Unit of Pathological Anatomy, University Hospital of Pisa, Pisa, Italy.
Department of Surgical, Medical, Molecular Pathology and Critical Area, University of Pisa, Pisa, Italy.
J Mol Diagn. 2020 Apr;22(4):457-466. doi: 10.1016/j.jmoldx.2019.12.009. Epub 2020 Feb 7.
Pleural effusions are among the first clinical manifestations of malignant pleural mesothelioma (MPM) and often constitute the only available material for diagnosis. Although an MPM diagnosis can be reliable on cytology, the reported sensitivity is low (30% to 75%). Particularly, it can be hard to discriminate epithelioid MPM, the most common histotype, from reactive mesothelial hyperplasia (MH). Currently, BRCA1-associated protein 1 (BAP1) and CDKN2A (p16), evaluated by immunohistochemistry and fluorescent in situ hybridization, respectively, are the most valuable markers to discriminate MPM and MH. Both markers have a high specificity, but their sensitivity is not always satisfying, even when used together. We have recently developed a 117-gene expression panel, based on Nanostring technology, able to differentiate epithelioid MPM from MH pleural tissues better than BAP1 and p16. Herein, we evaluated the efficacy of the same panel on an independent retrospective cohort of 23 MPM and 11 MH pleural effusions (cell blocks and smears). The overall sensitivity and specificity of the panel were equal to 0.9565 and 1, respectively. Moreover, the panel performance was compared with BAP1 and p16 on 25 cell blocks. Sensitivity levels of gene panel, BAP1 alone, p16 alone, and BAP1 plus p16 were 1, 0.5882, 0.4706, and 0.7647, respectively. Specificity was always 1. Although further validation is needed, this gene panel could really facilitate patients' management, allowing a definitive MPM diagnosis directly on pleural effusions.
胸腔积液是恶性胸膜间皮瘤(MPM)的最初临床表现之一,通常是诊断的唯一可用材料。尽管在细胞学上可以可靠地诊断 MPM,但报告的敏感性较低(30%至 75%)。特别是,区分最常见的组织学类型上皮样 MPM 和反应性间皮增生(MH)可能具有挑战性。目前,BRCA1 相关蛋白 1(BAP1)和 CDKN2A(p16)分别通过免疫组织化学和荧光原位杂交评估,是区分 MPM 和 MH 的最有价值的标志物。这两种标志物具有很高的特异性,但即使一起使用,其敏感性也并不总是令人满意。我们最近开发了一种基于 Nanostring 技术的 117 个基因表达面板,能够更好地区分上皮样 MPM 和 MH 胸膜组织,优于 BAP1 和 p16。在此,我们在 23 例 MPM 和 11 例 MH 胸腔积液(细胞块和涂片)的独立回顾性队列中评估了该面板的疗效。该面板的总体敏感性和特异性分别为 0.9565 和 1。此外,还将该面板的性能与 25 个细胞块上的 BAP1 和 p16 进行了比较。基因面板、BAP1 单独、p16 单独和 BAP1 加 p16 的敏感性水平分别为 1、0.5882、0.4706 和 0.7647,特异性均为 1。尽管还需要进一步验证,但该基因面板确实可以方便患者管理,允许直接从胸腔积液中明确诊断 MPM。