Ludwig Boltzmann Institute Applied Diagnostics, Vienna, Austria.
Department of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.
J Nucl Med. 2023 Jun;64(6):863-868. doi: 10.2967/jnumed.122.264981. Epub 2023 Jan 19.
The present study was carried out to investigate whether PET imaging can be used as a potential substitute for immunohistochemical analysis of tumor samples in prostate cancer (PC) patients. Correlation between imaging signals of 2 PET tracers and the corresponding target structures was assessed. The first tracer was [Ga]Ga-PSMA (prostate-specific membrane antigen)-HBED-CC (,'-bis [2-hydroxy-5-(carboxyethyl)benzyl]ethylenediamine-,'-diacetic acid) [Ga]Ga-PSMA ([Ga]PSMA), which is already implemented in clinical routines. The second tracer was 16β-[F]fluoro-5α-dihydrotestosterone (16β-[F]FDHT), which binds to the androgen receptor (AR). The AR is particularly interesting in PC, because AR expression status and its shift during therapy might directly influence patient care. This prospective, explorative clinical study included 10 newly diagnosed PC patients. Each patient underwent [Ga]PSMA PET/MRI and [F]FDHT PET/MRI scans before prostatectomy. Cancer SUVs were determined and related to background SUVs. After prostatectomy, tumor tissue was sampled, and AR and prostate-specific membrane antigen (PSMA) expression was determined. AR and PSMA expression was evaluated quantitatively with the open-source bioimage analysis software QuPath and with a 4-tier rating system. Correlation between imaging signals and marker expression was statistically assessed. For [F]FDHT, the SUV/SUV ratio showed a significant, strong correlation ( = 0.72; = 0.019) with the AR optical density of the correlating tissue sample. The correlation between PSMA optical density and the [Ga]PSMA SUV/SUV ratio was not significant ( = 0.061), yet a positive correlation trend could be observed ( = 0.61). SUV/SUV ratios were higher for [Ga]PSMA (mean ± SD, 34.9 ± 24.8) than for [F]FDHT (4.8 ± 1.2). In line with these findings, the tumor detection rates were 90% for the [Ga]PSMA PET scan but only 40% for the [F]FDHT PET scan. The 4-tier rating of PSMA staining intensity yielded very homogeneous results, with values of 3+ for most subjects (90%). AR staining was rated as 1+ in 2 patients (20%), 2+ in 4 patients (40%), and 3+ in 4 patients (40%). [F]FDHT PET may be useful for monitoring AR expression and alterations in AR expression during treatment of PC patients. This approach may facilitate early detection of treatment resistance and allows for adaptation of therapy to prevent cancer progression. [F]FDHT PET is inferior to [Ga]PSMA PET for primary PC diagnosis, but the correlation between [Ga]PSMA SUVs and PSMA expression is weaker than that between [F]FDHT and the AR.
本研究旨在探讨 PET 成像是否可以作为前列腺癌 (PC) 患者肿瘤样本免疫组织化学分析的潜在替代方法。评估了两种 PET 示踪剂的成像信号与相应靶结构之间的相关性。第一种示踪剂是 [Ga]Ga-PSMA(前列腺特异性膜抗原)-HBED-CC(双-[2-羟基-5-(羧乙基)苄基]乙二胺-N,N′-二乙酸)[Ga]Ga-PSMA ([Ga]PSMA),已经在临床常规中实施。第二种示踪剂是 16β-[F]氟-5α-二氢睾酮 (16β-[F]FDHT),它与雄激素受体 (AR) 结合。AR 在 PC 中特别有趣,因为 AR 表达状态及其在治疗过程中的变化可能直接影响患者的护理。 这项前瞻性、探索性临床研究纳入了 10 名新诊断的 PC 患者。每位患者在前列腺切除术前均进行 [Ga]PSMA PET/MRI 和 [F]FDHT PET/MRI 扫描。确定了癌症 SUV 并与背景 SUV 相关。前列腺切除术后,采集肿瘤组织,并测定 AR 和前列腺特异性膜抗原 (PSMA) 的表达。使用开源生物图像分析软件 QuPath 和 4 级评分系统对 AR 和 PSMA 表达进行定量评估。统计评估了成像信号与标志物表达之间的相关性。 对于 [F]FDHT,SUV/SUV 比值与相关组织样本的 AR 光密度呈显著、强相关性 (=0.72;=0.019)。PSMA 光密度与 [Ga]PSMA SUV/SUV 比值之间无显著相关性 (=0.061),但可观察到正相关趋势 (=0.61)。[Ga]PSMA 的 SUV/SUV 比值(平均值±标准差,34.9±24.8)高于 [F]FDHT(4.8±1.2)。与此发现一致,[Ga]PSMA PET 扫描的肿瘤检测率为 90%,而 [F]FDHT PET 扫描的肿瘤检测率仅为 40%。PSMA 染色强度的 4 级评分产生了非常均匀的结果,大多数受试者(90%)的值为 3+。AR 染色在 2 名患者(20%)中评为 1+,在 4 名患者(40%)中评为 2+,在 4 名患者(40%)中评为 3+。 [F]FDHT PET 可能有助于监测 AR 表达及其在 PC 患者治疗过程中的变化。这种方法可以促进对治疗耐药性的早期检测,并允许调整治疗以防止癌症进展。[F]FDHT PET 对原发性 PC 的诊断不如 [Ga]PSMA PET,但 [Ga]PSMA SUV 与 PSMA 表达之间的相关性弱于 [F]FDHT 与 AR 之间的相关性。