Compositions and methods for reducing major thrombotic events in cancer patients

1. A method for reducing soluble P-selectin in a patient with cancer comprising administering to the patient an effective amount of isoquercetin, vitamin B3, and vitamin C for a period of at least about 2 months; wherein the patient has been diagnosed with a cancer and is at an increased risk of bleeding; and exhibits an elevated level of soluble P-selectin prior to administration of isoquercetin, when compared to a reference or baseline level of soluble P-selectin; and wherein soluble p-selectin levels are reduced after administration of the effective amount of isoquercetin, vitamin B3, and vitamin C for a period of at least about 2 months.

2. A method for reducing or preventing formation of a thrombus in a patient with cancer comprising administering to the patient an effective amount of isoquercetin, vitamin B3, and vitamin C for a period of at least about 2 months; wherein the patient has been diagnosed with a cancer and is at an increased risk of bleeding; and exhibits an elevated level of soluble P-selectin prior to administration of isoquercetin, when compared to a reference or baseline level of soluble P-selectin; wherein the dose of isoquercetin is 500 mg per day wherein the patient does not exhibit primary venous thromboembolism (VTE) during treatment or after administration of the effective amount of isoquercetin, vitamin B3, and vitamin C for a period of at least about 2 months; and wherein soluble P-selectin is decreased at least about 30% when compared to a reference or baseline level of soluble P-selectin, following administration of the isoquercetin.

3. A method for promoting tumor regression in a patient with cancer comprising administering to the patient an effective amount of isoquercetin, vitamin B3, and vitamin C for a period of at least about 2 months; wherein the patient has been diagnosed with a cancer and is at an increased risk of bleeding; and exhibits an elevated level of soluble P-selectin prior to administration of isoquercetin, when compared to a reference or baseline level of soluble P-selectin; and wherein the patient exhibits tumor regression after administration of the effective amount of isoquercetin, vitamin B3, and vitamin C for a period of at least about 2 months.

4. A method for stabilizing or reducing metastatic cancer in a patient with cancer comprising administering to the patient an effective amount of isoquercetin, vitamin B3, and vitamin C for a period of at least about 2 months; wherein the patient has been diagnosed with a cancer and is at an increased risk of bleeding; and exhibits an elevated level of soluble P-selectin prior to administration of isoquercetin, when compared to a reference or baseline level of soluble P-selectin; and wherein administration results in stabilizing or reducing metastatic cancer in the patient after administration of the effective amount of isoquercetin, vitamin B3, and vitamin C for a period of at least about 2 months.

5. The method of claim 1 , wherein soluble P-selectin decrease ranges from 30-40%, 40-50%, 55-60%, 60-70%, 70-75%, or 75-80% when compared to a reference or baseline level of soluble P-selectin, following administration of the isoquercetin.

6. The method of claim 1 , wherein the wherein the cancer is metastatic cancer.

7. The method of claim 6 , wherein the metastatic cancer is colorectal cancer, pancreatic cancer, or non-small cell lung cancer.

8. The method of claim 6 , wherein the metastatic cancer is selected from the group consisting of metastasizing forms of Hodgkin lymphoma, colorectal cancer, cervical cancer, lung cancer, skin cancer such as squamous cell cancer or basal cell carcinoma, head and neck cancer, gastric cancer, and pancreatic cancer.

9. The method of claim 1 , wherein the cancer is selected from the group consisting of estrogen receptor-dependent breast cancer, estrogen receptor-independent breast cancer, hormone receptor-dependent prostate cancer, hormone receptor-independent prostate cancer, brain cancer, renal cancer, glioblastoma, colon cancer, familial adenomatous polyposis (FAP), colorectal cancer, pancreatic cancer, bladder cancer, esophageal cancer, stomach cancer, genitourinary cancer, gastrointestinal cancer, uterine cancer, ovarian cancer, astrocytomas, gliomas, skin cancer, squamous cell carcinoma, Keratoakantoma, Bowen disease, cutaneous T-Cell Lymphoma, melanoma, basal cell carcinoma, actinic keratosis; ichtiosis; acne, acne vulgaris, sarcomas, Kaposi's sarcoma, osteosarcoma, head and neck cancer, small cell lung carcinoma, non-small cell lung carcinoma, leukemia, lymphomas and/or other blood cell cancers.

10. The method of claim 1 , wherein the patient exhibits no severe adverse events (grade 3 or 4 toxicities) during treatment.

