IP Library Granted Patent US 10,105,090
Granted Patent B2
US 10,105,090 · App. 15/783,723 · Granted Oct 23, 2018

Method for representations of network-dependent features of the hemoglobin signal in living tissues for detection of breast cancer and other applications

Inventors: Randall L. Barbour (Glen Head, NY); Harry L. Graber (New York, NY); San-Lian S. Barbour (Glen Head, NY)
Assignees: Photon Migration Technologies Corp.; SLB Innovations Group, LLC
A61B5/4312A61B5/14546A61B5/14552A61B5/7225A61B5/7282A61B2562/0233A61B2576/02
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Quick Facts
Patent No.
US 10,105,090
App. No.
15/783,723
Granted
Oct 23, 2018
Kind
B2
Abstract

A non-invasive method of detecting anomalous tissue, such as cancerous or injured tissue, in a patient. At least two hemoglobin signal components of hemoglobin levels in at least one segment of tissue of the patient are non-invasively measured over time. Time varying changes of at least a first of the hemoglobin signal components are measured with respect to at least time varying changes of a second of the hemoglobin signal components. A co-varying coordinate system of the time varying changes is generated. Any anomalous tissue in the measured segment of tissue is detected from a signature of the measured segment of tissue in the co-varying coordinate system which differs from a signature of non-anomalous tissue in the co-varying coordinate system. Preferably, five hemoglobin signal components are measured: oxyHb, deoxyHb, total Hb (totalHb=oxyHb+deoxy Hb), Hb oxygen saturation (HbO 2 Sat=(oxyHb/totalHb)*100), and tissue-hemoglobin oxygen exchange HbO 2 Exc (deoxyHb−oxyHb).

Claims (44)

1. A non-invasive method of detecting breast cancer in a patient via time series measures of the hemoglobin signal, acquired under conditions of a substantially resting state, from at least one breast by comparing the values of coefficients obtained from a functional finite-state transition network representation of said signal, comprising the steps of:

non-invasively measuring at least two measured hemoglobin signal components of hemoglobin levels in at least one breast of the patient in a substantially resting state over time, the at least two measured hemoglobin signal components comprising oxygenated hemoglobin and deoxygenated hemoglobin;

transforming the measured hemoglobin signal components to yield relative changes in the levels of oxygenated and deoxygenated forms of hemoglobin and to compute at least three derived hemoglobin signal components;

specifying a multiaxis representation of the two measured hemoglobin signal components and the three derived hemoglobin signal components and determining the algebraic sign of each hemoglobin signal component based on their measured relative amplitudes;

defining the composite of these algebraic sign assignments as a hemoglobin state, of which ten such composites are uniquely defined;

determining when in time at least one hemoglobin signal component undergoes a change in its algebraic sign and identifying such occurrence as a State transition;

computing coefficient values for at least one of i) State transition rates, ii) State transition probabilities from the tabulation of unique transition types, or iii) State-dependent component flux of a given State; and

detecting any cancerous tissue in the measured breast from a signature of said State transitions of the measured breast which differs from a signature of State transitions of non-cancerous tissue.

2. A non-invasive method of detecting breast cancer in a patient according to claim 1 , wherein said at least two measured hemoglobin signal components comprise oxyHb and deoxyHb, and wherein said at least three derived hemoglobin signal components comprise total Hb (totalHb=oxyHb+deoxy Hb), Hb oxygen saturation (HbO 2 Sat=(oxyHb/totalHb)*100), and tissue-hemoglobin oxygen exchange (HbO 2 Exc=deoxyHb−oxyHb).

3. A non-invasive method of detecting breast cancer in a patient according to claim 1 , wherein said first measuring step further comprises the step of measuring the tissue optically.

4. A non-invasive method of detecting breast cancer in a patient according to claim 3 , wherein said optical measuring step further comprises the steps of:

illuminating the breast with light; and

measuring at least one of diffusely transmitted or back-reflected light from the breast.

5. A non-invasive method of detecting breast cancer in a patient according to claim 1 , wherein said first measuring step further comprises the step of measuring the tissue at least one of photoacoustically, holographically, via structured illumination, or via OCT.

6. A non-invasive method of detecting anomalous tissue in a patient via time series measures of the hemoglobin signal, acquired under conditions of a substantially resting state, by comparing the values of coefficients obtained from a functional finite-state transition network representation of said signal, comprising the steps of:

non-invasively measuring at least two measured hemoglobin signal components of hemoglobin levels in at least one segment of tissue of the patient in a substantially resting state over time, the at least two measured hemoglobin signal components comprising oxygenated hemoglobin and deoxygenated hemoglobin;

transforming the measured hemoglobin signal components to yield relative changes in the levels of oxygenated and deoxygenated forms of hemoglobin and to compute at least three derived hemoglobin signal components;

specifying a multiaxis representation of the two measured hemoglobin signal components and the three derived hemoglobin signal components and determining the algebraic sign of each hemoglobin signal component based on their measured relative amplitudes;

defining the composite of these algebraic sign assignments as a hemoglobin state, of which ten such composites are uniquely defined;

determining when in time at least one hemoglobin signal component undergoes a change in its algebraic sign and identifying such occurrence as a State transition;

computing coefficient values for at least one of i) State transition rates, ii) State transition probabilities from the tabulation of unique transition types, or iii) State-dependent component flux of a given State; and

detecting any anomalous tissue in the measured segment of tissue from a signature of said State transitions of the measured segment of tissue which differs from a signature of State transitions of non-anomalous tissue.

