IP Library Granted Patent US 12,215,390
Granted Patent B2
US 12,215,390 · App. 18/056,967 · Granted Feb 4, 2025

Integration of tumor characteristics with breast cancer index

Inventors: Yi Zhang (San Diego, CA); Catherine A. Schnabel (San Diego, CA)
Assignee: BIOTHERANOSTICS, INC.
C12Q1/6886A61K31/337A61K31/513A61K31/675A61K31/704A61K45/06C12Q2600/106C12Q2600/118C12Q2600/158
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,215,390
App. No.
18/056,967
Granted
Feb 4, 2025
Kind
B2
Abstract

Methods of determining risk of recurrence of a breast cancer of a subject are provided. Also provided are methods of predicting responsiveness to a therapy of a breast cancer of a subject. Additionally, methods of recommending treatment for a subject that has breast cancer are provided. Further provided are methods of treating a subject that has breast cancer. Systems for performing described methods are also provided.

Claims (44)

1. A method of treating breast cancer of a subject who is lymph node-positive, the method comprising

(i) determining that the subject has an MGIN+ score above an MGIN+ score cut point by:

assaying or having assayed a sample of breast cancer cells from the subject for the expression levels of BUB1B, CENPA, NEK2, RACGAP1 and RRM2;

summing or having summed the expression levels of BUB1B, CENPA, NEK2, RACGAP1 and RRM2 as a single index into a subject's MGI index;

determining or having determined one or more clinicopathological factor selected from tumor size and grade of the subject's breast cancer;

calculating or having calculated the MGIN+ score of the subject by combining the subject's MGI index with the one or more clinicopathological factor of the subject using a multivariate Cox-proportional model;

comparing or having compared the subject's MGIN+ score to the MGIN+ score cut point, wherein the MGIN+ score cut point has been pre-determined based on the MGIN+ scores calculated for a training set of samples containing breast cancer tissues from patients who had breast cancer recurrence and patients who did not have breast cancer recurrence; and

(ii) treating the subject with an MGIN+ score above the MGIN+ cut point with chemotherapy or endocrine therapy.

2. The method of claim 1 , wherein the subject has previously been treated for breast cancer with chemotherapy.

3. The method of claim 1 , wherein the subject has previously been treated for breast cancer with five years of endocrine therapy.

4. The method of claim 3 , wherein the previous endocrine therapy comprised treatment with tamoxifen or anastrozole.

5. The method of claim 1 , wherein the subject is treated with

(a) endocrine therapy, if the subject has previously been treated for breast cancer, or

(b) paclitaxel with 5-fluorouracil, doxorubicin and cyclophosphamide, if the subject has not previously been treated for breast cancer.

6. The method of claim 5 , wherein the endocrine therapy comprises tamoxifen or anastrozole.

7. The method of claim 1 , wherein combining or having combined the subject's expression levels of BUB1B, CENPA, NEK2, RACGAP1 and RRM2 as a single index into the subject's MGI index uses or has used coefficients determined from a Cox proportional hazards regression, an accelerated failure time model, a parametric survival model, a logistic model, or a linear discriminant analysis.

8. The method of claim 7 , wherein the coefficients are or have been determined from a Cox proportional hazards regression.

9. The method of claim 1 , wherein the patients from the training set with MGIN+ scores below the cut point have minimal 5-year breast cancer recurrence.

10. The method of claim 9 , wherein the recurrence is distant recurrence.

11. The method of claim 9 , wherein the recurrence is local recurrence.

12. The method of claim 1 , wherein the patients from the training set with MGIN+ scores below the cut point have minimal 10-year residual disease.

