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Elevated amylase in plasma represents an adverse prognostic marker in patients with metastatic pancreatic cancer: A retrospective analysis

BACKGROUND AND AIM: The aim of this study was to investigate the prognostic relevance of plasma amylase and lipase concerning survival of patients suffering from metastatic pancreatic cancer (PC). METHOD: This retrospective study included 351 patients with metastatic PC, who were treated in a single...

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Autores principales: Asamer, Eva, Szkandera, Joanna, Gibiser, Paul, Lembeck, Anna Lena, Stojakovic, Tatjana, Kornprat, Peter, Lackner, Caroline, Winder, Thomas, Schlick, Konstantin, Stöger, Herbert, Gerger, Armin, Pichler, Martin, Stotz, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Vienna 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6209010/
https://www.ncbi.nlm.nih.gov/pubmed/30132196
http://dx.doi.org/10.1007/s00508-018-1383-3
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author Asamer, Eva
Szkandera, Joanna
Gibiser, Paul
Lembeck, Anna Lena
Stojakovic, Tatjana
Kornprat, Peter
Lackner, Caroline
Winder, Thomas
Schlick, Konstantin
Stöger, Herbert
Gerger, Armin
Pichler, Martin
Stotz, Michael
author_facet Asamer, Eva
Szkandera, Joanna
Gibiser, Paul
Lembeck, Anna Lena
Stojakovic, Tatjana
Kornprat, Peter
Lackner, Caroline
Winder, Thomas
Schlick, Konstantin
Stöger, Herbert
Gerger, Armin
Pichler, Martin
Stotz, Michael
author_sort Asamer, Eva
collection PubMed
description BACKGROUND AND AIM: The aim of this study was to investigate the prognostic relevance of plasma amylase and lipase concerning survival of patients suffering from metastatic pancreatic cancer (PC). METHOD: This retrospective study included 351 patients with metastatic PC, who were treated in a single academic institution. Cancer-specific survival (CSS) was analyzed using the Kaplan-Meier method. To further evaluate the prognostic significance of lipase and amylase, univariate and multivariate values were calculated using Cox proportional models. RESULTS: In univariate analysis, an increased amylase level was associated with shorter CSS in PC patients (hazard ratio HR = 1.258; 95% confidence interval CI = 1.011–1.566; p = 0.039). In multivariate analysis, including gender, age, CA19-9 and administration of chemotherapy, increased amylase levels prevailed as an independent prognostic factor for CSS (HR = 1.373; 95%CI = 1.004–1.878; p = 0.047). CONCLUSIONS: Plasma amylase was found to be an independent prognostic factor in patients with metastatic PC. The results indicate that amylase might represent a novel and useful marker for better patient stratification in PC management.
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spelling pubmed-62090102018-11-13 Elevated amylase in plasma represents an adverse prognostic marker in patients with metastatic pancreatic cancer: A retrospective analysis Asamer, Eva Szkandera, Joanna Gibiser, Paul Lembeck, Anna Lena Stojakovic, Tatjana Kornprat, Peter Lackner, Caroline Winder, Thomas Schlick, Konstantin Stöger, Herbert Gerger, Armin Pichler, Martin Stotz, Michael Wien Klin Wochenschr Original Article BACKGROUND AND AIM: The aim of this study was to investigate the prognostic relevance of plasma amylase and lipase concerning survival of patients suffering from metastatic pancreatic cancer (PC). METHOD: This retrospective study included 351 patients with metastatic PC, who were treated in a single academic institution. Cancer-specific survival (CSS) was analyzed using the Kaplan-Meier method. To further evaluate the prognostic significance of lipase and amylase, univariate and multivariate values were calculated using Cox proportional models. RESULTS: In univariate analysis, an increased amylase level was associated with shorter CSS in PC patients (hazard ratio HR = 1.258; 95% confidence interval CI = 1.011–1.566; p = 0.039). In multivariate analysis, including gender, age, CA19-9 and administration of chemotherapy, increased amylase levels prevailed as an independent prognostic factor for CSS (HR = 1.373; 95%CI = 1.004–1.878; p = 0.047). CONCLUSIONS: Plasma amylase was found to be an independent prognostic factor in patients with metastatic PC. The results indicate that amylase might represent a novel and useful marker for better patient stratification in PC management. Springer Vienna 2018-08-21 2018 /pmc/articles/PMC6209010/ /pubmed/30132196 http://dx.doi.org/10.1007/s00508-018-1383-3 Text en © The Author(s) 2018 Open Access This 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.
spellingShingle Original Article
Asamer, Eva
Szkandera, Joanna
Gibiser, Paul
Lembeck, Anna Lena
Stojakovic, Tatjana
Kornprat, Peter
Lackner, Caroline
Winder, Thomas
Schlick, Konstantin
Stöger, Herbert
Gerger, Armin
Pichler, Martin
Stotz, Michael
Elevated amylase in plasma represents an adverse prognostic marker in patients with metastatic pancreatic cancer: A retrospective analysis
title Elevated amylase in plasma represents an adverse prognostic marker in patients with metastatic pancreatic cancer: A retrospective analysis
title_full Elevated amylase in plasma represents an adverse prognostic marker in patients with metastatic pancreatic cancer: A retrospective analysis
title_fullStr Elevated amylase in plasma represents an adverse prognostic marker in patients with metastatic pancreatic cancer: A retrospective analysis
title_full_unstemmed Elevated amylase in plasma represents an adverse prognostic marker in patients with metastatic pancreatic cancer: A retrospective analysis
title_short Elevated amylase in plasma represents an adverse prognostic marker in patients with metastatic pancreatic cancer: A retrospective analysis
title_sort elevated amylase in plasma represents an adverse prognostic marker in patients with metastatic pancreatic cancer: a retrospective analysis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6209010/
https://www.ncbi.nlm.nih.gov/pubmed/30132196
http://dx.doi.org/10.1007/s00508-018-1383-3
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