[18F]FAPI PET/CT in the evaluation of focal liver lesions with [18F]FDG non-avidity

被引:27
|
作者
Zhang, Jing [1 ]
He, Qiao [2 ]
Jiang, Shuqin [1 ]
Li, Mengsi [3 ]
Xue, Haibao [1 ]
Zhang, Donghui [4 ]
Li, Shuyi [1 ]
Peng, Hao [1 ]
Liang, Jiucen [1 ]
Liu, Zhidong [1 ]
Rao, Songquan [1 ]
Wang, Jin [3 ]
Zhang, Rusen [1 ]
Zhang, Linqi [1 ]
机构
[1] Guangzhou Med Univ, Dept Nucl Med, Affiliated Canc Hosp & Inst, 78 Hengzhigang Rd, Guangzhou 510095, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Dept Nucl Med, Affiliated Hosp 1, 58 Zhongshan 2nd Rd, Guangzhou 510080, Guangdong, Peoples R China
[3] Sun Yat Sen Univ, Dept Radiol, Affiliated Hosp 3, 600 Tianhe Rd, Guangzhou 510630, Guangdong, Peoples R China
[4] Guangzhou Med Univ, Dept Pathol, Affiliated Canc Hosp & Inst, 78 Hengzhigang Rd, Guangzhou 510095, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
F-18]FAPI; PET; CT; Focal liver lesions; Hepatocellular carcinoma; Cancer-associated fibroblasts; HEPATOCELLULAR-CARCINOMA; F-18-FDG; PROTEIN; EXPRESSION;
D O I
10.1007/s00259-022-06022-1
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Purpose: This prospective study was aimed to investigate the potential utility of [F-18]fibroblast activation protein inhibitor (FAPI) PET/CT for evaluating focal liver lesions (FLLs) with [F-18]FDG non-avidity. Methods: From January 2021 to March 2022, this prospective study included 80 FLLs that were not avid on [F-18]FDG PET/CT from 37 patients, then underwent [F-18]FAPI PET/CT. All patients with FLL(s) with biopsy-proof or follow-up confirmation were categorized into four subgroups (20 hepatocellular carcinomas [HCCs]/5 non-HCC malignancies/4 inflammatory FLLs/8 benign noninflammatory FLLs). The diagnostic value of [F-18]FAPI for detecting liver malignancy was determined by visual evaluation. Differences in the maximum standardized uptake value (SUVmax) and lesion-to-background ratio (LBR) obtained from [F-18]FAPI PET/CT among the four subgroups were analyzed by semiquantitative analysis. Results: Among the thirty-seven enrolled participants (34 males; median age 57 years, range 48-67 years), on visual evaluation, the sensitivity, specificity, and accuracy of [F-18]FAPI PET for detecting liver malignancy in the patient-based analysis were 96.0% (24/25), 58.3% (7/12), and 83.8% (31/37), respectively. On semiquantitative analysis, the SUVmax and LBR of [F-18]FAPI PET in liver malignancy (33 HCC lesions; 19 non-HCC malignant lesions) were significantly higher than those in 11 benign noninflammatory FLLs [HCC: SUVmax: 6.4 vs. 4.5, P = 0.017; LBR: 5.1 vs. 1.5, P = 0.003; non-HCC: SUVmax: 5.5 vs. 4.5, P = 0.008; LBR: 4.4 vs. 1.5, P = 0.042]. Notably, there was no significant difference in the SUVmax of [F-18]FAPI PET between 33 HCC lesions and 17 inflammatory FLLs (6.4 vs. 8.2, P = 0.37), but the LBR of [F-18]FAPI PET in HCC were significantly lower than that in inflammatory FLLs (5.1 vs. 9.1, P = 0.003). Conclusions: [F-18]FAPI PET/CT shows high sensitivity in detecting HCC and non-HCC malignancy with [F-18]FDG non-avidity. [F-18]FAPI might be a promising radiopharmaceutical for the differential diagnosis of benign noninflammatory FLLs and liver malignancy with [F-18]FDG non-avidity.
引用
收藏
页码:937 / 950
页数:14
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