Initial Evaluation of [<sup>18</sup>F]FAPI-74 PET for Various Histopathologically Confirmed Cancers and Benign Lesions.
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- Record sourced from PubMed, PMID 37268427.
- Also identified by DOI 10.2967/jnumed.123.265486 and PMC identifier 10394310.
- Licence recorded as CC BY.
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Abstract
The <sup>18</sup>F-labeled fibroblast activation protein inhibitor (FAPI) [<sup>18</sup>F]FAPI-74 has the benefit of a higher synthetic yield and better image resolution than <sup>68</sup>Ga-labeled FAPI. We preliminarily evaluated the diagnostic performance of [<sup>18</sup>F]FAPI-74 PET in patients with various histopathologically confirmed cancers or suspected malignancies. <b>Methods:</b> We enrolled 31 patients (17 men and 14 women) with lung cancer (<i>n</i> = 7), breast cancer (<i>n</i> = 5), gastric cancer (<i>n</i> = 5), pancreatic cancer (<i>n</i> = 3), other cancers (<i>n</i> = 5), and benign tumors (<i>n</i> = 6). Twenty-seven of the 31 patients were treatment-naïve or preoperative, whereas recurrence was suspected in the remaining 4 patients. Histopathologic confirmation was obtained for the primary lesions of 29 of the 31 patients. In the remaining 2 patients, the final diagnosis was based on the clinical course. [<sup>18</sup>F]FAPI-74 PET scanning was performed 60 min after the intravenous injection of [<sup>18</sup>F]FAPI-74 (240 ± 31 MBq). The [<sup>18</sup>F]FAPI-74 PET images were compared between the primary or local recurrent lesions of malignant tumors (<i>n</i> = 21) and nonmalignant lesions (<i>n</i> = 8: type-B1 thymomas, granuloma, solitary fibrous tumor, and postoperative or posttherapeutic changes). The uptake and number of detected lesions on [<sup>18</sup>F]FAPI-74 PET were also compared with those on [<sup>18</sup>F]FDG PET for available patients (<i>n</i> = 19). <b>Results:</b> [<sup>18</sup>F]FAPI-74 PET showed higher uptake in primary lesions of various cancers than in nonmalignant lesions (median SUV<sub>max</sub>, 9.39 [range, 1.83-25.28] vs. 3.49 [range, 2.21-15.58]; <i>P</i> = 0.053), but some of the nonmalignant lesions showed high uptake. [<sup>18</sup>F]FAPI-74 PET also showed significantly higher uptake than [<sup>18</sup>F]FDG PET (median SUV<sub>max</sub>, 9.44 [range, 2.50-25.28] vs. 5.45 [range, 1.22-15.06] in primary lesions [<i>P</i> = 0.010], 8.86 [range, 3.51-23.33] vs. 3.84 [range, 1.01-9.75] in lymph node metastases [<i>P</i> = 0.002], and 6.39 [range, 0.55-12.78] vs. 1.88 [range, 0.73-8.35] in other metastases [<i>P</i> = 0.046], respectively). In 6 patients, [<sup>18</sup>F]FAPI-74 PET detected more metastatic lesions than [<sup>18</sup>F]FDG PET. <b>Conclusion:</b> [<sup>18</sup>F]FAPI-74 PET showed higher uptake and detection rates in primary and metastatic lesions than did [<sup>18</sup>F]FDG PET. [<sup>18</sup>F]FAPI-74 PET is a promising novel diagnostic modality for various tumors, especially for precise staging before treatment, including characterization of tumor lesions before surgery. Moreover, <sup>18</sup>F-labeled FAPI ligand might serve a higher demand in clinical care in the future.
Medical subject headings
- Breast Neoplasms
- Pancreatic Neoplasms
- Lung Neoplasms
- Stomach Neoplasms
- Quinolines