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Ga-PSMA11 和 Ga-RM2 PET/MRI 引导前列腺癌疑似患者活检的初步研究。

A Pilot Study of Ga-PSMA11 and Ga-RM2 PET/MRI for Biopsy Guidance in Patients with Suspected Prostate Cancer.

机构信息

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.

出版信息

J Nucl Med. 2023 May;64(5):744-750. doi: 10.2967/jnumed.122.264448. Epub 2022 Nov 17.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6abe/10152125/87b7d6faa33e/jnumed.122.264448absf1.jpg

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