Results of a two-phased clinical study evaluating a new multiband mucosectomy device for early Barrett's neoplasia: a randomized pre-esophagectomy trial and a pilot therapeutic pilot study

被引:5
作者
Belghazi, K. [1 ]
Scholvinck, D. W. [1 ,2 ]
Henegouwen, M. I. van Berge [3 ]
Gisbertz, S. S. [3 ]
Weusten, B. L. [1 ,2 ]
Meijer, S. L. [4 ]
Bergman, J. J. [1 ]
Pouw, R. E. [1 ]
机构
[1] Univ Amsterdam, Amsterdam UMC, Dept Gastroenterol & Hepatol, Meibergdreef 9, NL-1105 AZ Amsterdam, Netherlands
[2] St Antonius Hosp, Dept Gastroenterol & Hepatol, Nieuwegein, Netherlands
[3] Univ Amsterdam, Amsterdam UMC, Dept Surg, Amsterdam, Netherlands
[4] Univ Amsterdam, Amsterdam UMC, Dept Pathol, Amsterdam, Netherlands
来源
SURGICAL ENDOSCOPY AND OTHER INTERVENTIONAL TECHNIQUES | 2019年 / 33卷 / 09期
关键词
Endoscopic mucosal resection; Multiband mucosectomy; Barrett's esophagus; High-grade dysplasia; Early cancer; ENDOSCOPIC RESECTION; ESOPHAGUS; CANCER;
D O I
10.1007/s00464-018-6582-5
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background Multiband mucosectomy (MBM) is the preferred technique for piecemeal resection of early neoplastic lesions in Barrett's esophagus (BE). The currently most widely used device for MBM is the Duette device. Recently, the Captivator EMR device has come available which might have practical advantages over the Duette device. Methods Phase I was a randomized pre-esophagectomy trial with a non-inferiority design aiming to compare EMR specimens obtained with the Captivator and the Duette device. Primary outcome: max diameter of the EMR specimens, secondary outcomes: min diameter, max thickness of the EMR specimens and resected submucosal stroma. Phase II were clinical pilot cases aiming to evaluate the feasibility of EMR using the Captivator device. Primary outcome was the successful EMR rate and secondary outcomes included procedure time and adverse events. Results Phase I: 24 EMR specimens (12 pairs) were obtained from six patients. The median max diameter of EMR specimens obtained with the Captivator device was 16 mm [IQR 12-21] versus 18 mm [IQR 13-23] for the Duette device. Non-inferiority of the max diameter of the Captivator specimens could not be demonstrated (median difference 1 mm, 95% CI - 3.26 to + 5.26). However, when using paired analysis, no significant difference was found (p 0.573). In addition, no statistically significant differences were found in the min diameter, max thickness of EMR specimens, and max thickness of resected submucosal stroma. Phase II: 5 BE patients with early neoplastic lesions were included. Successful EMR was achieved in 100%. Median procedure time was 33 min (IQR 25-39). One patient developed transient dysphagia, without signs of stenosis on endoscopy. Conclusions EMR of early Barrett's neoplasia using the Captivator device is comparable to Duette EMR when looking at size of resected specimens. In the first patients, EMR using the Captivator was feasible, resulting in successful resection without acute adverse events.
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收藏
页码:2864 / 2872
页数:9
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