{"title":"[68Ga] ga -成纤维细胞活化蛋白抑制剂- 04与[18F]FDG PET成像在孤立性纤维性肿瘤中的比较及fap靶向放射药物治疗的初步应用","authors":"Rongxi Wang, Jiarou Wang, Jialin Xiang, Huimin Sui, Linlin Li, Chenhao Jia, Xingtong Peng, Xiaoyuan Chen, Zhaohui Zhu, Jingjing Zhang","doi":"10.2967/jnumed.124.268258","DOIUrl":null,"url":null,"abstract":"<p>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. <strong>Methods:</strong> 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. <strong>Results:</strong> 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%, <em>P</em> < 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, <em>P</em> < 0.001; kidney and abdominopelvic cavity, <em>P</em> = 0.001; muscle and pericardium, <em>P</em> < 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. <strong>Conclusion:</strong> [<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.</p>","PeriodicalId":22820,"journal":{"name":"The Journal of Nuclear Medicine","volume":"7 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-03-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"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\",\"authors\":\"Rongxi Wang, Jiarou Wang, Jialin Xiang, Huimin Sui, Linlin Li, Chenhao Jia, Xingtong Peng, Xiaoyuan Chen, Zhaohui Zhu, Jingjing Zhang\",\"doi\":\"10.2967/jnumed.124.268258\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>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. <strong>Methods:</strong> 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. <strong>Results:</strong> 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%, <em>P</em> < 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, <em>P</em> < 0.001; kidney and abdominopelvic cavity, <em>P</em> = 0.001; muscle and pericardium, <em>P</em> < 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. <strong>Conclusion:</strong> [<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.</p>\",\"PeriodicalId\":22820,\"journal\":{\"name\":\"The Journal of Nuclear Medicine\",\"volume\":\"7 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-03-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Journal of Nuclear Medicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2967/jnumed.124.268258\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Nuclear Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2967/jnumed.124.268258","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
孤立性纤维性肿瘤是一种罕见的间质肉瘤。虽然通常是良性的,但SFTs有复发和转移的风险,有效的治疗选择有限。本研究的目的是比较成纤维细胞活化蛋白抑制剂(FAPI)、[68Ga]Ga-DOTA-FAPI-04(简称[68Ga]Ga-FAPI-04)与常规[18F]FDG PET/CT在复发或转移性SFT患者头对头的表现,并初步探讨FAPI靶向177Lu对SFT患者的放射性药物治疗价值。方法:31例疑似复发或转移性SFTs患者(21例男性,44±13岁)在1周内接受了[18F]FDG和[68Ga]Ga-FAPI-04 PET/CT检查。比较不同受累脏器2次PET/CT扫描的阳性病变率及摄取值(SUVmax)。4例[68Ga]Ga-FAPI-04摄取高的患者接受单周期2.22 GBq的[177Lu] lu标记、fap靶向的放射性药物[177Lu]Lu-Evans蓝- fapi治疗,随访4个月。结果:在31例522例局部复发和远处转移患者中,[68Ga]Ga-FAPI-04 PET检出的病灶明显多于[18F]FDG (87.0% vs. 45.4%, P <;0.001)。在病变摄取值方面,[68Ga]Ga-FAPI-04 PET在大多数复发或转移器官(骨、肺、中枢神经系统、胰腺和胸膜)的平均SUVmax高于[18F]FDG, P <;0.001;肾和腹腔,P = 0.001;肌和心包,P <;0.05)。4例患者对[177Lu]Lu-Evans blue-FAPI耐受良好。全身吸收剂量为4.02E−01±3.54E−02 Gy,有效剂量为4.01E+02±4.18E+01 mSv。随后的[68Ga]Ga-FAPI-04 PET随访显示患者病情稳定。结论:[68Ga]Ga-FAPI-04可能是一种很有前途的评价SFTs的PET试剂。鉴于晚期SFTs缺乏有效的治疗方法,FAP在这类肿瘤中的高表达有望成为潜在的治疗靶点。
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
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), [68Ga]Ga-DOTA-FAPI-04 (denoted as [68Ga]Ga-FAPI-04), and conventional [18F]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 177Lu for SFT patients. Methods: Thirty-one participants (21 men, 44 ± 13 y) with suspected recurrent or metastatic SFTs underwent both [18F]FDG and [68Ga]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 (SUVmax) were compared. Four patients with high [68Ga]Ga-FAPI-04 uptake received single-cycle therapy of 2.22 GBq of a [177Lu]Lu-labeled, FAP-targeted radiopharmaceutical, [177Lu]Lu-Evans blue–FAPI, and were followed up for 4 mo. Results: In 522 local recurrences and distant metastases in the 31 patients, [68Ga]Ga-FAPI-04 PET detected significantly more lesions than did [18F]FDG (87.0% vs. 45.4%, P < 0.001). In terms of lesion uptake values, [68Ga]Ga-FAPI-04 PET showed a mean SUVmax higher than that of [18F]FDG in most recurrence or metastatic organs (bone, lung, central nervous system, pancreas, and pleura, P < 0.001; kidney and abdominopelvic cavity, P = 0.001; muscle and pericardium, P < 0.05). Four patients tolerated [177Lu]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 [68Ga]Ga-FAPI-04 PET showed that these patients were in stable condition. Conclusion: [68Ga]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.