Combination cancer therapy with an AKT inhibitor and other anticancer agents
The invention relates to combination anticancer therapy with certain Akt inhibitor and other anticancer agents such as anticancer antimetabolites, anticancer antibiotics, plant-derived anticancer agents, anticancer platinum-coordinated complex compounds, anticancer camptothecin derivatives and anticancer tyrosine kinase inhibitors.
1. A combined anticancer agent for simultaneous, separate or successive administration in cancer therapy, comprising the following pharmaceutical preparations (a) and (b):
(a) a pharmaceutical preparation comprising 8-[4-(1-aminocyclobutyl)phenyl]-9phenyl[1,2,4]triazolo[3,4-f]-1,6-naphthyridin-3(2H)-one or a pharmaceutically acceptable salt thereof, together with a pharmaceutically acceptable carrier or diluent, and
(b) a pharmaceutical preparation comprising, together with a pharmaceutically acceptable carrier or diluent, at least one anticancer agent selected from the group consisting of anticancer antimetabolites, anticancer antibiotics, plant-derived anticancer agents, anticancer platinum-coordinated complex compounds, anticancer camptothecin derivatives and anticancer tyrosine kinase inhibitors, or a pharmaceutically acceptable salt thereof, wherein
the anticancer antimetabolites are 5-fluorouracil and gemcitabine;
the anticancer antibiotics is doxorubicin;
the plant-derived anticancer agents are docetaxel and paclitaxel;
the anticancer platinum-coordinated complex compounds are cisplatin and carboplatin;
the anticancer camptothecin derivatives is camptothecin; and
the anticancer tyrosine kinase inhibitors are lapatinib and erlotinib and wherein
the cancer is selected from breast cancer, endometrial cancer, non-small cell lung cancer, ovarian cancer and prostate cancer.
2. An anticancer agent comprising 8-[4-(1-aminocyclobutyl)phenyl]-9-phenyl[1,2,4]triazolo[3,4-f]-1,6-naphthyridin-3(2H)-one or a pharmaceutically acceptable salt thereof, and at least one anticancer agent selected from the group consisting of anticancer antimetabolites, anticancer antibiotics, plant-derived anticancer agents, anticancer platinum-coordinated complex compounds, anticancer camptothecin derivatives and anticancer tyrosine kinase inhibitors, wherein the definition of each anticancer agent is the same as defined in claim 1 , or a pharmaceutically acceptable salt thereof, together with a pharmaceutically acceptable carrier or diluent.
3. A pharmaceutical kit comprising in a first compartment 8-[4-(1-aminocyclobutyl)phenyl]-9-phenyl[1,2,4]triazolo[3,4-f]-1,6-naphthyridin-3(2H)-one or a pharmaceutically acceptable salt thereof together with a pharmaceutically acceptable carrier or diluent, and in a second compartment at least one anticancer agent selected from the group consisting of anticancer antimetabolites, anticancer antibiotics, plant-derived anticancer agents, anticancer platinum-coordinated complex compounds, anticancer camptothecin derivatives and anticancer tyrosine kinase inhibitors, wherein the definition of each anticancer agent is the same as defined in claim 1 , or a pharmaceutically acceptable salt thereof, together with a pharmaceutically acceptable carrier or diluent.
4. A method for the treatment of cancer, which comprises administering to a subject in need thereof a therapeutically-effective amount of 8-[4-(1-aminocyclobutyl)phenyl]-9-phenyl[1,2,4]triazolo[3,4-f]-1,6-naphthyridin-3(2H)-one or a pharmaceutically acceptable salt thereof, in combination with at least one anticancer agent selected from the group consisting of anticancer antimetabolites, anticancer antibiotics, plant-derived anticancer agents, anticancer platinum-coordinated complex compounds, anticancer camptothecin derivatives and anticancer tyrosine kinase inhibitors, wherein the definition of each anticancer agent is the same as defined in claim 1 , or a pharmaceutically acceptable salt thereof.
5. The method according to claim 4 , wherein the cancer is selected from breast cancer, endometrial cancer, non-small cell lung cancer, ovarian cancer and prostate cancer.