Department of Urology, Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia; Faculty of Medicine, The University of Queensland, Brisbane, Queensland, Australia.
University of Queensland Centre for Clinical Research, Faculty of Medicine, Brisbane, Queensland, Australia.
Eur Urol Focus. 2022 Sep;8(5):1256-1269. doi: 10.1016/j.euf.2021.07.016. Epub 2021 Aug 21.
Staging, restaging, and surveillance of urothelial carcinoma (UC) is challenging due to suboptimal accuracy of standard of care imaging modalities. Prostate-specific membrane antigen (PSMA) imaging may serve to improve characterisation of UC.
To appraise available literature regarding cellular, imaging, and prognostic implications of PSMA for UC.
A systematic review was performed considering all available literature (including conference abstracts) published from 1990 to 2020 and reported according to Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) guidelines following registration in PROSPERO (CRD42020186744). All relevant texts relating to immunohistochemical analysis and PSMA-based imaging in UC were included and collated. Additionally, FOLH1 (gene encoding PSMA) expression according to The Cancer Genome Atlas (TCGA) database was analysed as well as according to consensus and TCGA molecular classification subtypes and subsequently compared with clinical outcomes.
PSMA expression across UC tumour tissue was heterogeneous (0-100%) but appeared to decrease with increased grade and stage. The TCGA analysis demonstrated loss of FOLH1 expression with increasing T stage (p = 0.0180) and N stage (p = 0.0269), and reduced FOLH1 expression was associated with worse disease-free survival. PSMA expression in UC neovasculature was variable but mostly increased (44-100%). Eleven reports of PSMA-based imaging for UC were identified, reporting on 18 patients. PSMA positron emission tomography (PET) imaging was positive in 17 out of 18 patients. The included literature review data were limited by mostly low-quality, retrospective studies.
Tissue PSMA, or FOLH1 expression, may inversely be associated with pathological and survival outcomes in localised UC. PSMA PET imaging may improve detection of metastatic disease and response to systemic therapy due to PSMA expression in neovasculature. Available evidence is limited; thus, larger, prospective studies are required to confirm early results and define populations that benefit most.
In this systematic review, we assess the potential role of prostate-specific membrane antigen in urothelial cancer. We found that its utility is in expression of blood vessels surrounding metastasis. We conclude that it may be beneficial in detecting metastasis and response to systemic therapies.
由于标准护理成像方式的准确性不理想,尿路上皮癌(UC)的分期、再分期和监测具有挑战性。前列腺特异性膜抗原(PSMA)成像可能有助于提高 UC 的特征描述。
评估 PSMA 对 UC 的细胞、成像和预后意义的现有文献。
系统评价考虑了 1990 年至 2020 年期间发表的所有现有文献(包括会议摘要),并根据首选报告项目进行了报告系统评价和荟萃分析(PRISMA)指南在 PROSPERO(CRD42020186744)中注册后。所有与 UC 中的免疫组织化学分析和 PSMA 为基础的成像相关的文本均被包括并整理。此外,还根据癌症基因组图谱(TCGA)数据库分析了 FOLH1(编码 PSMA 的基因)的表达,以及根据共识和 TCGA 分子分类亚型进行了分析,并随后与临床结果进行了比较。
UC 肿瘤组织中 PSMA 的表达具有异质性(0-100%),但似乎随着分级和分期的增加而降低。TCGA 分析表明,随着 T 分期(p=0.0180)和 N 分期(p=0.0269)的增加,FOLH1 表达丢失,FOLH1 表达降低与无病生存期较差相关。UC 新生血管中 PSMA 的表达是可变的,但大多增加(44-100%)。确定了 11 项用于 UC 的 PSMA 为基础的成像报告,涉及 18 名患者。18 名患者中有 17 名 PSMA 正电子发射断层扫描(PET)成像阳性。纳入的文献综述数据主要受到低质量、回顾性研究的限制。
组织 PSMA 或 FOLH1 表达可能与局部 UC 的病理和生存结果呈负相关。PSMA PET 成像可能通过在新生血管中表达 PSMA 而提高转移性疾病的检测和对全身治疗的反应。现有证据有限;因此,需要更大的、前瞻性研究来证实早期结果,并确定受益最大的人群。
在这项系统评价中,我们评估了前列腺特异性膜抗原在尿路上皮癌中的潜在作用。我们发现,它的效用在于表达肿瘤周围的血管。我们得出结论,它可能有助于检测转移和对全身治疗的反应。