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Multiplatform Biomarker Discovery for Bladder Cancer Recurrence Diagnosis

Purpose. Nonmuscle invasive bladder cancer (BCa) has a high recurrence rate requiring lifelong surveillance. Urinary biomarkers are promising as simple alternatives to cystoscopy for the diagnosis of recurrent bladder cancer. However, no single marker can achieve the required accuracy. The purpose o...

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Autores principales: De Paoli, Marine, Gogalic, Selma, Sauer, Ursula, Preininger, Claudia, Pandha, Hardev, Simpson, Guy, Horvath, Andras, Marquette, Christophe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5021863/
https://www.ncbi.nlm.nih.gov/pubmed/27660385
http://dx.doi.org/10.1155/2016/4591910
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author De Paoli, Marine
Gogalic, Selma
Sauer, Ursula
Preininger, Claudia
Pandha, Hardev
Simpson, Guy
Horvath, Andras
Marquette, Christophe
author_facet De Paoli, Marine
Gogalic, Selma
Sauer, Ursula
Preininger, Claudia
Pandha, Hardev
Simpson, Guy
Horvath, Andras
Marquette, Christophe
author_sort De Paoli, Marine
collection PubMed
description Purpose. Nonmuscle invasive bladder cancer (BCa) has a high recurrence rate requiring lifelong surveillance. Urinary biomarkers are promising as simple alternatives to cystoscopy for the diagnosis of recurrent bladder cancer. However, no single marker can achieve the required accuracy. The purpose of this study was to select a multiparameter panel, comprising urinary biomarkers and clinical parameters, for BCa recurrence diagnosis. Experimental Design. Candidate biomarkers were measured in urine samples of BCa patients with recurrence and BCa patients without recurrence. A multiplatform strategy was used for marker quantification comprising a multiplexed microarray and an automated platform for ELISA analysis. A multivariate statistical analysis combined the results from both platforms with the collected clinical data. Results. The best performing combination of biomarkers and clinical parameters achieved an AUC value of 0.91, showing better performance than individual parameters. This panel comprises six biomarkers (cadherin-1, IL-8, ErbB2, IL-6, EN2, and VEGF-A) and three clinical parameters (number of past recurrences, number of BCG therapies, and stage at time of diagnosis). Conclusions. The multiparameter panel could be a useful noninvasive tool for BCa surveillance and potentially impact the clinical management of this disease. Validation of results in an independent cohort is warranted.
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spelling pubmed-50218632016-09-22 Multiplatform Biomarker Discovery for Bladder Cancer Recurrence Diagnosis De Paoli, Marine Gogalic, Selma Sauer, Ursula Preininger, Claudia Pandha, Hardev Simpson, Guy Horvath, Andras Marquette, Christophe Dis Markers Research Article Purpose. Nonmuscle invasive bladder cancer (BCa) has a high recurrence rate requiring lifelong surveillance. Urinary biomarkers are promising as simple alternatives to cystoscopy for the diagnosis of recurrent bladder cancer. However, no single marker can achieve the required accuracy. The purpose of this study was to select a multiparameter panel, comprising urinary biomarkers and clinical parameters, for BCa recurrence diagnosis. Experimental Design. Candidate biomarkers were measured in urine samples of BCa patients with recurrence and BCa patients without recurrence. A multiplatform strategy was used for marker quantification comprising a multiplexed microarray and an automated platform for ELISA analysis. A multivariate statistical analysis combined the results from both platforms with the collected clinical data. Results. The best performing combination of biomarkers and clinical parameters achieved an AUC value of 0.91, showing better performance than individual parameters. This panel comprises six biomarkers (cadherin-1, IL-8, ErbB2, IL-6, EN2, and VEGF-A) and three clinical parameters (number of past recurrences, number of BCG therapies, and stage at time of diagnosis). Conclusions. The multiparameter panel could be a useful noninvasive tool for BCa surveillance and potentially impact the clinical management of this disease. Validation of results in an independent cohort is warranted. Hindawi Publishing Corporation 2016 2016-08-31 /pmc/articles/PMC5021863/ /pubmed/27660385 http://dx.doi.org/10.1155/2016/4591910 Text en Copyright © 2016 Marine De Paoli et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
De Paoli, Marine
Gogalic, Selma
Sauer, Ursula
Preininger, Claudia
Pandha, Hardev
Simpson, Guy
Horvath, Andras
Marquette, Christophe
Multiplatform Biomarker Discovery for Bladder Cancer Recurrence Diagnosis
title Multiplatform Biomarker Discovery for Bladder Cancer Recurrence Diagnosis
title_full Multiplatform Biomarker Discovery for Bladder Cancer Recurrence Diagnosis
title_fullStr Multiplatform Biomarker Discovery for Bladder Cancer Recurrence Diagnosis
title_full_unstemmed Multiplatform Biomarker Discovery for Bladder Cancer Recurrence Diagnosis
title_short Multiplatform Biomarker Discovery for Bladder Cancer Recurrence Diagnosis
title_sort multiplatform biomarker discovery for bladder cancer recurrence diagnosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5021863/
https://www.ncbi.nlm.nih.gov/pubmed/27660385
http://dx.doi.org/10.1155/2016/4591910
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