Imaging of Solid Tumors Using FAP-2286

• ClinicalTrials.gov Identifier: NCT04621435
• Recruitment Status: Recruiting
• First Posted: November 9, 2020
• Last Update Posted: August 4, 2022
• Sponsor: Thomas Hope
• Collaborator: Clovis Oncology, Inc.
• Information provided by (Responsible Party): Thomas Hope, University of California, San Francisco

Study Description

Brief Summary:

This is a multi-arm prospective trial that evaluates the ability of a novel imaging radiolabeled agents to detect metastatic cancer in participants with solid tumors using a gallium 68 (68Ga-) or copper 64 (64Cu-) FAP-2286 tracer. FAP-2286 is a peptidomimetic molecule that that binds to Fibroblast Activation Protein (FAP). FAP is a transmembrane protein expressed on cancer-associated fibroblasts, and has been shown to be present on a number of solid tumors.

Condition or disease	Intervention/treatment	Phase
Solid Tumors, Adult; Metastatic Cancer	Drug: Gallium-68 labelled (68Ga-) FAP-2286; Procedure: Positron Emission Tomography (PET) imaging; Drug: Copper-64 labeled (64Cu-) FAP-2286	Phase 1

Detailed Description:

Initially the investigator(s) will focus on imaging breast, pancreas, sarcoma, prostate cancer, bladder cancer, colon cancer, and head and neck cancer.

STUDY AIMS

1. Determine the dosimetry for gallium-68 labelled (68Ga-) and 64Cu- FAP-2286.
2. Evaluate the uptake and retention of radiotracer in a variety of solid tumors with FAP-2286.
3. Evaluate the ability of FAP-2286 to detect metastatic disease.

PRIMARY OBJECTIVES

1. All cohorts: Safety of 68Ga- and 64Cu-FAP-2286.
2. Cohort 1a: determine the organ dosimetry of 68Ga-FAP-2286.
3. Cohort 1b: determine the organ dosimetry of 64Cu-FAP-2286.
4. Cohort 2: To assess the feasibility of detecting tumor uptake using FAP-2286.
5. Cohort 3: To determine the feasibility of detecting metastatic disease using FAP-2286.

EXPLORATORY OBJECTIVES

1. To detect the sensitivity of FAP-2286 PET compared to conventional imaging for the detection of metastatic disease, and when available sensitivity compared to Fluorodeoxyglucose (FDG) PET (FDG-PET).
2. Correlation of FAP-2286 uptake with FAP expression determined by immunohistochemistry.
3. Compare biodistribution of 68Ga-FAP-2286 and 64Cu-FAP-2286 in normal organs and blood pool based on renal function.
4. Determine impact of administered dose of FAP-2286 on image quality.
5. Compare the feasibility of detecting tumor uptake using 68Ga-FAP-2286 and 64Cu-FAP-2286

A repeat radiolabeled FAP-2286 PET may be obtained after initiation of subsequent treatment in order to evaluate changes in PET uptake due to treatment effect. Patients will be followed for up to 3 days after the injection of radiolabeled ligand for evaluation of adverse events.

Study Design

• Study Type: Interventional (Clinical Trial)
• Estimated Enrollment: 86 participants
• Allocation: Non-Randomized
• Intervention Model: Parallel Assignment
• Masking: None (Open Label)
• Primary Purpose: Diagnostic
• Official Title: Imaging of Solid Tumors Using FAP-2286
• Actual Study Start Date: December 14, 2020
• Estimated Primary Completion Date: June 30, 2023
• Estimated Study Completion Date: June 30, 2023

