Method of treating cancers and a pharmaceutical composition that may be used in practicing said method
Abstract
The method of treating a person having a cancer selected from carcinoma, sarcoma or hematopoietic cancer by administering (a) an effective amount of at least one anti-cancer drug selected from the group consisting of an epidermal growth factor receptor (EGFR) inhibitor, a vascular endothelial growth factor receptor (VEGFR) inhibitor and a Raf kinase inhibitor and (b) an effective amount of 5-(4-(6-(4-amino-3,5-dimethyl-phenoxy)-1-methyl-1H-benzimidazol-2-ylmethoxy)-benzyl)-thiazolidine-2,4-dione.dihydrochloride provided that said carcinoma is not lung cancer when an EGFR inhibitor is erlotinib. The invention also provides a pharmaceutical composition that may be used in practicing said method.
Claims
exact text as granted — not AI-modified1 . An anti-cancer pharmaceutical composition for treatment of carcinoma, sarcoma or hematopoietic cancer comprising:
(a) an effective amount of at least one anti-cancer drug selected from the group consisting of an epidermal growth factor receptor (EGFR) inhibitor, a vascular endothelial growth factor receptor (VEGFR) inhibitor and a Raf kinase inhibitor and (b) an effective amount of 5-(4-(6-(4-amino-3,5-dimethyl-phenoxy)-1-methyl-1H-benzimidazol-2-ylmethoxy)-benzyl)-thiazolidine-2,4-dione.dihydrochloride as active ingredients provided that said carcinoma is not lung cancer when an EGFR inhibitor is erlotinib.
2 . The pharmaceutical composition of claim 1 , wherein said anti-cancer drug (a) is at least one selected from the group consisting of cetuximab, panitumumab, erlotinib, lapatinib, bevacizumab, SU11248 and vatalanib.
3 . The pharmaceutical composition of claim 1 , wherein said anti-cancer drug (a) is at least one selected from the group consisting of gefitinib and sorafenib.
4 . The pharmaceutical composition of claim 1 , wherein said composition is for the treatment of breast cancer, pancreatic cancer, kidney cancer or prostate cancer.
5 . The pharmaceutical composition of claim 1 , wherein said composition is for the treatment of medulloblastoma, rhabdomyosarcoma, Ewing sarcoma or liposarcoma.
6 . The pharmaceutical composition of claim 1 , wherein said composition is for the treatment of liposarcoma.
7 . The pharmaceutical composition of claim 1 , wherein said composition is for the treatment of multiple myeloma or leukemia.
8 . A method of treating a person having a cancer selected from carcinoma, sarcoma or hematopoietic cancer comprising administering:
(a) an effective amount of at least one anti-cancer drug selected from the group consisting of an epidermal growth factor receptor (EGFR) inhibitor, a vascular endothelial growth factor receptor (VEGFR) inhibitor and a Raf kinase inhibitor and (b) an effective amount of 5-(4-(6-(4-amino-3,5-dimethyl-phenoxy)-1-methyl-1H-benzimidazol-2-ylmethoxy)-benzyl)-thiazolidine-2,4-dione.dihydrochloride provided that said carcinoma is not lung cancer when an EGFR inhibitor is erlotinib.
9 . The method of claim 8 , wherein said anti-cancer drug (a) is at least one selected from the group consisting of panitumumab, lapatinib, bevacizumab, SU11248 and vatalanib.
10 . The method of claim 8 , wherein said anti-cancer drug (a) is at least one selected from the group consisting of cetuximab, gefitinib, erlotinib and sorafenib.
11 . The method of claim 8 , wherein said method is for the treatment of lung cancer, and said anti-cancer drug (a) is gefitinib.
12 . The method of claim 8 , wherein said method is for the treatment of kidney cancer, and said anti-cancer drug (a) is sorafenib.
13 . The method of claim 8 , wherein said carcinoma is for the treatment of kidney cancer, and said anti-cancer drug (a) is sorafenib.
14 . The method of claim 8 , wherein said cancer is medulloblastoma, rhabdomyosarcoma, Ewing sarcoma or liposarcoma.
15 . The method of claim 8 , wherein said cancer is multiple myeloma or leukemia.
16 . The method of claim 8 , wherein said cancer is liposarcoma.Cited by (0)
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