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Diabetes and beta-adrenergic blockage are risk factors for metastatic prostate cancer

BACKGROUND: We evaluated the influence of comorbidity inferred risks for lymph node metastasis (pN1) and positive surgical margins (R1) after radical prostatectomy in order to optimize pretherapeutic risk classification. We analyzed 454 patients after radical prostatectomy (RP) between 2009 and 2014...

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Autores principales: Krönig, Malte, Haverkamp, Christian, Schulte, Antonia, Heinicke, Laura, Schaal, Kathrin, Drendel, Vanessa, Werner, Martin, Wetterauer, Ulrich, Schultze-Seemann, Wolfgang, Jilg, Cordula Annette
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5320736/
https://www.ncbi.nlm.nih.gov/pubmed/28222734
http://dx.doi.org/10.1186/s12957-017-1117-4
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author Krönig, Malte
Haverkamp, Christian
Schulte, Antonia
Heinicke, Laura
Schaal, Kathrin
Drendel, Vanessa
Werner, Martin
Wetterauer, Ulrich
Schultze-Seemann, Wolfgang
Jilg, Cordula Annette
author_facet Krönig, Malte
Haverkamp, Christian
Schulte, Antonia
Heinicke, Laura
Schaal, Kathrin
Drendel, Vanessa
Werner, Martin
Wetterauer, Ulrich
Schultze-Seemann, Wolfgang
Jilg, Cordula Annette
author_sort Krönig, Malte
collection PubMed
description BACKGROUND: We evaluated the influence of comorbidity inferred risks for lymph node metastasis (pN1) and positive surgical margins (R1) after radical prostatectomy in order to optimize pretherapeutic risk classification. We analyzed 454 patients after radical prostatectomy (RP) between 2009 and 2014. Comorbidities were defined by patients’ medication from our electronic patient chart and stratified according to the ATC WHO code. Endpoints were lymph node metastasis (pN1) and positive surgical margins (R1). RESULTS: Rates for pN1 and R1 were 21.4% (97/454) and 29.3% (133/454), respectively. In addition to CAPRA and Gleason score, we identified diabetes as a significant medication inferred risk factor for pN1 (OR 2.9, p = 0.004/OR 3.2, p = 0.001/OR 3.5, p = 0.001) and beta-blockers for R1 (OR 1.9, p = 0.020/OR 2.9, p = 0.004). Patients with diabetes showed no statistically significant difference in Gleason score, CAPRA Score, PSA, and age compared to non-diabetic patients. CONCLUSIONS: We identified diabetes and beta1 adrenergic blockage as significant risk factors for lymph node metastasis and positive surgical margins in prostate cancer (PCa). Patients at risk will need intensive pretherapeutic staging for optimal therapeutic stratification. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12957-017-1117-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-53207362017-02-24 Diabetes and beta-adrenergic blockage are risk factors for metastatic prostate cancer Krönig, Malte Haverkamp, Christian Schulte, Antonia Heinicke, Laura Schaal, Kathrin Drendel, Vanessa Werner, Martin Wetterauer, Ulrich Schultze-Seemann, Wolfgang Jilg, Cordula Annette World J Surg Oncol Research BACKGROUND: We evaluated the influence of comorbidity inferred risks for lymph node metastasis (pN1) and positive surgical margins (R1) after radical prostatectomy in order to optimize pretherapeutic risk classification. We analyzed 454 patients after radical prostatectomy (RP) between 2009 and 2014. Comorbidities were defined by patients’ medication from our electronic patient chart and stratified according to the ATC WHO code. Endpoints were lymph node metastasis (pN1) and positive surgical margins (R1). RESULTS: Rates for pN1 and R1 were 21.4% (97/454) and 29.3% (133/454), respectively. In addition to CAPRA and Gleason score, we identified diabetes as a significant medication inferred risk factor for pN1 (OR 2.9, p = 0.004/OR 3.2, p = 0.001/OR 3.5, p = 0.001) and beta-blockers for R1 (OR 1.9, p = 0.020/OR 2.9, p = 0.004). Patients with diabetes showed no statistically significant difference in Gleason score, CAPRA Score, PSA, and age compared to non-diabetic patients. CONCLUSIONS: We identified diabetes and beta1 adrenergic blockage as significant risk factors for lymph node metastasis and positive surgical margins in prostate cancer (PCa). Patients at risk will need intensive pretherapeutic staging for optimal therapeutic stratification. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12957-017-1117-4) contains supplementary material, which is available to authorized users. BioMed Central 2017-02-21 /pmc/articles/PMC5320736/ /pubmed/28222734 http://dx.doi.org/10.1186/s12957-017-1117-4 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Krönig, Malte
Haverkamp, Christian
Schulte, Antonia
Heinicke, Laura
Schaal, Kathrin
Drendel, Vanessa
Werner, Martin
Wetterauer, Ulrich
Schultze-Seemann, Wolfgang
Jilg, Cordula Annette
Diabetes and beta-adrenergic blockage are risk factors for metastatic prostate cancer
title Diabetes and beta-adrenergic blockage are risk factors for metastatic prostate cancer
title_full Diabetes and beta-adrenergic blockage are risk factors for metastatic prostate cancer
title_fullStr Diabetes and beta-adrenergic blockage are risk factors for metastatic prostate cancer
title_full_unstemmed Diabetes and beta-adrenergic blockage are risk factors for metastatic prostate cancer
title_short Diabetes and beta-adrenergic blockage are risk factors for metastatic prostate cancer
title_sort diabetes and beta-adrenergic blockage are risk factors for metastatic prostate cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5320736/
https://www.ncbi.nlm.nih.gov/pubmed/28222734
http://dx.doi.org/10.1186/s12957-017-1117-4
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