Copyright: ©Author(s) 2026.
World J Gastroenterol. Jun 28, 2026; 32(24): 119127
Published online Jun 28, 2026. doi: 10.3748/wjg.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 | ||||
| CA724 | 33.0% | 94.0% | Simple to detect and noninvasive, suitable for monitoring therapeutic efficacy and prognostic assessments | Low sensitivity and specificity, high false-positive rate, not suitable for early screening |
| CEA | 25.5% | 97.9% | ||
| CA125 | 31.1% | 97.3% | ||
| CA199 | 38.7% | 92.6% | ||
| Gastric function biomarkers | ||||
| PG | 57%-59% | 73%-87% | Noninvasive, convenient, low-cost | Sensitivity and specificity are limited due to interference from benign gastric conditions |
| G-17 | 70% | 93% | ||
| GastroPanel | 51%-59% | 61%-66% | Noninvasive and convenient; aids in diagnosing gastric mucosal diseases | Low sensitivity and specificity; threshold optimization requires a consideration of baseline population characteristics |
| Liquid biopsy | ||||
| CTCs | 85.3% | 90.3% | High tumor specificity; noninvasive; aids in early diagnosis and prognostic assessments | Enrichment and identification techniques lack uniform standards; low blood levels; prone to interference from epithelial-mesenchymal transition processes or benign inflammation |
| CtDNA | 51.5% | 99.5% | Noninvasive with high patient compliance; predicts postoperative recurrence | Low sensitivity; lack of standardized operating procedures |
| DNA methylation | 56%-63% | 91%-100% | Noninvasive; high specificity; combined testing increases detection efficacy | Testing techniques need standardization; testing costs remain relatively high; multicenter studies are needed for validation |
| MiRNA | 87.0% | 68.4% | Good serum stability, high diagnostic accuracy | Research heterogeneity and inconsistent results; high costs |
| LncRNAs | 80% | 70% | Predict tumor invasion/metastasis/prognosis; their combination with protein markers increases diagnostic efficacy | The specificity of standalone testing is limited, and further research is needed to validate their clinical utility |
| CircRNAs | 78% | 84% | Noninvasive; high stability; early diagnosis | Detection technology requires standardization; clinical implementation data are insufficient |
| Imaging examinations | ||||
| Gastric ultrasound | 60.8%-88.7% | 83.5%-91% | Noninvasive, radiation-free; clearly displays gastric wall layers, supplements T staging | EGC detection has low sensitivity; it is significantly affected by gastric gas and operator technique; biopsy is not feasible |
| Upper gastrointestinal series | 36.7% | 96.1% | Dynamic observation of gastrointestinal motility; relatively simple to operate | Radioactive, biopsy cannot be performed; low sensitivity; high false-negative rate |
| CT | 77.1%-88.9% | 80.0%-96.8% | Assesses the depth of invasion and metastasis | Limited sensitivity in detecting EGC; radiation exposure; requires large-scale prospective validation |
| MRI | 71.4%-82.6% | 91.4%-100% | High soft tissue resolution with no radiation exposure; diffusion-weighted imaging demonstrates high accuracy in detecting lymph node metastasis | The examination is time-consuming, with insufficient sensitivity for detecting early mucosal lesions; biopsy is not feasible |
| Endoscopic examinations | ||||
| EUS | 50%-90% | NA | Accurately determines the depth of invasion and peri-gastric lymph nodes; guides endoscopic resection | High technical demands and time-consuming; biopsy is not feasible; low accuracy in T2 lesion assessments |
| MCCE | 92% | 90% | Noninvasive, no anesthesia needed; excellent tolerability; capable of detecting lesions missed by gastroscopy | Unsuitable for biopsy/treatment; difficult to control through the pylorus; relies on gastrointestinal motility |
| EGD | 74.6% | 94.0% | Intuitive visualization and precise localization; high diagnostic accuracy; biopsy confirmation | Invasive, low compliance; potential risk of complications; high cost |
- Citation: Jiang JJ, Chen K, Weng T, Hong JM, Qin WY. Early screening and risk factors for gastric cancer. World J Gastroenterol 2026; 32(24): 119127
- URL: https://www.wjgnet.com/1007-9327/full/v32/i24/119127.htm
- DOI: https://dx.doi.org/10.3748/wjg.119127