Cytotoxic agents for the treatment of cancer
The present invention relates to a method of treating brain cancer comprising administering a therapeutically effective substance to a patient, wherein the therapeutically effective substance comprises: (I), or a pharmaceutically acceptable salt thereof, wherein X is a. moiety that can be cleaved hydrolytically or enzymatically in the body of the patient in a pH-dependent manner.
1. A method for the treatment of brain cancer comprising administering a therapeutically effective substance to a patient, wherein the therapeutically effective substance comprises DOXO-EMCH or a pharmaceutically acceptable salt thereof, wherein the therapeutically effective substance binds to serum albumin; and wherein the therapeutically effective substance is administered to the patient by an administration route selected from the group consisting of intravenous, intra-arterial and intramuscular.
2. The method according to claim 1 , wherein the therapeutically effective substance is cleaved in the body of the patient, with the release of doxorubicin or a pharmaceutically acceptable salt thereof.
3. The method according to claim 1 , wherein the therapeutically effective substance is (E)- N′-(1-((2S,4S)-4-(4-amino-5-hydroxy-6-methyl-tetrahydro-2H-pyran-2-yloxy)-2,5,12-trihydroxy-7-methoxy-6,11-dioxo-1,2,3,4,6,11-hexahydrotetracen-2-yl)-2-hydroxyethylidene)-6-(2,5-dioxo-2H-pyrrol-1(5H)yl)hexanehydrazide.HCl.
4. The method according to any one of claim 1 , 2 or 3 , wherein the brain cancer is a primary brain cancer.
5. The method of claim 4 , wherein the primary brain cancer is glioma, astrocytoma, oligodendroglioma, ependymoma, meningioma, craniopharyngioma, germinoma, pineocytoma, pineoblastoma and glioblastoma multiforme.
6. The method of claim 5 , wherein the primary brain cancer is glioblastoma multiforme.
7. The method according to any one of claim 1 or 3 , wherein the brain cancer is a secondary or metastatic cancer.
8. The method of claim 7 , wherein the secondary or metastatic cancer is selected from bladder cancer, breast cancer, lung cancer, stomach cancer, endometrial cancer, ovarian cancer, pancreatic cancer, pancreatic ductal adenocarcinoma, cancer of the adrenal cortex, non-Hodgkin's lymphoma, multiple myeloma, leukemia, Kaposi's sarcoma, Ewing's sarcoma, soft tissue sarcoma, nephroblastoma, prostate cancer, liver cancer, bone cancer, chondrosarcoma, renal cancer, bladder cancer, thyroid cancer and gastric cancer.
9. The method according to any one of claims 1 , 2 or 3 , wherein the therapeutically effective substance is administered in combination with an anti-cancer agent.
10. The method of claim 9 , wherein the anti-cancer agent is selected from doxorubicin, cisplatin, carboplatin, paclitaxel, docetaxel, temozolomide, nitrosoureas, bortezomib, gemcitabine, etoposide, topotecan, or a pharmaceutically acceptable salt thereof.