Cargando…
Bladder Cancer Diagnosis and Identification of Clinically Significant Disease by Combined Urinary Detection of Mcm5 and Nuclear Matrix Protein 22
BACKGROUND: Urinary biomarkers for bladder cancer detection are constrained by inadequate sensitivity or specificity. Here we evaluate the diagnostic accuracy of Mcm5, a novel cell cycle biomarker of aberrant growth, alone and in combination with NMP22. METHODS: 1677 consecutive patients under inves...
Autores principales: | , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3392249/ https://www.ncbi.nlm.nih.gov/pubmed/22792272 http://dx.doi.org/10.1371/journal.pone.0040305 |
_version_ | 1782237608845246464 |
---|---|
author | Kelly, John D. Dudderidge, Tim J. Wollenschlaeger, Alex Okoturo, Odu Burling, Keith Tulloch, Fiona Halsall, Ian Prevost, Teresa Prevost, Andrew Toby Vasconcelos, Joana C. Robson, Wendy Leung, Hing Y. Vasdev, Nikhil Pickard, Robert S. Williams, Gareth H. Stoeber, Kai |
author_facet | Kelly, John D. Dudderidge, Tim J. Wollenschlaeger, Alex Okoturo, Odu Burling, Keith Tulloch, Fiona Halsall, Ian Prevost, Teresa Prevost, Andrew Toby Vasconcelos, Joana C. Robson, Wendy Leung, Hing Y. Vasdev, Nikhil Pickard, Robert S. Williams, Gareth H. Stoeber, Kai |
author_sort | Kelly, John D. |
collection | PubMed |
description | BACKGROUND: Urinary biomarkers for bladder cancer detection are constrained by inadequate sensitivity or specificity. Here we evaluate the diagnostic accuracy of Mcm5, a novel cell cycle biomarker of aberrant growth, alone and in combination with NMP22. METHODS: 1677 consecutive patients under investigation for urinary tract malignancy were recruited to a prospective blinded observational study. All patients underwent ultrasound, intravenous urography, cystoscopy, urine culture and cytologic analysis. An immunofluorometric assay was used to measure Mcm5 levels in urine cell sediments. NMP22 urinary levels were determined with the FDA-approved NMP22® Test Kit. RESULTS: Genito-urinary tract cancers were identified in 210/1564 (13%) patients with an Mcm5 result and in 195/1396 (14%) patients with an NMP22 result. At the assay cut-point where sensitivity and specificity were equal, the Mcm5 test detected primary and recurrent bladder cancers with 69% sensitivity (95% confidence interval = 62–75%) and 93% negative predictive value (95% CI = 92–95%). The area under the receiver operating characteristic curve for Mcm5 was 0.75 (95% CI = 0.71–0.79) and 0.72 (95% CI = 0.67–0.77) for NMP22. Importantly, Mcm5 combined with NMP22 identified 95% (79/83; 95% CI = 88–99%) of potentially life threatening diagnoses (i.e. grade 3 or carcinoma in situ or stage ≥pT1) with high specificity (72%, 95% CI = 69–74%). CONCLUSIONS: The Mcm5 immunoassay is a non-invasive test for identifying patients with urothelial cancers with similar accuracy to the FDA-approved NMP22 ELISA Test Kit. The combination of Mcm5 plus NMP22 improves the detection of UCC and identifies 95% of clinically significant disease. Trials of a commercially developed Mcm5 assay suitable for an end-user laboratory alongside NMP22 are required to assess their potential clinical utility in improving diagnostic and surveillance care pathways. |
format | Online Article Text |
id | pubmed-3392249 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33922492012-07-12 Bladder Cancer Diagnosis and Identification of Clinically Significant Disease by Combined Urinary Detection of Mcm5 and Nuclear Matrix Protein 22 Kelly, John D. Dudderidge, Tim J. Wollenschlaeger, Alex Okoturo, Odu Burling, Keith Tulloch, Fiona Halsall, Ian Prevost, Teresa Prevost, Andrew Toby Vasconcelos, Joana C. Robson, Wendy Leung, Hing Y. Vasdev, Nikhil Pickard, Robert S. Williams, Gareth H. Stoeber, Kai PLoS One Research Article BACKGROUND: Urinary biomarkers for bladder cancer detection are constrained by inadequate sensitivity or specificity. Here we evaluate the diagnostic accuracy of Mcm5, a novel cell cycle biomarker of aberrant growth, alone and in combination with NMP22. METHODS: 1677 consecutive patients under investigation for urinary tract malignancy were recruited to a prospective blinded observational study. All patients underwent ultrasound, intravenous urography, cystoscopy, urine culture and cytologic analysis. An immunofluorometric assay was used to measure Mcm5 levels in urine cell sediments. NMP22 urinary levels were determined with the FDA-approved NMP22® Test Kit. RESULTS: Genito-urinary tract cancers were identified in 210/1564 (13%) patients with an Mcm5 result and in 195/1396 (14%) patients with an NMP22 result. At the assay cut-point where sensitivity and specificity were equal, the Mcm5 test detected primary and recurrent bladder cancers with 69% sensitivity (95% confidence interval = 62–75%) and 93% negative predictive value (95% CI = 92–95%). The area under the receiver