Intraoperative and endoscopic tumor detection and therapy

• US 4,932,412 A
• Filed: 12/18/1986
• Issued: 06/12/1990
• Est. Priority Date: 12/18/1986
• Status: Expired due to Term

• Current Assignee: Immunomedics, Inc.
• Original Assignee: Immunomedics, Inc.
• Inventors: Goldenberg, Milton D.
• Primary Examiner(s): NOT, DEFINED
• Assistant Examiner(s): Rose, Sharon
• Application Number:
  US06/943,561
• Time in Patent Office: 1,272 Days
• Field of Search: 128/1.1, 128/630, 128/631, 128/654, 128/659, 424/1.1, 424/4, 424/9
• US Class Current: 600/431
• CPC Class Codes: A61B 6/4258 for detecting non x-ray radiation, e.g. gamma radiation A61B6/037 takes precedence
• CPC Class Codes: A61K 2123/00 Preparations for testing in vivo
• CPC Class Codes: A61K 51/1045 against animal or human tumor cells or tumor cell determinants

Abstract

Methods are provided for short-range intraoperative and endoscopic detection and therapy of tumors using radiolabeled antibodies and, in some cases, techniques for reducing or correcting for non-specific background radiation to improve resolution. Therapy using external radiation and/or laser or mechanical endoscopically introduced tumor removal means can be combined with the detection methods to increase precision of the tumor removal operations.

Claims

1. In a method for short-range intraoperative detection of a tumor, wherein a surgical patient is injected parenterally with a radiolabeled primary antibody which specifically binds a marker produced by or associated with a tumor, the surgically exposed interior of a body cavity of said patient is scanned at close range with a radiation detection probe, and the sites of accretion of said labeled antibody are located by detecting elevated levels of radiation at said sites with said probe,

the improvement comprising compensating for or reducing non-target background radiation by injecting said patient parenterally, either concurrently or sequentially, with:

(a) a contrast or subtraction agent radiolabeled with a radioisotope emitting at an energy which is separately detectable from the primary antibody label using a radiation detection probe;

radiation detected from emission of the contrast or subtraction agent being used to better define the tumor, wherein;

(i) said contrast or subtraction agent comprises an organ, blood pool or interstitial fluid non-tumor-specific contrast agent, and the resultant diffuse distribution of the contrast agent is used to define the organ, blood pool or interstitial region, whereby foci of labeled primary antibody activity are enhanced and better discriminated against a background of reduced diffuse contrast agent label activity;

or

(ii) said contrast or subtraction agent is a dual isotope correction agent comprising irrelevant immunoglobulin from the same or different species as that used to prepare the primary antibody, the irrelevant immunoglobulin being so labeled that the kinetics and distribution of the radiolabeled primary antibody and irrelevant immunoglobulin in the patient are substantially the same during the time period required for scanning; and

wherein the ratio of primary antibody label activity to irrelevant immunoglobulin label activity at a selected site is compared to said ratio at a known non-tumor site, whereby an elevated level of primary antibody label accretion due to antigen-antibody complex formation at said selected site can be discriminated;

(b) unlabeled second antibody which specifically binds the primary antibody or the labeling moiety thereof, the second antibody being injected at a time after the injection of the primary antibody sufficient to permit specific uptake of the primary antibody by a tumor in the body cavity, and in an amount sufficent to reduce the circulating level of the primary antibody label by at least about 10-85%, or to increase the localization ratio of the labeled primary antibody by at least about 20%, within about 2-72 hours following injection of the second antibody, whereby background levels of nonspecifically distributed primary antibody and/or label are reduced in the body cavity, and the sites of accretion of labeled primary antibody as well as the level of specific uptake thereof are more effectively discriminated.

