Effective treatment of esophageal adenocarcinoma using triciribine and related compounds

Patent metadata

Field	Value
Publication number	US-9457040-B2
Application number	US-201514832400-A
Country	US
Kind code	B2
Filing date	Aug 21, 2015
Priority date	Sep 7, 2007
Publication date	Oct 4, 2016
Grant date	Oct 4, 2016

Abstract

The inventors have determined, contrary to the prior art and experience, how to successfully use triciribine to treat esophogeal adenocarcinoma by one or a combination of (i) administering triciribine only to patients which according to a diagnostic test described below, exhibit enhanced sensitivity to the drug; (ii) use of a described dosage level that minimizes the toxicity of the drug but yet still exhibits efficacy; or (iii) use of a described dosage regimen that minimizes the toxicity of the drug.

First claim

What is claimed is:

1. A method for treating esophogeal adenocarcinoma, which overexpresses Akt kinase, in a mammal comprising treating the mammal with an effective amount of a compound of the formula:

wherein each R 2 ′, R 3 ′ and R 5 ′ are independently hydrogen, optionally substituted phosphate or phosphonate; acyl; alkyl; amide, sulfonate ester, alkyl sulfonate ester, arylalkyl sulfonate ester; sulfonyl, methanesulfonyl, benzyl sulfonyl, wherein the phenyl group is optionally substituted with one or more substituents; optionally substituted arylsulfonyl; a lipid, a phospholipid; an amino acid; a carbohydrate; a peptide; or cholesterol; or other pharmaceutically acceptable leaving group that, in vivo, provides a compound wherein R 2 ′, R 3 ′ or R 5 ′ is independently H or mono-, di- or tri-phosphate;
wherein R x and R y are independently hydrogen, optionally substituted phosphate; acyl; amide, alkyl; aromatic, polyoxyalkylene, polyethyleneglycol, optionally substituted arylsulfonyl; a lipid, a phospholipid; an amino acid; a carbohydrate; a peptide; or cholesterol; or other pharmaceutically acceptable leaving group;
wherein R 1 and R 2 each are independently H, optionally substituted straight chained, branched or cyclic alkyl, alkenyl, or alkynyl, CO-alkyl, CO-alkenyl, CO-alkynyl, CO-aryl or heteroaryl, CO-alkoxyalkyl, CO-aryloxyalkyl, CO-substituted aryl, sulfonyl, alkyl sulfonyl, aryl sulfonyl, aralkylsulfonyl.

2. The method of claim 1 , wherein the mammal has been diagnosed with esophogeal adenocarcinoma.

3. The method of claim 1 , comprising first obtaining a biological sample from the tumor or cancer; then determining whether the tumor or cancer overexpresses an Akt kinase, wherein the level of Akt kinase expression is determined by assaying the cancer for the presence of a phosphorylated Akt kinase.

4. The method of claim 3 , wherein the level of Akt kinase expression is determined by assaying the cancer for the presence of a phosphorylated Akt kinase with an antibody.

5. A method of treating esophogeal adenocarcinoma, which overexpresses Akt kinase, in a mammal comprising administering to the mammal an effective amount of a compound of formula:

wherein each R 2 ′, R 3 ′ and R 5 ′ are independently hydrogen, optionally substituted phosphate or phosphonate; acyl; alkyl; amide, sulfonate ester, alkyl sulfonate ester, arylalkyl sulfonate ester; sulfonyl, methanesulfonyl, benzyl sulfonyl, wherein the phenyl group is optionally substituted with one or more substituents; optionally substituted arylsulfonyl; a lipid, a phospholipid; an amino acid; a carbohydrate; a peptide; or cholesterol; or other pharmaceutically acceptable leaving group that, in vivo, provides a compound wherein R 2 ′, R 3 ′ or R 5 ′ is independently H or mono-, di- or tri-phosphate;
wherein R x and R y are independently hydrogen, optionally substituted phosphate; acyl; amide, alkyl; aromatic, polyoxyalkylene, polyethyleneglycol, optionally substituted arylsulfonyl; a lipid, a phospholipid; an amino acid; a carbohydrate; a peptide; or cholesterol; or other pharmaceutically acceptable leaving group;
wherein R 1 and R 2 each are independently H, optionally substituted straight chained, branched or cyclic alkyl, alkenyl, or alkynyl, CO-alkyl, CO-alkenyl, CO-alkynyl, CO-aryl or heteroaryl, CO-alkoxyalkyl, CO-aryloxyalkyl, CO-substituted aryl, sulfonyl, alkyl sulfonyl, aryl sulfonyl, aralkyl sulfonyl;
wherein the compound is administered one time per week via intravenous infusion for three weeks followed by a one week period wherein the compound is not administered.

