Clinical—Alimentary TractEndoscopic and Surgical Treatment of Mucosal (T1a) Esophageal Adenocarcinoma in Barrett's Esophagus
Section snippets
Study Design
This was a retrospective cohort study. Patients were either referred for endoscopic treatment of mucosal EAC to the Barrett's Esophagus Unit by physicians or were under surveillance for high-grade dysplasia (HGD) in the BE Unit. All patients seen in the BE Unit for endoscopic therapy had received consultation either with thoracic surgeons at the Mayo Clinic or at their local hospitals. Patients referred for esophagectomy usually were referred directly by their physicians or were elected to
Results
A total of 132 patients underwent endoscopic therapy (ENDO group) and 46 patients underwent esophagectomy (SURG group) for mucosal EAC between 1998 and 2007 at the Mayo Clinic (Rochester, MN) and were included in this study. The baseline characteristics of these patients are summarized in Table 1. As is evident from Table 1, patients treated endoscopically were older and had more medical comorbidities than those treated surgically. In addition, patients in the SURG group also had a longer BE
Discussion
Early stage EAC (T1 stage disease confined to the mucosa or submucosa) comprises approximately 20% of all cases of EAC diagnosed in the United States.21, 22 Endoscopic therapy of mucosal EAC has been proposed as an alternative to surgical resection given the low risk of metastatic lymphadenopathy in these patients.6 In this large cohort study we studied outcomes after the endoscopic and surgical treatment of mucosal (T1a) EAC and found that overall survival and cumulative mortality rates were
Acknowledgments
The authors appreciate the assistance of Ross Dierkhising, MS (Division of Biostatistics) for statistical analysis, and Yutaka Tomizawa, MD (Division of Gastroenterology) for assistance with data extraction.
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Conflicts of interest The authors disclose no conflicts.
Funding Supported by National Institutes of Health grants R01CA111603-01A1 (K.K.W.), R01CA097048 (K.K.W.), R21CA122426-01 (K.K.W.), and R03CA135991-01 (G.A.P.), and the Shirley and Miles Fiterman Digestive Disease Center.