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New observations on the utility of CA19-9 as a biomarker in Lewis negative patients with pancreatic cancer

Authors :
Qiuyi Huang
Quanxing Ni
Chen Liu
Jin Xu
Jiang Long
Meng Guo
Xianjun Yu
Yu Lu
Chao Yang
Zhiyao Fan
Andrew L. Warshaw
Liang Liu
Renquan Lu
Kun Fan
Kaizhou Jin
Guopei Luo
He Cheng
Source :
Pancreatology. 18:971-976
Publication Year :
2018
Publisher :
Elsevier BV, 2018.

Abstract

Background Carbohydrate antigen 19-9 (CA19-9) is the best-validated biomarker for pancreatic cancer. The National Comprehensive Cancer Network (NCCN) guideline asserts that “CA19-9 will be undetectable in Lewis antigen-negative individuals”. However, reports of CA19-9 secretion and its significance in Lewis (-) patients with pancreatic cancer have been inconsistent. This study was to examine serum CA19-9 levels in patients with pancreatic cancer according to Lewis status. Methods Patients with pancreatic cancer (1482 cases) were retrieved from a prospectively maintained database. Patients with benign pancreatic disease (210 cases) and normal subjects (315 cases) were used as controls. Lewis genotypes were examined by fucosyltransferase 3 (FUT3) sequencing. Results In patients with pancreatic cancer, 8.4% of subjects were Lewis (-), but only 41.9% of Lewis (-) subjects had CA19-9 values ≤ 2 U/mL. CA19-9 was even elevated (>37 U/mL) in 27.4% of Lewis (-) patients. The area under the receiver operating characteristic (ROC) curve for CA19-9 as a diagnostic biomarker was 0.842 in Lewis (-) patients with pancreatic cancer, which is closing to that of CA19-9 applied in all of patients with pancreatic cancer (0.898). Lewis (-) status was an independent prognostic factor for shorter survival in a multivariable analysis (hazard ratio (HR), 1.30, 95% confidence interval (CI), 1.03–1.64; P = 0.028). Conclusions Not all Lewis (-) patients with pancreatic cancer are non-secretors of CA19-9. Contrary to general understanding, CA19-9 can retain its utility as a biomarker in these patients in spite of Lewis (-) genotype.

Details

ISSN :
14243903
Volume :
18
Database :
OpenAIRE
Journal :
Pancreatology
Accession number :
edsair.doi.dedup.....2c7dd985c4fc05a973a9804a7c3b3a2d