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Evaluation of PSMA in HER2- AR+ Metastatic Breast Cancer

Primary Purpose

Breast Cancer, HER2-negative Breast Cancer, Metastatic Breast Cancer

Status
Recruiting
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
18F-DCFPyL
Sponsored by
University of Wisconsin, Madison
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Breast Cancer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients diagnosed with metastatic HER2-negative breast cancer AR expression of ≥ 10%

Exclusion Criteria:

  • Other (non-breast) known active malignancy. Participants with previously treated cancers which are in remission or have no evidence of disease are eligible.
  • Unable to lie flat during or tolerate PET/CT
  • Participants with any medical condition or other circumstances that, in the opinion of the investigator, compromise the safety or compliance of the subject to produce reliable data or completing the study
  • Women of childbearing potential must not be pregnant or breast feeding (pregnancy test negative within 7 days prior to PET/CT

Sites / Locations

  • University of Wisconsin School of Medicine and Public HealthRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

18F-DCFPyL PSMA-based PET/CT

Arm Description

18F-DCFPyL whole body PET/CT scan Review of relevant imaging and medical record information Blood draw for circulating tumor cells (CTCs) Analysis of diagnostic tissue specimens

Outcomes

Primary Outcome Measures

PSMA Expression as measured by 18F-DCFPyL SUV
Quantitative analysis of 18F-DCFPyL PSMA PET uptake will be performed at the lesion-level. Standardized uptake values (SUV) will be measured by manually drawing a region of interest (ROI) to encompass the entire lesion guided by the lesion extent visualized on conventional imaging. PET SUV based quantitative tumor uptake parameters will be obtained.

Secondary Outcome Measures

Expression of PSMA in CTCs
Expression of PSMA in CTCs will be measured via immunofluorescence.
Expression of PSMA in diagnostic metastatic tissue
PSMA expression in tumors will be semi-quantitatively scored by a study pathologist using published methods including separate assessment of tumor-associated and non-tumor vasculature, with the endothelium highlighted by a CD31 immunostain to facilitate definitive recognition.
Change in PSMA Expression on CTCs after 2 weeks of bicalutamide
The change in PSMA expression on CTCs will be measured pre and post treatment via immunofluorescence.

Full Information

First Posted
September 28, 2020
Last Updated
September 14, 2023
Sponsor
University of Wisconsin, Madison
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1. Study Identification

Unique Protocol Identification Number
NCT04573231
Brief Title
Evaluation of PSMA in HER2- AR+ Metastatic Breast Cancer
Official Title
Evaluation of Prostate Specific Membrane Antigen (PSMA) in HER2-negative, Androgen Receptor (AR)-Positive Metastatic Breast Cancer With 18F-DCFPyL PSMA-based PET/CT
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 24, 2021 (Actual)
Primary Completion Date
November 2025 (Anticipated)
Study Completion Date
November 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Wisconsin, Madison

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this research is to determine the expression of prostate specific membrane antigen (PSMA) in human epidermal growth factor receptor 2 (HER2)-negative, androgen receptor (AR)-positive metastatic breast cancer, and to determine its role in resistance to the anti-androgen, bicalutamide. The investigators hypothesize that PSMA expression will correlate with resistance to anti-androgen therapies, as has been documented in prostate cancer, and this can be used to select patients most likely to benefit from these therapies in future clinical trials. 15 people with HER2-negative, AR-positive metastatic breast cancer will be enrolled and be on study for about 3 days.
Detailed Description
Primary Objective: To evaluate the expression of PSMA via 18F-DCFPyL PSMA-based PET/CT in patients with metastatic HER2-negative, AR-positive breast cancer. Expression of PSMA will be quantified using PSMA-based PET imaging using a novel agent, 18F-DCFPyL, as a non-invasive imaging biomarker of tumor neovasculature in HER2-negative, AR-positive metastatic breast cancer. Secondary Objectives: PSMA PET will be compared with the expression of PSMA in CTCs and diagnostic metastatic tissue from patients with HER2-negative, AR-positive metastatic breast cancer. PSMA expression will be correlated with clinical benefit (objective response and progression-free survival) to bicalutamide and ribociclib for patients enrolled in NCT03090165.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer, HER2-negative Breast Cancer, Metastatic Breast Cancer

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Model Description
Phase 2, single-center, open-label study
Masking
None (Open Label)
Allocation
N/A
Enrollment
15 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
18F-DCFPyL PSMA-based PET/CT
Arm Type
Experimental
Arm Description
18F-DCFPyL whole body PET/CT scan Review of relevant imaging and medical record information Blood draw for circulating tumor cells (CTCs) Analysis of diagnostic tissue specimens
Intervention Type
Drug
Intervention Name(s)
18F-DCFPyL
Intervention Description
PSMA is highly expressed on prostate cancer and is associated with metastasis and resistance to anti-androgen therapies. Researchers have evaluated the expression of PSMA in the tumor and tumor-associated neovasculature in primary tumors and distant metastases in patients with breast cancer.
Primary Outcome Measure Information:
Title
PSMA Expression as measured by 18F-DCFPyL SUV
Description
Quantitative analysis of 18F-DCFPyL PSMA PET uptake will be performed at the lesion-level. Standardized uptake values (SUV) will be measured by manually drawing a region of interest (ROI) to encompass the entire lesion guided by the lesion extent visualized on conventional imaging. PET SUV based quantitative tumor uptake parameters will be obtained.
Time Frame
up to 3 days
Secondary Outcome Measure Information:
Title
Expression of PSMA in CTCs
Description
Expression of PSMA in CTCs will be measured via immunofluorescence.
Time Frame
up to 2 weeks
Title
Expression of PSMA in diagnostic metastatic tissue
Description
PSMA expression in tumors will be semi-quantitatively scored by a study pathologist using published methods including separate assessment of tumor-associated and non-tumor vasculature, with the endothelium highlighted by a CD31 immunostain to facilitate definitive recognition.
Time Frame
up to 3 days
Title
Change in PSMA Expression on CTCs after 2 weeks of bicalutamide
Description
The change in PSMA expression on CTCs will be measured pre and post treatment via immunofluorescence.
Time Frame
baseline and up to 2 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients diagnosed with metastatic HER2-negative breast cancer AR expression of ≥ 10% Exclusion Criteria: Other (non-breast) known active malignancy. Participants with previously treated cancers which are in remission or have no evidence of disease are eligible. Unable to lie flat during or tolerate PET/CT Participants with any medical condition or other circumstances that, in the opinion of the investigator, compromise the safety or compliance of the subject to produce reliable data or completing the study Women of childbearing potential must not be pregnant or breast feeding (pregnancy test negative within 7 days prior to PET/CT
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Gemma Gliori
Phone
608-262-7269
Email
radstudy@uwhealth.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Steve Y Cho, MD
Organizational Affiliation
University of Wisconsin, Madison
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Wisconsin School of Medicine and Public Health
City
Madison
State/Province
Wisconsin
ZIP/Postal Code
53705
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gemma Gliori
Phone
608-262-7269
Email
ggliori@uwhealth.org

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Evaluation of PSMA in HER2- AR+ Metastatic Breast Cancer

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