IP Library Granted Patent US 8,932,649
Granted Patent B2
US 8,932,649 · App. 10/576,568 · Granted Jan 13, 2015

Methods for treating a neoplastic disease in a subject using inorganic selenium-containing compounds

Inventors: Susan J. Knox (Stanford, CA); Bryan Husbeck (Palo Alto, CA)
Assignee: The Board of Trustees of the Leland Stanford Junior University
A61K45/06A61K33/04
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Quick Facts
Patent No.
US 8,932,649
App. No.
10/576,568
Granted
Jan 13, 2015
Kind
B2
Abstract

The invention features methods and selenium-containing compositions for treating a neoplastic disease in a subject. In particular, the invention features methods for enhancing sensitivity of a tumor to cancer therapy by treating the tumor with an inorganic selenium-containing (iSe) compound and with a cancer therapy, particularly a cancer therapy that also affects the cellular redox status of a tumor cell (e.g., radiation).

Claims (34)

1. A method of treating prostate cancer in a subject, the method comprising:

administering to a subject having prostate cancer a pharmaceutically acceptable salt of an inorganic selenium-containing compound (iSe compound) in an amount effective to alter a reduction-oxidation state of a prostate cancer cell toward oxidation; and

administering radiation therapy to the subject within 6 hours after administering the iSe compound;

wherein administering the iSe compound and radiation therapy provides for a synergistic effect in treating the prostate cancer in the subject.

2. The method of claim 1 , wherein the iSe compound is inorganic selenite.

3. The method of claim 1 , wherein the radiation therapy is external beam radiation therapy, brachytherapy or systemically targeted radiation.

4. The method of claim 1 , wherein said administering of the iSe compound is intravenous, tumor targeted, intratumoral, peritumoral, or oral.

5. The method of claim 1 , wherein the iSe compound is administered within 2 hours prior to administering the radiation therapy.

6. The method of claim 1 , wherein the iSe compound is selenite.

7. The method of claim 6 , wherein the pharmaceutically acceptable salt of the iSe compound is a sodium salt.

8. The method of claim 1 , wherein the prostate cancer is androgen-responsive.

9. The method of claim 1 , wherein the prostate cancer is androgen-resistant.

10. The method of claim 1 , wherein the iSe compound is inorganic selenate.

11. The method of claim 1 , wherein the administering comprises intravenously administering about 0.25 mg/Kg of the pharmaceutically acceptable salt of iSe compound.

12. A method of enhancing sensitivity of prostate cancer in a subject to radiation therapy, the method comprising:

administering to a subject having prostate cancer a pharmaceutically acceptable salt of an inorganic selenium-containing compound (iSe compound) in an amount effective to sensitize the prostate cancer to radiation therapy; and

administering the radiation therapy to the subject within 6 hours after administering the iSe compound;

wherein administration of the iSe compound is effective to enhance sensitivity of the tumor to the radiation therapy by providing a synergistic effect in enhancing sensitivity of the prostate cancer to the radiation therapy.

13. The method of claim 12 , wherein inorganic selenium-containing compound is inorganic selenite.

14. The method of claim 12 , wherein the prostate cancer is androgen-responsive.

15. The method of claim 12 , wherein the prostate cancer is androgen- resistant.

16. The method of claim 12 , wherein the radiation therapy is external beam radiation therapy, brachytherapy or systemically targeted radiation.

17. The method of claim 12 , wherein the administering of the iSe compound is intravenous, tumor targeted, intratumoral, peritumoral, or oral.

18. The method of claim 12 , wherein the administering comprises intravenously administering about 0.25 mg/Kg or more of the pharmaceutically acceptable salt of iSe compound.

19. The method of claim 12 , wherein the pharmaceutically acceptable salt of an iSe compound is sodium selenite.

20. A method of treating prostate cancer, the method comprising:

administering to a subject having prostate cancer a pharmaceutically acceptable salt of an inorganic selenite, wherein the salt of the inorganic selenite is sodium selenite; and

administering radiation therapy to the subject within 6 hours after administering the pharmaceutically acceptable salt of an inorganic selenite;

wherein administering the pharmaceutically acceptable salt of an inorganic selenite and the radiation therapy provides for a synergistic effect in prostate cancer cell growth inhibition to treat the prostate cancer.

21. The method of claim 20 , wherein the radiation therapy is external beam radiation therapy, brachytherapy or systemically targeted radiation.

22. The method of claim 20 , wherein the administering of the iSe compound is intravenous, tumor targeted, intratumoral, peritumoral, or oral.

23. The method of claim 20 , wherein the administering comprises intravenously administering about 0.25 mg/Kg or more of the pharmaceutically acceptable salt of an inorganic selenite.

24. The method of claim 20 , wherein the prostate cancer is androgen-responsive.

25. The method of claim 20 , wherein the prostate cancer is androgen- resistant.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 3, 2007
From: KNOX, SUSAN J.; HUSBECK, BRYAN
To: THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY
Reel/Frame 018702/0297 →
Continuity (2)
Provisional Application 60520539 · Nov 14, 2003
Related Publication 20070160685A1 · Jul 12, 2007