IP Library Granted Patent US 8,435,489
Granted Patent B2
US 8,435,489 · App. 13/309,972 · Granted May 7, 2013

Non-invasive diagnostic agents of cancer and methods of diagnosing cancer, especially leukemia and lymphoma

Inventors: Jeffrey P. Norenberg (Albuquerque, NM); Richard S. Larson (Albuquerque, NM)
Assignee: STC.UNM
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Quick Facts
Patent No.
US 8,435,489
App. No.
13/309,972
Granted
May 7, 2013
Kind
B2
Abstract

The present invention is directed to novel non-invasive diagnostic tools to image cancers, especially, leukemia and non-Hodgkin's lymphomas (NHL) with minimal toxicity in vivo. The present invention represents a clear advance in the art which presently relies on tissue biopsy for diagnoses of these cancers. The novel imaging probe is capable of detecting precancerous cells, as well as their metastatic spread in tissues. This represents a quantum step forward in the diagnosis and staging of NHL using non-invasively molecular imaging techniques. This novel probe will also be useful to monitor patients response to chemotherapy treatments and other interventions or therapies used in the treatment of NHL. Compounds according to the present invention may be used as diagnostic tools for a number of conditions and diseases states as well as therapeutic agents for treating such conditions and disease states.

Claims (28)

1. A method of diagnosing the existence of a disease state or condition in tissue of a patient in which levels of LFA-1 or ICAM receptors are suspected of being elevated comprising administering to said patient an effective amount of at least one compound according to the following chemical structure:

wherein Y is a —(CH 2 ) n Z— group where n is 4, Z is a NR group and R is H, and which group links the nitrogen of said NR group to a 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA) group and wherein said DOTA group incorporates or complexes with a radioisotope selected from the group consisting of 90 Y, 111 In, 177 Lu, 67 Ga, 68 Ga, and 213 Bi, or a pharmaceutically acceptable salt thereof, measuring the amount of said compound which binds to said tissue in said patient, and comparing said measurement from said measuring step with a standard, wherein an elevated measurement in comparison to said standard is indicative of the existence of said disease state or condition in said patient and said disease state or condition is an inflammatory disease, an autoimmune disease or a hyperproliferative disease, wherein said inflammatory disease is arthritis, rheumatoid arthritis or osteoarthritis, adult respiratory distress syndrome, shock, oxygen toxicity, septic shock, multiple organ injury syndrome secondary to septicemia or multiple organ injury syndrome secondary to trauma, said autoimmune disease is Raynaud's syndrome, autoimmune thyroiditis, dermatitis, multiple sclerosis, insulin-dependent diabetes mellitus, diabetes retinopathy, uveitis, inflammatory bowel disease, Crohn's disease, ulcerative colitis or systemic lupus erythematosus and said hyperproliferative disease is psoriasis, hyperkeratosis, ichthyoisis, keratoderma, lichen planus or warts.

2. The method according to claim 1 wherein X incorporates a radioisotope selected from the group consisting of 90 Y, 111 In, 177 Lu, 225 Ac, 213 Bi, 67 Ga, 68 Ga, 64 Cu, 67 Cu, 71 As, 72 As, 76 As, 77 As, 65 Zn, 76 Br, 48 V, 49 V, 203 Pb, 209 Pb, 212 Pb, 166 Ho, 153 Pm, 201 Tl, 188 Re, 186 Re, 99m Tc or a mixture thereof.

3. The method according to claim 1 wherein said radioisotope is 90 Y, 213 Bi, 177 Lu or 111 In.

4. The method according to claim 1 wherein said radioisotope is 213 Bi, 177 Lu or 111 In.

5. The method according to claim 1 wherein said radioisotope is 213 Bi, 90 Y, or 177 Lu.

6. The method according to claim 1 wherein said radioisotope is 213 Bi.

7. The method according to claim 1 wherein said compound is

or a pharmaceutically acceptable salt thereof.

8. The method according to claim 1 wherein said disease state or condition is arthritis, rheumatoid arthritis or osteoarthritis, adult respiratory distress syndrome, shock, oxygen toxicity, septic shock, multiple organ injury syndrome secondary to septicemia or multiple organ injury syndrome secondary to trauma.

9. The method according to claim 1 wherein said disease state or condition is Raynaud's syndrome, autoimmune thyroiditis, dermatitis, multiple sclerosis, insulin-dependent diabetes mellitus, diabetes retinopathy, uveitis, inflammatory bowel disease, Crohn's disease, ulcerative colitis or systemic lupus erythematosus.

10. The method according to claim 1 wherein said disease state or condition is psoriasis, hyperkeratosis, ichthyoisis, keratoderma, lichen planus or warts.

