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Large cribriform growth pattern identifies ISUP grade 2 prostate cancer at high risk for recurrence and metastasis

Invasive cribriform and intraductal carcinoma are associated with adverse clinical outcome in patients with Gleason score 7 prostate cancer. It is yet unclear whether invasive cribriform and intraductal carcinoma of the prostate both have independent prognostic value, or whether field size of invasi...

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Autores principales: Hollemans, Eva, Verhoef, Esther I., Bangma, Chris H., Rietbergen, John, Helleman, Jozien, Roobol, Monique J., van Leenders, Geert J.L.H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6300553/
https://www.ncbi.nlm.nih.gov/pubmed/30349027
http://dx.doi.org/10.1038/s41379-018-0157-9
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author Hollemans, Eva
Verhoef, Esther I.
Bangma, Chris H.
Rietbergen, John
Helleman, Jozien
Roobol, Monique J.
van Leenders, Geert J.L.H.
author_facet Hollemans, Eva
Verhoef, Esther I.
Bangma, Chris H.
Rietbergen, John
Helleman, Jozien
Roobol, Monique J.
van Leenders, Geert J.L.H.
author_sort Hollemans, Eva
collection PubMed
description Invasive cribriform and intraductal carcinoma are associated with adverse clinical outcome in patients with Gleason score 7 prostate cancer. It is yet unclear whether invasive cribriform and intraductal carcinoma of the prostate both have independent prognostic value, or whether field size of invasive cribriform carcinoma has impact on disease outcome. Our objective was to determine the prognostic impact of intraductal and invasive cribriform prostate cancer histological subtypes in radical prostatectomies. We reviewed 420 prostatectomy specimens with ISUP grade 2 prostate cancer, assessed the percentages of Gleason grade 4 and tertiary 5, and performed immunohistochemistry for basal cells to discriminate intraductal from invasive cribriform growth. Small and large invasive cribriform fields were distinguished based on a diameter of at least twice the size of adjacent pre-existent normal glands. Clinicopathological parameters and biochemical recurrence-free survival were used as endpoints. Cribriform architecture was observed in 228 (54.3%) men, 103 (24.5%) of whom had intraductal, 194 (46.2%) small invasive, and 34 (8.1%) large invasive cribriform growth. Large invasive cribriform architecture was associated with older age (P < 0.001), higher percentage Gleason grade 4 (P = 0.001), extraprostatic expansion (P < 0.001), and more frequent lymph node metastases (P = 0.002), when compared with small invasive cribriform and/or intraductal carcinoma. Univariate analysis identified PSA, pT-stage, surgical margin status, and intraductal and invasive cribriform growth as significant predictors for biochemical recurrence-free survival. In multivariable Cox regression analysis, pT-stage (hazard ratio = 1.64, 95% CI: 1.02–2.63, P = 0.04), positive surgical margins (hazard ratio = 3.28, 95% CI: 2.06–5.23, P < 0.001), and large cribriform growth (hazard ratio = 4.36, 95% CI: 2.08–9.17, P < 0.001) were independent predictors for biochemical recurrence-free survival, while intraductal carcinoma, small cribriform growth, and percentage of Gleason grade 4 were not. In conclusion, large cribriform fields represent an aggressive subpattern of invasive cribriform prostate cancer and are an independent predictive factor for biochemical recurrence-free survival in ISUP grade 2 prostate cancer patients.
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spelling pubmed-63005532019-02-01 Large cribriform growth pattern identifies ISUP grade 2 prostate cancer at high risk for recurrence and metastasis Hollemans, Eva Verhoef, Esther I. Bangma, Chris H. Rietbergen, John Helleman, Jozien Roobol, Monique J. van Leenders, Geert J.L.H. Mod Pathol Article Invasive cribriform and intraductal carcinoma are associated with adverse clinical outcome in patients with Gleason score 7 prostate cancer. It is yet unclear whether invasive cribriform and intraductal carcinoma of the prostate both have independent prognostic value, or whether field size of invasive cribriform carcinoma has impact on disease outcome. Our objective was to determine the prognostic impact of intraductal and invasive cribriform prostate cancer histological subtypes in radical prostatectomies. We reviewed 420 prostatectomy specimens with ISUP grade 2 prostate cancer, assessed the percentages of Gleason grade 4 and tertiary 5, and performed immunohistochemistry for basal cells to discriminate intraductal from invasive cribriform growth. Small and large invasive cribriform fields were distinguished based on a diameter of at least twice the size of adjacent pre-existent normal glands. Clinicopathological parameters and biochemical recurrence-free survival were used as endpoints. Cribriform architecture was observed in 228 (54.3%) men, 103 (24.5%) of whom had intraductal, 194 (46.2%) small invasive, and 34 (8.1%) large invasive cribriform growth. Large invasive cribriform architecture was associated with older age (P < 0.001), higher percentage Gleason grade 4 (P = 0.001), extraprostatic expansion (P < 0.001), and more frequent lymph node metastases (P = 0.002), when compared with small invasive cribriform and/or intraductal carcinoma. Univariate analysis identified PSA, pT-stage, surgical margin status, and intraductal and invasive cribriform growth as significant predictors for biochemical recurrence-free survival. In multivariable Cox regression analysis, pT-stage (hazard ratio = 1.64, 95% CI: 1.02–2.63, P = 0.04), positive surgical margins (hazard ratio = 3.28, 95% CI: 2.06–5.23, P < 0.001), and large cribriform growth (hazard ratio = 4.36, 95% CI: 2.08–9.17, P < 0.001) were independent predictors for biochemical recurrence-free survival, while intraductal carcinoma, small cribriform growth, and percentage of Gleason grade 4 were not. In conclusion, large cribriform fields represent an aggressive subpattern of invasive cribriform prostate cancer and are an independent predictive factor for biochemical recurrence-free survival in ISUP grade 2 prostate cancer patients. Nature Publishing Group US 2018-10-22 2019 /pmc/articles/PMC6300553/ /pubmed/30349027 http://dx.doi.org/10.1038/s41379-018-0157-9 Text en © The Author(s) 2019 Open Access 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 http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Hollemans, Eva
Verhoef, Esther I.
Bangma, Chris H.
Rietbergen, John
Helleman, Jozien
Roobol, Monique J.
van Leenders, Geert J.L.H.
Large cribriform growth pattern identifies ISUP grade 2 prostate cancer at high risk for recurrence and metastasis
title Large cribriform growth pattern identifies ISUP grade 2 prostate cancer at high risk for recurrence and metastasis
title_full Large cribriform growth pattern identifies ISUP grade 2 prostate cancer at high risk for recurrence and metastasis
title_fullStr Large cribriform growth pattern identifies ISUP grade 2 prostate cancer at high risk for recurrence and metastasis
title_full_unstemmed Large cribriform growth pattern identifies ISUP grade 2 prostate cancer at high risk for recurrence and metastasis
title_short Large cribriform growth pattern identifies ISUP grade 2 prostate cancer at high risk for recurrence and metastasis
title_sort large cribriform growth pattern identifies isup grade 2 prostate cancer at high risk for recurrence and metastasis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6300553/
https://www.ncbi.nlm.nih.gov/pubmed/30349027
http://dx.doi.org/10.1038/s41379-018-0157-9
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