Original article
Clinical endoscopy
Long-term outcomes of a primary complete endoscopic resection strategy for short-segment Barrett’s esophagus with high-grade dysplasia and/or early esophageal adenocarcinoma

https://doi.org/10.1016/j.gie.2015.04.044Get rights and content

Background and Aims

Complete endoscopic resection (CER) of Barrett’s esophagus (BE) with high-grade dysplasia (HGD) and early esophageal adenocarcinoma (EEA) is a comprehensive and precise staging tool and may produce a sustained treatment response, preventing metachronous disease. There are limited data on long-term clinical outcomes and the sustainability of dysplasia eradication after CER. We aimed to describe long-term outcomes of a primary CER strategy of BE with HGD/EEA.

Methods

Patients with biopsy-proven HGD and EEA in short-segment BE (≤3 cm in circumferential length and ≤5 cm in maximal length) underwent staged CER by multiband mucosectomy or the cap method. The primary endpoint was remission of HGD or EEA (complete resection of HGD/EEA), dysplasia (complete resection of any dysplasia), and complete resection of intestinal metaplasia.

Results

Of 153 patients (126 HGD, 27 EEA; 83.7% male, median age of 66 years) considered suitable for CER, 138 met all inclusion criteria. CER was technically successful in all patients and was established after a median of 2 sessions. Covert synchronous EEA was found in 1 patient. At a mean follow-up of 40.7 months by intention-to-treat analysis, complete remission of HGD/EEA, dysplasia, and intestinal metaplasia was achieved in 98.5%, 89.1%, and 71.0%, respectively. In 47.1% of patients, CER changed the histological grade compared with pretreatment biopsies (28.1% downstaged and 19.0% upstaged). Esophageal dilation was performed in 36.8% in a mean of 2.5 sessions. At the end of follow-up, 96.4% of patients had no or minimal dysphagia and 90.6% of patients found CER an acceptable treatment.

Conclusions

On long-term follow-up, a primary CER strategy was a highly effective, safe, and durable treatment for HGD and EEA. Despite the need for post-CER dilation in one-third of patients, the majority found it an acceptable treatment on long-term follow-up.

Section snippets

Data collection

Data were prospectively collected for patients referred to 2 Australian tertiary referral centers for endoscopic management of biopsy-proven HGD and EEA between January 2004 and January 2014. Follow-up of these patients was extended to May 2014. The same data collection form was used at both study centers. In a minority of patients (7 patients), data such as lesion location and histology was not recorded. For all of these patients, medical records, endoscopy, and histology reports were

Results

The flow of patients is depicted in Figure 1. Patient baseline characteristics of patients considered for CER are shown in Table 1.

During the study period (January 2004 to January 2014), 246 patients were referred for management of HGD/EEA; 153 patients were considered suitable for treatment by CER. Focal ER was performed in 19 patients who were suspected of having invasive carcinoma. Fourteen patients were found to have high-risk histological features and were referred for surgical

Discussion

Our study demonstrated that CER is a highly effective strategy to eliminate residual BE after focal ER. It is durable, safe, and acceptable to patients. We have documented outcomes in a large, prospective, and well-characterized cohort of patients with short-segment BE and early neoplasia. The mean follow-up time of our CER cohort is more than 40 months. Clinicians not uncommonly encounter patients with HGD/EEA, and currently there is limited high-level evidence of the optimal management of the

Acknowledgment

The authors acknowledge the work of Karen Byth, PhD, who assisted with the statistical analysis of the study.

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    DISCLOSURE: All authors disclosed no financial relationships relevant to this article. Drs Bahin, Jayanna, and Whiteman were supported by grants from the National Health and Medical Research Council of Australia (NHMRC). The Cancer Institute of New South Wales (CINSW) provided funding for a research nurse and data manager to assist with the administration of the study. There was no influence from the NHMRC or the CINSW on study design or conduct, data collection and management, analysis, interpretation, and preparation and review or approval of the manuscript.

    See CME section; p. 212.

    If you would like to chat with an author of this article, you may contact Dr Bourke at [email protected].

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