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一项使用逐步圆周和局部消融(HALO系统)对伴有低度异型增生的巴雷特食管进行消融的前瞻性试点试验。

A prospective pilot trial of ablation of Barrett's esophagus with low-grade dysplasia using stepwise circumferential and focal ablation (HALO system).

作者信息

Sharma V K, Kim H Jae, Das A, Dean P, DePetris G, Fleischer D E

机构信息

Division of Gastroenterology and Hepatology, Department of Medicine, Mayo Clinic, Scottsdale, Arizona 85253, USA.

出版信息

Endoscopy. 2008 May;40(5):380-7. doi: 10.1055/s-2007-995587.

DOI:10.1055/s-2007-995587
PMID:18459074
Abstract

BACKGROUND AND STUDY AIMS

Yearly surveillance endoscopy is carried out for Barrett's esophagus with low-grade dysplasia (LGD) so that progression to high-grade dysplasia and adenocarcinoma can be detected at the earliest stage. The aim of the study was to assess the long-term safety and effectiveness of circumferential ablation followed by focal ablation (HALO system) for eliminating Barrett's esophagus and LGD.

PATIENTS AND METHODS

Patients with 2 - 6 cm of Barrett's esophagus with histology demonstrating LGD on their last two sequential endoscopies over the previous 2 years and confirmed by two pathologists were enrolled in this prospective, single-center trial. Circumferential ablation was carried out at baseline and at 4 months (if residual Barrett's esophagus present). Endoscopy with 4-quadrant biopsies every 1 cm was performed at 1, 3, 6, 12, and 24 months. After 1 year, focal ablation was applied to any visible Barrett's esophagus or irregularity of the squamocolumnar junction. Patients received lansoprazole 30 mg bid. Complete responses for dysplasia (CR-dysplasia) and intestinal metaplasia (CR-IM) at 2-year follow-up, with complete response defined as "all biopsies negative for dysplasia or intestinal metaplasia" were the main outcomes.

RESULTS

Ten patients (nine men, mean age 66.9 years, range 48 - 79) with confirmed LGD (median 4.4 cm, range 3 - 6) underwent circumferential ablation with focal ablation after 1 year as necessary. At 2 years, CR-dysplasia was 100 % and CR-IM was 90 %. There were no strictures or buried intestinal metaplasia at follow-up.

CONCLUSION

A stepwise regimen of circumferential ablation followed by focal ablation appears to eradicate intestinal metaplasia (90 % CR-IM) and dysplasia (100 % CR-dysplasia) at 2-year follow-up in this trial, without stricture formation or buried intestinal metaplasia.

摘要

背景与研究目的

对于伴有低级别异型增生(LGD)的巴雷特食管,每年进行监测性内镜检查,以便能在最早阶段检测到其进展为高级别异型增生和腺癌。本研究的目的是评估采用环形消融联合局部消融(HALO系统)消除巴雷特食管及LGD的长期安全性和有效性。

患者与方法

本前瞻性单中心试验纳入了过去2年中连续两次内镜检查组织学显示LGD且经两名病理学家确诊、巴雷特食管长度为2 - 6 cm的患者。在基线时及4个月时(如果存在残留巴雷特食管)进行环形消融。在1、3、6、12和24个月时进行内镜检查,每1 cm进行4象限活检。1年后,对任何可见的巴雷特食管或鳞柱状交界处的不规则部位进行局部消融。患者接受兰索拉唑30 mg,每日两次。主要结局是2年随访时异型增生的完全缓解(CR-异型增生)和肠化生的完全缓解(CR-IM),完全缓解定义为“所有活检均未发现异型增生或肠化生”。

结果

10例确诊为LGD(中位长度4.4 cm,范围3 - 6 cm)的患者(9例男性,平均年龄66.9岁,范围48 - 79岁)接受了环形消融,必要时在1年后进行局部消融。2年时,CR-异型增生为100%,CR-IM为90%。随访期间未出现狭窄或隐匿性肠化生。

结论

在本试验中,采用先环形消融后局部消融的分步方案在2年随访时似乎能根除肠化生(CR-IM为90%)和异型增生(CR-异型增生为100%),且未形成狭窄或隐匿性肠化生。

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