TY - JOUR
T1 - Comparative Outcomes of Cap Assisted Endoscopic Resection and Endoscopic Submucosal Dissection in Dysplastic Barrett's Esophagus
AU - Codipilly, D. Chamil
AU - Dhaliwal, Lovekirat
AU - Oberoi, Meher
AU - Gandhi, Parth
AU - Johnson, Michele L.
AU - Lansing, Ramona M.
AU - Harmsen, W. Scott
AU - Wang, Kenneth K.
AU - Iyer, Prasad G.
N1 - Funding Information:
Funding Supported in part by National Cancer Institute grant CA 241162 (P.G.I.), and by the Freeman Foundation .
Publisher Copyright:
© 2022 AGA Institute
PY - 2022/1
Y1 - 2022/1
N2 - Background & Aims: Endoscopic resection is an important component of the endoscopic treatment of Barrett's esophagus (BE) with dysplasia and intramucosal adenocarcinoma. Endoscopic resection can be performed by cap-assisted endoscopic mucosal resection (cEMR) or endoscopic submucosal dissection (ESD). We compared the histologic outcomes of ESD vs cEMR, followed by ablation. Methods: We queried a prospectively maintained database of all patients undergoing cEMR and ESD followed by ablation at our institution from January 2006 to March 2020 and abstracted relevant demographic and clinical data. Our primary outcomes included the rate of complete remission of dysplasia (CRD): absence of dysplasia on surveillance histology, and complete remission of intestinal metaplasia (CRIM): absence of intestinal metaplasia. Our secondary outcome included complication rates. Results: We included 537 patients in the study: 456 underwent cEMR and 81 underwent ESD. The cumulative probabilities of CRD at 2 years were 75.8% and 85.6% in the cEMR and ESD groups, respectively (P <.01). Independent predictors of CRD were as follows: ESD (hazard ratio [HR], 2.38; P <.01) and shorter BE segment length (HR, 1.11; P <.01). The cumulative probabilities of CRIM at 2 years were 59.3% and 50.6% in the cEMR and ESD groups, respectively (P >.05). The only independent predictor of CRIM was a shorter BE segment (HR, 1.16; P <.01). Conclusions: BE patients with dysplasia or intramucosal adenocarcinoma undergoing ESD reach CRD at higher rates than those treated with cEMR, although CRIM rates at 2 years and complication rates were similar between the 2 groups.
AB - Background & Aims: Endoscopic resection is an important component of the endoscopic treatment of Barrett's esophagus (BE) with dysplasia and intramucosal adenocarcinoma. Endoscopic resection can be performed by cap-assisted endoscopic mucosal resection (cEMR) or endoscopic submucosal dissection (ESD). We compared the histologic outcomes of ESD vs cEMR, followed by ablation. Methods: We queried a prospectively maintained database of all patients undergoing cEMR and ESD followed by ablation at our institution from January 2006 to March 2020 and abstracted relevant demographic and clinical data. Our primary outcomes included the rate of complete remission of dysplasia (CRD): absence of dysplasia on surveillance histology, and complete remission of intestinal metaplasia (CRIM): absence of intestinal metaplasia. Our secondary outcome included complication rates. Results: We included 537 patients in the study: 456 underwent cEMR and 81 underwent ESD. The cumulative probabilities of CRD at 2 years were 75.8% and 85.6% in the cEMR and ESD groups, respectively (P <.01). Independent predictors of CRD were as follows: ESD (hazard ratio [HR], 2.38; P <.01) and shorter BE segment length (HR, 1.11; P <.01). The cumulative probabilities of CRIM at 2 years were 59.3% and 50.6% in the cEMR and ESD groups, respectively (P >.05). The only independent predictor of CRIM was a shorter BE segment (HR, 1.16; P <.01). Conclusions: BE patients with dysplasia or intramucosal adenocarcinoma undergoing ESD reach CRD at higher rates than those treated with cEMR, although CRIM rates at 2 years and complication rates were similar between the 2 groups.
KW - Barrett's Esophagus
KW - Endoscopic Eradication Therapy
KW - Endoscopic Mucosal Resection
KW - Endoscopic Submucosal Dissection
KW - Esophageal Adenocarcinoma
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U2 - 10.1016/j.cgh.2020.11.017
DO - 10.1016/j.cgh.2020.11.017
M3 - Article
C2 - 33220523
AN - SCOPUS:85103700858
SN - 1542-3565
VL - 20
SP - 65-73.e1
JO - Clinical Gastroenterology and Hepatology
JF - Clinical Gastroenterology and Hepatology
IS - 1
ER -