18F-Fibroblast Activation Protein Inhibitor ([18F]FAPI-74) PET Imaging for Cancer Detection

Trial Title: 18F-Fibroblast Activation Protein Inhibitor ([18F]FAPI-74) PET Imaging for Cancer Detection

NCT ID: NCT06503146

Condition: Pancreatic Ductal Adenocarcinoma
Cholangiocarcinoma
Gastric Cancer
Bladder Cancer
Hepatocellular Carcinoma
Pheochromocytoma
Ovarian Cancer

Conditions: Official terms:
Cholangiocarcinoma
Pheochromocytoma

Conditions: Keywords:
Fluorodeoxyglucose F18
PET Imaging
18F-Fibroblast Activation Protein Inhibitor

Study type: Interventional

Study phase: Phase 2

Overall status: Not yet recruiting

Study design:

Allocation: N/A

Intervention model: Parallel Assignment

Primary purpose: Diagnostic

Masking: None (Open Label)

Intervention:

Intervention type: Drug
Intervention name: [18F]FAPI-74
Description: Participants will receive a single intravenous (IV) dose of [18F]FAPI-74 prior to PET/CT imaging.
Arm group label: 1/Arm 1

Intervention type: Drug
Intervention name: [18F]FDG
Description: 18F-FDG PET/CT or PET/MRI imaging will be done per standard of care.
Arm group label: 1/Arm 1

Summary: Background: Fibroblast-activation protein (FAP) is an enzyme that appears in high numbers in certain cancer cells. [18F]FAPI-74 is a new tracer-a substance that is injected into a person s body before an imaging scan. Researchers believe that [18F]FAPI-74 may be able to highlight FAP enzymes more effectively than approved tracers. If so, the new tracer would make it easier to find FAP-positive tumors in the body. Objective: To see if [18F]FAPI-74 PET scans are as good or better than other methods for detecting certain cancers. Eligibility: People aged 18 years or older with cancer in 1 of these places: the ducts of the pancreas, liver, gallbladder, or small intestine; stomach; bladder; ovaries; or adrenal glands. They must be enrolled in an NIH treatment study for their cancer. Design: Participants will have 2 baseline scans: 1 with [18F]FAPI-74; 1 with an approved tracer. The [18F]FAPI-74 will be infused through a tube attached to a needle inserted into a vein. About 1 hour later, the participant will undergo 1 or more imaging scans. Within 1 week, participants will undergo the same scanning procedures with the approved tracer. If the baseline scan with [18F]FAPI-74 shows the tumors, scans with this tracer will be repeated when their regular treatment regimen calls for scans again. If the scans with the regular tracer also showed tumors, this scan will be repeated within the same week as the repeated [18F]FAPI-74 scans. If either type of scan showed no tumors, that scan will not be repeated. If the participant s cancer progresses within 2 years, both types of scan may be repeated. Follow-up calls will continue for 2 years.

