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Validation of a contemporary prostate cancer grading system using prostate cancer death as outcome
BACKGROUND: Gleason scoring (GS) has major deficiencies and a novel system of five grade groups (GS⩽6; 3+4; 4+3; 8; ⩾9) has been recently agreed and included in the WHO 2016 classification. Although verified in radical prostatectomies using PSA relapse for outcome, it has not been validated using pr...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4865975/ https://www.ncbi.nlm.nih.gov/pubmed/27100731 http://dx.doi.org/10.1038/bjc.2016.86 |
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author | Berney, Daniel M Beltran, Luis Fisher, Gabrielle North, Bernard V Greenberg, David Møller, Henrik Soosay, Geraldine Scardino, Peter Cuzick, Jack |
author_facet | Berney, Daniel M Beltran, Luis Fisher, Gabrielle North, Bernard V Greenberg, David Møller, Henrik Soosay, Geraldine Scardino, Peter Cuzick, Jack |
author_sort | Berney, Daniel M |
collection | PubMed |
description | BACKGROUND: Gleason scoring (GS) has major deficiencies and a novel system of five grade groups (GS⩽6; 3+4; 4+3; 8; ⩾9) has been recently agreed and included in the WHO 2016 classification. Although verified in radical prostatectomies using PSA relapse for outcome, it has not been validated using prostate cancer death as an outcome in biopsy series. There is debate whether an ‘overall' or ‘worst' GS in biopsies series should be used. METHODS: Nine hundred and eighty-eight prostate cancer biopsy cases were identified between 1990 and 2003, and treated conservatively. Diagnosis and grade was assigned to each core as well as an overall grade. Follow-up for prostate cancer death was until 31 December 2012. A log-rank test assessed univariable differences between the five grade groups based on overall and worst grade seen, and using univariable and multivariable Cox proportional hazards. Regression was used to quantify differences in outcome. RESULTS: Using both ‘worst' and ‘overall' GS yielded highly significant results on univariate and multivariate analysis with overall GS slightly but insignificantly outperforming worst GS. There was a strong correlation with the five grade groups and prostate cancer death. CONCLUSIONS: This is the largest conservatively treated prostate cancer cohort with long-term follow-up and contemporary assessment of grade. It validates the formation of five grade groups and suggests that the ‘worst' grade is a valid prognostic measure. |
format | Online Article Text |
id | pubmed-4865975 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48659752017-05-10 Validation of a contemporary prostate cancer grading system using prostate cancer death as outcome Berney, Daniel M Beltran, Luis Fisher, Gabrielle North, Bernard V Greenberg, David Møller, Henrik Soosay, Geraldine Scardino, Peter Cuzick, Jack Br J Cancer Clinical Study BACKGROUND: Gleason scoring (GS) has major deficiencies and a novel system of five grade groups (GS⩽6; 3+4; 4+3; 8; ⩾9) has been recently agreed and included in the WHO 2016 classification. Although verified in radical prostatectomies using PSA relapse for outcome, it has not been validated using prostate cancer death as an outcome in biopsy series. There is debate whether an ‘overall' or ‘worst' GS in biopsies series should be used. METHODS: Nine hundred and eighty-eight prostate cancer biopsy cases were identified between 1990 and 2003, and treated conservatively. Diagnosis and grade was assigned to each core as well as an overall grade. Follow-up for prostate cancer death was until 31 December 2012. A log-rank test assessed univariable differences between the five grade groups based on overall and worst grade seen, and using univariable and multivariable Cox proportional hazards. Regression was used to quantify differences in outcome. RESULTS: Using both ‘worst' and ‘overall' GS yielded highly significant results on univariate and multivariate analysis with overall GS slightly but insignificantly outperforming worst GS. There was a strong correlation with the five grade groups and prostate cancer death. CONCLUSIONS: This is the largest conservatively treated prostate cancer cohort with long-term follow-up and contemporary assessment of grade. It validates the formation of five grade groups and suggests that the ‘worst' grade is a valid prognostic measure. Nature Publishing Group 2016-05-10 2016-04-21 /pmc/articles/PMC4865975/ /pubmed/27100731 http://dx.doi.org/10.1038/bjc.2016.86 Text en Copyright © 2016 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Clinical Study Berney, Daniel M Beltran, Luis Fisher, Gabrielle North, Bernard V Greenberg, David Møller, Henrik Soosay, Geraldine Scardino, Peter Cuzick, Jack Validation of a contemporary prostate cancer grading system using prostate cancer death as outcome |
title | Validation of a contemporary prostate cancer grading system using prostate cancer death as outcome |
title_full | Validation of a contemporary prostate cancer grading system using prostate cancer death as outcome |
title_fullStr | Validation of a contemporary prostate cancer grading system using prostate cancer death as outcome |
title_full_unstemmed | Validation of a contemporary prostate cancer grading system using prostate cancer death as outcome |
title_short | Validation of a contemporary prostate cancer grading system using prostate cancer death as outcome |
title_sort | validation of a contemporary prostate cancer grading system using prostate cancer death as outcome |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4865975/ https://www.ncbi.nlm.nih.gov/pubmed/27100731 http://dx.doi.org/10.1038/bjc.2016.86 |
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