Sorino Claudio, Mondoni Michele, Marchetti Giampietro, Agati Sergio, Inchingolo Riccardo, Mei Federico, Flamini Sara, Lococo Filippo, Feller-Kopman David
Division of Pulmonology, Sant'Anna Hospital of Como, University of Insubria, 21100 Varese, Italy.
Respiratory Unit, ASST Santi Paolo e Carlo, Department of Health Sciences, Università degli Studi di Milano, 20122 Milan, Italy.
J Clin Med. 2023 Nov 9;12(22):7006. doi: 10.3390/jcm12227006.
Pleural mesothelioma (PM) is a type of cancer that is highly related to exposure to asbestos fibers. It shows aggressive behavior, and the current therapeutic approaches are usually insufficient to change the poor prognosis. Moreover, apart from staging and histological classification, there are no validated predictors of its response to treatment or its long-term outcomes. Numerous studies have investigated minimally invasive biomarkers in pleural fluid or blood to aid in earlier diagnosis and prognostic assessment of PM. The most studied marker in pleural effusion is mesothelin, which exhibits good specificity but low sensitivity, especially for non-epithelioid PM. Other biomarkers found in pleural fluid include fibulin-3, hyaluronan, microRNAs, and CYFRA-21.1, which have lower diagnostic capabilities but provide prognostic information and have potential roles as therapeutic targets. Serum is the most investigated matrix for biomarkers of PM. Several serum biomarkers in PM have been studied, with mesothelin, osteopontin, and fibulin-3 being the most often tested. A soluble mesothelin-related peptide (SMRP) is the only FDA-approved biomarker in patients with suspected mesothelioma. With different serum and pleural fluid cut-offs, it provides useful information on the diagnosis, prognosis, follow-up, and response to therapy in epithelioid PM. Panels combining different markers and proteomics technologies show promise in terms of improving clinical performance in the diagnosis and monitoring of mesothelioma patients. However, there is still no evidence that early detection can improve the treatment outcomes of PM patients.
胸膜间皮瘤(PM)是一种与接触石棉纤维高度相关的癌症。它具有侵袭性,目前的治疗方法通常不足以改变其不良预后。此外,除了分期和组织学分类外,尚无经过验证的预测其治疗反应或长期预后的指标。许多研究已经调查了胸水或血液中的微创生物标志物,以帮助早期诊断和评估PM的预后。胸水中研究最多的标志物是间皮素,其具有良好的特异性,但敏感性较低,尤其是对于非上皮样PM。胸水中发现的其他生物标志物包括纤维连接蛋白-3、透明质酸、微小RNA和细胞角蛋白19片段(CYFRA-21.1),它们的诊断能力较低,但可提供预后信息,并具有作为治疗靶点的潜在作用。血清是PM生物标志物研究最多的基质。已经研究了PM中的几种血清生物标志物,其中间皮素、骨桥蛋白和纤维连接蛋白-3是最常检测的。可溶性间皮素相关肽(SMRP)是美国食品药品监督管理局(FDA)批准的唯一用于疑似间皮瘤患者的生物标志物。通过不同的血清和胸水临界值,它为上皮样PM的诊断、预后、随访和治疗反应提供了有用信息。结合不同标志物和蛋白质组学技术的检测组合在提高间皮瘤患者诊断和监测的临床性能方面显示出前景。然而,仍然没有证据表明早期检测可以改善PM患者的治疗结果。