13. The method of claim 1 , wherein 1 to 3 lymph nodes are positive.

14. The method of claim 1 , wherein the subject's breast cancer is estrogen receptor positive.

15. A method of treating breast cancer of a subject who is lymph node-positive, the method comprising

(i) determining that the subject has an MGIN+ score above 7 by:

assaying or having assayed a sample of breast cancer cells from the subject for the expression levels of BUB1B, CENPA, NEK2, RACGAP1 and RRM2;

summing or having summed the expression levels of BUB1B, CENPA, NEK2, RACGAP1 and RRM2 as a single index into a subject's MGI index;

determining or having determined one or more clinicopathological factor selected from tumor size and grade of the subject's breast cancer;

calculating or having calculated the MGIN+ score of the subject by combining the subject's MGI index with the one or more clinicopathological factor of the subject using a multivariate Cox-proportional model; and

(ii) treating the subject with an MGIN+ score above 7 with chemotherapy or endocrine therapy.

16. The method of claim 15 , wherein the subject is treated with

(a) endocrine therapy, if the subject has previously been treated for breast cancer, or

(b) paclitaxel with 5-fluorouracil, doxorubicin and cyclophosphamide, if the subject has not previously been treated for breast cancer.

17. The method of claim 16 , wherein the endocrine therapy comprises tamoxifen or anastrozole.

18. A method of treating breast cancer of a subject who is lymph node-positive, the method comprising

(i) determining that the subject has an MGIN+score above an MGIN+score cut point by:

assaying or having assayed a sample of breast cancer cells from the subject for the expression levels of BUB1B, CENPA, NEK2, RACGAP1 and RRM2;

summing or having summed the expression levels of BUB1B, CENPA, NEK2, RACGAP1 and RRM2 as a single index into a subject's MGI index;

determining or having determined one or more clinicopathological factor selected from tumor size and grade of the subject's breast cancer;

calculating or having calculated the MGIN+ score of the subject by combining the subject's MGI index with the one or more clinicopathological factor of the subject using a multivariate Cox-proportional model;

comparing or having compared the subject's MGIN+ score to the MGIN+ score cut point, wherein the MGIN+ score cut point has been pre-determined based on the MGIN+ scores calculated for a training set of samples containing breast cancer tissues from patients who were responsive to endocrine therapy and patients who were not responsive to endocrine therapy; and

(ii) treating the subject with an MGIN+ score above the MGIN+ cut point with endocrine therapy.

19. The method of claim 18 , wherein the endocrine therapy comprises tamoxifen or anastrozole.

20. The method of claim 18 , wherein the subject's breast cancer is estrogen receptor positive.

Assignments (5)
RELEASE OF SECURITY INTEREST RECORDED AT REEL/FRAME 065286/0407 Recorded Apr 24, 2026
From: BANK OF AMERICA, N.A., AS COLLATERAL AGENT
To: HOLOGIC, INC.; GEN-PROBE INCORPORATED; FAXITRON BIOPTICS, LLC; BIOTHERANOSTICS, INC.; GEN-PROBE PRODESSE, INC.
Reel/Frame 075457/0767 →
SECURITY INTEREST Recorded Apr 8, 2026
From: BIOTHERANOSTICS, INC.; GEN-PROBE INCORPORATED; GEN-PROBE PRODESSE, INC.; CYTYC CORPORATION; SUROS SURGICAL SYSTEMS, INC.; GYNESONICS, INC.; BOLDER SURGICAL, LLC; FAXITRON BIOPTICS, LLC; HEALTH BEACONS, INC.; HOLOGIC, INC.
To: ROYAL BANK OF CANADA, AS COLLATERAL AGENT
Reel/Frame 075462/0440 →
CHANGE OF ADDRESS Recorded Jun 24, 2024
From: BIOTHERANOSTICS, INC.
To: BIOTHERANOSTICS, INC.
Reel/Frame 067824/0243 →
SECURITY INTEREST Recorded Oct 19, 2023
From: HOLOGIC, INC.; FAXITRON BIOPTICS, LLC; BIOTHERANOSTICS, INC.; GEN-PROBE INCORPORATED; GEN-PROBE PRODESSE, INC.
To: BANK OF AMERICA, N.A., AS COLLATERAL AGENT
Reel/Frame 065286/0407 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 29, 2022
From: ZHANG, YI; SCHNABEL, CATHERINE A.
To: BIOTHERANOSTICS, INC.
Reel/Frame 062233/0962 →