cancerous tissue.
4. The method or composition of claim 3 , wherein the BCL-2 expression is protein expression or gene expression.
5. The method of claim 1 , wherein the amount of the HSP90 inhibitor is less than 90% of the recommended phase 2 dose of the HSP90 inhibitor.
6. The method of claim 1 , wherein the cancer is a leukemia selected from acute lymphoblastic leukemia (ALL), acute myelogenous leukemia (AML), chronic lymphocytic leukemia (CLL), chronic myelogenous leukemia (CML), and acute monocytic leukemia.
7. The method of claim 6 , wherein the cancer is AML.
8. The method of claim 1 , wherein the cancer is a lymphoma selected from a Hodgkins and a Non-Hodgkin's lymphoma.
9. The method of claim 8 , wherein the cancer is a Non-Hodgkin's B cell lymphoma, preferably selected from a diffuse large B cell lymphoma (DLBCL), Burkitt lymphoma, lymphoblastic lymphoma, and mantle cell lymphoma, and most preferably selected from a diffuse large B cell lymphoma (DLBCL) and a mantle cell lymphoma.
10. The method of claim 1 , wherein the cancer is a multiple myeloma.
11. The method of claim 1 , wherein the HSP90 inhibitor is MPC-0767 or tanespimycin, and pharmaceutically acceptable salts thereof.
12. The method of claim 1 , wherein the subject is human.