Despite guidelines recommending screening for esophageal adenocarcinoma (OAC) and its precursor, Barrett’s esophagus (BO), uptake remains low due to the invasive nature and cost of endoscopy. Emerging non-endoscopic, swallowable cell collection devices combined with biomarker analysis have shown promising accuracy and safety, leading to their inclusion in screening guidelines. Pragmatic trials indicate patient interest, with up to 60% favoring capsule sponge-based screening, suggesting that minimally invasive alternatives could significantly enhance early detection and intervention efforts.
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