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Copyright: ©Author(s) 2026. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution-NonCommercial (CC BY-NC 4.0) license. No commercial re-use. See permissions. Published by Baishideng Publishing Group Inc.
World J Gastrointest Oncol. May 15, 2026; 18(5): 119610
Published online May 15, 2026. doi: 10.4251/wjgo.v18.i5.119610
Diagnostic and prognostic values of pancreatic juice carbohydrate antigen 19-9 and carcinoembryonic antigen levels in patients with pancreatic cancer
Bojan Trogrlić, Zrinka Požgain, Goran Augustin, Borna Kovačić, Dejan Hil, Ivan Šerić, Veronika Šikić
Bojan Trogrlić, Borna Kovačić, Dejan Hil, Ivan Šerić, Veronika Šikić, Department of Abdominal Surgery, University Hospital Centre Osijek, Osijek 31000, Croatia
Bojan Trogrlić, Zrinka Požgain, Borna Kovačić, Dejan Hil, Veronika Šikić, Faculty of Medicine, J.J. Strossmayer University Osijek, Osijek 31000, Croatia
Zrinka Požgain, Department of Abdominal Surgery, University Hospital Centre, Osijek 31000, Croatia
Goran Augustin, Department of Surgery, University Hospital Centre Zagreb, Zagreb 10000, Croatia
Author contributions: Trogrlić B and Kovačić B designed the research; Trogrlić B, Požgain Z, and Hil D performed the research; Augustin G, Hil D, and Šerić I analyzed the data; Trogrlić B, Augustin G, Požgain Z, and Šikić V wrote the paper. All authors have read and approved the final manuscript.
Institutional review board statement: The study followed the principles of the Declaration of Helsinki. It received approval from the Ethics Committee of University Hospital Centre Osijek in Osijek, Croatia (No. R2:17233-5/2017).
Informed consent statement: All participants signed the informed consent before the intervention.
Conflict-of-interest statement: All the authors report no relevant conflicts of interest for this article.
STROBE statement: The authors have read the STROBE Statement-checklist of items, and the manuscript was prepared and revised according to the STROBE Statement-checklist of items.
Data sharing statement: No additional data are available.
Corresponding author: Goran Augustin, MD, PhD, Consultant Physician-Scientist, Staff Physician, Surgeon, Department of Surgery, University Hospital Centre Zagreb, Kišpatićeva 12, Zagreb 10000, Croatia. augustin.goran@gmail.com
Received: February 3, 2026
Revised: February 7, 2026
Accepted: February 26, 2026
Published online: May 15, 2026
Processing time: 102 Days and 10.7 Hours
Abstract
BACKGROUND

The estimated 5-year survival rate of pancreatic cancer is 13%, with a median survival of 4 months. Therefore, early detection and personalized treatment are essential. Carbohydrate antigen 19-9 (CA 19-9) and carcinoembryonic antigen (CEA) help diagnose the disease and predict metastasis and recurrence. Pancreatic juice (PJ) contains tumor-specific proteins released by pancreatic cancer cells, which can be collected during surgical resection or endoscopic retrograde cholangiopancreatography (ERCP). The prognostic significance of CA 19-9 and CEA levels in PJ remains uncertain.

AIM

To hypothesize that CA 19-9 and CEA concentrations in PJ are significantly higher in pancreatic cancer patients than in those with benign conditions, even when serum levels are normal, suggesting potential predictive value for 2-year and 5-year survival outcomes.

METHODS

A prospective cohort study conducted over 10 years involved patients with resectable pancreatic cancer who underwent pancreaticoduodenectomy (Whipple procedure), along with a control group with benign conditions. PJ was collected during the Whipple procedure from the main pancreatic duct after the resection of the pancreatic head and during ERCP in patients with benign hepatobiliary conditions. The samples were analyzed using the “ECLIA” method (Roche Elecsys 1010/2010). Data analysis involved Fisher’s exact test, the Mann-Whitney U test, and the log-rank test.

RESULTS

The study involved 24 patients, of whom 17 (71%) underwent surgery for pancreatic cancer, and 7 (29%) had ERCP. Two-year survival was seen in 8 (47%) patients, and 5-year survival in 5 (29%). Significantly higher levels of PJ CA 19-9 and CEA were found in the operated group. All patients with serum CA 19-9 < 25 U/mL survived at least 2 years after surgery, which was a statistically significant difference (Fisher’s exact test, P = 0.03). Patients with CA 19-9 levels ≥ 25 U/mL had significantly shorter 2-year and 5-year survival than those with CA 19-9 < 25 U/mL (Log-rank test, P = 0.04). There were no significant differences in serum and PJ CEA levels or PJ CA 19-9 concentrations based on 2-year and 5-year survival outcomes.

CONCLUSION

CA 19-9 is a prognostic biomarker that enables a personalized approach to adjuvant therapy. Furthermore, these findings have significant clinical implications for future research. CA 19-9 levels in PJ may help more accurately distinguish pancreatic adenocarcinoma from pancreatitis. Additionally, levels below 25 mL/U PJ CA19-9 suggest a better prognosis and survival, which could be used to enhance patient monitoring during current procedures. Collecting specimens during ERCP can help distinguish pancreatic cancer from pancreatic inflammation, preventing unnecessary surgeries and guiding appropriate interventions.

Keywords: Pancreatic cancer; Tumor markers; Pancreatic juice; Survival; Carbohydrate-antigen 19-9; Carcinoembryonic antigen

Core Tip: Early detection and personalized treatment are crucial for managing pancreatic cancer. Carbohydrate antigen 19-9 (CA 19-9) and carcinoembryonic antigen (CEA) help diagnose and predict metastases and recurrence. Pancreatic juice (PJ) contains tumor-specific proteins released by pancreatic cancer cells and can be collected during surgical resection or endoscopic retrograde cholangiopancreatography. The prognostic value of CA 19-9 and CEA levels in PJ remains uncertain. CA 19-9 levels in PJ may help more accurately distinguish pancreatic adenocarcinoma from pancreatitis. Additionally, levels below 25 mL/U PJ CA 19-9 indicate a better prognosis and survival, which could help improve patient monitoring during current procedures.

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