Comparison of [<sup>68</sup>Ga]Ga-Fibroblast Activation Protein Inhibitor–04 and [<sup>18</sup>F]FDG PET Imaging for Solitary Fibrous Tumor and Preliminary Application of FAP-Targeted Radiopharmaceutical Therapy

Solitary fibrous tumor (SFT) is a rare sarcoma of mesenchymal origin. Although generally benign, SFTs carry the risk of recurrence and metastasis, with limited effective treatment options. The aims of this study are to compare the performance of fibroblast activation protein inhibitor (FAPI), [<sup>68</sup>Ga]Ga-DOTA-FAPI-04 (denoted as [<sup>68</sup>Ga]Ga-FAPI-04), and conventional [<sup>18</sup>F]FDG PET/CT in patients with recurrent or metastatic SFTs head to head and to preliminarily explore the value of FAP-targeted radiopharmaceutical therapy with <sup>177</sup>Lu for SFT patients. <b>Methods:</b> Thirty-one participants (21 men, 44 ± 13 y) with suspected recurrent or metastatic SFTs underwent both [<sup>18</sup>F]FDG and [<sup>68</sup>Ga]Ga-FAPI-04 PET/CT within 1 wk. The positive-lesion rates of the 2 PET/CT scans in the different organs involved and the uptake values (SUV<sub>max</sub>) were compared. Four patients with high [<sup>68</sup>Ga]Ga-FAPI-04 uptake received single-cycle therapy of 2.22 GBq of a [<sup>177</sup>Lu]Lu-labeled, FAP-targeted radiopharmaceutical, [<sup>177</sup>Lu]Lu-Evans blue-FAPI, and were followed up for 4 mo. <b>Results:</b> In 522 local recurrences and distant metastases in the 31 patients, [<sup>68</sup>Ga]Ga-FAPI-04 PET detected significantly more lesions than did [<sup>18</sup>F]FDG (87.0% vs. 45.4%, <i>P</i> < 0.001). In terms of lesion uptake values, [<sup>68</sup>Ga]Ga-FAPI-04 PET showed a mean SUV<sub>max</sub> higher than that of [<sup>18</sup>F]FDG in most recurrence or metastatic organs (bone, lung, central nervous system, pancreas, and pleura, <i>P</i> < 0.001; kidney and abdominopelvic cavity, <i>P</i> = 0.001; muscle and pericardium, <i>P</i> < 0.05). Four patients tolerated [<sup>177</sup>Lu]Lu-Evans blue-FAPI well. The total-body absorbed dose and the effective dose were 4.02E-01 ± 3.54E-02 Gy and 4.01E+02 ± 4.18E+01 mSv, respectively. Subsequent follow-up with [<sup>68</sup>Ga]Ga-FAPI-04 PET showed that these patients were in stable condition. <b>Conclusion:</b> [<sup>68</sup>Ga]Ga-FAPI-04 may be a promising PET agent for the assessment of SFTs. Given the lack of effective treatments for advanced SFTs, high FAP expression in this type of tumor is expected to become a potential treatment target.

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Journal
Journal of Nuclear Medicine
Published
2025-03-06
DOI
https://doi.org/10.2967/jnumed.124.268258
Citations
6
Primary Topic
Peptidase Inhibition and Analysis
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article
Field-Weighted Citation Impact
6.27
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article

Comparison of [68Ga]Ga-Fibroblast Activation Protein Inhibitor–04 and [18F]FDG PET Imaging for Solitary Fibrous Tumor and Preliminary Application of FAP-Targeted Radiopharmaceutical Therapy

Jiarou Wang, Jialin Xiang, Huimin Sui, Chenhao Jia et al.
6 citations
Journal of Nuclear Medicine
Peptidase Inhibition and Analysis
6.27
article

Comparison of [68Ga]Ga-Fibroblast Activation Protein Inhibitor–04 and [18F]FDG PET Imaging for Solitary Fibrous Tumor and Preliminary Application of FAP-Targeted Radiopharmaceutical Therapy

Jiarou Wang, Jialin Xiang, Huimin Sui, Chenhao Jia, Linlin Li, Xiaoyuan Shawn Chen, Zhaohui Zhu, Rongxi Wang, Xingtong Peng, Jingjing Zhang
article en
6 citations

Abstract

Solitary fibrous tumor (SFT) is a rare sarcoma of mesenchymal origin. Although generally benign, SFTs carry the risk of recurrence and metastasis, with limited effective treatment options. The aims of this study are to compare the performance of fibroblast activation protein inhibitor (FAPI), [<sup>68</sup>Ga]Ga-DOTA-FAPI-04 (denoted as [<sup>68</sup>Ga]Ga-FAPI-04), and conventional [<sup>18</sup>F]FDG PET/CT in patients with recurrent or metastatic SFTs head to head and to preliminarily explore the value of FAP-targeted radiopharmaceutical therapy with <sup>177</sup>Lu for SFT patients. <b>Methods:</b> Thirty-one participants (21 men, 44 ± 13 y) with suspected recurrent or metastatic SFTs underwent both [<sup>18</sup>F]FDG and [<sup>68</sup>Ga]Ga-FAPI-04 PET/CT within 1 wk. The positive-lesion rates of the 2 PET/CT scans in the different organs involved and the uptake values (SUV<sub>max</sub>) were compared. Four patients with high [<sup>68</sup>Ga]Ga-FAPI-04 uptake received single-cycle therapy of 2.22 GBq of a [<sup>177</sup>Lu]Lu-labeled, FAP-targeted radiopharmaceutical, [<sup>177</sup>Lu]Lu-Evans blue-FAPI, and were followed up for 4 mo. <b>Results:</b> In 522 local recurrences and distant metastases in the 31 patients, [<sup>68</sup>Ga]Ga-FAPI-04 PET detected significantly more lesions than did [<sup>18</sup>F]FDG (87.0% vs. 45.4%, <i>P</i> < 0.001). In terms of lesion uptake values, [<sup>68</sup>Ga]Ga-FAPI-04 PET showed a mean SUV<sub>max</sub> higher than that of [<sup>18</sup>F]FDG in most recurrence or metastatic organs (bone, lung, central nervous system, pancreas, and pleura, <i>P</i> < 0.001; kidney and abdominopelvic cavity, <i>P</i> = 0.001; muscle and pericardium, <i>P</i> < 0.05). Four patients tolerated [<sup>177</sup>Lu]Lu-Evans blue-FAPI well. The total-body absorbed dose and the effective dose were 4.02E-01 ± 3.54E-02 Gy and 4.01E+02 ± 4.18E+01 mSv, respectively. Subsequent follow-up with [<sup>68</sup>Ga]Ga-FAPI-04 PET showed that these patients were in stable condition. <b>Conclusion:</b> [<sup>68</sup>Ga]Ga-FAPI-04 may be a promising PET agent for the assessment of SFTs. Given the lack of effective treatments for advanced SFTs, high FAP expression in this type of tumor is expected to become a potential treatment target.

Journal of Nuclear MedicineVol. 66(4)
Agency for Science, Technology and Research (SG), National University of Singapore (SG), Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Peking Union Medical College Hospital (CN), Institute of Molecular and Cell Biology (SG)
Zero hunger
Openalex Percentile: Top 3%
Peptidase Inhibition and Analysis
6.27
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