Institute of Pathology and Neuropathology and Comprehensive Cancer Center Tuebingen, Eberhard-Karls-University, 72076 Tuebingen, Germany.
Department of Urology, Eberhard-Karls-University, 72076 Tuebingen, Germany.
Int J Mol Sci. 2022 Jul 23;23(15):8133. doi: 10.3390/ijms23158133.
Diagnosis and grading of non-invasive papillary urothelial tumors according to the current WHO classification poses some challenges for pathologists. The diagnostic reproducibility of separating low-grade and high-grade lesions is low, which impacts their clinical management. Whereas papillary urothelial neoplasms with low malignant potential (PUN-LMP) and low-grade papillary non-invasive carcinoma (LG-PUC) are comparable and show frequent local recurrence but rarely metastasize, high-grade papillary non-invasive carcinoma (HG-PUC) has a poor prognosis. The main objective of this work is to develop a multiparametric classification to unambiguously distinguish low-grade and high-grade tumors, considering immunohistochemical stains for p53, FGFR3, CK20, MIB-1, p16, p21 and p-HH3, and pathogenic mutations in , , , , , and . We reviewed and analyzed the clinical and histological data of 45 patients with a consensus diagnosis of PUN-LMP ( = 8), non-invasive LG-PUC ( = 23), and HG-PUC ( = 14). The proliferation index and mitotic count assessed with MIB-1 and P-HH3 staining, respectively correlated with grading and clinical behavior. Targeted sequencing confirmed frequent mutations in non-invasive papillary tumors and identified mutations in as high-risk. Cluster analysis of the different immunohistochemical and molecular parameters allowed a clear separation in two different clusters: cluster 1 corresponding to PUN-LMP and LG-PUC (low MIB-1 and mitotic count/ and mutations) and cluster 2, HG-PUC (high MIB-1 and mitosis count/CK20 +++ expression, WT and mutation). Further analysis is required to validate and analyze the reproducibility of these clusters and their biological and clinical implication.
根据现行世界卫生组织分类诊断和分级非浸润性乳头状尿路上皮肿瘤对病理学家提出了一些挑战。低级别和高级别病变的诊断可重复性低,这影响了它们的临床管理。而低恶性潜能的乳头状尿路上皮肿瘤(PUN-LMP)和低级别乳头状非浸润性癌(LG-PUC)具有可比性,表现为频繁的局部复发但很少转移,而高级别乳头状非浸润性癌(HG-PUC)则预后较差。这项工作的主要目的是开发一种多参数分类方法,以明确区分低级别和高级别肿瘤,同时考虑 p53、FGFR3、CK20、MIB-1、p16、p21 和 p-HH3 的免疫组织化学染色,以及 、 、 、 、 、 中的致病突变。我们回顾和分析了 45 例患者的临床和组织学数据,这些患者的共识诊断为 PUN-LMP(n=8)、非浸润性 LG-PUC(n=23)和 HG-PUC(n=14)。用 MIB-1 和 P-HH3 染色评估的增殖指数和有丝分裂计数分别与分级和临床行为相关。靶向测序证实非浸润性乳头状肿瘤中频繁存在 突变,并鉴定出 中的突变是高危的。不同免疫组织化学和分子参数的聚类分析允许在两个不同的簇中进行明确的分离:簇 1 对应于 PUN-LMP 和 LG-PUC(低 MIB-1 和有丝分裂计数/和 突变),簇 2 对应于 HG-PUC(高 MIB-1 和有丝分裂计数/CK20+++表达,WT 和 突变)。需要进一步分析以验证和分析这些簇的重现性及其生物学和临床意义。