Department of Urology, Hospital de Braga, Hospitais CUF, Faculty of Medicine, University of Coimbra, Coimbra, Portugal.
Department of Urology, University Hospitals Leuven, Leuven, Belgium.
Eur Urol. 2021 Oct;80(4):456-466. doi: 10.1016/j.eururo.2021.06.006. Epub 2021 Jun 24.
Clinical management of testicular germ cell tumours (GCTs) is hampered by low sensitivity and specificity of the biomarkers currently in use. Circulating microRNAs (miRs) might offer the potential to address areas of unmet clinical need.
To systematically evaluate the evidence for clinical applications of serum levels of miR302/367 and miR371-3 in adult testicular GCTs in terms of primary diagnosis, various clinical scenarios, and the costs of clinical implementation.
We performed a critical review of PubMed/Medline, Embase and the Cochrane Library in January 2021 in accordance with Preferred Reporting Items for Systematic Review and Meta-analysis (PRISMA) statement.
Thirty-one manuscripts addressed miR performance and potential clinical use in testicular GCT. Of these, 23 evaluated the utility in primary diagnosis, seven in early-stage disease, and 13 in metastatic disease, and two addressed the costs of clinical implementation. Of the various miRs studied, miR-371a-3p appears the most useful and potentially the only one that needs to be assayed, with an area under the receiver operating characteristic curve >0.90, sensitivity of 89-96%, and specificity of >90% for both seminoma and nonseminoma, surpassing the classic serum tumour markers. The miRs studied to date are not elevated in cases with teratoma only. Levels of miR-371a-3p correlate with primary tumour mass, clinical stage, and International Germ Cell Cancer Collaborative Group risk groups. Serial measurements mirror treatment efficacy in all clinical stages.
Circulating miRNA levels, particularly of miR-371a-3p, have potential for incorporation in clinical practice and may aid in clinical decision-making in various clinical scenarios in GCT.
We analysed the current evidence on the usefulness of blood levels of molecules called microRNAs in the management of testicular tumours. The microRNA-371a-3p molecule has better sensitivity and specificity than the markers currently being measured. This new biomarker may soon have a place in clinical practice.
目前使用的生物标志物的灵敏度和特异性较低,这阻碍了睾丸生殖细胞肿瘤(GCT)的临床管理。循环 microRNAs(miRs)可能有潜力解决临床需求未得到满足的领域。
根据原发性诊断、各种临床情况以及临床实施成本,系统评估血清 miR302/367 和 miR371-3 水平在成人睾丸 GCT 中的临床应用的证据。
我们根据系统评价和荟萃分析的首选报告项目(PRISMA)声明,于 2021 年 1 月在 PubMed/Medline、Embase 和 Cochrane 图书馆进行了批判性审查。
31 篇文献探讨了 miR 的表现和在睾丸 GCT 中的潜在临床应用。其中 23 篇评估了原发性诊断的效用,7 篇评估了早期疾病,13 篇评估了转移性疾病,2 篇评估了临床实施成本。在研究的各种 miRs 中,miR-371a-3p 似乎最有用,并且可能是唯一需要检测的,其受试者工作特征曲线下面积>0.90,灵敏度为 89-96%,特异性为>90%,适用于精原细胞瘤和非精原细胞瘤,超过了经典的血清肿瘤标志物。迄今为止,这些 miRs 在仅存在畸胎瘤的病例中并未升高。miR-371a-3p 的水平与原发肿瘤质量、临床分期和国际生殖细胞癌症协作组风险组相关。在所有临床阶段,连续测量均可反映治疗效果。
循环 miRNA 水平,特别是 miR-371a-3p 的水平,具有纳入临床实践的潜力,并可能有助于 GCT 中各种临床情况下的临床决策。
我们分析了血液中称为 microRNAs 的分子在睾丸肿瘤管理中的有用性的现有证据。miR-371a-3p 分子比目前正在测量的标志物具有更高的灵敏度和特异性。这种新的生物标志物可能很快就会在临床实践中占有一席之地。