Cargando…

A Panel of CA19-9, Ca125, and Ca15-3 as the Enhanced Test for the Differential Diagnosis of the Pancreatic Lesion

Background. Proper diagnosis of pancreatic lesion etiology is a challenging clinical dilemma. Studies suggest that surgery for suspected pancreatic ductal adenocarcinoma (PDAC) reveals a benign lesion in 5% to 13% of cases. The aim of our study was to assess whether routinely used biomarkers such as...

Descripción completa

Detalles Bibliográficos
Autores principales: Hogendorf, Piotr, Skulimowski, Aleksander, Durczyński, Adam, Kumor, Anna, Poznańska, Grażyna, Oleśna, Aleksandra, Rut, Joanna, Strzelczyk, Janusz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5357521/
https://www.ncbi.nlm.nih.gov/pubmed/28356610
http://dx.doi.org/10.1155/2017/8629712
_version_ 1782516053586214912
author Hogendorf, Piotr
Skulimowski, Aleksander
Durczyński, Adam
Kumor, Anna
Poznańska, Grażyna
Oleśna, Aleksandra
Rut, Joanna
Strzelczyk, Janusz
author_facet Hogendorf, Piotr
Skulimowski, Aleksander
Durczyński, Adam
Kumor, Anna
Poznańska, Grażyna
Oleśna, Aleksandra
Rut, Joanna
Strzelczyk, Janusz
author_sort Hogendorf, Piotr
collection PubMed
description Background. Proper diagnosis of pancreatic lesion etiology is a challenging clinical dilemma. Studies suggest that surgery for suspected pancreatic ductal adenocarcinoma (PDAC) reveals a benign lesion in 5% to 13% of cases. The aim of our study was to assess whether routinely used biomarkers such as CA19-9, Ca125, Ca15-3, and CEA, when combined, can potentially yield an accurate test predicting pancreatic lesion etiology. Methods. We retrospectively analyzed data of 326 patients who underwent a diagnostic process due to pancreatic lesions of unknown etiology. Results. We found statistically significant differences in mean levels of all biomarkers. In logistic regression model, we applied levels CA19-9, Ca125, and Ca15-3 as variables. Two validation methods were used, namely, random data split into training and validation groups and bootstrapping. Afterward, we built ROC curve using the model that we had created, reaching AUC = 0,801. With an optimal cut-off point, it achieved specificity of 81,2% and sensitivity of 63,10%. Our proposed model has superior diagnostic accuracy to both CA19-9 (p = 0,0194) and CA125 (p = 0,0026). Conclusion. We propose a test that is superior to CA19-9 in a differential diagnosis of pancreatic lesion etiology. Although our test fails to reach exceptionally high accuracy, its feasibility and cost-effectiveness make it clinically useful.
format Online
Article
Text
id pubmed-5357521
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Hindawi
record_format MEDLINE/PubMed
spelling pubmed-53575212017-03-29 A Panel of CA19-9, Ca125, and Ca15-3 as the Enhanced Test for the Differential Diagnosis of the Pancreatic Lesion Hogendorf, Piotr Skulimowski, Aleksander Durczyński, Adam Kumor, Anna Poznańska, Grażyna Oleśna, Aleksandra Rut, Joanna Strzelczyk, Janusz Dis Markers Research Article Background. Proper diagnosis of pancreatic lesion etiology is a challenging clinical dilemma. Studies suggest that surgery for suspected pancreatic ductal adenocarcinoma (PDAC) reveals a benign lesion in 5% to 13% of cases. The aim of our study was to assess whether routinely used biomarkers such as CA19-9, Ca125, Ca15-3, and CEA, when combined, can potentially yield an accurate test predicting pancreatic lesion etiology. Methods. We retrospectively analyzed data of 326 patients who underwent a diagnostic process due to pancreatic lesions of unknown etiology. Results. We found statistically significant differences in mean levels of all biomarkers. In logistic regression model, we applied levels CA19-9, Ca125, and Ca15-3 as variables. Two