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Imaging tumor microenvironment: clinical experience with 68Ga-FAPI PET/CT across multiple cancer types
Ahmed K Al-Timeemi1, Alzahraa I Al-Timeemi2, Jasim Al-Ibraheemi3
1Department of Nuclear Medicine, Al-Loaloa PET Center, Al-Kafeel Hospital, College of Medicine, University of Kerbala, Kerbala, Iraq.
Background:
Fibroblast activation protein (FAP) is highly expressed in the stroma of various cancers, making it a promising target for positron emission tomography (PET) imaging. This study aimed to evaluate the clinical performance of 68Ga-labeled fibroblast activation protein inhibitor (FAPI)-46 PET/CT across multiple cancer types.
Methods:
In this single-center, retrospective study, we included 22 patients (mean age 43 years, range 10-69) with histopathologically confirmed primary or metastatic cancers in whom 18F-FDG PET/CT or conventional imaging yielded inconclusive results. All patients underwent 68Ga-FAPI-46 PET/CT. Scan positivity was determined by two experienced nuclear medicine physicians based on non-physiologic tracer uptake. Malignancy was confirmed by histopathology (the reference standard) or correlative imaging follow-up. Analysis was performed on both a per-patient and per-lesion basis. Tumor uptake was quantified using maximum standardized uptake value (SUV
Results:
A total of 115 lesions were identified and evaluated across 12 different cancer types. The highest 68Ga-FAPI-46 avidity (SUV
Conclusions:
68Ga-FAPI-46 PET/CT provides high-contrast imaging across a wide spectrum of malignancies, demonstrating particularly strong potential for visualizing tumors with prominent stromal components. These findings suggest a significant clinical role for this modality in improving tumor staging, restaging, and therapy assessment, especially in cases where 18F-FDG PET/CT is suboptimal.
Insights
68Ga-FAPI-46 PET/CT imaging shows high contrast across many cancer types, especially those with significant stromal components. This technique offers a promising alternative to 18F-FDG PET/CT for improved tumor visualization and assessment.
Area of Science:
- Nuclear Medicine
- Oncology Imaging
- Radiopharmaceuticals
Background:
- Fibroblast activation protein (FAP) is a stromal marker highly expressed in various cancers.
- FAP-targeted positron emission tomography (PET) imaging offers a potential diagnostic avenue.
- 68Ga-labeled fibroblast activation protein inhibitor (FAPI)-46 is a novel PET tracer.
Purpose of the Study:
- To evaluate the clinical performance of 68Ga-FAPI-46 PET/CT in a diverse cancer patient cohort.
- To assess the diagnostic utility of 68Ga-FAPI-46 PET/CT in cases with inconclusive conventional imaging or 18F-FDG PET/CT results.
Main Methods:
- Retrospective analysis of 22 patients with histopathologically confirmed cancers.
- All patients underwent 68Ga-FAPI-46 PET/CT.
- Tumor uptake was quantified using SUVmax and tumor-to-background ratio (TBR); malignancy was confirmed by histopathology or follow-up.
Main Results:
- 115 lesions across 12 cancer types were evaluated.
- Highest 68Ga-FAPI-46 avidity was observed in sarcoma, breast cancer, and cholangiocarcinoma.
- High TBRs were achieved due to low background activity, indicating excellent image contrast.
Conclusions:
- 68Ga-FAPI-46 PET/CT provides high-contrast imaging across a broad range of malignancies.
- The modality shows particular promise for visualizing tumors with significant stromal components.
- This technique may enhance tumor staging, restaging, and therapy assessment, especially when 18F-FDG PET/CT is suboptimal.
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