68Ga-FAPi-46 PET/CT Scan in Imaging Patients With Sarcoma
Primary Purpose
Metastatic Sarcoma, Recurrent Sarcoma, Sarcoma
Status
Recruiting
Phase
Early Phase 1
Locations
United States
Study Type
Interventional
Intervention
Computed Tomography
Gallium Ga 68 FAPi-46
Positron Emission Tomography
18F-FDG
Sponsored by
About this trial
This is an interventional diagnostic trial for Metastatic Sarcoma
Eligibility Criteria
Inclusion Criteria:
- Patients who are scheduled to undergo surgical excision or biopsy of a suspected sarcoma primary, or a suspected recurrent or metastatic lesion.
- Patients who are ≥ 18 years old at the time of the radiotracer administration.
- Patients who can provide written informed consent.
- Patients who are able to remain still for duration of imaging procedures (up to one hour for each).
Exclusion Criteria:
- Patient is pregnant or nursing.
- Patients with any new cancer therapy between the baseline 18F-FDG PET/CT and the investigational FAPI PET/CT
- Patient has underlying disease which, based on the judgment of the investigator, might interfere with the collection of high quality data.
Sites / Locations
- UCLA / Jonsson Comprehensive Cancer CenterRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Diagnostic (68Ga-FAPI-46 PET/CT)
Arm Description
Patients receive 68Ga-FAPi-46 intravenously (IV), and then undergo PET/computed tomography (CT) over 20-90 minutes. On another day, patients receive 18F-FDG and then undergo PET/computed tomography (CT) according to standard of care procedures (if applicable).
Outcomes
Primary Outcome Measures
Biodistribution of gallium Ga 68 fibroblast activation protein inhibitor (FAPi)-46 (68Ga-FAPi-46) in normal and cancer tissues
Will be quantified by mean and maximum standardized uptake values (SUVmean and SUVmax).
Secondary Outcome Measures
68Ga-FAPi-46 accumulation observed by positron emission tomography (PET)/computed tomography (CT)
Will be correlated with and validated by FAP expression in surgically removed or biopsy derived tumor tissue.
Frequency of the following phenotypes (FAP positive [+]/ fludeoxyglucose [FDG]+, FAP negative [-]/ FDG+, FAP+/ FDG-, FAP-/ FDG-)
To assess the 68Ga-FAPI-46 biodistribution correlation with 18F-FDG biodistribution and to define the frequency of the following phenotypes (FAP+/ FDG+, FAP-/ FDG+, FAP+/ FDG-, FAP-/ FDG-)
Full Information
NCT ID
NCT04457258
First Posted
June 30, 2020
Last Updated
October 11, 2023
Sponsor
Jonsson Comprehensive Cancer Center
Collaborators
National Cancer Institute (NCI)
1. Study Identification
Unique Protocol Identification Number
NCT04457258
Brief Title
68Ga-FAPi-46 PET/CT Scan in Imaging Patients With Sarcoma
Official Title
PET Biodistribution Study of 68Ga-FAPI-46 in Patients With Sarcoma: An Exploratory Biodistribution Study With Histopathology Validation
Study Type
Interventional
2. Study Status
Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 8, 2020 (Actual)
Primary Completion Date
July 1, 2024 (Anticipated)
Study Completion Date
July 21, 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Jonsson Comprehensive Cancer Center
Collaborators
National Cancer Institute (NCI)
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This early phase I trial studies an imaging technique called 68Ga-FAPi-46 PET/CT to determine where and to which degree the FAPI tracer (68Ga-FAPi-46) accumulates in normal and cancer tissues in patients with sarcoma. PET is an established imaging technique that utilizes small amounts of radioactivity attached to very minimal amounts of tracer, in the case of this research, 68Ga-FAPi. Because some cancers take up 68Ga-FAPi it can be seen with PET. CT utilizes x-rays that traverse body from the outside. CT images provide an exact outline of organs and potential inflammatory tissue where it occurs in patient's body.
Detailed Description
PRIMARY OBJECTIVE:
I. To define the biodistribution of gallium Ga 68 fibroblast activation protein inhibitor (FAPi)-46 (68Ga-FAPi-46) in normal and cancer tissues of patients with sarcoma with histopathology validation.
SECONDARY OBJECTIVES:
I. To evaluate whether 68Ga-FAPi-46 accumulation observed by positron emission tomography (PET) reflects geography, extent and degree of FAP expression determined by immuno-histochemistry (IHC).
II. To assess the 68Ga-FAPI-46 biodistribution correlation with fludeoxyglucose F-18 (18F-FDG) biodistribution and to define the frequency of the following phenotypes (FAP positive [+]/ FDG+, FAP negative [-]/ FDG+, FAP+/ FDG-, FAP-/ FDG-).
