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Prediction of progression in pTa and pT1 bladder carcinomas with p53, p16 and pRb

Currently available prognostic tools appear unable to adequately predict recurrence and progression in non muscle-invasive bladder carcinomas. We aimed to assess the prognostic value of immunohistochemical evaluation of the cell cycle markers p53, p16 and pRb. Paraffin blocks were obtained from 78 c...

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Autores principales: Hitchings, A W, Kumar, M, Jordan, S, Nargund, V, Martin, J, Berney, D M
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2409830/
https://www.ncbi.nlm.nih.gov/pubmed/15226775
http://dx.doi.org/10.1038/sj.bjc.6601954
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author Hitchings, A W
Kumar, M
Jordan, S
Nargund, V
Martin, J
Berney, D M
author_facet Hitchings, A W
Kumar, M
Jordan, S
Nargund, V
Martin, J
Berney, D M
author_sort Hitchings, A W
collection PubMed
description Currently available prognostic tools appear unable to adequately predict recurrence and progression in non muscle-invasive bladder carcinomas. We aimed to assess the prognostic value of immunohistochemical evaluation of the cell cycle markers p53, p16 and pRb. Paraffin blocks were obtained from 78 cases of pTa and pT1 transitional cell carcinomas, for which long-term follow-up was available. Representative sections were stained using antibodies against p53, p16 and pRb. Altered marker expression was found in 45, 17 and 30% of cases, respectively. Concurrent alteration of two or three markers occurred in 19% of cases, and was significantly associated with grade and stage. In univariate survival analysis, the concurrent alteration of any two markers was significantly associated with progression. The greatest risk was produced by alteration of both p53 and p16, which increased the risk of progression by 14.45 times (95% confidence interval (CI) 3.10–67.35). After adjusting for grade and stage, this risk was 7.73 (CI 1.13–52.70). The markers did not generally predict tumour recurrence, except in the 25 pT1 tumours. In these, p16 alteration was associated with a univariate risk of 2.83 (CI 1.01–7.91), and concurrent p53 and p16 alteration with a risk of 9.29 (CI 1.24–69.50). Overall, we conclude that the immunohistochemical evaluation of p53 and p16 may have independent prognostic value for disease progression, and may help guide management decisions in these tumours.
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spelling pubmed-24098302009-09-10 Prediction of progression in pTa and pT1 bladder carcinomas with p53, p16 and pRb Hitchings, A W Kumar, M Jordan, S Nargund, V Martin, J Berney, D M Br J Cancer Molecular and Cellular Pathology Currently available prognostic tools appear unable to adequately predict recurrence and progression in non muscle-invasive bladder carcinomas. We aimed to assess the prognostic value of immunohistochemical evaluation of the cell cycle markers p53, p16 and pRb. Paraffin blocks were obtained from 78 cases of pTa and pT1 transitional cell carcinomas, for which long-term follow-up was available. Representative sections were stained using antibodies against p53, p16 and pRb. Altered marker expression was found in 45, 17 and 30% of cases, respectively. Concurrent alteration of two or three markers occurred in 19% of cases, and was significantly associated with grade and stage. In univariate survival analysis, the concurrent alteration of any two markers was significantly associated with progression. The greatest risk was produced by alteration of both p53 and p16, which increased the risk of progression by 14.45 times (95% confidence interval (CI) 3.10–67.35). After adjusting for grade and stage, this risk was 7.73 (CI 1.13–52.70). The markers did not generally predict tumour recurrence, except in the 25 pT1 tumours. In these, p16 alteration was associated with a univariate risk of 2.83 (CI 1.01–7.91), and concurrent p53 and p16 alteration with a risk of 9.29 (CI 1.24–69.50). Overall, we conclude that the immunohistochemical evaluation of p53 and p16 may have independent prognostic value for disease progression, and may help guide management decisions in these tumours. Nature Publishing Group 2004-08-02 2004-06-29 /pmc/articles/PMC2409830/ /pubmed/15226775 http://dx.doi.org/10.1038/sj.bjc.6601954 Text en Copyright © 2004 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Molecular and Cellular Pathology
Hitchings, A W
Kumar, M
Jordan, S
Nargund, V
Martin, J
Berney, D M
Prediction of progression in pTa and pT1 bladder carcinomas with p53, p16 and pRb
title Prediction of progression in pTa and pT1 bladder carcinomas with p53, p16 and pRb
title_full Prediction of progression in pTa and pT1 bladder carcinomas with p53, p16 and pRb
title_fullStr Prediction of progression in pTa and pT1 bladder carcinomas with p53, p16 and pRb
title_full_unstemmed Prediction of progression in pTa and pT1 bladder carcinomas with p53, p16 and pRb
title_short Prediction of progression in pTa and pT1 bladder carcinomas with p53, p16 and pRb
title_sort prediction of progression in pta and pt1 bladder carcinomas with p53, p16 and prb
topic Molecular and Cellular Pathology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2409830/
https://www.ncbi.nlm.nih.gov/pubmed/15226775
http://dx.doi.org/10.1038/sj.bjc.6601954
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