Co-administration of a polysaccharide with a chemotherapeutic agent for the treatment of cancer
View Patent ↗Methods and compositions for treating cancer with a formulation are provided in which a polysaccharide, galactomannan, is co-administered with a therapeutic agent to a subject to reduce toxicity and/or enhance efficacy of the agent for the subject.
1. A method for treating a cancer in a subject, comprising:
obtaining a mixture of galactomannan polysaccharide and an effective dose of a chemotherapeutic agent in a pharmaceutically acceptable formulation; and
administering the formulation to the subject so as to treat the cancer.
2. A method according to claim 1 , wherein the mixture contains an amount of galactomannan and the chemotherapeutic agent in a ratio suitable for reducing a toxic effect in the subject, the toxic effect associated with administration of the chemotherapeutic agent absent galactomannan.
3. A method according to claim 1 , wherein the mixture contains an amount of galactomannan and the chemotherapeutic agent in a ratio suitable for enhancing efficacy of chemotherapeutic effect for treating the cancer.
4. A method according to claim 1 , wherein the size of the galactomannan is in the range of 20,000 to 600,000 D.
5. A method according to claim 4 , wherein the galactomannan has a molecular weight in the range of 90,000 to 415,000 D.
6. A method according to claim 4 , wherein the galactomannan has a molecular weight in the range of 40,000-200,000 D.
7. A method according to claim 4 , wherein the galactomannan has an average molecular weight of 48,000 D.
8. A method according to claim 4 , wherein the galactomannan has an average molecular weight of 83,000 D.
9. A method according to claim 4 , wherein the galactomannan has an average molecular weight of 215,000 D.
10. A method according to claim 1 , wherein the galactomannan is β 1,4 D-galactomannan.
11. A method according to claim 4 , wherein galactomannan includes a ratio of mannose to galactose in the range of 1.0-3.0.
12. A method according to claim 11 , wherein galactomannan includes a ratio of 2.6 mannose to 1.5 galactose.
13. A method according to claim 11 , wherein galactomannan includes a ratio of 2.2 mannose to 0.9 galactose.
14. A method according to claim 11 , wherein the galactomannan includes a ratio of 1.13 mannose to 1 galatose.
15. A method according to claim 11 , wherein the galactomannan includes a ratio of 2.2 mannose to 1 galactose.
16. A method according to claim 1 , wherein the galactomannan and the chemotherapeutic agent are present in the mixture in a ratio of 0.1:1 w/w to 10:1 w/w.
17. A method according to claim 2 , wherein the mixture has a reduced toxicity of greater than 50% compared with the same dose of the agent absent galactomannan.
18. A method according to claim 2 , wherein the mixture has a reduced toxicity of greater than 80% compared with the same dose of the agent absent galactomannan.
19. A method according to claim 3 , wherein the mixture has an enhanced efficacy of greater than 50% compared with the same dose of the agent absent galactomannan.
20. A method according to claim 3 , wherein the mixture has an enhanced efficacy of greater than 80% compared with the same dose of the agent absent galactomannan.
21. A method according to claim 1 , wherein the chemotherapeutic agent is adriamycin.
22. A method according to claim 1 , wherein the chemotherapeutic agent is 5-FU.
23. A method according to claim 1 , wherein the cancer is any of chronic leukemia, breast cancer, sarcoma, ovarian carcinoma, rectal cancer, throat cancer, melanoma, colon cancer, bladder cancer, lung cancer, mammary adenocarcinoma, gastrointestinal cancer, stomach cancer, prostate cancer, pancreatic cancer, or Kaposi's sarcoma.
24. The method according to claim 1 , wherein the cancer is any of breast cancer, colon cancer, or pancreatic cancer.
25. The method according to claim 23 , wherein the subject is a human subject.