III. 3. To determine FAP expression profile and identify activating and loss of function mutations and gene rearrangement in available tumor tissue samples from patients with localized or metastatic sarcoma using RNA sequencing
OUTLINE:
Patients receive 68Ga-FAPi-46 intravenously (IV), and then undergo PET/computed tomography (CT) over 20-90 minutes. On another day, patients receive 18F-FDG and then undergo PET/computed tomography (CT) according to standard of care procedures (if applicable).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Metastatic Sarcoma, Recurrent Sarcoma, Sarcoma
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Early Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Diagnostic (68Ga-FAPI-46 PET/CT)
Arm Type
Experimental
Arm Description
Patients receive 68Ga-FAPi-46 intravenously (IV), and then undergo PET/computed tomography (CT) over 20-90 minutes. On another day, patients receive 18F-FDG and then undergo PET/computed tomography (CT) according to standard of care procedures (if applicable).
Intervention Type
Procedure
Intervention Name(s)
Computed Tomography
Other Intervention Name(s)
CAT, CAT Scan, Computerized Axial Tomography, Computerized Tomography, CT, CT Scan, tomography
Intervention Description
Undergo PET/CT
Intervention Type
Drug
Intervention Name(s)
Gallium Ga 68 FAPi-46
Other Intervention Name(s)
68Ga-FAPi-46, Gallium-68-FAPi-46
Intervention Description
Given IV
Intervention Type
Procedure
Intervention Name(s)
Positron Emission Tomography
Other Intervention Name(s)
Medical Imaging, Positron Emission Tomography, PET, PET Scan, Positron Emission Tomography Scan, Positron-Emission Tomography, proton magnetic resonance spectroscopic imaging
Intervention Description
Undergo PET/CT
Intervention Type
Radiation
Intervention Name(s)
18F-FDG
Other Intervention Name(s)
18F-fluorodeoxyglucose
Intervention Description
Given IV
Primary Outcome Measure Information:
Title
Biodistribution of gallium Ga 68 fibroblast activation protein inhibitor (FAPi)-46 (68Ga-FAPi-46) in normal and cancer tissues
Description
Will be quantified by mean and maximum standardized uptake values (SUVmean and SUVmax).
Time Frame
At 20-90 minutes after injection
Secondary Outcome Measure Information:
Title
68Ga-FAPi-46 accumulation observed by positron emission tomography (PET)/computed tomography (CT)
Description
Will be correlated with and validated by FAP expression in surgically removed or biopsy derived tumor tissue.
Time Frame
Up to year 2
Title
Frequency of the following phenotypes (FAP positive [+]/ fludeoxyglucose [FDG]+, FAP negative [-]/ FDG+, FAP+/ FDG-, FAP-/ FDG-)
Description
To assess the 68Ga-FAPI-46 biodistribution correlation with 18F-FDG biodistribution and to define the frequency of the following phenotypes (FAP+/ FDG+, FAP-/ FDG+, FAP+/ FDG-, FAP-/ FDG-)
Time Frame
Up to year 2
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients who are scheduled to undergo surgical excision or biopsy of a suspected sarcoma primary, or a suspected recurrent or metastatic lesion.
Patients who are ≥ 18 years old at the time of the radiotracer administration.
Patients who can provide written informed consent.
Patients who are able to remain still for duration of imaging procedures (up to one hour for each).
Exclusion Criteria:
Patient is pregnant or nursing.
Patients with any new cancer therapy between the baseline 18F-FDG PET/CT and the investigational FAPI PET/CT
Patient has underlying disease which, based on the judgment of the investigator, might interfere with the collection of high quality data.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ethan Lam
Phone
310-206-7372
Email
clam@mednet.ucla.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Stephanie Lira
Phone
310-206-7372
Email
StephanieLira@mednet.ucla.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jeremie Calais, MD
Organizational Affiliation
UCLA / Jonsson Comprehensive Cancer Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
UCLA / Jonsson Comprehensive Cancer Center
City
Los Angeles
State/Province
California
ZIP/Postal Code
90095
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ethan Lam
Phone
310-206-7372
Email
clam@mednet.ucla.edu
First Name & Middle Initial & Last Name & Degree
Stephanie Lira
Phone
310-206-7372
Email
StephanieLira@mednet.ucla.edu
First Name & Middle Initial & Last Name & Degree
Jeremie Calais, MD
12. IPD Sharing Statement
Learn more about this trial
68Ga-FAPi-46 PET/CT Scan in Imaging Patients With Sarcoma
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