6. The method of claim 5 , wherein the dosing schedule is repeated at least twice.

7. The method of claim 5 , wherein the dosing schedule is repeated at least 4 times.

8. The method of claim 5 , wherein at least 10 mg/m 2 of the compound is administered.

9. The method of claim 5 , wherein 10 mg/m 2 or less of the compound is administered.

10. A method of treating esophogeal adenocarcinoma, which overexpresses Akt kinase, in a mammal comprising administering to the mammal a dose of 10 mg/m 2 or less of a compound of the formula:

wherein each R2′, R3′ and R5′ are independently hydrogen, optionally substituted phosphate or phosphonate; acyl; alkyl; amide, sulfonate ester, alkyl sulfonate ester, arylalkyl sulfonate ester; sulfonyl, methanesulfonyl, benzyl sulfonyl, wherein the phenyl group is optionally substituted with one or more substituents; optionally substituted arylsulfonyl; a lipid, a phospholipid; an amino acid; a carbohydrate; a peptide; or cholesterol; or other pharmaceutically acceptable leaving group that, in vivo, provides a compound wherein R 2 ′, R 3 ′ or R 5 ′ is independently H or mono-, di- or tri-phosphate;
wherein R x and R y are independently hydrogen, optionally substituted phosphate; acyl; amide, alkyl; aromatic, polyoxyalkylene, polyethyleneglycol, optionally substituted arylsulfonyl; a lipid, a phospholipid; an amino acid; a carbohydrate; a peptide; or cholesterol; or other pharmaceutically acceptable leaving group;
wherein R 1 and R 2 each are independently H, optionally substituted straight chained, branched or cyclic alkyl, alkenyl, or alkynyl, CO-alkyl, CO-alkenyl, CO-alkynyl, CO-aryl or heteroaryl, CO-alkoxyalkyl, CO-aryloxyalkyl, CO-substituted aryl, sulfonyl, alkyl sulfonyl, aryl sulfonyl, aralkyl sulfonyl;
wherein the compound is administered one time per week.

11. The method of claim 10 , wherein the dosing regimen is repeated for at least two weeks.

12. The method of claim 10 , wherein the dosing regimen is repeated for three weeks, and wherein the three week period is followed by a one week period wherein no drug is administered.

13. The method of claim 12 , wherein the dosing regimen represents a dosing cycle.

14. The method of claim 13 , wherein the dosing cycle is repeated at least twice.

15. The method of claim 13 wherein the dosing cycle is repeated until regression of the cancer is achieved.

16. The method of claim 1 , wherein the drug is administered intravenously.

17. The method of claim 1 , wherein the mammal is a human.

18. The method of claim 1 , wherein the compound is the compound of Formula IB:

19. The method of claim 1 , wherein the compound is the compound of Formula IIA:

Assignees

• Univ South Florida

Inventors

• Cheng Jin Q

Classifications

• A61K31/7052

  having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides · CPC title

• G01N2333/912

  transferring phosphorus containing groups, e.g. kinases (2.7) · CPC title

• A61P35/02

  specific for leukemia · CPC title

• A61K31/70

  Carbohydrates; Sugars; Derivatives thereof (sorbitol A61K31/047) · CPC title

• C07H19/23

  Heterocyclic radicals containing two or more heterocyclic rings condensed among themselves or condensed with a common carbocyclic ring system, not provided for in groups C07H19/14 - C07H19/22 · CPC title