Characterizing Breast Cancer With Al18F-NOTA-FAPI-04 PET/CT

Sponsor
Peking Union Medical College Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05574920
Collaborator
(none)
100
1
1
13.7
7.3

Study Details

Study Description

Brief Summary

Fibroblast activation protein (FAP) is overexpressed in cancer-associated fibroblasts (CAFs), which constitute a major proportion of cells within the tumor microenvironment, especially in breast cancer. Previous studies have demonstrated that FAPI PET/CT performs well in cases of epithelial tumors, including breast cancer. This prospective study is going to investigate the performance and value of Al18F-NOTA-FAPI-04 PET/CT in patients with breast cancer.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Al18F-NOTA-FAPI-04 PET/CT scan
N/A

Detailed Description

Breast cancer is a complex, heterogeneous disease comprising numerous distinct biological subtypes characterized by variant pathobiological features and clinical behaviors. 18F-fluorodeoxyglucose (18F-FDG) PET/CT, an essential imaging modality in the characterization of metabolism within the tumor, has successfully evolved in the diagnosis, staging, and assessment of treatment response in patients with breast cancer. Cancer-associated fibroblasts (CAFs) are a crucial component of the tumor stroma with diverse functions. Fibroblast activation protein (FAP), a type II membrane-bound glycoprotein from the dipeptidyl peptidase-4 family, is highly expressed in the CAFs of several epithelial carcinomas, including breast cancer, coupled with relatively low expression in normal tissue. Based on this characteristic, many small-molecule inhibitors of FAP (FAPIs) labeled with radioactive tracers (68Ga, 18F, or 177Lu) have been synthesized as theranostic radiotracers for cancer. Previous studies on FAPI PET/CT tumor imaging have focused on the 68Ga radionuclide rather than 18F. As 18F-labeled FAPI has more favorable physical properties, high production capacity, and good imaging characteristics, it may be an ideal agent for PET imaging. Therefore, this study aims to evaluate the performance and value of Al18F-NOTA-FAPI-04 PET/CT in patients with breast cancer.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
A Prospective Pilot Study to Explore Performance and Efficacy of Al18F-NOTA-FAPI-04 PET/CT in Breast Cancer Patients
Actual Study Start Date :
May 10, 2022
Anticipated Primary Completion Date :
Dec 31, 2022
Anticipated Study Completion Date :
Jun 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Al18F-NOTA-FAPI-04 PET/CT

Inject Al18F-NOTA-FAPI-04 and then perform PET/CT scan.

Diagnostic Test: Al18F-NOTA-FAPI-04 PET/CT scan
Patients enrolled underwent PET/CT after injection of Al18F-NOTA-FAPI-04 to image lesions of breast cancer.

Outcome Measures

Primary Outcome Measures

  1. The maximum standard uptake value (SUVmax ) was measured in the breast cancer lesions on Al18F-NOTA-FAPI-04 PET/CT. [through study completion, an average of 1 year]

    Standardized uptake value of Al18F-NOTA-FAPI-04 in BC

  2. Standardized uptake value of Al18F-NOTA-FAPI-04 in BC [through study completion, an average of 1 year]

    The mean standard uptake value ( SUVmean) was measured in the breast cancer lesions on Al18F-NOTA-FAPI-04 PET/CT.

Secondary Outcome Measures

  1. Lesions detected by Al18F-NOTA-FAPI-04 PET/CT [through study completion, an average of 1 year]

    The number of target lesions in each organ system was calculated by Al18F-NOTA-FAPI-04 PET/CT.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 90 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • suspected or confirmed untreated breast cancer;

  • signed written consent.

Exclusion Criteria:
  • pregnancy;

  • breastfeeding;

  • any medical condition that in the opinion of the investigator may significantly interfere with study compliance.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Peking Union Medical College Hospital Beijing Beijing China 100730

Sponsors and Collaborators

  • Peking Union Medical College Hospital

Investigators

  • Principal Investigator: Li Huo, M.D., Peking Union Medical College Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Peking Union Medical College Hospital
ClinicalTrials.gov Identifier:
NCT05574920
Other Study ID Numbers:
  • PekingUMCH-FAPI-BC-2
First Posted:
Oct 12, 2022
Last Update Posted:
Oct 12, 2022
Last Verified:
Oct 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 12, 2022