Division of Nuclear Medicine and Molecular Imaging, Department of Radiology, Stanford University, Stanford, California.
Division of Body MRI, Department of Radiology, Stanford University, Stanford, California.
J Nucl Med. 2023 May;64(5):744-750. doi: 10.2967/jnumed.122.264448. Epub 2022 Nov 17.
Targeting of lesions seen on multiparametric MRI (mpMRI) improves prostate cancer (PC) detection at biopsy. However, 20%-65% of highly suspicious lesions on mpMRI (PI-RADS [Prostate Imaging-Reporting and Data System] 4 or 5) are false-positives (FPs), while 5%-10% of clinically significant PC (csPC) are missed. Prostate-specific membrane antigen (PSMA) and gastrin-releasing peptide receptors (GRPRs) are both overexpressed in PC. We therefore aimed to evaluate the potential of Ga-PSMA11 and Ga-RM2 PET/MRI for biopsy guidance in patients with suspected PC. A highly selective cohort of 13 men, aged 58.0 ± 7.1 y, with suspected PC (persistently high prostate-specific antigen [PSA] and PSA density) but negative or equivocal mpMRI results or negative biopsy were prospectively enrolled to undergo Ga-PSMA11 and Ga-RM2 PET/MRI. PET/MRI included whole-body and dedicated pelvic imaging after a delay of 20 min. All patients had targeted biopsy of any lesions seen on PET followed by standard 12-core biopsy. The SUV of suspected PC lesions was collected and compared with gold standard biopsy. PSA and PSA density at enrollment were 9.8 ± 6.0 (range, 1.5-25.5) ng/mL and 0.20 ± 0.18 (range, 0.06-0.68) ng/mL, respectively. Standardized systematic biopsy revealed a total of 14 PCs in 8 participants: 7 were csPC and 7 were nonclinically significant PC (ncsPC). Ga-PSMA11 identified 25 lesions, of which 11 (44%) were true-positive (TP) (5 csPC). Ga-RM2 showed 27 lesions, of which 14 (52%) were TP, identifying all 7 csPC and also 7 ncsPC. There were 17 concordant lesions in 11 patients versus 14 discordant lesions in 7 patients between Ga-PSMA11 and Ga-RM2 PET. Incongruent lesions had the highest rate of FP (12 FP vs. 2 TP). SUV was significantly higher for TP than FP lesions in delayed pelvic imaging for Ga-PSMA11 (6.49 ± 4.14 vs. 4.05 ± 1.55, = 0.023) but not for whole-body images, nor for Ga-RM2. Our results show that Ga-PSMA11 and Ga-RM2 PET/MRI are feasible for biopsy guidance in suspected PC. Both radiopharmaceuticals detected additional clinically significant cancers not seen on mpMRI in this selective cohort. Ga-RM2 PET/MRI identified all csPC confirmed at biopsy.
靶向多参数 MRI(mpMRI)上可见的病变可提高前列腺癌(PC)活检的检出率。然而,mpMRI(前列腺成像报告和数据系统[PI-RADS] 4 或 5 级)上 20%-65%的高度可疑病变为假阳性(FP),而 5%-10%的临床显著 PC(csPC)漏诊。前列腺特异性膜抗原(PSMA)和胃泌素释放肽受体(GRPR)在 PC 中均过度表达。因此,我们旨在评估 Ga-PSMA11 和 Ga-RM2 PET/MRI 用于有疑似 PC 患者活检指导的潜力。
我们前瞻性地招募了 13 名年龄为 58.0±7.1 岁的疑似 PC(持续高前列腺特异性抗原[PSA]和 PSA 密度)但 mpMRI 结果阴性或不确定或活检阴性的高度选择性患者,进行 Ga-PSMA11 和 Ga-RM2 PET/MRI 检查。PET/MRI 在 20 分钟延迟后包括全身和专用骨盆成像。所有患者均对 PET 上见到的任何病变进行靶向活检,然后进行标准的 12 针活检。采集可疑 PC 病变的 SUV,并与金标准活检进行比较。
入组时的 PSA 和 PSA 密度分别为 9.8±6.0(范围,1.5-25.5)ng/mL 和 0.20±0.18(范围,0.06-0.68)ng/mL。标准化系统活检显示 8 名参与者中有 14 例 PC:7 例为 csPC,7 例为非临床显著 PC(ncsPC)。Ga-PSMA11 发现 25 个病变,其中 11 个(44%)为真阳性(TP)(5 个 csPC)。Ga-RM2 显示 27 个病变,其中 14 个(52%)为 TP,可识别所有 7 个 csPC 和 7 个 ncsPC。在 11 名患者中有 17 个一致的病变,在 7 名患者中有 14 个不一致的病变,Ga-PSMA11 和 Ga-RM2 PET 之间存在差异。不一致的病变中 FP 的发生率最高(12 个 FP 对 2 个 TP)。在 Ga-PSMA11 延迟盆腔成像中,TP 病变的 SUV 明显高于 FP 病变(6.49±4.14 对 4.05±1.55, = 0.023),但全身成像和 Ga-RM2 则不然。
我们的结果表明,Ga-PSMA11 和 Ga-RM2 PET/MRI 可用于疑似 PC 的活检指导。这两种放射性药物在这个选择性队列中都检测到了 mpMRI 上未见的额外的临床显著癌症。Ga-RM2 PET/MRI 可识别活检证实的所有 csPC。