Zhou Xing, Li YingChun, Jiang Xiao, Wang XiaoXiong, Chen ShiRong, Shen TaiPeng, You JinHui, Lu Hao, Liao Hong, Li Zeng, Cheng ZhuZhong
Radiation Oncology Key Laboratory of Sichuan Province, PET/CT Centre, Sichuan Cancer Hospital, Chengdu, China.
Department of Nuclear Medicine, Affiliated Hospital of North Sichuan Medical College, Nanchong, China.
Front Oncol. 2021 Feb 1;10:585213. doi: 10.3389/fonc.2020.585213. eCollection 2020.
18F labelled PSMA-1007 presents promising results in detecting prostate cancer (PC), while some pitfalls exists meanwhile. An intra-individual comparison of 18F-FDG and 18F-PSMA-1007 in patients with prostate cancer were aimed to be performed in the present study. Then, the pitfalls of 18F-PSMA-1007 PET/CT in imaging of patients with prostate cancer were analyzed.
21 prostate cancer patients underwent 18F-PSMA-1007 PET/CT as well as 18F-FDG PET/CT before treatment. All positive lesions were noticed in both 18F-PSMA-1007 PET/CT and 18F-FDG PET/CT, then differentiated PC metastasis from benign lesions. the SUVmax, SUVmean and TBR of lesions, up to 10 metastases and 10 benign lesions per patients were recorded (5 for bone, 5 for soft tissue metastasis ). The distribution of positive lesions were analyzed for two imaging. Detection rates, SUVmax, SUVmean and TBR in 18F-PSMA-1007 PET/CT and 18F-FDG PET/CT were compared, respectively. The optimal cut-off values of SUVmax, SUVmean for metastases vs. benign lesions was found through areas under ROC in 18F-PSMA-1007.
The detection rates of primary lesions in 18F-PSMA-1007 PET/CT was higher than that of 18F-FDG PET/CT(100% (21/21) vs. 67%(14/21)). For extra- prostatic lesions, 18F-PSMA-1007 PET/CT revealed 124 positive lesions, 49(49/124, 40%) attributed to a benign origin; 18F-FDG PET/CT revealed 68 positive lesions, 14(14/68, 21%) attributed to a benign origin. The SUVmax, SUVmean, TBR of primary tumor in 18F-PSMA-1007 PET/CT was higher than that in 18F-FDG PET/CT (15.20 vs. 4.20 for SUVmax; 8.70 vs. 2.80 for SUVmean; 24.92 vs. 4.82 for TBR, respectively); The SUVmax, SUVmean, TBR of metastases in 18F-PSMA-1007 PET/CT was higher than that in 18F-FDG PET/CT (10.72 vs. 4.42 for SUVmax; 6.67 vs. 2.59 for SUVmean; The TBR of metastases was 13.3 vs. 7.91). For 18F-FDG PET/CT, the SUVmax, SUVmean in metastases was higher than that in benign lesions (4.42 vs. 3.04 for SUVmax, 2.59 vs. 1.75 for SUVmean, respectively). Similarly, for 18F-PSMA-1007 PET/CT, the SUVmax, SUVmean in metastases was significantly higher than that in benign lesions(10.72 vs. 3.14 for SUVmax, 6.67 vs. 1.91 for SUVmean, respectively), ROC suggested that SUVmax=7.71, SUVmean=5.35 might be the optimal cut-off values for metastases vs. benign lesions.
The pilot study suggested that 18F-PSMA-1007 showed superiority over 18F-FDG because its high detecting rate of PC lesions and excellent tumor uptake. While non-tumor uptake in 18F-PSMA-1007 may lead to misdiagnosis, recognizing these pitfalls and careful analysis can improve the accuracy of diagnosis.
18F标记的PSMA - 1007在检测前列腺癌(PC)方面显示出有前景的结果,但同时也存在一些缺陷。本研究旨在对前列腺癌患者进行18F - FDG和18F - PSMA - 1007的个体内比较。然后,分析18F - PSMA - 1007 PET/CT在前列腺癌患者成像中的缺陷。
21例前列腺癌患者在治疗前接受了18F - PSMA - 1007 PET/CT以及18F - FDG PET/CT检查。在18F - PSMA - 1007 PET/CT和18F - FDG PET/CT中均发现所有阳性病变,然后区分PC转移灶与良性病变。记录病变的SUVmax、SUVmean和TBR,每位患者最多记录10个转移灶和10个良性病变(5个骨转移灶,5个软组织转移灶)。分析两种成像中阳性病变的分布情况。分别比较18F - PSMA - 1007 PET/CT和18F - FDG PET/CT的检测率、SUVmax、SUVmean和TBR。通过18F - PSMA - 1007的ROC曲线下面积找到转移灶与良性病变的SUVmax、SUVmean的最佳截断值。
18F - PSMA - 1007 PET/CT对原发灶的检测率高于18F - FDG PET/CT(100%(21/21)对67%(14/21))。对于前列腺外病变,18F - PSMA - 1007 PET/CT显示124个阳性病变,49个(49/124,40%)为良性起源;18F - FDG PET/CT显示68个阳性病变,14个(14/68,21%)为良性起源。18F - PSMA - 1007 PET/CT中原发肿瘤的SUVmax、SUVmean、TBR高于18F - FDG PET/CT(SUVmax分别为15.20对4.20;SUVmean分别为8.70对2.80;TBR分别为24.92对4.82);18F - PSMA - 1007 PET/CT中转移灶的SUVmax、SUVmean、TBR高于18F - FDG PET/CT(SUVmax分别为10.72对4.42;SUVmean分别为6.67对2.59;转移灶的TBR分别为13.3对7.91)。对于18F - FDG PET/CT,转移灶中的SUVmax、SUVmean高于良性病变(SUVmax分别为4.42对3.04,SUVmean分别为2.59对1.75)。同样,对于18F - PSMA - 1007 PET/CT,转移灶中的SUVmax、SUVmean显著高于良性病变(SUVmax分别为10.72对3.14,SUVmean分别为6.67对1.91),ROC曲线表明SUVmax = 7.71,SUVmean = 5.35可能是转移灶与良性病变的最佳截断值。
初步研究表明,18F - PSMA - 1007在PC病变检测率和肿瘤摄取方面优于18F - FDG。虽然18F - PSMA - 1007中的非肿瘤摄取可能导致误诊,但认识到这些缺陷并仔细分析可以提高诊断准确性。