Treatment of cancer with TOR kinase inhibitors
US-9493466-B2 · Nov 15, 2016 · US
US9782427B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9782427-B2 |
| Application number | US-201414254009-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 16, 2014 |
| Priority date | Apr 17, 2013 |
| Publication date | Oct 10, 2017 |
| Grant date | Oct 10, 2017 |
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Provided herein are methods for treating or preventing a cancer, comprising administering an effective amount of a TOR kinase inhibitor having the following formula (I): and an effective amount of a cytidine analog, such as 5-azacytidine, to a patient having a cancer.
Opening claim text (preview).
What is claimed is: 1. A method for treating liver cancer or breast cancer, comprising administering an effective amount of a TOR kinase inhibitor in combination with an effective amount of 5 azacytidine to a patient having liver cancer or breast cancer, wherein the TOR kinase inhibitor is 1-ethyl-7-(2-methyl-6-(4H-1,2,4-triazol-3-yl)pyridin-3-yl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1H)-one or 7-(6-(2-hydroxypropan-2-yl)pyridin-3 -yl)-1-(trans-4-methoxycyclohexyl)-3,4-dihydropyrazino[2,3 -b]pyrazin-2(1H)-one or a pharmaceutically acceptable salt, stereoisomer, or tautomer thereof. 2. The method of claim 1 , wherein the cancer is a relapsed or refractory cancer. 3. The method of claim 1 , wherein the cancer is an advanced cancer. 4. The method of claim 1 , wherein the breast cancer is, hormone receptor positive, estrogen receptor positive (ER+, ER+/Her2 or ER+/Her2+), estrogen receptor negative (ER−/Her2+) or triple negative (TN). 5. The method of claim 1 , wherein the cancer is a cancer associated with the pathways involving mTOR, PI3K, or Akt kinases and mutants or isoforms thereof. 6. The method of claim 1 , wherein the cancer is liver cancer. 7. The method of claim 1 , wherein the cancer is breast cancer. 8. The method of claim 1 , wherein the TOR kinase inhibitor is 1-ethyl-7-(2-methyl-6-(4H-1,2,4-triazol-3-yl)pyridin-3-yl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1H)-one or a pharmaceutically acceptable salt, stereoisomer, or tautomer thereof. 9. The method of claim 1 , wherein the TOR kinase inhibitor is 7-(6-(2-hydroxypropan-2-yl)pyridin-3-yl)-1-(trans-4-methoxycyclohexyl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1H)-one or a pharmaceutically acceptable salt, stereoisomer, or tautomer thereof.
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