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Improved preoperative risk stratification in endometrial carcinoma patients: external validation of the ENDORISK Bayesian network model in a large population-based case series

PURPOSE: Preoperative risk stratification of newly diagnosed endometrial carcinoma (EC) patients has been hindered by only moderate prediction performance for many years. Recently ENDORISK, a Bayesian network model, showed high predictive performance. It was the aim of this study to validate ENDORIS...

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Autores principales: Grube, Marcel, Reijnen, Casper, Lucas, Peter J. F., Kommoss, Frieder, Kommoss, Felix K. F., Brucker, Sara Y., Walter, Christina B., Oberlechner, Ernst, Krämer, Bernhard, Andress, Jürgen, Neis, Felix, Staebler, Annette, Pijnenborg, Johanna M. A., Kommoss, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10314833/
https://www.ncbi.nlm.nih.gov/pubmed/35939115
http://dx.doi.org/10.1007/s00432-022-04218-4
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author Grube, Marcel
Reijnen, Casper
Lucas, Peter J. F.
Kommoss, Frieder
Kommoss, Felix K. F.
Brucker, Sara Y.
Walter, Christina B.
Oberlechner, Ernst
Krämer, Bernhard
Andress, Jürgen
Neis, Felix
Staebler, Annette
Pijnenborg, Johanna M. A.
Kommoss, Stefan
author_facet Grube, Marcel
Reijnen, Casper
Lucas, Peter J. F.
Kommoss, Frieder
Kommoss, Felix K. F.
Brucker, Sara Y.
Walter, Christina B.
Oberlechner, Ernst
Krämer, Bernhard
Andress, Jürgen
Neis, Felix
Staebler, Annette
Pijnenborg, Johanna M. A.
Kommoss, Stefan
author_sort Grube, Marcel
collection PubMed
description PURPOSE: Preoperative risk stratification of newly diagnosed endometrial carcinoma (EC) patients has been hindered by only moderate prediction performance for many years. Recently ENDORISK, a Bayesian network model, showed high predictive performance. It was the aim of this study to validate ENDORISK by applying the model to a population-based case series of EC patients. METHODS: ENDORISK was applied to a retrospective cohort of women surgically treated for EC from 2003 to 2013. Prediction accuracy for LNM as well as 5-year DSS was investigated. The model’s overall performance was quantified by the Brier score, discriminative performance by area under the curve (AUC). RESULTS: A complete dataset was evaluable from 247 patients. 78.1% cases were endometrioid histotype. The majority of patients (n = 156;63.2%) had stage IA disease. Overall, positive lymph nodes were found in 20 (8.1%) patients. Using ENDORISK predicted probabilities, most (n = 156;63.2%) patients have been assigned to low or very low risk group with a false-negative rate of 0.6%. AUC for LNM prediction was 0.851 [95% confidence interval (CI) 0.761–0.941] with a Brier score of 0.06. For 5-year DSS the AUC was 0.698 (95% CI 0.595–0.800) as Brier score has been calculated 0.09. CONCLUSIONS: We were able to successfully validate ENDORISK for prediction of LNM and 5-year DSS. Next steps will now have to focus on ENDORISK performance in daily clinical practice. In addition, incorporating TCGA-derived molecular subtypes will be of key importance for future extended use. This study may support further promoting of data-based decision-making tools for personalized treatment of EC.
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spelling pubmed-103148332023-07-03 Improved preoperative risk stratification in endometrial carcinoma patients: external validation of the ENDORISK Bayesian network model in a large population-based case series Grube, Marcel Reijnen, Casper Lucas, Peter J. F. Kommoss, Frieder Kommoss, Felix K. F. Brucker, Sara Y. Walter, Christina B. Oberlechner, Ernst Krämer, Bernhard Andress, Jürgen Neis, Felix Staebler, Annette Pijnenborg, Johanna M. A. Kommoss, Stefan J Cancer Res Clin Oncol Research PURPOSE: Preoperative risk stratification of newly diagnosed endometrial carcinoma (EC) patients has been hindered by only moderate prediction performance for many years. Recently ENDORISK, a Bayesian network model, showed high predictive performance. It was the aim of this study to validate ENDORISK by applying the model to a population-based case series of EC patients. METHODS: ENDORISK was applied to a retrospective cohort of women surgically treated for EC from 2003 to 2013. Prediction accuracy for LNM as well as 5-year DSS was investigated. The model’s overall performance was quantified by the Brier score, discriminative performance by area under the curve (AUC). RESULTS: A complete dataset was evaluable from 247 patients. 78.1% cases were endometrioid histotype. The majority of patients (n = 156;63.2%) had stage IA disease. Overall, positive lymph nodes were found in 20 (8.1%) patients. Using ENDORISK predicted probabilities, most (n = 156;63.2%) patients have been assigned to low or very low risk group with a false-negative rate of 0.6%. AUC for LNM prediction was 0.851 [95% confidence interval (CI) 0.761–0.941] with a Brier score of 0.06. For 5-year DSS the AUC was 0.698 (95% CI 0.595–0.800) as Brier score has been calculated 0.09. CONCLUSIONS: We were able to successfully validate ENDORISK for prediction of LNM and 5-year DSS. Next steps will now have to focus on ENDORISK performance in daily clinical practice. In addition, incorporating TCGA-derived molecular subtypes will be of key importance for future extended use. This study may support further promoting of data-based decision-making tools for personalized treatment of EC. Springer Berlin Heidelberg 2022-08-08 2023 /pmc/articles/PMC10314833/ /pubmed/35939115 http://dx.doi.org/10.1007/s00432-022-04218-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research
Grube, Marcel
Reijnen, Casper
Lucas, Peter J. F.
Kommoss, Frieder
Kommoss, Felix K. F.
Brucker, Sara Y.
Walter, Christina B.
Oberlechner, Ernst
Krämer, Bernhard
Andress, Jürgen
Neis, Felix
Staebler, Annette
Pijnenborg, Johanna M. A.
Kommoss, Stefan
Improved preoperative risk stratification in endometrial carcinoma patients: external validation of the ENDORISK Bayesian network model in a large population-based case series
title Improved preoperative risk stratification in endometrial carcinoma patients: external validation of the ENDORISK Bayesian network model in a large population-based case series
title_full Improved preoperative risk stratification in endometrial carcinoma patients: external validation of the ENDORISK Bayesian network model in a large population-based case series
title_fullStr Improved preoperative risk stratification in endometrial carcinoma patients: external validation of the ENDORISK Bayesian network model in a large population-based case series
title_full_unstemmed Improved preoperative risk stratification in endometrial carcinoma patients: external validation of the ENDORISK Bayesian network model in a large population-based case series
title_short Improved preoperative risk stratification in endometrial carcinoma patients: external validation of the ENDORISK Bayesian network model in a large population-based case series
title_sort improved preoperative risk stratification in endometrial carcinoma patients: external validation of the endorisk bayesian network model in a large population-based case series
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10314833/
https://www.ncbi.nlm.nih.gov/pubmed/35939115
http://dx.doi.org/10.1007/s00432-022-04218-4
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