IP Library Granted Patent US 7,125,541
Granted Patent B2
US 7,125,541 · App. 09/738,970 · Granted Oct 24, 2006

Combined methods for tumor vasculature targeting and tumor treatment with radiotherapy

Assignee: The University of Texas System Board of Regents
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Quick Facts
Patent No.
US 7,125,541
App. No.
09/738,970
Granted
Oct 24, 2006
Kind
B2
Abstract

The present invention relates generally to methods and compositions for targeting the vasculature of solid tumors using immunological- and growth factor-based reagents. In particular aspects, antibodies carrying diagnostic or therapeutic agents are targeted to the vasculature of solid tumor masses through recognition of tumor vasculature-associated antigens, such as, for example, through endoglin binding, or through the specific induction of endothelial cell surface antigens on vascular endothelial cells in solid tumors.

Claims (17)

1. A method for treating an animal having a vascularized tumor, comprising:

(a) administering to said animal an amount of a construct effective to treat said vascularized tumor; said construct comprising a selected therapeutic agent linked to a targeting agent that binds to a marker expressed, accessible to binding or localized on the cell surfaces of intratumoral blood vessels of the vascularized tumor; and

(b) treating said animal with radiotherapy.

2. The method of claim 1 , wherein said targeting agent is a monoclonal antibody or monoclonal antibody fragment.

3. The method of claim 2 , wherein said antibody recognizes ELAM-1, VCAM-1, ICAM-1, a ligand reactive with LAM-1 or endoglin.

4. The method of claim 2 , wherein said antibody binds to a growth factor localized on the cell surface of intratumoral blood vessels of a vascularized tumor, wherein said growth factor binds to an intratumoral vasculature cell surface receptor.

5. The method of claim 2 , wherein said antibody binds to a complex of a growth factor and a growth factor receptor present on the surface of intratumoral blood vessels of the vascularized tumor, but that does not bind to the individual growth factor or growth factor receptor.

6. The method of claim 1 , wherein said targeting agent is a growth factor.

7. The method of claim 6 , wherein said targeting agent is a VEGF growth factor.

8. The method of claim 1 , wherein said targeting agent is linked to an anticellular agent capable of killing or suppressing the growth or cell division of endothelial cells.

9. The method of claim 8 , wherein said anticellular agent is a chemotherapeutic agent, radioisotope or cytotoxin.

10. The method of claim 9 , wherein said anticellular agent is a steroid, a cytokine, an antimetabolite, an anthracycline, a vinca alkaloid, an antibiotic, an alkylating agent, an epipodophyllotoxin, a plant-, fungus- or bacteria-derived toxin, an A chain toxin, bacterial endotoxin, the lipid A moiety of bacterial endotoxin, a ribosome inactivating protein, gelonin, α-sarcin, aspergillin, restrictocin, a ribonuclease, diphtheria toxin, Pseudomonas exotoxin, ricin A chain or deglycosylated ricin A chain.

11. The method of claim 1 , wherein the therapeutic agent of said construct is gelonin and the targeting agent of said construct is VEGF.

12. The method of claim 1 , wherein said animal is a human patient.

13. The method of claim 3 , wherein said antibody recognizes ELAM-1.

14. The method of claim 3 , wherein said antibody recognizes VCAM-1.

15. The method of claim 3 , wherein said antibody recognizes endoglin.

Assignments (2)
CONFIRMATORY LICENSE Recorded Feb 4, 2015
From: BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 034894/0765 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 16, 2008
From: THORPE, PHILIP E.; BURROWS, FRANCIS J.
To: BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM
Reel/Frame 021985/0281 →
Continuity (5)
Continuation 0920727700 · Dec 8, 1998
Continuation 0835021200 · Dec 5, 1994
Continuation In Part 0820533000 · Mar 2, 1994
Continuation In Part 0784634900 · Mar 5, 1992
Related Publication 20020037289A1 · Mar 28, 2002