validation methods were used, namely, random data split into training and validation groups and bootstrapping. Afterward, we built ROC curve using the model that we had created, reaching AUC = 0,801. With an optimal cut-off point, it achieved specificity of 81,2% and sensitivity of 63,10%. Our proposed model has superior diagnostic accuracy to both CA19-9 (p = 0,0194) and CA125 (p = 0,0026). Conclusion. We propose a test that is superior to CA19-9 in a differential diagnosis of pancreatic lesion etiology. Although our test fails to reach exceptionally high accuracy, its feasibility and cost-effectiveness make it clinically useful. Hindawi 2017 2017-03-05 /pmc/articles/PMC5357521/ /pubmed/28356610 http://dx.doi.org/10.1155/2017/8629712 Text en Copyright © 2017 Piotr Hogendorf et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Hogendorf, Piotr
Skulimowski, Aleksander
Durczyński, Adam
Kumor, Anna
Poznańska, Grażyna
Oleśna, Aleksandra
Rut, Joanna
Strzelczyk, Janusz
A Panel of CA19-9, Ca125, and Ca15-3 as the Enhanced Test for the Differential Diagnosis of the Pancreatic Lesion
title A Panel of CA19-9, Ca125, and Ca15-3 as the Enhanced Test for the Differential Diagnosis of the Pancreatic Lesion
title_full A Panel of CA19-9, Ca125, and Ca15-3 as the Enhanced Test for the Differential Diagnosis of the Pancreatic Lesion
title_fullStr A Panel of CA19-9, Ca125, and Ca15-3 as the Enhanced Test for the Differential Diagnosis of the Pancreatic Lesion
title_full_unstemmed A Panel of CA19-9, Ca125, and Ca15-3 as the Enhanced Test for the Differential Diagnosis of the Pancreatic Lesion
title_short A Panel of CA19-9, Ca125, and Ca15-3 as the Enhanced Test for the Differential Diagnosis of the Pancreatic Lesion
title_sort panel of ca19-9, ca125, and ca15-3 as the enhanced test for the differential diagnosis of the pancreatic lesion
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5357521/
https://www.ncbi.nlm.nih.gov/pubmed/28356610
http://dx.doi.org/10.1155/2017/8629712
work_keys_str_mv AT hogendorfpiotr apanelofca199ca125andca153astheenhancedtestforthedifferentialdiagnosisofthepancreaticlesion
AT skulimowskialeksander apanelofca199ca125andca153astheenhancedtestforthedifferentialdiagnosisofthepancreaticlesion
AT durczynskiadam apanelofca199ca125andca153astheenhancedtestforthedifferentialdiagnosisofthepancreaticlesion
AT kumoranna apanelofca199ca125andca153astheenhancedtestforthedifferentialdiagnosisofthepancreaticlesion
AT poznanskagrazyna apanelofca199ca125andca153astheenhancedtestforthedifferentialdiagnosisofthepancreaticlesion
AT olesnaaleksandra apanelofca199ca125andca153astheenhancedtestforthedifferentialdiagnosisofthepancreaticlesion
AT rutjoanna apanelofca199ca125andca153astheenhancedtestforthedifferentialdiagnosisofthepancreaticlesion
AT strzelczykjanusz apanelofca199ca125andca153astheenhancedtestforthedifferentialdiagnosisofthepancreaticlesion
AT hogendorfpiotr panelofca199ca125andca153astheenhancedtestforthedifferentialdiagnosisofthepancreaticlesion
AT skulimowskialeksander panelofca199ca125andca153astheenhancedtestforthedifferentialdiagnosisofthepancreaticlesion
AT durczynskiadam panelofca199ca125andca153astheenhancedtestforthedifferentialdiagnosisofthepancreaticlesion
AT kumoranna panelofca199ca125andca153astheenhancedtestforthedifferentialdiagnosisofthepancreaticlesion
AT poznanskagrazyna panelofca199ca125andca153astheenhancedtestforthedifferentialdiagnosisofthepancreaticlesion
AT olesnaaleksandra panelofca199ca125andca153astheenhancedtestforthedifferentialdiagnosisofthepancreaticlesion
AT rutjoanna panelofca199ca125andca153astheenhancedtestforthedifferentialdiagnosisofthepancreaticlesion
AT strzelczykjanusz panelofca199ca125andca153astheenhancedtestforthedifferentialdiagnosisofthepancreaticlesion