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Prognostic Value of Ki67 Percentage, WT-1 Expression and p16/CDKN2A Deletion in Diffuse Malignant Peritoneal Mesothelioma: A Single-Centre Cohort Study

Diffuse malignant peritoneal mesothelioma (DMPM) is a rare malignant neoplasm with a poor survival. Although some advances in knowledge have been obtained for the pleural form, much less is known about DMPM. Advantages in terms of prognosis are still limited and strong efforts need to be made. The a...

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Autores principales: Pezzuto, Federica, Serio, Gabriella, Fortarezza, Francesco, Scattone, Anna, Caporusso, Concetta, Punzi, Alessandra, Cavone, Domenica, Pennella, Antonio, Marzullo, Andrea, Vimercati, Luigi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7345555/
https://www.ncbi.nlm.nih.gov/pubmed/32526924
http://dx.doi.org/10.3390/diagnostics10060386
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author Pezzuto, Federica
Serio, Gabriella
Fortarezza, Francesco
Scattone, Anna
Caporusso, Concetta
Punzi, Alessandra
Cavone, Domenica
Pennella, Antonio
Marzullo, Andrea
Vimercati, Luigi
author_facet Pezzuto, Federica
Serio, Gabriella
Fortarezza, Francesco
Scattone, Anna
Caporusso, Concetta
Punzi, Alessandra
Cavone, Domenica
Pennella, Antonio
Marzullo, Andrea
Vimercati, Luigi
author_sort Pezzuto, Federica
collection PubMed
description Diffuse malignant peritoneal mesothelioma (DMPM) is a rare malignant neoplasm with a poor survival. Although some advances in knowledge have been obtained for the pleural form, much less is known about DMPM. Advantages in terms of prognosis are still limited and strong efforts need to be made. The aim of our study was to correlate several histological and molecular factors with survival in a large cohort of 45 DMPMs. We evaluated histotype, nuclear grade, mitotic count, necrosis, inflammation, desmoplastic reaction, Ki67 percentage, WT-1 expression, p16 protein by immunohistochemistry and CDKN2A deletion by FISH. Our results showed that epithelioid histotype, nuclear grade 2, mitotic count ≤5 x mm(2), absence of desmoplasia and p16/CDKN2A deletion, low Ki67 value, and high WT-1 expression were correlated with the most prolonged survival (p = 0.0001). Moreover, p16 loss in immunohistochemistry reflected CDKN2A deletion detected with FISH, and both were correlated with the worst survival (p = 0.0001). At multivariate analysis, Ki67 value, WT-1 expression and p16/CDKN2A deletion emerged as independent prognostic factors (p = 0.01, p = 0.0001 and p = 0.01, respectively). These parameters are easy to analyse at the time of DMPM diagnosis and may support better patient stratification, prediction of treatment effectiveness and therapeutic optimization.
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spelling pubmed-73455552020-07-09 Prognostic Value of Ki67 Percentage, WT-1 Expression and p16/CDKN2A Deletion in Diffuse Malignant Peritoneal Mesothelioma: A Single-Centre Cohort Study Pezzuto, Federica Serio, Gabriella Fortarezza, Francesco Scattone, Anna Caporusso, Concetta Punzi, Alessandra Cavone, Domenica Pennella, Antonio Marzullo, Andrea Vimercati, Luigi Diagnostics (Basel) Article Diffuse malignant peritoneal mesothelioma (DMPM) is a rare malignant neoplasm with a poor survival. Although some advances in knowledge have been obtained for the pleural form, much less is known about DMPM. Advantages in terms of prognosis are still limited and strong efforts need to be made. The aim of our study was to correlate several histological and molecular factors with survival in a large cohort of 45 DMPMs. We evaluated histotype, nuclear grade, mitotic count, necrosis, inflammation, desmoplastic reaction, Ki67 percentage, WT-1 expression, p16 protein by immunohistochemistry and CDKN2A deletion by FISH. Our results showed that epithelioid histotype, nuclear grade 2, mitotic count ≤5 x mm(2), absence of desmoplasia and p16/CDKN2A deletion, low Ki67 value, and high WT-1 expression were correlated with the most prolonged survival (p = 0.0001). Moreover, p16 loss in immunohistochemistry reflected CDKN2A deletion detected with FISH, and both were correlated with the worst survival (p = 0.0001). At multivariate analysis, Ki67 value, WT-1 expression and p16/CDKN2A deletion emerged as independent prognostic factors (p = 0.01, p = 0.0001 and p = 0.01, respectively). These parameters are easy to analyse at the time of DMPM diagnosis and may support better patient stratification, prediction of treatment effectiveness and therapeutic optimization. MDPI 2020-06-09 /pmc/articles/PMC7345555/ /pubmed/32526924 http://dx.doi.org/10.3390/diagnostics10060386 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Pezzuto, Federica
Serio, Gabriella
Fortarezza, Francesco
Scattone, Anna
Caporusso, Concetta
Punzi, Alessandra
Cavone, Domenica
Pennella, Antonio
Marzullo, Andrea
Vimercati, Luigi
Prognostic Value of Ki67 Percentage, WT-1 Expression and p16/CDKN2A Deletion in Diffuse Malignant Peritoneal Mesothelioma: A Single-Centre Cohort Study
title Prognostic Value of Ki67 Percentage, WT-1 Expression and p16/CDKN2A Deletion in Diffuse Malignant Peritoneal Mesothelioma: A Single-Centre Cohort Study
title_full Prognostic Value of Ki67 Percentage, WT-1 Expression and p16/CDKN2A Deletion in Diffuse Malignant Peritoneal Mesothelioma: A Single-Centre Cohort Study
title_fullStr Prognostic Value of Ki67 Percentage, WT-1 Expression and p16/CDKN2A Deletion in Diffuse Malignant Peritoneal Mesothelioma: A Single-Centre Cohort Study
title_full_unstemmed Prognostic Value of Ki67 Percentage, WT-1 Expression and p16/CDKN2A Deletion in Diffuse Malignant Peritoneal Mesothelioma: A Single-Centre Cohort Study
title_short Prognostic Value of Ki67 Percentage, WT-1 Expression and p16/CDKN2A Deletion in Diffuse Malignant Peritoneal Mesothelioma: A Single-Centre Cohort Study
title_sort prognostic value of ki67 percentage, wt-1 expression and p16/cdkn2a deletion in diffuse malignant peritoneal mesothelioma: a single-centre cohort study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7345555/
https://www.ncbi.nlm.nih.gov/pubmed/32526924
http://dx.doi.org/10.3390/diagnostics10060386
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