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.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9330009 | PMC |
http://dx.doi.org/10.3390/ijms23158133 | DOI Listing |
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