IP Library Patent Application 12593160
Patent Application
App. No. 12/593,160

DETECTION OF ELEVATED LEVELS OF HER-2/NEU PROTEIN FROM NON-ISOLATED CIRCULATING CANCER CELLS AND TREATMENT

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Patent No.
US None
App. No.
12/593,160
Abstract

The expression of Her-2/neu protein on circulating cancer cells in a sample of blood or peripheral blood mononuclear cells (PBMCs) is detected by performing a sensitive Her-2/neu immunoassay. There is no need to isolate the cancer cells before performing the immunoassay. A positive result indicates the expression of Her-2/neu on cancer cells in the blood sample. This method can be used to identify cancer patients who are likely to benefit from treatment with an anticancer agent that targets Her-2/neu, such as trastuzumab (HERCEPTIN), lapatinib, CP-724,714, NKI-272, and BMS-599626

Claims (29)

1 . A method of detecting the expression of Her-2/neu protein on circulating cancer cells in a whole blood sample, comprising performing on the blood sample an immunoassay capable of detecting cancer cell-associated Her-2/neu, in which a positive immunoassay result indicates the presence of Her-2/neu on the cancer cells;

wherein the circulating cancer cells are not isolated from the whole blood prior to the performance of the immunoassay;

and wherein the immunoassay:

a) is capable of detecting Her-2/neu from SK-BR-3 breast cancer cells when spiked into blood at a concentration of less than or equal to 100 SK-

b) BR-3 cells per milliliter of blood; and

is capable of detecting Her-2/neu from 10 SK-BR-3 breast cancer cells when assayed in the presence of at least 1 million human peripheral blood mononuclear cells.

2 . A method of detecting the expression of Her-2/neu protein on circulating cancer cells in a blood sample, comprising performing on the blood sample an immunoassay capable of detecting cancer cell-associated Her-2/neu, in which a positive immunoassay result indicates the presence of Her-2/neu on the cancer cells;

wherein the circulating cancer cells are not isolated from peripheral blood mononuclear cells prior to the performance of the immunoassay;

and wherein the immunoassay:

a) is capable of detecting Her-2/neu from SK-BR-3 breast cancer cells when spiked into blood at a concentration of less than or equal to 100 SK-BR-3 cells per milliliter of blood; and

b) is capable of detecting Her-2/neu from 10 SK-BR-3 breast cancer cells when assayed in the presence of at least 1 million human peripheral blood mononuclear cells.

3 . The method of claim 1 , wherein the immunoassay is a solution-based immunoassay, and said immunoassay uses a technique selected from the group consisting of electrochemiluminescence, chemiluminescence, fluorogenic chemiluminescence, fluorescence polarization, and time-resolved fluorescence, for detection.

4 . (canceled)

5 . The method of claim 1 , wherein the immunoassay is a sandwich immunoassay and said immunoassay uses a technique selected from the group consisting of electrochemiluminescence, chemiluminescence, and fluorogenic chemiluminescence, for detection.

6 . (canceled)

7 . The method of claim 1 , wherein the immunoassay generates a signal proportional to the number of cancer cell-associated Her-2/neu molecules present in the blood sample.

8 - 11 . (canceled)

12 . The method of claim 1 , wherein the immunoassay uses a monoclonal antibody against Her-2/neu.

13 . The method of claim 12 , wherein the immunoassay uses a secondary antibody against said monoclonal antibody.

14 . The method of claim 12 , wherein the monoclonal antibody is a humanized mouse monoclonal antibody.

15 . The method of claim 14 , wherein the monoclonal antibody is trastuzumab.

16 - 25 . (canceled)

26 . The method of claim 2 , wherein the immunoassay is a solution-based immunoassay, and said immunoassay uses a technique selected from the group consisting of electrochemiluminescence, chemiluminescence, fluorogenic chemiluminescence, fluorescence polarization, and time-resolved fluorescence, for detection.

27 . The method of claim 2 , wherein the immunoassay is a sandwich immunoassay and said immunoassay uses a technique selected from the group consisting of electrochemiluminescence, chemiluminescence, and fluorogenic chemiluminescence, for detection.

28 . The method of claim 2 , wherein the immunoassay generates a signal proportional to the number of cancer cell-associated Her-2/neu molecules present in the blood sample.

29 . The method of claim 2 , wherein the immunoassay uses a monoclonal antibody against Her-2/neu.

30 . The method of claim 29 , wherein the immunoassay uses a secondary antibody against said monoclonal antibody.

31 . The method of claim 29 , wherein the monoclonal antibody is a humanized mouse monoclonal antibody.

32 . The method of claim 31 , wherein the monoclonal antibody is trastuzumab.

Assignments (3)
RELEASE OF SECURITY INTEREST Recorded Jan 21, 2021
From: WHITE OAK GLOBAL ADVISORS, LLC, AS ADMINISTRATIVE AGENT
To: WELLSTAT BIOLOGICS CORPORATION
Reel/Frame 055060/0338 →
SECURITY AGREEMENT Recorded Sep 17, 2013
From: WELLSTAT BIOLOGICS CORPORATION
To: PDL BIOPHARMA, INC.
Reel/Frame 031288/0530 →
SECURITY AGREEMENT Recorded Aug 15, 2013
From: WELLSTAT BIOLOGICS CORPORATION
To: WHITE OAK GLOBAL ADVISORS, LLC, AS ADMINISTRATIVE AGENT
Reel/Frame 031029/0801 →