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Development and validation of a novel risk score for the detection of insignificant prostate cancer in unscreened patient cohorts

BACKGROUND: Active surveillance is recommended for insignificant prostate cancer (PCa). Tools exist to identify suitable candidates using clinical variables. We aimed to develop and validate a novel risk score (NRS) predicting which patients are harbouring insignificant PCa. METHODS: We used prospec...

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Autores principales: Dutto, Lorenzo, Ahmad, Amar, Urbanova, Katerina, Wagner, Christian, Schuette, Andreas, Addali, Mustafa, Kelly, John D., Sridhar, Ashwin, Nathan, Senthil, Briggs, Timothy P., Witt, Joern H., Shaw, Gregory L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288120/
https://www.ncbi.nlm.nih.gov/pubmed/30478408
http://dx.doi.org/10.1038/s41416-018-0316-2
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author Dutto, Lorenzo
Ahmad, Amar
Urbanova, Katerina
Wagner, Christian
Schuette, Andreas
Addali, Mustafa
Kelly, John D.
Sridhar, Ashwin
Nathan, Senthil
Briggs, Timothy P.
Witt, Joern H.
Shaw, Gregory L.
author_facet Dutto, Lorenzo
Ahmad, Amar
Urbanova, Katerina
Wagner, Christian
Schuette, Andreas
Addali, Mustafa
Kelly, John D.
Sridhar, Ashwin
Nathan, Senthil
Briggs, Timothy P.
Witt, Joern H.
Shaw, Gregory L.
author_sort Dutto, Lorenzo
collection PubMed
description BACKGROUND: Active surveillance is recommended for insignificant prostate cancer (PCa). Tools exist to identify suitable candidates using clinical variables. We aimed to develop and validate a novel risk score (NRS) predicting which patients are harbouring insignificant PCa. METHODS: We used prospectively collected data from 8040 consecutive unscreened patients who underwent radical prostatectomy between 2006 and 2016. Of these, data from 2799 patients with Gleason 3 + 3 on biopsy were used to develop a multivariate model predicting the presence of insignificant PC at radical prostatectomy (ERSPC updated definition(3): Gleason 3 + 3 only, index tumour volume < 1.3 cm(3) and total tumour volume < 2.5 cm(3)). This was used to develop a novel risk score (NRS) which was validated in an equivalent independent cohort (n = 441). We compared the accuracy of existing predictive tools and the NRS in these cohorts. RESULTS: The NRS (incorporating PSA, prostate volume, age, clinical T Stage, percent and number of positive biopsy cores) outperformed pre-existing predictive tools in derivation and validation cohorts (AUC 0.755 and 0.76, respectively). Selection bias due to analysis of a surgical cohort is acknowledged. CONCLUSIONS: The advantage of the NRS is that it can be tailored to patient characteristics and may prove to be valuable tool in clinical decision-making.
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spelling pubmed-62881202019-11-27 Development and validation of a novel risk score for the detection of insignificant prostate cancer in unscreened patient cohorts Dutto, Lorenzo Ahmad, Amar Urbanova, Katerina Wagner, Christian Schuette, Andreas Addali, Mustafa Kelly, John D. Sridhar, Ashwin Nathan, Senthil Briggs, Timothy P. Witt, Joern H. Shaw, Gregory L. Br J Cancer Article BACKGROUND: Active surveillance is recommended for insignificant prostate cancer (PCa). Tools exist to identify suitable candidates using clinical variables. We aimed to develop and validate a novel risk score (NRS) predicting which patients are harbouring insignificant PCa. METHODS: We used prospectively collected data from 8040 consecutive unscreened patients who underwent radical prostatectomy between 2006 and 2016. Of these, data from 2799 patients with Gleason 3 + 3 on biopsy were used to develop a multivariate model predicting the presence of insignificant PC at radical prostatectomy (ERSPC updated definition(3): Gleason 3 + 3 only, index tumour volume < 1.3 cm(3) and total tumour volume < 2.5 cm(3)). This was used to develop a novel risk score (NRS) which was validated in an equivalent independent cohort (n = 441). We compared the accuracy of existing predictive tools and the NRS in these cohorts. RESULTS: The NRS (incorporating PSA, prostate volume, age, clinical T Stage, percent and number of positive biopsy cores) outperformed pre-existing predictive tools in derivation and validation cohorts (AUC 0.755 and 0.76, respectively). Selection bias due to analysis of a surgical cohort is acknowledged. CONCLUSIONS: The advantage of the NRS is that it can be tailored to patient characteristics and may prove to be valuable tool in clinical decision-making. Nature Publishing Group UK 2018-11-27 2018-12-11 /pmc/articles/PMC6288120/ /pubmed/30478408 http://dx.doi.org/10.1038/s41416-018-0316-2 Text en © Cancer Research UK 2018 https://creativecommons.org/licenses/by/4.0/ This work is published under the standard license to publish agreement. After 12 months the work will become freely available and the license terms will switch to a Creative Commons Attribution 4.0 International (CC BY 4.0)
spellingShingle Article
Dutto, Lorenzo
Ahmad, Amar
Urbanova, Katerina
Wagner, Christian
Schuette, Andreas
Addali, Mustafa
Kelly, John D.
Sridhar, Ashwin
Nathan, Senthil
Briggs, Timothy P.
Witt, Joern H.
Shaw, Gregory L.
Development and validation of a novel risk score for the detection of insignificant prostate cancer in unscreened patient cohorts
title Development and validation of a novel risk score for the detection of insignificant prostate cancer in unscreened patient cohorts
title_full Development and validation of a novel risk score for the detection of insignificant prostate cancer in unscreened patient cohorts
title_fullStr Development and validation of a novel risk score for the detection of insignificant prostate cancer in unscreened patient cohorts
title_full_unstemmed Development and validation of a novel risk score for the detection of insignificant prostate cancer in unscreened patient cohorts
title_short Development and validation of a novel risk score for the detection of insignificant prostate cancer in unscreened patient cohorts
title_sort development and validation of a novel risk score for the detection of insignificant prostate cancer in unscreened patient cohorts
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288120/
https://www.ncbi.nlm.nih.gov/pubmed/30478408
http://dx.doi.org/10.1038/s41416-018-0316-2
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