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Multifocal nitrous oxide cryoballoon ablation with or without EMR for treatment of neoplastic Barrett’s esophagus (with video) - 15/08/18

Doi : 10.1016/j.gie.2018.03.024 
Marcia Irene Canto, MD, MHS 1, , Nicholas J. Shaheen, MD 2, Jose Alejandro Almario, BS 1, Lysandra Voltaggio, MD 1, Elizabeth Montgomery, MD 1, Charles J. Lightdale, MD 3
1 Division of Gastroenterology and Hepatology, Johns Hopkins Medical Institutions, Baltimore, Maryland, USA 
2 Division of Gastroenterology, University North Carolina, Chapel Hill, Chapel Hill, North Carolina, USA 
3 Digestive and Liver Disease, Columbia University Medical Center, New York, New York, USA 

Reprint requests: Marcia Irene Canto, MD, MHS, Johns Hopkins University School of Medicine, Division of Gastroenterology and Hepatology, The Johns Hopkins Hospital, 1800 Orleans Street, Blalock 407, Baltimore, MD 21287.Johns Hopkins University School of MedicineDivision of Gastroenterology and HepatologyThe Johns Hopkins Hospital1800 Orleans Street, Blalock 407BaltimoreMD21287

Abstract

Background and Aims

Endoscopic cryotherapy can eradicate neoplastic Barrett’s esophagus (BE). A new contact cryoballoon focal ablation system (CbFAS)) freezes esophageal mucosa with nitrous oxide. We studied the safety and efficacy of CbFAS for complete eradication of neoplastic Barrett's esophagus.

Methods

In a prospective clinical trial, consecutive BE patients with confirmed neoplasia (low-grade dysplasia [LGD], high-grade dysplasia [HGD], and/or intramucosal adenocarcinoma [ImCA]), at least 1 cm of BE, with or without prior ablation, were treated with a dose 10 seconds of spray per site. EMR was performed for nodular lesions. Treatments were repeated every 10 to 12 weeks until complete eradication, with a maximum of 5 treatments. Primary outcomes were complete eradication of all dysplasia (CE-D) and complete eradication of intestinal metaplasia (CE-IM) at 1 year (intention-to-treat analysis).

Results

Forty-one assessable patients (22 treatment naive, 19 previously ablated) with LGD (n = 13), HGD (n = 23), or ImCA (n = 5) were treated. The median procedure time was 30 minutes. The median number of ablation procedures for CE-IM was 3 (interquartile range, 2-4). Overall 1-year CE-D and CE-IM rates were 95% and 88%, respectively. CE-D rate was significantly lower (67%) in those with ultra-long BE compared with those with <8 cm (100%, P = .02). Median pain scores were zero at day 1. Four patients (9.7%) developed mild dysphagia from stenoses requiring dilation. One patient on aspirin developed upper GI bleeding that did not require therapy.

Conclusions

Multifocal nitrous oxide cryotherapy using CbFAS is a promising, highly effective, and safe endoscopic treatment for primary or rescue therapy of BE-associated neoplasia and IM. (Clinical trial registration number: NCT02534233.)

Il testo completo di questo articolo è disponibile in PDF.

Abbreviations : APC, BE, CbFAS, CE-D, CE-IM, HGD, IM, ImCA, LGD, RFA


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 DISCLOSURE: The following authors disclosed financial relationships relevant to this publication: M. I. Canto: Royalty from UpToDate; research grant recipient from C2 Therapeutics and Cosmo Pharmaceuticals; speaker for Cook Medical. N. J. Shaheen: Consultant for Boston Scientific, Cook Medical, and Shire; research grant recipient from CDX Medical, C2 Therapeutics, and CSA Medical. C. J. Lightdale: Consultant for C2 Therapeutics, Boston Scientific, and CDx Diagnostics; L. Voltaggio: Research Grant Salary Support from C2 Therapeutics. All other authors disclosed no financial relationships relevant to this publication. Research support for this study was provided by an unrestricted research grant from C2 Therapeutics, Inc.
 See CME section; p. 542.
 If you would like to chat with an author of this article, you may contact Dr Canto at mcanto@jhmi.edu.


© 2018  American Society for Gastrointestinal Endoscopy. Pubblicato da Elsevier Masson SAS. Tutti i diritti riservati.
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Vol 88 - N° 3

P. 438 - settembre 2018 Ritorno al numero
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