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前列腺特异性膜抗原报告和数据系统第 2.0 版。

Prostate-specific Membrane Antigen Reporting and Data System Version 2.0.

机构信息

Department of Nuclear Medicine, University Hospital Würzburg, Würzburg, Germany; The Russell H Morgan Department of Radiology and Radiological Science, Division of Nuclear Medicine and Molecular Imaging, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Department of Nuclear Medicine, University Hospital Würzburg, Würzburg, Germany.

出版信息

Eur Urol. 2023 Nov;84(5):491-502. doi: 10.1016/j.eururo.2023.06.008. Epub 2023 Jul 4.

Abstract

Prostate-specific Membrane Antigen Reporting and Data System (PSMA-RADS) was introduced for standardized reporting, and PSMA-RADS version 1.0 allows classification of lesions based on their likelihood of representing a site of prostate cancer on PSMA-targeted positron emission tomography (PET). In recent years, this system has extensively been investigated. Increasing evidence has accumulated that the different categories reflect their actual meanings, such as true positivity in PSMA-RADS 4 and 5 lesions. Interobserver agreement studies demonstrated high concordance among a broad spectrum of Ga- or F-labeled, PSMA-directed radiotracers, even for less experienced readers. Moreover, this system has also been applied to challenging clinical scenarios and to assist in clinical decision-making, for example, to avoid overtreatment in oligometastatic disease. Nonetheless, with an increasing use of PSMA-RADS 1.0, this framework has shown not only benefits, but also limitations, for example, for follow-up assessment of locally treated lesions. Thus, we aimed to update the PSMA-RADS framework to include a refined set of categories in order to optimize lesion-level characterization and best assist in clinical decision-making (PSMA-RADS version 2.0).

摘要

前列腺特异性膜抗原报告和数据系统(PSMA-RADS)用于标准化报告,PSMA-RADS 版本 1.0 允许根据 PSMA 靶向正电子发射断层扫描(PET)上代表前列腺癌部位的可能性对病变进行分类。近年来,该系统得到了广泛的研究。越来越多的证据表明,不同类别反映了它们的实际意义,例如 PSMA-RADS 4 和 5 病变中的真正阳性。观察者间一致性研究表明,在广泛的 Ga 或 F 标记、PSMA 导向的放射性示踪剂中,即使是经验较少的读者,也具有很高的一致性。此外,该系统还应用于具有挑战性的临床情况,并辅助临床决策,例如,避免寡转移疾病的过度治疗。尽管如此,随着 PSMA-RADS 1.0 的使用越来越多,该框架不仅显示出了益处,也显示出了局限性,例如,对局部治疗病变的随访评估。因此,我们旨在更新 PSMA-RADS 框架,以纳入一套更精细的类别,以便优化病变水平的特征描述,并最好地辅助临床决策(PSMA-RADS 版本 2.0)。

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