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Prognostic Impact of Tumor Budding in Intrahepatic Cholangiocellular Carcinoma

Background: Intrahepatic cholangiocarcinoma (ICC) represents an aggressive carcinoma with a dismal prognosis. For resection specimens, histopathological prognosticators are limited to standard AJCC parameters. Tumor budding (TB), a quantitative leviable parameter for tumor cell separation and infilt...

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Autores principales: Budau, Klara-Luisa, Sigel, Carlie S., Bergmann, Luise, Lüchtenborg, Anne-Marie, Wellner, Ulrich, Schilling, Oliver, Werner, Martin, Tang, Laura, Bronsert, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9174844/
https://www.ncbi.nlm.nih.gov/pubmed/35711834
http://dx.doi.org/10.7150/jca.63008
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author Budau, Klara-Luisa
Sigel, Carlie S.
Bergmann, Luise
Lüchtenborg, Anne-Marie
Wellner, Ulrich
Schilling, Oliver
Werner, Martin
Tang, Laura
Bronsert, Peter
author_facet Budau, Klara-Luisa
Sigel, Carlie S.
Bergmann, Luise
Lüchtenborg, Anne-Marie
Wellner, Ulrich
Schilling, Oliver
Werner, Martin
Tang, Laura
Bronsert, Peter
author_sort Budau, Klara-Luisa
collection PubMed
description Background: Intrahepatic cholangiocarcinoma (ICC) represents an aggressive carcinoma with a dismal prognosis. For resection specimens, histopathological prognosticators are limited to standard AJCC parameters. Tumor budding (TB), a quantitative leviable parameter for tumor cell separation and infiltration is a promising prognostic factor for several cancers. This retrospective study investigated the prognostic impact of tumor budding in ICC, using a semi-automated approach. Method: From the Memorial Sloan-Kettering Cancer Center pathology archives, tissue specimens from ICC patients were HE stained and digitized. Tumor budding was analyzed according to the International Tumor Budding Consensus Conference 2016 via QuPath in ten 0.785 mm² vision fields within the tumor center and the tumor-host interface. Within each field, automated QuPath cell detection was conducted and manually reviewed. Tumor budding was correlated with clinico-pathological parameters including AJCC 8(th) edition classification, hepatitis status, age, ethnicity, treatment, sex, patient overall (OS) and recurrence free survival (RFS) via uni- and multivariate analyses. Results: From 89 patients, 1780 Vision fields comprising 6006 tumor buds were analyzed and correlated with patients' OS and RFS. The median value for tumor budding in tumor budding hot spots was five within the tumor-host interface and six within the tumor center. Tumor budding correlated significantly with patient OS and RFS in uni- and multivariate analyses (p<0.001). Conclusion: Our data supports tumor budding, assessed using a digitally enhanced technique, as an independent prognosticator in ICCs for patient's OS and RFS.
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spelling pubmed-91748442022-06-15 Prognostic Impact of Tumor Budding in Intrahepatic Cholangiocellular Carcinoma Budau, Klara-Luisa Sigel, Carlie S. Bergmann, Luise Lüchtenborg, Anne-Marie Wellner, Ulrich Schilling, Oliver Werner, Martin Tang, Laura Bronsert, Peter J Cancer Research Paper Background: Intrahepatic cholangiocarcinoma (ICC) represents an aggressive carcinoma with a dismal prognosis. For resection specimens, histopathological prognosticators are limited to standard AJCC parameters. Tumor budding (TB), a quantitative leviable parameter for tumor cell separation and infiltration is a promising prognostic factor for several cancers. This retrospective study investigated the prognostic impact of tumor budding in ICC, using a semi-automated approach. Method: From the Memorial Sloan-Kettering Cancer Center pathology archives, tissue specimens from ICC patients were HE stained and digitized. Tumor budding was analyzed according to the International Tumor Budding Consensus Conference 2016 via QuPath in ten 0.785 mm² vision fields within the tumor center and the tumor-host interface. Within each field, automated QuPath cell detection was conducted and manually reviewed. Tumor budding was correlated with clinico-pathological parameters including AJCC 8(th) edition classification, hepatitis status, age, ethnicity, treatment, sex, patient overall (OS) and recurrence free survival (RFS) via uni- and multivariate analyses. Results: From 89 patients, 1780 Vision fields comprising 6006 tumor buds were analyzed and correlated with patients' OS and RFS. The median value for tumor budding in tumor budding hot spots was five within the tumor-host interface and six within the tumor center. Tumor budding correlated significantly with patient OS and RFS in uni- and multivariate analyses (p<0.001). Conclusion: Our data supports tumor budding, assessed using a digitally enhanced technique, as an independent prognosticator in ICCs for patient's OS and RFS. Ivyspring International Publisher 2022-05-06 /pmc/articles/PMC9174844/ /pubmed/35711834 http://dx.doi.org/10.7150/jca.63008 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Budau, Klara-Luisa
Sigel, Carlie S.
Bergmann, Luise
Lüchtenborg, Anne-Marie
Wellner, Ulrich
Schilling, Oliver
Werner, Martin
Tang, Laura
Bronsert, Peter
Prognostic Impact of Tumor Budding in Intrahepatic Cholangiocellular Carcinoma
title Prognostic Impact of Tumor Budding in Intrahepatic Cholangiocellular Carcinoma
title_full Prognostic Impact of Tumor Budding in Intrahepatic Cholangiocellular Carcinoma
title_fullStr Prognostic Impact of Tumor Budding in Intrahepatic Cholangiocellular Carcinoma
title_full_unstemmed Prognostic Impact of Tumor Budding in Intrahepatic Cholangiocellular Carcinoma
title_short Prognostic Impact of Tumor Budding in Intrahepatic Cholangiocellular Carcinoma
title_sort prognostic impact of tumor budding in intrahepatic cholangiocellular carcinoma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9174844/
https://www.ncbi.nlm.nih.gov/pubmed/35711834
http://dx.doi.org/10.7150/jca.63008
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