Laboratory for Radiopharmacy, Ghent University, Ghent, Belgium.
Department of Diagnostic Sciences, Ghent University, Ghent, Belgium.
Sci Rep. 2021 Nov 19;11(1):22623. doi: 10.1038/s41598-021-02104-6.
This two-part preclinical study aims to evaluate prostate specific membrane antigen (PSMA) as a valuable target for expression-based imaging applications and to determine changes in target binding in function of varying apparent molar activities (MA) of [F]AlF-PSMA-11. For the evaluation of PSMA expression levels, male NOD/SCID mice bearing prostate cancer (PCa) xenografts of C4-2 (PSMA+++), 22Rv1 (PSMA+) and PC-3 (PSMA-) were administered [F]AlF-PSMA-11 with a medium MA (20.24 ± 3.22 MBq/nmol). SUV and SUV values were respectively 3.22 and 3.17 times higher for the high versus low PSMA expressing tumors (p < 0.0001). To evaluate the effect of varying MA, C4-2 and 22Rv1 xenograft bearing mice underwent additional [F]AlF-PSMA-11 imaging with a high (211.2 ± 38.9 MBq/nmol) and/or low MA (1.92 ± 0.27 MBq/nmol). SUV values showed a significantly increasing trend with higher MA. Significant changes were found for SUV and SUV between the high versus low MA and medium versus low MA (both p < 0.05), but not between the high versus medium MA (p = 0.055 and 0.25, respectively). The effect of varying MA was more pronounced in low expressing tumors and PSMA expressing tissues (e.g. salivary glands and kidneys). Overall, administration of a high MA increases the detection of low expression tumors while also increasing uptake in PSMA expressing tissues, possibly leading to false positive findings. In radioligand therapy, a medium MA could reduce radiation exposure to dose-limiting organs with only limited effect on radionuclide accumulation in the tumor.
本研究分为两部分,旨在评估前列腺特异膜抗原(PSMA)作为表达为基础的成像应用的有价值的靶标,并确定[F]AlF-PSMA-11 的表观摩尔活性(MA)变化时,靶标结合的变化。为了评估 PSMA 表达水平,用具有中 MA(20.24 ± 3.22 MBq/nmol)的[F]AlF-PSMA-11 处理携带有前列腺癌(PCa)异种移植物的雄性 NOD/SCID 小鼠,这些异种移植物包括 C4-2(PSMA+++)、22Rv1(PSMA+)和 PC-3(PSMA-)。高表达 PSMA 的肿瘤的 SUV 和 SUV 值分别比低表达 PSMA 的肿瘤高 3.22 和 3.17 倍(p<0.0001)。为了评估 MA 变化的影响,在 C4-2 和 22Rv1 异种移植瘤小鼠中进行了另外的[F]AlF-PSMA-11 成像,使用高(211.2 ± 38.9 MBq/nmol)和/或低 MA(1.92 ± 0.27 MBq/nmol)。SUV 值显示出随 MA 增加而呈明显上升趋势。高 MA 与低 MA 相比和中 MA 与低 MA 相比,SUV 和 SUV 值均有显著变化(均 p<0.05),但高 MA 与中 MA 相比无显著变化(p=0.055 和 0.25)。MA 变化的影响在低表达肿瘤和 PSMA 表达组织中更为明显(例如唾液腺和肾脏)。总的来说,高 MA 的给药增加了低表达肿瘤的检测,同时也增加了 PSMA 表达组织的摄取,这可能导致假阳性发现。在放射性配体治疗中,中等 MA 可减少对剂量限制器官的辐射暴露,而对肿瘤中放射性核素的积累影响有限。