Table 5:
Pros and Cons of Non-endoscopic Screening Methods
Pros | Cons | |
---|---|---|
Esophageal mucosal sampling devices (brushes, balloons, sponges) | • Minimally invasive direct tissue sampling •Can be combined with any molecular test • Low operating cost • High specificity |
• Cytology-only yields low sensitivity • Devices are hard to swallow and may lead to poor compliance |
Auto-antibodies (blood) | • Non-invasive (serum) • Stable assay |
• Low sensitivity |
Circulating tumor cells (blood) | • Non-invasive • High specificity • Prognostic value |
• Low sensitivity • Not found in early disease |
Circulating miRNA (blood | • Non-invasive (detected from plasma or serum) • Stable and consistently expressed • High sensitivity and specificity |
•Limited number of studies |
Methylated DNA (cell sample or blood) | • Can be non-invasively detected in plasma • Stable and consistently expressed |
• Limited number of studies |
Volatile Organic Compounds (breath) | • Non-invasive | • Limited number of studies |