11. The method of claim 1 , wherein the patient exhibits no VTE for at least 30-60 days following treatment.

12. The method of claim 1 , wherein the patient exhibits no major hemorrhages during treatment.

13. The method of claim 1 , wherein the patient exhibits a decrease in platelet-dependent thrombin generation of from about 30-60% when compared to a reference or baseline level of platelet dependent thrombin, following administration of the isoquercetin.

14. The method of claim 1 , wherein the isoquercetin is administered in a composition comprising about 20 micrograms to about 3 grams of Vitamin B3, and optionally further comprises about 200 micrograms to about 3 grams of Vitamin C.

15. The method of claim 1 , further comprising administering between about 1 000 micrograms to about 3 000 micrograms of folic acid.

16. The method of claim 2 , further comprising administering between about 1 000 micrograms to about 3 000 micrograms of folic acid.

17. The method of claim 3 , further comprising administering between about 1 000 micrograms to about 3 000 micrograms of folic acid.

18. The method of claim 4 , further comprising administering between about 1 000 micrograms to about 3 000 micrograms of folic acid.

19. The method of claim 2 , wherein the wherein the cancer is metastatic cancer.

20. The method of claim 19 , wherein the metastatic cancer is colorectal cancer, pancreatic cancer, or non-small cell lung cancer.

21. The method of claim 19 , wherein the metastatic cancer is selected from the group consisting of metastasizing forms of Hodgkin lymphoma, colorectal cancer, cervical cancer, lung cancer, skin cancer such as squamous cell cancer or basal cell carcinoma, head and neck cancer, gastric cancer, and pancreatic cancer.

22. The method of claim 2 , wherein the cancer is selected from the group consisting of estrogen receptor-dependent breast cancer, estrogen receptor-independent breast cancer, hormone receptor-dependent prostate cancer, hormone receptor-independent prostate cancer, brain cancer, renal cancer, glioblastoma, colon cancer, familial adenomatous polyposis (FAP), colorectal cancer, pancreatic cancer, bladder cancer, esophageal cancer, stomach cancer, genitourinary cancer, gastrointestinal cancer, uterine cancer, ovarian cancer, astrocytomas, gliomas, skin cancer, squamous cell carcinoma, Keratoakantoma, Bowen disease, cutaneous T-Cell Lymphoma, melanoma, basal cell carcinoma, actinic keratosis; ichtiosis; acne, acne vulgaris, sarcomas, Kaposi's sarcoma, osteosarcoma, head and neck cancer, small cell lung carcinoma, non-small cell lung carcinoma, leukemia, lymphomas and/or other blood cell cancers.

23. The method of claim 3 , wherein the wherein the cancer is metastatic cancer.

24. The method of claim 23 , wherein the metastatic cancer is colorectal cancer, pancreatic cancer, or non-small cell lung cancer.

25. The method of claim 23 , wherein the metastatic cancer is selected from the group consisting of metastasizing forms of Hodgkin lymphoma, colorectal cancer, cervical cancer, lung cancer, skin cancer such as squamous cell cancer or basal cell carcinoma, head and neck cancer, gastric cancer, and pancreatic cancer.

26. The method of claim 3 , wherein the cancer is selected from the group consisting of estrogen receptor-dependent breast cancer, estrogen receptor-independent breast cancer, hormone receptor-dependent prostate cancer, hormone receptor-independent prostate cancer, brain cancer, renal cancer, glioblastoma, colon cancer, familial adenomatous polyposis (FAP), colorectal cancer, pancreatic cancer, bladder cancer, esophageal cancer, stomach cancer, genitourinary cancer, gastrointestinal cancer, uterine cancer, ovarian cancer, astrocytomas, gliomas, skin cancer, squamous cell carcinoma, Keratoakantoma, Bowen disease, cutaneous T-Cell Lymphoma, melanoma, basal cell carcinoma, actinic keratosis; ichtiosis; acne, acne vulgaris, sarcomas, Kaposi's sarcoma, osteosarcoma, head and neck cancer, small cell lung carcinoma, non-small cell lung carcinoma, leukemia, lymphomas and/or other blood cell cancers.

27. The method of claim 4 , wherein the metastatic cancer is colorectal cancer, pancreatic cancer, or non-small cell lung cancer.

28. The method of claim 4 , wherein the metastatic cancer is selected from the group consisting of metastasizing forms of Hodgkin lymphoma, colorectal cancer, cervical cancer, lung cancer, skin cancer such as squamous cell cancer or basal cell carcinoma, head and neck cancer, gastric cancer, and pancreatic cancer.