Division of Nuclear Medicine and Molecular Imaging, Department of Radiology, Stanford University, Stanford, California.
Department of Radiation Oncology, Stanford University, Stanford, California.
J Nucl Med. 2018 May;59(5):803-808. doi: 10.2967/jnumed.117.197624. Epub 2017 Oct 30.
Ga-labeled DOTA-4-amino-1-carboxymethyl-piperidine-d-Phe-Gln-Trp-Ala-Val-Gly-His-Sta-Leu-NH (Ga-RM2) is a synthetic bombesin receptor antagonist that targets gastrin-releasing peptide receptor (GRPr). GRPr proteins are highly overexpressed in several human tumors, including prostate cancer (PCa). We present data from the use of Ga-RM2 in patients with biochemical recurrence (BCR) of PCa and negative findings on conventional imaging. We enrolled 32 men with BCR of PCa, who were 59-83 y old (mean ± SD, 68.7 ± 6.4 y). Imaging started at 40-69 min (mean, 50.5 ± 6.8 min) after injection of 133.2-151.7 MBq (mean, 140.6 ± 7.4 MBq) of Ga-RM2 using a time-of-flight-enabled simultaneous PET/MRI scanner. T1-weighted, T2-weighted, and diffusion-weighted images were acquired. All patients had a rising level of prostate-specific antigen (PSA) (range, 0.3-119.0 ng/mL; mean, 10.1 ± 21.3 ng/mL) and negative findings on conventional imaging (CT or MRI, and a Tc-methylene diphosphonate bone scan) before enrollment. The observed Ga-RM2 PET detection rate was 71.8%. Ga-RM2 PET identified recurrent PCa in 23 of the 32 participants, whereas the simultaneous MRI scan identified findings compatible with recurrent PCa in 11 of the 32 patients. PSA velocity was 0.32 ± 0.59 ng/mL/y (range, 0.04-1.9 ng/mL/y) in patients with negative PET findings and 2.51 ± 2.16 ng/mL/y (range, 0.13-8.68 ng/mL/y) in patients with positive PET findings ( = 0.006). Ga-RM2 PET can be used for assessment of GRPr expression in patients with BCR of PCa. High uptake in multiple areas compatible with cancer lesions suggests that Ga-RM2 is a promising PET radiopharmaceutical for localization of disease in patients with BCR of PCa and negative findings on conventional imaging.
Ga 标记的 DOTA-4-氨基-1-羧甲基-哌啶-d-Phe-Gln-Trp-Ala-Val-Gly-His-Sta-Leu-NH(Ga-RM2)是一种合成的蛙皮素受体拮抗剂,其靶向胃泌素释放肽受体(GRPr)。GRPr 蛋白在包括前列腺癌(PCa)在内的几种人类肿瘤中高度过表达。我们报告了 Ga-RM2 在生化复发(BCR)的 PCa 患者和常规影像学阴性发现中的使用数据。
我们纳入了 32 名 BCR 的 PCa 男性患者,年龄为 59-83 岁(平均值±标准差,68.7±6.4 岁)。在注射 133.2-151.7 MBq(平均值,140.6±7.4 MBq)Ga-RM2 后 40-69 分钟(平均值,50.5±6.8 分钟)开始进行成像,使用配备飞行时间功能的同时 PET/MRI 扫描仪。采集 T1 加权、T2 加权和弥散加权图像。所有患者在入组前均有前列腺特异性抗原(PSA)水平升高(范围,0.3-119.0 ng/mL;平均值,10.1±21.3 ng/mL)和常规影像学(CT 或 MRI 及 Tc-亚甲基二膦酸盐骨扫描)阴性发现。观察到的 Ga-RM2 PET 检测率为 71.8%。Ga-RM2 PET 在 32 名参与者中的 23 名中识别出复发性 PCa,而同时进行的 MRI 扫描在 32 名患者中的 11 名中识别出与复发性 PCa 相符的发现。PET 结果阴性的患者 PSA 速度为 0.32±0.59 ng/mL/y(范围,0.04-1.9 ng/mL/y),而 PET 结果阳性的患者 PSA 速度为 2.51±2.16 ng/mL/y(范围,0.13-8.68 ng/mL/y)(=0.006)。Ga-RM2 PET 可用于评估 BCR 的 PCa 患者中 GRPr 的表达。在与癌症病变多处兼容的高摄取提示 Ga-RM2 是一种有前途的 PET 放射性药物,可用于定位 BCR 的 PCa 患者和常规影像学阴性发现的疾病。