Radiofrequency ablation for Barrett's oesophagus related neoplasia with the 360 Express catheter: initial experience from the United Kingdom and Ireland-preliminary results.


Journal

Surgical endoscopy
ISSN: 1432-2218
Titre abrégé: Surg Endosc
Pays: Germany
ID NLM: 8806653

Informations de publication

Date de publication:
01 2022
Historique:
received: 29 06 2020
accepted: 13 01 2021
pubmed: 7 2 2021
medline: 3 3 2022
entrez: 6 2 2021
Statut: ppublish

Résumé

Radio-frequency ablation (RFA) for Barrett's oesophagus (BE)-related neoplasia is currently used after endoscopic resection of visible neoplasia. The HALO 360 balloon has been used to ablate long segment BE. The Barrx™ 360 Express RFA self-sizing catheter ('RFA Express') may potentially allow quicker ablation times and improved treatment outcomes. The aim of this paper is to present real world data on the use of the 360 Express Device. Centres in the UK and Ireland submitted cases where the RFA Express was used. The primary outcome was regression of BE at 3 months. Secondary outcomes were the rate of symptomatic stricture formation and resolution of intestinal metaplasia (CR-IM) and dysplasia (CR-D) at End of Treatment (EoT). 11 centres submitted 123 consecutive patients. 112 had a follow up endoscopy. The median age was 67 years (IQR 62-75). 3 dosimetries were used. The mean reduction in Circumferential (C) length was 78% ± 36 and mean reduction in Maximal length (M) was 55% ± 36. 17 patients (15%) developed strictures requiring dilation. There was a higher rate of stricture formation when the 12 J energy was used (p < 0.05). 47 patients had EoT biopsies, 40 (85%) had CR-D and 34(76%) had CR-IM. The RFA 360 Express catheter shows reduction in length of baseline BE at 3 months after index treatment, and eradication of intestinal metaplasia and dysplasia at 12 months similar to other studies with earlier devices. It appears that the symptomatic stricture rate is slightly higher than previous series with the HALO 360 catheter. This study was performed as part of the HALO registry and has been approved by the Research Ethics Committee - MREC Number 08/H0714/27 Local project reference 08/0104 Project ID 15,033 IRAS Number 54678 EudraCT 2009-015980-1. Registered on ISRCTN as below: ISRCTN93069556. https://doi.org/10.1186/ISRCTN93069556.

Sections du résumé

BACKGROUND
Radio-frequency ablation (RFA) for Barrett's oesophagus (BE)-related neoplasia is currently used after endoscopic resection of visible neoplasia. The HALO 360 balloon has been used to ablate long segment BE. The Barrx™ 360 Express RFA self-sizing catheter ('RFA Express') may potentially allow quicker ablation times and improved treatment outcomes. The aim of this paper is to present real world data on the use of the 360 Express Device.
METHODS
Centres in the UK and Ireland submitted cases where the RFA Express was used. The primary outcome was regression of BE at 3 months. Secondary outcomes were the rate of symptomatic stricture formation and resolution of intestinal metaplasia (CR-IM) and dysplasia (CR-D) at End of Treatment (EoT).
RESULTS
11 centres submitted 123 consecutive patients. 112 had a follow up endoscopy. The median age was 67 years (IQR 62-75). 3 dosimetries were used. The mean reduction in Circumferential (C) length was 78% ± 36 and mean reduction in Maximal length (M) was 55% ± 36. 17 patients (15%) developed strictures requiring dilation. There was a higher rate of stricture formation when the 12 J energy was used (p < 0.05). 47 patients had EoT biopsies, 40 (85%) had CR-D and 34(76%) had CR-IM.
CONCLUSIONS
The RFA 360 Express catheter shows reduction in length of baseline BE at 3 months after index treatment, and eradication of intestinal metaplasia and dysplasia at 12 months similar to other studies with earlier devices. It appears that the symptomatic stricture rate is slightly higher than previous series with the HALO 360 catheter. This study was performed as part of the HALO registry and has been approved by the Research Ethics Committee - MREC Number 08/H0714/27 Local project reference 08/0104 Project ID 15,033 IRAS Number 54678 EudraCT 2009-015980-1. Registered on ISRCTN as below: ISRCTN93069556. https://doi.org/10.1186/ISRCTN93069556.

Identifiants

pubmed: 33547491
doi: 10.1007/s00464-021-08325-0
pii: 10.1007/s00464-021-08325-0
pmc: PMC8741663
doi:

Banques de données

ISRCTN
['ISRCTN93069556']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

598-606

Informations de copyright

© 2021. The Author(s).

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Auteurs

Cormac G Magee (CG)

University College London Hospital, London, UK.
Centre for Obesity Research, University College London, London, UK.

David Graham (D)

University College London Hospital, London, UK.
Division of Surgery and Interventional Sciences, University College London, London, UK.

Charles Gordon (C)

Royal Bournemouth and Christchurch Hospitals, Bournemouth, UK.

Jason Dunn (J)

Guy's and St Thomas' Hospital, London, UK.

Ian Penman (I)

Royal Infirmary of Edinburgh, Edinburgh, UK.

Robert Willert (R)

Manchester Royal Infirmary, Manchester, UK.

Howard Smart (H)

Royal Liverpool University Hospital, Liverpool, UK.

Jacobo Ortiz-Fernandez-Sordo (J)

Nottingham Digestive Diseases Centre, NIHR Biomedical Research Centre, Nottingham University Hospitals NHS Trust, Nottingham, UK.

Krish Ragunath (K)

Nottingham Digestive Diseases Centre, NIHR Biomedical Research Centre, Nottingham University Hospitals NHS Trust, Nottingham, UK.

Martin Everson (M)

Division of Surgery and Interventional Sciences, University College London, London, UK.

Durayd Alzoubaidi (D)

Division of Surgery and Interventional Sciences, University College London, London, UK.

Matthew Banks (M)

University College London Hospital, London, UK.
Division of Surgery and Interventional Sciences, University College London, London, UK.

Danielle Morris (D)

University College London Hospital, London, UK.

Sarmed Sami (S)

University College London Hospital, London, UK.
Division of Surgery and Interventional Sciences, University College London, London, UK.

Allan J Morris (AJ)

Glasgow Royal Infirmary, Glasgow, UK.

Pradeep Bhandari (P)

Portsmouth University Hospital, Portsmouth, UK.

Ravi Narayanasamy (R)

St James' Hospital, Dublin, Ireland.

Massimiliano Di Pietro (M)

Cambridge University Hospitals, Cambridge, UK.

Laurence B Lovat (LB)

University College London Hospital, London, UK.
Division of Surgery and Interventional Sciences, University College London, London, UK.

Rehan Haidry (R)

University College London Hospital, London, UK. r.haidry@ucl.ac.uk.
Division of Surgery and Interventional Sciences, University College London, London, UK. r.haidry@ucl.ac.uk.

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Classifications MeSH