Wen YR, Lin XW, Zhou YW, Xu L, Zhang JL, Chen CY, He J. N-glycan biosignatures as a potential diagnostic biomarker for early-stage pancreatic cancer. World J Gastrointest Oncol 2024; 16(3): 659-669 [PMID: 38577461 DOI: 10.4251/wjgo.v16.i3.659]
Corresponding Author of This Article
Jian He, Doctor, PhD, Chief Doctor, Department of Nuclear Medicine, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, No. 321 Zhongshan Road, Nanjing 210008, Jiangsu Province, China. hjxueren@126.com
Research Domain of This Article
Oncology
Article-Type of This Article
Case Control Study
Open-Access Policy of This Article
This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
World J Gastrointest Oncol. Mar 15, 2024; 16(3): 659-669 Published online Mar 15, 2024. doi: 10.4251/wjgo.v16.i3.659
Table 1 Patient demographics and clinical characteristics of the study cohort
Characteristics
PDAC (n = 93)
Non-PDAC (n = 64)
Control (n = 88)
Men, n (%)
59 (63.4)
35 (54.7)
38 (43.2)
Women, n (%)
34 (36.6)
29 (45.3)
50 (56.8)
Age (yr)
64 (54.74)
54 (40.68)
57 (43, 71)
CEA, n (%)
93 (100)
64 (100)
82 (93.18)
CA19-9, n (%)
93 (100)
64 (100)
69 (78.41)
CA125, n (%)
93 (100)
63 (98.44)
42 (47.73)
CA242, n (%)
93 (100)
63 (98.33)
0 (0.00)
CA724, n (%)
93 (100)
63 (98.44)
0 (0.00)
AFP, n (%)
93 (100)
64 (100)
82 (93.18)
Stage I, n (%)
29 (31.18)
-
-
Stage II, n (%)
22 (23.66)
-
-
Stage III, n (%)
4 (4.30)
-
-
Stage IV, n (%)
16 (17.20)
-
-
Unknown, n (%)
22 (23.66)
-
-
Table 2 Diagnostic performance of N-glycans, tumor markers in distinguishing patients with pancreatic ductal adenocarcinoma
Biomarker
AUC
Cut-off
Sensitivity
Specificity
N-glycan
0.86
0.28
84.90%
73.00%
CA19-9
0.75
37
55.91%
95.49%
CEA
0.72
5.0
22.58%
100.00%
CA125
0.76
35
32.26%
98.10%
CA242
0.67
30
30.11%
98.41%
CA724
0.56
6.9
20.43%
87.30%
Table 3 Sensitivity of the Glyco-model in detecting patients with pancreatic ductal adenocarcinoma of different stages
Subgroup
Sensitivity
Overall
84.95% (79/93)
Stage I
89.66% (26/29)
Stage II
77.27% (17/22)
Stage III & IV
90.00% (18/20)
Unknown
81.82% (18/22)
Table 4 Sensitivity of the N-glycan model in non-pancreatic ductal adenocarcinoma individuals
Subgroup
Specificity
Overall
73.03% (111/152)
Healthy
79.55% (70/88)
SPN
83.33% (10/12)
PNET
50.00% (5/10)
SCN
91.67% (11/12)
IPMN
50.00% (13/26)
MCN
50.00% (2/4)
Table 5 The positivity rate of Glyco-model among patients with pancreatic ductal adenocarcinoma with tumor markers-negative
Tumor marker negative
Glyco-model positivity rate
CEA ≤ 5 (72)
87.50% (63/72)
CA19-9 ≤ 37 (41)
82.93% (34/41)
CA125 ≤ 35 (63)
88.89% (56/63)
CA242 ≤ 30 (65)
83.08% (54/65)
CA724 ≤ 6.9 (74)
86.49% (64/74)
Citation: Wen YR, Lin XW, Zhou YW, Xu L, Zhang JL, Chen CY, He J. N-glycan biosignatures as a potential diagnostic biomarker for early-stage pancreatic cancer. World J Gastrointest Oncol 2024; 16(3): 659-669