Gastrointestinal Endoscopy
Volume 68, Issue 5 , Pages 867-876, November 2008

Endoscopic ablation of Barrett's esophagus: a multicenter study with 2.5-year follow-up

Current affiliations: Mayo Clinic (D.E.F., V.K.S.), Scottsdale, Arizona, Gastrointestinal Associates (B.F.O.), Knoxville, Tennessee, Ponce Gastroenterology (A.R., N.S.), Ponce, Puerto Rico, Tacoma Digestive Disease Center (M.B.K.) Tacoma, Washington, Beth Israel Deaconess Medical Center (R.C., D.K.P.), Boston, Massachusetts, University of California – Irvine (K.J.C.), Irvine, California, Columbia Presbyterian Medical Center (C.J.L.), New York, NY, GI Pathology (P.J.D.), Memphis, Tennessee, Mayo Clinic (K.K.W.) Rochester, Minnesota

Received 13 August 2007; accepted 3 March 2008. published online 18 June 2008.

Scottsdale, Arizona, Knoxville, Memphis, Tennessee, Tacoma, Washington, Boston, Massachusetts, Irvine, California, New York, New York, Rochester, Minnesota, USA, Ponce, Puerto Rico

Background

For patients with Barrett's esophagus (BE), life-long surveillance endoscopy is recommended because of an elevated risk for developing dysplasia and esophageal adenocarcinoma. Various endoscopic therapies have been used to eradicate BE. Recently circumferential radiofrequency ablation has been used with encouraging short-term results.

Objective

To provide longer follow-up and to assess the long-term safety and efficacy of step-wise circumferential ablation with the addition of focal ablation for BE.

Design

Prospective, multicenter clinical trial (NCT00489268).

Setting

Eight U.S. centers, between May 2004 and February 2007.

Patients

Seventy subjects with 2 to 6 cm of BE and histologic evidence of intestinal metaplasia (IM).

Interventions

Circumferential ablation was performed at baseline and repeated at 4 months if there was residual IM. Follow-up biopsy specimens were obtained at 1, 3, 6, 12, and 30 months. Specimens were reviewed by a central pathology board. Focal ablation was performed after the 12-month follow-up for histological evidence of IM at the 12-month biopsy (absolute indication) or endoscopic appearance suggestive of columnar-lined esophagus (relative indication). Subjects received esomeprazole for control of esophageal reflux.

Main outcome measurements

Complete absence of IM per patient from biopsy specimens obtained at 12 and 30 months, defined as complete remission–IM (CR-IM).

Results

At 12 months, CR-IM was achieved in 48 of 69 available patients (70% per protocol [PP], 69% intention to treat [ITT]). At 30 months after additional focal ablative therapy, CR-IM was achieved in 60 of 61 available patients (98% PP, 97% ITT). There were no strictures or buried glandular mucosa detected by the standardized biopsy protocol at 12 or 30 months, and there were no serious adverse events.

Limitations

This was an uncontrolled clinical trial with 2.5-year follow-up.

Conclusion

Stepwise circumferential and focal ablation resulted in complete eradication of IM in 98% of patients at 2.5-year follow-up.

Abbreviations: AIM, Ablation Intestinal Metaplasia trial, APC, argon plasma coagulation, BE, Barrett's esophagus, CR, complete remission, CR-IM, complete remission of intestinal metaplasia, EAC, early esophageal cancer, GERD, gastroesophageal reflux disease, HGD, high-grade dysplasia, ID, inner diameter, IM, intestinal metaplasia, ITT, intention to treat, LGD, low-grade dysplasia, MPEC, multipolar electrocoagulation, PDT, photodynamic therapy, PP, per protocol, SCJ, squamocolumnar junction, TGF, top of the gastric folds, VAS, visual analog scale

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 Presented at Digestive Disease Week, May 20-23, 2007, Washington, DC (Gastrointest Endosc 2007;65:AB135).

 See CME section; p. 960.

PII: S0016-5107(08)00381-7

doi:10.1016/j.gie.2008.03.008

Gastrointestinal Endoscopy
Volume 68, Issue 5 , Pages 867-876, November 2008