operating characteristic curve for Mcm5 was 0.75 (95% CI = 0.71–0.79) and 0.72 (95% CI = 0.67–0.77) for NMP22. Importantly, Mcm5 combined with NMP22 identified 95% (79/83; 95% CI = 88–99%) of potentially life threatening diagnoses (i.e. grade 3 or carcinoma in situ or stage ≥pT1) with high specificity (72%, 95% CI = 69–74%). CONCLUSIONS: The Mcm5 immunoassay is a non-invasive test for identifying patients with urothelial cancers with similar accuracy to the FDA-approved NMP22 ELISA Test Kit. The combination of Mcm5 plus NMP22 improves the detection of UCC and identifies 95% of clinically significant disease. Trials of a commercially developed Mcm5 assay suitable for an end-user laboratory alongside NMP22 are required to assess their potential clinical utility in improving diagnostic and surveillance care pathways. Public Library of Science 2012-07-09 /pmc/articles/PMC3392249/ /pubmed/22792272 http://dx.doi.org/10.1371/journal.pone.0040305 Text en Kelly et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Kelly, John D. Dudderidge, Tim J. Wollenschlaeger, Alex Okoturo, Odu Burling, Keith Tulloch, Fiona Halsall, Ian Prevost, Teresa Prevost, Andrew Toby Vasconcelos, Joana C. Robson, Wendy Leung, Hing Y. Vasdev, Nikhil Pickard, Robert S. Williams, Gareth H. Stoeber, Kai Bladder Cancer Diagnosis and Identification of Clinically Significant Disease by Combined Urinary Detection of Mcm5 and Nuclear Matrix Protein 22 |
title | Bladder Cancer Diagnosis and Identification of Clinically Significant Disease by Combined Urinary Detection of Mcm5 and Nuclear Matrix Protein 22 |
title_full | Bladder Cancer Diagnosis and Identification of Clinically Significant Disease by Combined Urinary Detection of Mcm5 and Nuclear Matrix Protein 22 |
title_fullStr | Bladder Cancer Diagnosis and Identification of Clinically Significant Disease by Combined Urinary Detection of Mcm5 and Nuclear Matrix Protein 22 |
title_full_unstemmed | Bladder Cancer Diagnosis and Identification of Clinically Significant Disease by Combined Urinary Detection of Mcm5 and Nuclear Matrix Protein 22 |
title_short | Bladder Cancer Diagnosis and Identification of Clinically Significant Disease by Combined Urinary Detection of Mcm5 and Nuclear Matrix Protein 22 |
title_sort | bladder cancer diagnosis and identification of clinically significant disease by combined urinary detection of mcm5 and nuclear matrix protein 22 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3392249/ https://www.ncbi.nlm.nih.gov/pubmed/22792272 http://dx.doi.org/10.1371/journal.pone.0040305 |
work_keys_str_mv | AT kellyjohnd bladdercancerdiagnosisandidentificationofclinicallysignificantdiseasebycombinedurinarydetectionofmcm5andnuclearmatrixprotein22 AT dudderidgetimj bladdercancerdiagnosisandidentificationofclinicallysignificantdiseasebycombinedurinarydetectionofmcm5andnuclearmatrixprotein22 AT wollenschlaegeralex bladdercancerdiagnosisandidentificationofclinicallysignificantdiseasebycombinedurinarydetectionofmcm5andnuclearmatrixprotein22 AT okoturoodu bladdercancerdiagnosisandidentificationofclinicallysignificantdiseasebycombinedurinarydetectionofmcm5andnuclearmatrixprotein22 AT burlingkeith bladdercancerdiagnosisandidentificationofclinicallysignificantdiseasebycombinedurinarydetectionofmcm5andnuclearmatrixprotein22 AT tullochfiona bladdercancerdiagnosisandidentificationofclinicallysignificantdiseasebycombinedurinarydetectionofmcm5andnuclearmatrixprotein22 AT halsallian bladdercancerdiagnosisandidentificationofclinicallysignificantdiseasebycombinedurinarydetectionofmcm5andnuclearmatrixprotein22 AT prevostteresa bladdercancerdiagnosisandidentificationofclinicallysignificantdiseasebycombinedurinarydetectionofmcm5andnuclearmatrixprotein22 AT prevostandrewtoby bladdercancerdiagnosisandidentificationofclinicallysignificantdiseasebycombinedurinarydetectionofmcm5andnuclearmatrixprotein22 AT vasconcelosjoanac bladdercancerdiagnosisandidentificationofclinicallysignificantdiseasebycombinedurinarydetectionofmcm5andnuclearmatrixprotein22 AT robsonwendy bladdercancerdiagnosisandidentificationofclinicallysignificantdiseasebycombinedurinarydetectionofmcm5andnuclearmatrixprotein22 AT leunghingy bladdercancerdiagnosisandidentificationofclinicallysignificantdiseasebycombinedurinarydetectionofmcm5andnuclearmatrixprotein22 AT vasdevnikhil bladdercancerdiagnosisandidentificationofclinicallysignificantdiseasebycombinedurinarydetectionofmcm5andnuclearmatrixprotein22 AT pickardroberts bladdercancerdiagnosisandidentificationofclinicallysignificantdiseasebycombinedurinarydetectionofmcm5andnuclearmatrixprotein22 AT williamsgarethh bladdercancerdiagnosisandidentificationofclinicallysignificantdiseasebycombinedurinarydetectionofmcm5andnuclearmatrixprotein22 AT stoeberkai bladdercancerdiagnosisandidentificationofclinicallysignificantdiseasebycombinedurinarydetectionofmcm5andnuclearmatrixprotein22 |