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[前列腺特异性膜抗原(PSMA)配体PET/CT前列腺癌成像操作指南]

[Procedure Guideline for Prostate Cancer Imaging with PSMA-ligand PET/CT].

作者信息

Afshar-Oromieh Ali, Eiber Matthias, Fendler Wolfgang, Schmidt Matthias, Rahbar Kambiz, Ahmadzadehfar Hojjat, Umutlu Lale, Hadaschik Boris, Hakenberg Oliver W, Fornara Paolo, Kurth Jens, Neels O, Wester Hans-Jürgen, Schwaiger Markus, Kopka Klaus, Haberkorn Uwe, Herrmann Ken, Krause Bernd J

机构信息

Universitätsklinikum Bern, Inselspital, Klinik für Nuklearmedizin, Universität Bern, Schweiz.

Technische Universität München, Klinik für Nuklearmedizin.

出版信息

Nuklearmedizin. 2023 Feb;62(1):5-19. doi: 10.1055/a-1984-8167. Epub 2023 Feb 6.

Abstract

PSMA-PET/CT for imaging prostate cancer (PC) has spread worldwide since its clinical introduction in 2011. The majority of experiences have been collected for PSMA-PET-imaging of recurrent PC. Data for primary staging of high-risk PC are highly promising. Meanwhile, a plethora of PSMA-ligands are available for clinical use (e. g. Ga-PSMA-11, Ga-PSMA-I&T, Ga-PSMA-617, F-DCFBC, F-DCFPyL, F-PSMA-1007, F-rhPSMA-7 and F-JK-PSMA-7). However, an official approval is available only for Ga-PSMA-11 (approved by the US FDA in 2020) and F-DCFPyL (approved by the US FDA in 2021).Recommendations for acquisition times vary from 1-2 h p. i. It has been shown that for the majority of tumour lesions, the contrast in PSMA-PET/CT increases with time. Therefore, additional late imaging can help to clarify unclear findings. PSMA-PET/CT should be performed prior to commencing an androgen deprivation therapy (ADT) since (long term) ADT reduces the visibility of PC lesions. Following injection of PSMA-ligands, hydration and forced diuresis are recommended for PSMA-ligands with primarily excretion via the kidneys in order to increase the visibility of tumour lesions adjacent to the urinary bladder.PSMA-ligands are physiologically taken up in multiple normal organs. For some F-labelled PSMA-ligands, presence of unspecific focal bone uptake has been reported. When using these tracers, focal bone uptake without CT-correlate should be interpreted with great caution. Besides prostate cancer, practically all solid tumors express PSMA in their neovasculature thereby taking up PSMA-ligands, although usually at a lower extent compared to PC. Also multiple benign lesions and inflammatory processes (e. g. lymph nodes) take up PSMA-ligands, also usually at lower extent compared to PC.

摘要

自2011年临床应用以来,用于前列腺癌(PC)成像的PSMA-PET/CT已在全球范围内广泛应用。大多数经验是关于复发性PC的PSMA-PET成像收集的。高危PC的初始分期数据非常有前景。同时,有大量PSMA配体可用于临床(例如,Ga-PSMA-11、Ga-PSMA-I&T、Ga-PSMA-617、F-DCFBC、F-DCFPyL、F-PSMA-1007、F-rhPSMA-7和F-JK-PSMA-7)。然而,目前只有Ga-PSMA-11(2020年获得美国食品药品监督管理局批准)和F-DCFPyL(2021年获得美国食品药品监督管理局批准)获得了官方批准。采集时间的建议从注射后1-2小时不等。研究表明,对于大多数肿瘤病变,PSMA-PET/CT中的对比度会随时间增加。因此,额外的延迟成像有助于澄清不明确的发现。PSMA-PET/CT应在开始雄激素剥夺治疗(ADT)之前进行,因为(长期)ADT会降低PC病变的可见性。注射PSMA配体后,对于主要通过肾脏排泄的PSMA配体,建议进行水化和强制利尿,以提高膀胱附近肿瘤病变的可见性。PSMA配体在多个正常器官中会被生理性摄取。对于一些F标记的PSMA配体,已报道存在非特异性局灶性骨摄取。使用这些示踪剂时,对于无CT相关性的局灶性骨摄取应极其谨慎地进行解读。除了前列腺癌,实际上所有实体瘤在其新生血管中都表达PSMA,从而摄取PSMA配体,尽管通常程度低于PC。此外,多种良性病变和炎症过程(如淋巴结)也摄取PSMA配体,通常程度也低于PC。

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