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[(18)F] AlF‑NOTA‑FAPI‑04 PET/CT as a promising tool for imaging fibroblast activation protein in gastrointestinal system cancers: a prospective investigation of comparative analysis with (18)F-FDG

PURPOSE: The radiopharmaceutical [(18)F]AlF-NOTA-FAPI-04 presents a promising alternative to (68) Ga-FAPI owing to its relatively longer half-life. This study aimed to evaluate the clinical usefulness of [(18)F]AlF-NOTA-FAPI-04 PET/CT for the diagnosis of primary and metastatic lesions in various ty...

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Detalles Bibliográficos
Autores principales: Yang, Liping, Xu, Shichuan, Cheng, Liang, Gao, Chao, Cao, Shaodong, Chang, Zhengsong, Wang, Kezheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10611594/
https://www.ncbi.nlm.nih.gov/pubmed/37542659
http://dx.doi.org/10.1007/s00259-023-06351-9
Descripción
Sumario:PURPOSE: The radiopharmaceutical [(18)F]AlF-NOTA-FAPI-04 presents a promising alternative to (68) Ga-FAPI owing to its relatively longer half-life. This study aimed to evaluate the clinical usefulness of [(18)F]AlF-NOTA-FAPI-04 PET/CT for the diagnosis of primary and metastatic lesions in various types of gastrointestinal system cancers, compared with (18)F-FDG PET/CT. METHODS: Patients diagnosed with gastrointestinal system malignancies were prospectively enrolled. All patients underwent both (18)F-FDG and (18)F-FAPI-04 PET/CT scans within one week, with 44 (73.3%) for cancer staging and 16 (26.7%) for tumor restaging. Diagnostic efficacy of the primary tumor, as well as the presence and number of lymph nodes and distant metastases, were assessed. Tumor uptake was quantified by the maximum standard uptake value (SUVmax). RESULTS: For detection of primary tumor, the diagnostic sensitivity of (18)F-FDG PET/CT was 72.7%, while it was 97.7% for (18)F-FAPI-04 PET/CT. Based on per-lymph node analysis, the sensitivity, specificity, and accuracy of (18)F-FAPI-04 PET/CT in diagnosing metastatic lymph nodes were 91.89%, 92.00%, and 91.96%, respectively. These values were notably higher than those (18)F-FDG PET/CT (79.72%, 81.33% and 80.80%, respectively). The (18)F-FAPI-04 PET/CT surpassed (18)F-FDG PET/CT in detecting suspected metastases in the brain (7 vs. 3), liver (39 vs. 20), bone (79 vs. 51), lung (11 vs. 4), and peritoneal carcinoma (48 vs. 22). Based on per-patient analysis, differential diagnostic accuracies ((18)F-FAPI-04 vs. (18)F-FDG PET/CT) were observed in all patients (91.7% vs. 76.7%), the initial staging group (90.9% vs. 79.5%), and the re-staging group (93.8% vs. 68.7%). Additionally, (18)F-FAPI-04 PET/CT revised final diagnosis in 31.7% of patients, contrasting with (18)F-FDG PET/CT, and prompted changes in clinical management for 21.7% of the patients. CONCLUSION: (18)F-FAPI-04 PET/CT outperforms (18)F-FDG PET/CT in delineating the primary gastrointestinal tumors and detecting suspected metastatic lesions due to a higher target-to-background ratio (TBR). Moreover, (18)F-FAPI-04 PET/CT could provide valuable guidance for tumor staging, thereby having a potential impact on patient management. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00259-023-06351-9.