7. A non-invasive method of detecting anomalous tissue in a patient according to claim 6 , wherein said at least two measured hemoglobin signal components comprise oxyHb and deoxyHb, and wherein said at least three derived hemoglobin signal components comprise total Hb (totalHb=oxyHb+deoxy Hb), Hb oxygen saturation (HbO 2 Sat=(oxyHb/totalHb)*100), and tissue-hemoglobin oxygen exchange (HbO 2 Exc=deoxyHb−oxyHb).

8. A non-invasive method of detecting anomalous tissue in a patient according to claim 6 , wherein said first measuring step further comprises the step of measuring the tissue optically.

9. A non-invasive method of detecting anomalous tissue in a patient according to claim 8 , wherein said optical measuring step further comprises the steps of:

illuminating the segment of tissue with light; and

measuring at least one of diffusely transmitted or back-reflected light from the segment of tissue.

10. A non-invasive method of detecting anomalous tissue in a patient according to claim 6 , wherein the anomalous tissue to be detected comprises at least one of cancerous tissue or injured tissue.

11. A non-invasive method of detecting anomalous tissue in a patient according to claim 6 , wherein said first measuring step further comprises the step of measuring the tissue at least one of photoacoustically, holographically, via structured illumination, or via OCT.

12. A non-invasive method of detecting changes in tissue in a living subject in response to physical and/or chemical stimuli patient via time series measures of the hemoglobin signal, acquired under conditions of a substantially resting state, by comparing the values of coefficients obtained from a functional finite-state transition network representation of said signal, comprising the steps of:

applying at least one physical or chemical stimulus to the living subject;

non-invasively measuring at least two hemoglobin signal components of hemoglobin levels in at least one segment of tissue of the living subject in a substantially resting state over time, the at least two measured hemoglobin signal components comprising oxygenated hemoglobin and deoxygenated hemoglobin;

transforming the measured hemoglobin signal components to yield relative changes in the levels of oxygenated and deoxygenated forms of hemoglobin and to compute at least three derived hemoglobin signal components;

specifying a multiaxis representation of the two measured hemoglobin signal components and the three derived hemoglobin signal components and determining the algebraic sign of each hemoglobin signal component based on their measured relative amplitudes;

defining the composite of these algebraic sign assignments as a hemoglobin state, of which ten such composites are uniquely defined;

determining when in time at least one hemoglobin signal component undergoes a change in its algebraic sign and identifying such occurrence as a State transition;

computing coefficient values for at least one of i) State transition rates, ii) State transition probabilities from the tabulation of unique transition types, or iii) State-dependent component flux of a given State; and

detecting any changes in the measured segment of tissue from a signature of said State transitions of the measured segment of tissue after the at least one stimulus is applied with respect to a signature of State transitions of the measured segment of tissue before the at least one stimulus is applied.

13. A non-invasive method of detecting changes in tissue in a living subject in response to physical and/or chemical stimuli according to claim 12 , wherein said at least two measured hemoglobin signal components comprise oxyHb and deoxyHb, and wherein said at least three derived hemoglobin signal components comprise total Hb (totalHb=oxyHb+deoxy Hb), Hb oxygen saturation (HbO 2 Sat=(oxyHb/totalHb)*100), and tissue-hemoglobin oxygen exchange (HbO 2 Exc=deoxyHb−oxyHb).

14. A non-invasive method of detecting changes in tissue in a living subject in response to physical and/or chemical stimuli according to claim 12 , wherein said first measuring step further comprises the step of measuring the tissue optically.

15. A non-invasive method of detecting changes in tissue in a living subject in response to physical and/or chemical stimuli according to claim 14 , wherein said optical measuring step further comprises the steps of:

illuminating the segment of tissue with light; and

measuring at least one of diffusely transmitted or back-reflected light from the segment of tissue.

16. A non-invasive method of detecting changes in tissue in a living subject in response to physical and/or chemical stimuli according to claim 12 , wherein said first measuring step further comprises the step of measuring the tissue at least one of photoacoustically, holographically, via structured illumination, or via OCT.

Assignments (4)
CORRECTIVE ASSIGNMENT TO CORRECT THE NATURE OF CONVEYANCE, ASSIGNMENT DOCUMENTATION RECEIVING PARTY DATA AND CONVEYING PARTY DATA PREVIOUSLY RECORDED ON REEL 70774 FRAME 721. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Jul 2, 2025
From: SLB INNOVATIONS GROUP, LLC
To: SLB INSPIRATIONS LTD
Reel/Frame 071942/0538 →
CHANGE OF NAME Recorded Apr 8, 2025
From: PHOTON MIGRATION TECHNOLOGIES CORP; SLB INNOVATIONS GROUP LLC
To: SLB INSPIRATIONS LTD
Reel/Frame 070774/0721 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 25, 2025
From: PHOTON MIGRATION TECHNOLOGIES CORP.
To: SLB INNOVATIONS GROUP, LLC
Reel/Frame 070322/0224 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 18, 2017
From: BARBOUR, RANDALL L.; GRABER, HARRY L.; BARBOUR, SAN-LIAN S.
To: PHOTON MIGRATION TECHNOLOGIES CORP.; SLB INNOVATIONS GROUP, LLC
Reel/Frame 044365/0708 →
Continuity (2)
Provisional Application 62407883 · Oct 13, 2016
Related Publication 20180110458A1 · Apr 26, 2018
Cited By (1)
US 12,310,726