2. The method of claim 1, wherein said improvement comprises injecting said patient parenterally, either concurrently or sequentially, with a contrast agent radiolabeled with a radioisotope emitting at an energy which is separately detectable from the primary antibody label using a radiation detection probe;

radiation detected from emission of the contrast agent being used to better define the tumor, and wherein said contrast agent comprises an organ, blood pool or interstitial fluid non-tumor-specific contrast agent, and the resultant diffuse distribution of the contrast agent is used to define the organ, blood pool or interstitial region, whereby foci of labeled primary antibody activity are enhanced and better discriminated against a background of reduced diffuse contrast agent label activity.

3. The method of claim 2, wherein said contrast agent comprises at least one of a radiocolloid, a radiolabeled liposome, a radiolabeled soluble salt, a radiolabeled soluble protein or a radiolabeled blood cell.

4. The method of claim 1, wherein said improvement comprises injecting said patient parenterally, either concurrently or sequentially, with a subtraction agent radiolabeled with a radioisotope emitting at an energy which is separately detectable from the primary antibody label using a radiation detection probe;

radiation detected from emission of the subtraction agent being used to better define the tumor, and wherein said subtraction agent is a dual isotope correction agent comprising irrelevant immunoglobulin from the same or different species as that used to prepare the primary antibody, the irrelevant immunoglobulin being so labeled that the kinetics and distribution of the radiolabeled primary antibody and irrelevant immunoglobulin in the patient are substantially the same during the time period required for scanning; and

wherein the ratio of primary antibody label activity to irrelevant immunoglobulin label activity at a selected site is compared to said ratio at a known non-tumor site, whereby an elevated level of primary antibody label accretion due to antigen-antibody complex formation at said selected site can be discriminated.

5. The method of claim 1, wherein said improvement comprises injecting said patient parenterally, either concurrently or sequentially, with unlabeled second antibody which specifically binds the primary antibody or the labeling moiety thereof, the second antibody being injected at a time after the injection of the primary antibody sufficient to permit specific uptake of the primary antibody by a tumor in the body cavity, and in an amount sufficent to reduce the circulating level of the primary antibody label by at least about 10-85%, or to increase the localization ratio of the labeled primary antibody by at least about 20%, within about 2-72 hours following injection of the second antibody, whereby background levels of nonspecifically distributed primary antibody and/or label are reduced in the body cavity, and the sites of accretion of labeled primary antibody as well as the level of specific uptake thereof are more effectively discriminated.

6. The method of claim 5, wherein a blood sample is taken at periodic intervals after injection of said second antibody, the level of circulating primary antibody label activity in the blood is determined for each sample, and the time for surgery is optimized by selecting a time when the level of circulating primary antibody label activity is reduced by at least about 85%.

16. The method of claim 2, wherein said contrast agent is a radiolabeled organ- or tissue-specific antibody.

7. A method for short-range endoscopic tumor detection, comprising injecting an endoscopy patient parenterally with a radiolabeled primary antibody which specifically binds a marker produced by or associated with a tumor, scanning the endoscopically accessed interior of a body cavity of said patient at close range with a radiation detection probe, and locating the sites of accretion of said labeled antibody by detecting elevated levels of radiation at said sites with said probe.

8. The method of claim 7, which further comprises compensating for or reducing non-target background radiation by injecting said patient parenterally, either concurrently or sequentially, with:

(a) a contrast or subtraction agent radiolabeled with a radioisotope emitting at an energy which is separately detectable from the primary antibody label using a radiation detection probe;

the radiation detected from emission of the contrast or subtraction agent being used to better define the tumor, wherein;

(i) said contrast or subtraction agent comprises an organ, blood pool or interstitial fluid non-tumor-specific contrast agent, and the resultant diffuse distribution of the contrast agent is used to define the organ, blood pool or interstitial region, whereby foci of labeled primary antibody activity are enhanced and better discriminated against a background of reduced diffuse contrast agent label activity;

or

(ii) said contrast or subtraction agent is a dual isotope correction agent comprising irrelevant immunoglobulin from the same or different species as that used to prepare the primary antibody, the irrelevant immunoglobulin being so labeled that the kinetics and distribution of the radiolabeled primary antibody and irrelevant immunoglobulin in the patient are substantially the same during the time period required for scanning; and