Detailed description: Background: - Fibroblast-activation protein (FAP) is a transmembrane type 2 serine protease with dipeptidyl peptidase and endopeptidase activity that is overexpressed on the surface of cancer-associated fibroblasts (CAFs), a major constituent of the tumor stroma, which correlates with a poor prognosis. - FAP-positive CAFs are present in the stromal tissue of more than 90% of epithelial carcinomas, including pancreatic, colorectal, ovarian, lung, and breast cancer among others. - FAP has emerged in recent years as a promising target for molecular imaging with PET/Computed Tomography (CT), using radiolabeled FAP inhibitors (FAPI). FAPI labeled with 68Ga or 18F has shown great promise in cancer detection demonstrating high tumor-to-background ratios in patients across a wide array of cancers. - While there is much clinical data with 68Ga-FAPI, there is much less data on the efficacy of [18F]FAPI-74, which is a more practical version of this PET agent due to its longer half-life. Objective: -To compare [18F]FAPI-74 PET imaging to 18F-fluorodeoxyglucose (18F-FDG) PET imaging and other imaging considered standard of care (SOC) (e.g., CT, and/or magnetic resonance imaging [MRI]) to detect sites of cancer in several malignancies. Eligibility: - >= 18 years old. - Histologically confirmed pancreatic ductal adenocarcinoma (PDAC), cholangiocarcinoma, hepatocellular carcinoma (HCC), gastric cancer, bladder cancer, ovarian cancer, or pheochromocytoma, small cell lung or extrapulmonary neuroendocrine cancer, mesothelioma or sarcoma. - Participants must be co-enrolled in an NIH parent cancer treatment clinical trial with the planned evaluation of response per Response Evaluation Criteria in Solid Tumors (RECIST) v.1.1 and other imaging considered SOC. - Eastern Cooperative Oncology Group (ECOG) Performance score <= 2. Design: - This is a single-site imaging study enrolling participants with PDAC, cholangiocarcinoma, HCC, gastric cancer, bladder cancer, ovarian cancer, pheochromocytoma, small cell lung or extrapulmonary neuroendocrine cancers, mesothelioma or sarcoma. - All participants will undergo baseline [18F]FAPI-74 PET and 18F-FDG PET imaging. - Participants with a positive baseline [18F]FAPI-74 PET scan (i.e., with the presence of FAPIpositive tumor/s) will undergo the second [18F]FAPI-74 PET imaging at the time of the next re-staging performed on the parent treatment protocol. Participants with a negative baseline [18F]FAPI-74 PET scan will not have post-treatment [18F]FAPI-74 PET or 18F-FDG PET scans performed on this protocol but will remain in follow-up. - Participants with a negative baseline 18F-FDG PET scan will not be re-scanned with 18F-FDG PET but may be re-scanned with [18F]FAPI-74 PET if baseline [18F]FAPI-74 PET imaging is positive. - All participants will be followed for 2 years following the first [18F]FAPI-74 PET scan to assess progression-free survival and 2-year overall survival. During this period, participants may undergo the additional [18F]FAPI-74 and 18F-FDG PET imaging in case of suspicion for recurrence/disease progression. These scans may be done even if the baseline [18F]FAPI-74 and/or 18F-FDG PET imaging are negative.

Criteria for eligibility:
Criteria:
- INCLUSION CRITERIA: - Histologically confirmed pancreatic ductal adenocarcinoma (PDAC), cholangiocarcinoma, hepatocellular carcinoma (HCC), gastric cancer, bladder cancer, ovarian cancer, pheochromocytoma, small cell lung cancer (SCLC) or extrapulmonary neuroendocrine cancer (EP-NEC), mesothelioma or sarcoma. - Participants must be co-enrolled in an NIH parent cancer treatment clinical trial with planned evaluation of response per RECIST v.1.1 and other imaging considered standard of care (SOC). - Evaluable disease - >= 18 years old. - Eastern Cooperative Oncology Group (ECOG) performance score <= 2. - Individuals of child-bearing potential (IOCBP) and individuals that can father children must agree to use effective contraception (barrier, hormonal, intrauterine device [IUD], surgical sterilization, abstinence) at the study entry and for 2 months after each [18F]FAPI-74 imaging. Sperm may not be frozen or donated within the same period. - Must be willing to discontinue breastfeeding for 2 months after each study imaging. - The ability of participant to understand and the willingness to sign a written informed consent document. EXCLUSION CRITERIA: - History of allergic reactions attributed to compounds of similar chemical or biologic composition to [18F]FAPI-74 or other agents used in the study. - History of severe claustrophobia unresponsive to oral anxiolytics or history of any other condition preventing the ability to lie on the imaging scanner for up to 45 minutes. - Weight > 350 lbs., or inability to fit within the imaging gantry. - Positive Beta-human chorionic gonadotropin (Beta-HCG) serum or urine pregnancy test performed in IOCBP at screening. - Uncontrolled intercurrent illness, or medical condition(s) including but not limited to renal failure, liver failure, or psychiatric illness/social situations evaluated by medical history and physical exam that would limit compliance with study requirements and potentially increase risk for the participant. - Serum creatinine > 2 times the upper limit of normal. - Liver transaminases (ALT, AST) greater than 3 times the upper limit of normal.

Gender: All

Minimum age: 18 Years

Maximum age: 120 Years

Healthy volunteers: No

Locations:

Facility:
Name: National Institutes of Health Clinical Center

Address:
City: Bethesda
Zip: 20892
Country: United States

Contact:
Last name: National Cancer Institute Referral Office

Phone: 888-624-1937
Email: ncimo_referrals@mail.nih.gov

Start date: November 17, 2024

Completion date: June 1, 2030

Lead sponsor:
Agency: National Cancer Institute (NCI)
Agency class: NIH

Source: National Institutes of Health Clinical Center (CC)

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT06503146
https://clinicalstudies.info.nih.gov/cgi/detail.cgi?B_001731-C.html