Naeimi Mahnoosh, Choyke Peter L, Dendl Katharina, Mori Yuriko, Staudinger Fabian, Watabe Tadashi, Koerber Stefan A, Röhrich Manuel, Debus Jürgen, Kratochwil Clemens, Haberkorn Uwe, Giesel Frederik L
Department of Nuclear Medicine, University Hospital Heidelberg, Heidelberg, Germany.
Molecular Imaging Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
J Nucl Med. 2023 Apr;64(4):618-622. doi: 10.2967/jnumed.122.264941. Epub 2022 Nov 10.
A growing family of Ga-fibroblast activation protein inhibitor (FAPI) PET probes has shown promise in imaging a variety of medical conditions. Ga-FAPI-46, in particular, has emerged as unique for both its diagnostic and its theranostic applications; however, the optimal timing of PET remains unclear. Therefore, we evaluated uptake at 3 time points after Ga-FAPI-46 administration in a spectrum of tumor types. The cohort consisted of 43 patients with diverse cancer diagnoses undergoing Ga-FAPI-46 PET/CT at 3 time points (10 min, 1 h, and 3 h). We determined the tracer uptake based on SUV and SUV and on tumor-to-background-ratios (TBRs) (SUV/SUV). There were 171 lesions in the 43 patients. Comparing all lesions at different time points, the mean SUV was maximal at 10 min (8.2) and declined slightly at 1 h (8.15) and 3 h (7.6) after tracer administration. Similarly, the mean SUV log still had a similar pattern in primary lesions at 10 min, 1 h, and 3 h ( = 30; 0.98, 1.01, and 0.98, respectively), lymph node metastases ( = 37; 0.82, 0.84, and 0.81, respectively), and distant metastases ( = 104; 0.81, 0.79, and 0.74, respectively). TBR also showed nonsignificant differences at the 3 times. Ga-FAPI-46 PET/CT imaging revealed remarkably stable tumor and background uptake as determined by SUV metrics and maintained high TBRs within 3 h of injection. Thus, it may be possible to scan with Ga-FAPI-46 within 10-20 min of injection, improving workflow and decreasing patient wait times. Confirmation of these findings in a larger cohort is under way.
越来越多的镓-成纤维细胞激活蛋白抑制剂(FAPI)PET探针在多种医疗状况的成像中显示出前景。特别是镓-FAPI-46,因其诊断和治疗诊断应用而独具特色;然而,PET的最佳时间仍不明确。因此,我们在一系列肿瘤类型中评估了注射镓-FAPI-46后3个时间点的摄取情况。该队列由43例患有不同癌症诊断的患者组成,在3个时间点(10分钟、1小时和3小时)接受镓-FAPI-46 PET/CT检查。我们基于SUV和SUV以及肿瘤与背景比值(TBRs)(SUV/SUV)来确定示踪剂摄取情况。43例患者中有171个病灶。比较不同时间点的所有病灶,注射示踪剂后10分钟时平均SUV最大(8.2),1小时(8.15)和3小时(7.6)时略有下降。同样,在10分钟、1小时和3小时时,原发灶(n = 30;分别为0.98、1.01和0.98)、淋巴结转移灶(n = 37;分别为0.82、0.84和0.81)以及远处转移灶(n = 104;分别为0.81、0.79和0.74)的平均SUV log也有类似模式。TBR在这3个时间点也显示出无显著差异。镓-FAPI-46 PET/CT成像显示,通过SUV指标确定,肿瘤和背景摄取非常稳定,且在注射后3小时内保持高TBRs。因此,有可能在注射镓-FAPI-46后10 - 20分钟内进行扫描,改善工作流程并减少患者等待时间。正在更大队列中对这些发现进行验证。