Barrett's esophagus (BE) is the precursor for esophageal adenocarcinoma (EAC). The risk of progression from nondysplastic BE (NDBE) to EAC is 30-fold to 125-fold greater than in the general population, increasing progressively with different stages of dysplasia. 1,2 Progression occurs stepwise from nondysplastic intestinal metaplasia to low-grade to high-grade dysplasia and ultimately to adenocarcinoma. 3
KEYWORDS • Barrett's esophagus • Radiofrequency ablation • Outcomes
KEY POINTS• Barrett's esophagus (BE) is the precursor for esophageal adenocarcinoma (EAC). The risk of progression from non-dysplastic BE to EAC increases progressively with stages of dysplasia.• If early-stage cancer or high-grade dysplasia is diagnosed, endoscopic therapy is the treatment of choice with better safety profile and similar efficacy compared with esophagectomy.• Endoscopic therapy is based on a "2-step concept": visible lesions are endoscopically removed and the remaining flat BE is ablated to prevent metachronous neoplasia.• Radiofrequency ablation (RFA) effectively eradicates dysplastic Barrett esophagus (BE) and reduces the metachronous risk of esophageal adenocarcinoma (EAC), with an acceptable low complication rate.• After achieving complete eradication of intestinal metaplasia (CE-IM) by RFA, dysplasia recurrence rate is approximately 2% per patient year of follow-up time, justifying postablation surveillance.