wherein the ratio of primary antibody label activity to irrelevant immunoglobulin label activity at a selected site is compared to said ratio at a known non-tumor site, whereby an elevated level of primary antibody label accretion due to antigen-antibody complex formation at said selected site can be discriminated;

or

(b) unlabeled second antibody which specifically binds the primary antibody or the labeling moiety thereof, the second antibody being injected at a time after the injection of the primary antibody sufficient to permit specific uptake of the primary antibody by a tumor in the body cavity, and in an amount sufficient to reduce the circulating level of the primary antibody label by at least about 10-85%, or to increase the localization ratio of the labeled primary antibody by at least about 20%, within about 2-72 hours following injection of the second antibody, whereby background levels of nonspecifically distributed primary antibody and/or label are reduced in the body cavity, and the sites of accretion of labeled primary antibody as well as the level of specific uptake thereof are more effectively discriminated.

9. The method of claim 7, wherein a laser is used to remove tumor tissue at sites of elevated primary antibody label accretion.

10. The method of claim 8, wherein a laser is used to remove tumor tissue at sites of elevated primary antibody label accretion.

11. The method of claim 7, which further comprises injecting said patient parenterally, either concurrently or sequentially, with a contrast agent radiolabeled with a radioisotope emitting at an energy which is separately detectable from the primary antibody label using a radiation detection probe;

radiation detected from emission of the contrast agent being used to better define the tumor, and wherein said contrast agent comprises an organ, blood pool or interstitial fluid non-tumor-specific contrast agent, and the resultant diffuse distribution of the contrast agent is used to define the organ, blood pool or interstitial region, whereby foci of labeled primary antibody activity are enhanced and better discriminated against a background of reduced diffuse contrast agent label activity.

12. The method of claim 11, wherein said contrast agent comprises at least one of a radiocolloid, a radiolabeled liposome, a radiolabeled soluble salt, a radiolabeled soluble protein or a radiolabeled blood cell.

13. The method of claim 7, which further comprises injecting said patient parenterally, either concurrently or sequentially, with a subtraction agent radiolabeled with a radioisotope emitting at an energy which is separately detectable from the primary antibody label using a radiation detection probe;

radiation detected from emission of the subtraction agent being used to better define the tumor, and wherein said subtraction agent is a dual isotope correction agent comprising irrelevant immunoglobulin from the same or different species as that used to prepare the primary antibody, the irrelevant immunoglobulin being so labeled that the kinetics and distribution of the radiolabeled primary antibody and irrelevant immunoglobulin in the patient are substantially the same during the time period required for scanning; and

wherein the ratio of primary antibody label activity to irrelevant immunoglobulin label activity at a selected site is compared to said ratio at a known non-tumor site, whereby an elevated level of primary antibody label accretion due to antigen-antibody complex formation at said selected site can be discriminated.

14. The method of claim 7, which further comprises injecting said patient parenterally, either concurrently or sequentially, with unlabeled second antibody which specifically binds the primary antibody or the labeling moiety thereof, the second antibody being injected at a time after the injection of the primary antibody sufficient to permit specific uptake of the primary antibody by a tumor in the body cavity, and in an amount sufficent to reduce the circulating level of the primary antibody label by at least about 10-85%, or to increase the localization ratio of the labeled primary antibody by at least about 20%, within about 2-72 hours following injection of the second antibody, whereby background levels of nonspecifically distributed primary antibody and/or label are reduced in the body cavity, and the sites of accretion of labeled primary antibody as well as the level of specific uptake thereof are more effectively discriminated.

15. The method of claim 14, wherein a blood sample is taken at periodic intervals after injection of said second antibody, the level of circulating primary antibody label activity in the blood is determined for each sample, and the time for surgery is optimized by selecting a time when the level of circulating primary antibody label activity is reduced by at least about 85%.

17. The method of claim 11, wherein said contrast agent is a radiolabeled organ- or tissue-specific antibody.