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Piloting 18F-FAPI PET/MRI for Applications in Breast Cancer

Piloting 18F-FAPI PET/MRI for Applications in Breast Cancer

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07180433
Enrollment
60
Registered
2025-09-18
Start date
2025-10-01
Completion date
2038-12-31
Last updated
2025-09-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Neoplasm Female

Brief summary

Breast cancer is the most common type of cancer in Norwegian women, with 4,224 new cases in 2022. More precise diagnosis are expected to result in more accurate assessment of treatment effect, and to contribute to both providing better treatment and reducing overtreatment. Fibroblast activating protein (FAP) is expressed in the tumor stroma of 90% of all epithelial-based tumors, including breast tumors. Inhibitors for this protein (FAPI) has been developed for use as radioactive tracers. Breast tumors of various histopathological types, and local metastatic lymph nodes, have shown high uptake for such tracers. The main aim of this project is to establish 18F-FAPI PET/MRI for use in breast cancer in a wide range of disease stages. We will evaluate how FAPI PET/MRI correlates with histopathological assessment, the method's ability to grade tumors - including assessment of treatment - compared to CT, scintigraphy and FDG PET/CT, and ability to detect local recurrence.

Interventions

DIAGNOSTIC_TESTFAPI PET/MR

The patients will be injected intravenously with 2 MBq/kg 18F-FAPI, 60 minutes before the PET/MRI acquisition. The PET/MRI examinations will be performed on a Siemens Biograph mMR (Siemens Healthcare, Erlangen, Germany) with software version VE11P. Static PET will be acquired simultaneously with MRI using two protocols; a one bed position protocol in prone position covering the breast and a whole body 4-5 bed position protocol in supine position covering brain to thighs. Total acquisition time of the breast protocol will be approximately 20 minutes. Total acquisition time of the whole-body protocol will be approximately 30 minutes.

Sponsors

Norwegian University of Science and Technology
CollaboratorOTHER
St. Olavs Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Inclusion criteria are accepting to undergo 18F-FAPI PET/MRI examinations and 1. diagnosed with local invasive breast cancer, 2. scheduled for neoadjuvant therapy as primary treatment, 3. has recurrent or new breast cancer, or 4. scheduled for neoadjuvant therapy as primary treatment with FDG-PET/CT applied for staging.

Exclusion criteria

* other primary malignancies than breast cancer, renal insufficiency or know allergy towards contrast agents, and MR incompatible implants.

Design outcomes

Primary

MeasureTime frameDescription
Diagnostic accuracy of 18F-FAPI-PET/MRI in detection of breast cancer lesionsBaselineDiagnostic accuracy (sensitivity, specificity, positive predictive value, negative predictive value) of 18F-FAPI-PET/MRI in detecting breast cancer lesions, including primary tumors, regional lymph node metastases, distant metastases, and local/distant recurrences. Interpretation will be based on consensus assessment by nuclear medicine physicians and radiologists. Histopathology and/or conventional imaging (CT, FDG-PET, bone scintigraphy) will serve as the reference standards.

Secondary

MeasureTime frameDescription
Correlation of standardized uptake values of 18F-FAPI to histologically proven characteristics of the breast cancer lesionsBaselineQuantitative PET compared to standard histopathology of breast tumours and axillary lymph nodes, including number and size, grading, receptor status, and histological type
Diagnostic accuracy of 18F-FAPI PET/MR compared to MR only in prediction/evaluation of response to neoadjuvant chemotherapyFrom baseline to surgery (~3-6 months)PET/MRI data compared to clinical response to chemotherapy (cR), pathologic complete response (pCR) and residual cancer burden (RCB)
Diagnostic accuracy of 18F-FAPI PET/MR compared to standard CT/bone scintigraphy in staging of breast cancerBaselineComparison of detection rates by PET/MR data to standard CT/bone scintigraphy.
Diagnostic accuracy of 18F-FAPI PET/MR compared to CT/bone scintigraphy in detection of recurrence.BaselineComparison of detection rates by PET/MR data to standard CT/bone scintigraphy.
Diagnostic accuracy of 18F-FAPI PET/MR compared to 18F-FDG PET/CT.BaselineComparisons of consesus readings by radiologists and nuclear medcine physisians.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026