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Review
Copyright: ©Author(s) 2026.
World J Gastroenterol. Jun 28, 2026; 32(24): 119127
Published online Jun 28, 2026. doi: 10.3748/wjg.119127
Table 1 Comparison of gastric cancer screening methods
Screening methods
Sensitivity
Specificity
Advantages
Limitations
Tumor markers
CA72433.0%94.0%Simple to detect and noninvasive, suitable for monitoring therapeutic efficacy and prognostic assessmentsLow sensitivity and specificity, high false-positive rate, not suitable for early screening
CEA25.5%97.9%
CA12531.1%97.3%
CA19938.7%92.6%
Gastric function biomarkers
PG57%-59%73%-87%Noninvasive, convenient, low-costSensitivity and specificity are limited due to interference from benign gastric conditions
G-1770%93%
GastroPanel51%-59%61%-66%Noninvasive and convenient; aids in diagnosing gastric mucosal diseasesLow sensitivity and specificity; threshold optimization requires a consideration of baseline population characteristics
Liquid biopsy
CTCs85.3%90.3%High tumor specificity; noninvasive; aids in early diagnosis and prognostic assessmentsEnrichment and identification techniques lack uniform standards; low blood levels; prone to interference from epithelial-mesenchymal transition processes or benign inflammation
CtDNA51.5%99.5%Noninvasive with high patient compliance; predicts postoperative recurrenceLow sensitivity; lack of standardized operating procedures
DNA methylation56%-63%91%-100%Noninvasive; high specificity; combined testing increases detection efficacyTesting techniques need standardization; testing costs remain relatively high; multicenter studies are needed for validation
MiRNA87.0%68.4%Good serum stability, high diagnostic accuracyResearch heterogeneity and inconsistent results; high costs
LncRNAs80%70%Predict tumor invasion/metastasis/prognosis; their combination with protein markers increases diagnostic efficacyThe specificity of standalone testing is limited, and further research is needed to validate their clinical utility
CircRNAs78%84%Noninvasive; high stability; early diagnosisDetection technology requires standardization; clinical implementation data are insufficient
Imaging examinations
Gastric ultrasound60.8%-88.7%83.5%-91%Noninvasive, radiation-free; clearly displays gastric wall layers, supplements T stagingEGC detection has low sensitivity; it is significantly affected by gastric gas and operator technique; biopsy is not feasible
Upper gastrointestinal series36.7%96.1%Dynamic observation of gastrointestinal motility; relatively simple to operateRadioactive, biopsy cannot be performed; low sensitivity; high false-negative rate
CT77.1%-88.9%80.0%-96.8%Assesses the depth of invasion and metastasisLimited sensitivity in detecting EGC; radiation exposure; requires large-scale prospective validation
MRI71.4%-82.6%91.4%-100%High soft tissue resolution with no radiation exposure; diffusion-weighted imaging demonstrates high accuracy in detecting lymph node metastasisThe examination is time-consuming, with insufficient sensitivity for detecting early mucosal lesions; biopsy is not feasible
Endoscopic examinations
EUS50%-90%NAAccurately determines the depth of invasion and peri-gastric lymph nodes; guides endoscopic resectionHigh technical demands and time-consuming; biopsy is not feasible; low accuracy in T2 lesion assessments
MCCE92%90%Noninvasive, no anesthesia needed; excellent tolerability; capable of detecting lesions missed by gastroscopyUnsuitable for biopsy/treatment; difficult to control through the pylorus; relies on gastrointestinal motility
EGD74.6%94.0%Intuitive visualization and precise localization; high diagnostic accuracy; biopsy confirmationInvasive, low compliance; potential risk of complications; high cost


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