Arms and Interventions

Arm	Intervention/treatment
Experimental: 68Ga-Dosimetry population (Cohort 1a); PET imaging will begin 30 +/-10 minutes, 60 +/-15 minutes and 120 +/-20 minutes after injection of 68Ga-FAP-2286. Contrast may be administered if clinically indicated.	Drug: Gallium-68 labelled (68Ga-) FAP-2286; The dose will be 3 to 8 millicurie (mCi) +/- 10% given intravenously at a single time prior to imaging; Other Name: 68Ga-FAP-2286; Procedure: Positron Emission Tomography (PET) imaging; Participants will be scanned for approximately 30 to 45 minutes; Other Name: PET
Experimental: 64Cu-Dosimetry population (Cohort 1b); PET imaging will begin 60±15 minutes, 240±30 minutes after injection,and 24±2 hours after injection of 64Cu-FAP-2286. Contrast may be administered if clinically indicated.	Procedure: Positron Emission Tomography (PET) imaging; Participants will be scanned for approximately 30 to 45 minutes; Other Name: PET; Drug: Copper-64 labeled (64Cu-) FAP-2286; The dose will be 3.5 to 5.5 millicurie (mCi) +/- 10% given intravenously at a single time prior to imaging; Other Name: 64Cu-FAP-2286
Experimental: Participants with metastatic disease (Cohort 2); Participants with metastatic disease will have PET imaging 50-100 minutes after injection of 68Ga- or 64Cu- FAP-2286. Contrast may be administered if clinically indicated.	Drug: Gallium-68 labelled (68Ga-) FAP-2286; The dose will be 3 to 8 millicurie (mCi) +/- 10% given intravenously at a single time prior to imaging; Other Name: 68Ga-FAP-2286; Procedure: Positron Emission Tomography (PET) imaging; Participants will be scanned for approximately 30 to 45 minutes; Other Name: PET; Drug: Copper-64 labeled (64Cu-) FAP-2286; The dose will be 3.5 to 5.5 millicurie (mCi) +/- 10% given intravenously at a single time prior to imaging; Other Name: 64Cu-FAP-2286
Experimental: Participants without metastatic disease (Cohort 3); Participants without metastatic disease will have PET imaging 50-100 minutes after injection of 68Ga- or 64Cu- FAP-2286. Contrast may be administered if if clinically indicated.	Drug: Gallium-68 labelled (68Ga-) FAP-2286; The dose will be 3 to 8 millicurie (mCi) +/- 10% given intravenously at a single time prior to imaging; Other Name: 68Ga-FAP-2286; Procedure: Positron Emission Tomography (PET) imaging; Participants will be scanned for approximately 30 to 45 minutes; Other Name: PET; Drug: Copper-64 labeled (64Cu-) FAP-2286; The dose will be 3.5 to 5.5 millicurie (mCi) +/- 10% given intravenously at a single time prior to imaging; Other Name: 64Cu-FAP-2286

Outcome Measures

Primary Outcome Measures :

1. Count of participants with treatment-emergent adverse events [ Time Frame: Up to 3 days ]
   The frequency and severity of treatment emergent adverse events following FAP-2286 injection will be descriptively reported as classified and graded by National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) version 5.0
2. Proportion of radiation-absorbed doses of radiolabeled FAP-2286 (Cohorts 1a/1b only) [ Time Frame: Up to 3 days ]
   Volumes of interest of 68Ga- and 64Cu- will be drawn around regions identified on the scans, including the liver, spleen, kidneys, urinary bladder, the central sacrum (for hematopoietic marrow) and whole body. Data will be fitted using the Simulation, Analysis, and Modeling Software II (SAAM II) software. Time integrals of activity will be entered into the Organ Level INternal Dose Assessment/EXponential Modeling (OLINDA/EXM) software, using the reference adult model. The results from all patients enrolled will be combined to allow the calculation of mean, standard deviation (SD), and range of radiation-absorbed doses to individual organs
3. Standardized Uptake Values (SUVs) (Cohort 2 only) [ Time Frame: Up to 3 days ]
   The maximum Standardized Uptake Value (SUVmax) will be calculated for up to five lesions in each patient, with mediastinal blood pool being used as background activity.
4. Tumor-to-background (TBR) Ratio (Cohort 2 only) [ Time Frame: Up to 3 days ]
   TBR ratios will be calculated for up to five lesions in each patient, with mediastinal blood pool being used as background activity. The median and range of the measured TBRs will be reported across all RECIST measurable lesions as a table broken down by location (organ metastases, nodal metastases and bone metastases).
5. Proportion of positive lesions on FAP-2286 PET (Cohort 3 only) [ Time Frame: Up to 3 days ]
   Conventional imaging will be reviewed in conjunction with the FAP-2286 PET images. Lesions will be characterized as positive on FAP-2286 PET if uptake is greater than 1.5 times higher than mediastinal blood pool and uptake cannot be attributed to physiologic or inflammatory reasons. Conventional imaging will be interpreted as positive by each lesion if the short axis dimension of lymph nodes is greater than 1 centimeter (cm), and organ metastases measure greater than 1 cm in long axis. The gold standard will be the combination of conventional imaging and FAP-2286 PET in combination with clinical follow-up and histopathology (if available). The number of lesions detected by each modality will be compared and sensitivity will be computed. Since this is a proof-of-concept study, it is not powered for the test of agreement. Nevertheless, the agreement will be tested using McNemar's test.