11. A method of treating an ICAM-1/LFA-1 mediated disease state or condition in a patient in need comprising administering to said patient an effective amount of at least one compound according to the following chemical structure:

wherein Y is a —(CH 2 ) n Z— group where n is 4, Z is a NR group and R is H, and which group links the nitrogen of said NR group to a 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA) group and wherein said DOTA group incorporates or complexes with a radioisotope selected from the group consisting of 90 Y, 111 In, 177 Lu, 67 Ga, 68 Ga, and 213 Bi, or a pharmaceutically acceptable salt thereof, and said disease state or condition is an inflammatory disease, an autoimmune disease or a hyperproliferative disease, wherein said inflammatory disease is arthritis, rheumatoid arthritis or osteoarthritis, adult respiratory distress syndrome, shock, oxygen toxicity, septic shock, multiple organ injury syndrome secondary to septicemia or multiple organ injury syndrome secondary to trauma, said autoimmune disease is Raynaud's syndrome, autoimmune thyroiditis, dermatitis, multiple sclerosis, insulin-dependent diabetes mellitus, diabetes retinopathy, uveitis, inflammatory bowel disease, Crohn's disease, ulcerative colitis or systemic lupus erythematosus and said hyperproliferative disease is psoriasis, hyperkeratosis, ichthyoisis, keratoderma, lichen planus or warts.

12. The method according to claim 11 wherein X incorporates a radioisotope selected from the group consisting of 90 Y, 111 In, 177 Lu, 225 Ac, 213 Bi, 67 Ga, 68 Ga, 64 Cu, 67 Cu, 71 As, 72 As, 76 As, 77 As, 65 Zn, 76 Br, 48 V, 49 V, 203 Pb, 209 Pb, 212 Pb, 166 Ho, 153 Pm, 201 Tl, 188 Re, 186 Re, 99m Tc or a mixture thereof.

13. The method according to claim 11 wherein said radioisotope is 90 Y, 213 Bi, 177 Lu or 111 In.

14. The method according to claim 11 wherein said radioisotope is 213 Bi, 177 Lu or 111 In.

15. The method according to claim 11 wherein said radioisotope is 213 Bi, 90 Y, or 177 Lu.

16. The method according to claim 11 wherein said radioisotope is 213 Bi or 111 In.

17. The method according to claim 11 wherein said radioisotope is 213 Bi or 90 Y.

18. The method according to claim 11 wherein said compound is

or a pharmaceutically acceptable salt thereof.

19. The method according to claim 11 wherein said disease state or condition is arthritis, rheumatoid arthritis or osteoarthritis, adult respiratory distress syndrome, shock, oxygen toxicity, septic shock, multiple organ injury syndrome secondary to septicemia or multiple organ injury'syndrome secondary to trauma.

20. The method according to claim 11 wherein said disease state or condition is Raynaud's syndrome, autoimmune thyroiditis, dermatitis, multiple sclerosis, insulin-dependent diabetes mellitus, diabetes retinopathy, uveitis, inflammatory bowel disease, Crohn's disease, ulcerative colitis or systemic lupus erythematosus.

21. The method according to claim 11 wherein said disease state or condition is psoriasis, hyperkeratosis, ichthyoisis, keratoderma, lichen planus or warts.

22. The method according to claim 13 wherein said disease state or condition is arthritis, rheumatoid arthritis or osteoarthritis, adult respiratory distress syndrome, shock, oxygen toxicity, septic shock, multiple organ injury syndrome secondary to septicemia or multiple organ injury syndrome secondary to trauma.

23. The method according to claim 13 wherein said disease state or condition is Raynaud's syndrome, autoimmune thyroiditis, dermatitis, multiple sclerosis, insulin-dependent diabetes mellitus, diabetes retinopathy, uveitis, inflammatory bowel disease, Crohn's disease, ulcerative colitis or systemic lupus erythematosus.

24. The method according to claim 13 wherein, said disease state or condition is psoriasis, hyperkeratosis, ichthyoisis, keratoderma, lichen planus or warts.

Assignments (3)
CONFIRMATORY LICENSE Recorded Mar 2, 2022
From: UNIVERSITY OF NEW MEXICO
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 059709/0675 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 19, 2012
From: LARSON, RICHARD; NORENBERG, JEFFREY
To: THE REGENTS OF THE UNIVERSITY OF NEW MEXICO C/O RESEARCH & TECHNOLOGY LAW
Reel/Frame 027889/0057 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 19, 2012
From: THE REGENTS OF THE UNIVERSITY OF NEW MEXICO C/O RESEARCH & TECHNOLOGY LAW
To: STC.UNM
Reel/Frame 027889/0077 →
Continuity (3)
Division 11507846 · Aug 22, 2006
Provisional Application 60710665 · Aug 23, 2005
Related Publication 20120070372A1 · Mar 22, 2012