IP Library Granted Patent US 9,365,640
Granted Patent B2
US 9,365,640 · App. 13/459,005 · Granted Jun 14, 2016

Methods for the treatment of cancer and inflammatory diseases using cereblon as a predictor

Inventors: Antonia Lopez-Girona (San Diego, CA); Peter H. Schafer (Somerset, NJ); Anita Gandhi (Bernardsville, NJ); Derek Mendy (San Diego, CA); Thomas O. Daniel (La Jolla, CA)
Assignee: CELGENE CORPORATION
C07K16/18C12Q1/6886G01N33/5743G01N33/57426G01N33/57484C12Q2600/106C12Q2600/156C12Q2600/158G01N21/6428G01N2800/52G01N2800/60
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Quick Facts
Patent No.
US 9,365,640
App. No.
13/459,005
Granted
Jun 14, 2016
Kind
B2
Abstract

Uses of the protein cereblon as a predictor of clinical sensitivity to cancer, inflammatory diseases, and patient response to drug treatment.

Claims (25)

1. A method of selecting the group of cancer patients based on the level of CRBN expression within the cancer, wherein said method comprises:

obtaining a biological sample of the cancer from the patient;

determining whether CRBN is present in the sample, wherein said determining is performed by contacting the cancer with an isolated antibody that immunospecifically binds to an epitope in CRBN, wherein the epitope has the amino acid sequence SEQ ID NO:1, and wherein the antibody comprises: (i) a heavy chain having the amino acid sequence depicted in SEQ ID NO:5 or 9, or (ii) a light chain having the amino acid sequence depicted in SEQ ID NO:7 or 11;

diagnosing the patient as having a drug-sensitive cancer if a higher than baseline level of the CRBN is determined to be present in the sample; and

administering a therapeutically effective amount of the drug to a patient diagnosed as having a drug-sensitive cancer;

wherein the cancer patients are multiple myeloma, non-Hodgkin's lymphoma, diffuse large B-cell lymphoma, melanoma or solid tumor patients; and

wherein the drug is thalidomide, lenalidomide, pomalidomide or 3-(5-amino-2-methyl-4-oxo-4H-quinazolin-3-yl)-piperidine-2,6-dione, a stereoisomer thereof, or a pharmaceutically acceptable salt, solvate, hydrate, co-crystal, clathrate, or polymorph thereof.

2. The method of claim 1 , wherein the antibody is polyclonal.

3. The method of claim 1 , wherein the antibody comprises: a heavy chain having the amino acid sequence depicted in SEQ ID NO:5 or 9.

4. The method of claim 1 , wherein the antibody comprises a light chain having the amino acid sequence depicted in SEQ ID NO:7 or 11.

5. The method of claim 1 , wherein the antibody comprises a heavy chain having the amino acid sequence depicted in SEQ ID NO:5 and a light chain having the amino acid sequence depicted in SEQ ID NO:7.

6. The method of claim 1 , wherein the antibody comprises a heavy chain having the amino acid sequence depicted in SEQ ID NO:9 and a light chain having the amino acid sequence depicted in SEQ ID NO:11.

7. The method of claim 1 , wherein the cancer patients are non-Hodgkin's lymphoma patients.

8. The method of claim 1 , wherein the level of CRBN expression is within the patient's T cells, B cells, or plasma cells of the patient.

9. The method of claim 8 , wherein the cancer patients are multiple myeloma patients.

10. The method of claim 8 , wherein the cancer patients are diffuse large B-cell lymphoma patients.

11. The method of claim 10 , wherein the diffuse large B-cell lymphoma is of the activated B-cell-like subtype.

12. The method of claim 1 , wherein the drug is thalidomide.

13. The method of claim 1 , wherein the drug is a stereoisomer of thalidomide, or a pharmaceutically acceptable salt, solvate, hydrate, co-crystal, clathrate, or polymorph of thalidomide.

14. The method of claim 1 , wherein the drug is pomalidomide.

15. The method of claim 1 , wherein is a stereoisomer of pomalidomide, or a pharmaceutically acceptable salt, solvate, hydrate, co-crystal, clathrate, or polymorph of pomalidomide.

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

17. The method of claim 1 , wherein is a stereoisomer of lenalidomide, or a pharmaceutically acceptable salt, solvate, hydrate, co-crystal, clathrate, or polymorph of lenalidomide.

18. The method of claim 1 , wherein the drug is 3-(5-amino-2-methyl-4-oxo-4H-quinazolin-3-yl)-piperidine-2,6-dione.

19. The method of claim 1 , wherein is a stereoisomer of 3-(5-amino-2-methyl-4-oxo-4H-quinazolin-3-yl)-piperidine-2,6-dione, or a pharmaceutically acceptable salt, solvate, hydrate, co-crystal, clathrate, or polymorph of 3-(5-amino-2-methyl-4-oxo-4H-quinazolin-3-yl)-piperidine-2,6-dione.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 23, 2012
From: LOPEZ-GIRONA, ANTONIA; SCHAFER, PETER H.; GANDHI, ANITA; MENDY, DEREK; DANIEL, THOMAS O.
To: CELGENE CORPORATION
Reel/Frame 028839/0648 →
Continuity (4)
Provisional Application 61481066 · Apr 29, 2011
Provisional Application 61511986 · Jul 26, 2011
Provisional Application 61579600 · Dec 22, 2011
Related Publication 20120322073A1 · Dec 20, 2012