Eligibility Criteria

• Ages Eligible for Study: 18 Years and older (Adult, Older Adult)
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Criteria

Inclusion Criteria:

1. Age >= 18 years

2. Histopathologically confirmed solid tumors in one of the following cohorts:

   a. Cohort 1 (n=16): measurable disease is not required for this cohort. i. Agnostic to tumor type. b. Cohort 2 (n=40): Metastatic disease present on conventional imaging defined as having RECIST 1.1 measurable disease or multiple bone metastases.

   i. Pathologically confirmed breast cancer, pancreatic adenocarcinoma, sarcoma, castrate-resistant prostate cancer, bladder cancer, or colon cancer.

   ii. Pathologically confirmed cancer other than noted above (basket subgroup, n=10).

   c. Cohort 3 (n=30): No evidence of metastatic disease as defined as the absence of RECIST 1.1 measurable disease or bone metastases.

   i. Patients can be imaged at initial staging with what is judged by the treating physician to be high risk disease and where the presence of metastatic disease would greatly impact treatment planning and prognosis. Patients may also be imaged after definitive therapy (surgery, chemotherapy or radiation therapy) if in the determination of the treating physician or investigator there is a high risk of disease recurrence that would also impact treatment plan and/or prognosis.

   ii. Pathologically confirmed head and neck cancer or bladder cancer.

3. Ability to understand a written informed consent document, and the willingness to sign it.

Exclusion Criteria:

1. Unlikely to comply with protocol procedures, restrictions and requirements and judged by the Investigator to be unsuitable for participation.
2. Known pregnancy.

Contacts and Locations

Contacts

Contact: Maya Aslam; 877-827-3222; Maya.Aslam@ucsf.edu

Locations

United States, California

University of California, San Francisco; Recruiting

San Francisco, California, United States, 94143

Contact: Maya Aslam 877-827-3222 Maya.Aslam@ucsf.edu

Contact cancertrials@ucsf.edu

Principal Investigator: Thomas Hope, MD

Sponsors and Collaborators

Thomas Hope

Clovis Oncology, Inc.

Investigators

• Principal Investigator: Thomas Hope, MD; University of California, San Francisco

More Information

• Responsible Party: Thomas Hope, Principal Investigator, University of California, San Francisco
• ClinicalTrials.gov Identifier: NCT04621435
• Other Study ID Numbers: 20929; NCI-2020-11728 ( Registry Identifier: NCI Clinical Trials Reporting Program (CTRP) )
• First Posted: November 9, 2020
• Last Update Posted: August 4, 2022
• Last Verified: August 2022

Individual Participant Data (IPD) Sharing Statement:

• Plan to Share IPD: No

• Studies a U.S. FDA-regulated Drug Product: Yes
• Studies a U.S. FDA-regulated Device Product: No

Keywords provided by Thomas Hope, University of California, San Francisco:

PET; 68Ga-FAP-2286; 64Cu-FAP-2286

Additional relevant MeSH terms:

Neoplasm Metastasis; Neoplasms; Neoplastic Processes; Pathologic Processes; Copper; Trace Elements; Micronutrients; Physiological Effects of Drugs