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Improvement over time in outcomes for patients undergoing endoscopic therapy for Barrett's oesophagus-related neoplasia: 6-year experience from the first 500 patients treated in the UK patient registry.
Haidry, R J; Butt, M A; Dunn, J M; Gupta, A; Lipman, G; Smart, H L; Bhandari, P; Smith, L; Willert, R; Fullarton, G; Di Pietro, M; Gordon, C; Penman, I; Barr, H; Patel, P; Kapoor, N; Hoare, J; Narayanasamy, R; Ang, Y; Veitch, A; Ragunath, K; Novelli, M; Lovat, L B.
Affiliation
  • Haidry RJ; Research Department of Tissue and Energy, Division of Surgery and Interventional Science, University College London, London, UK Department of Gastroenterology, University College Hospital NHS Foundation Trust, London, UK.
  • Butt MA; Research Department of Tissue and Energy, Division of Surgery and Interventional Science, University College London, London, UK.
  • Dunn JM; Guy's and St Thomas' NHS foundation Trust, London, UK Institute for Cancer Genetics and Informatics, Oslo University, Oslo, Norway.
  • Gupta A; Department of Gastroenterology, University College Hospital NHS Foundation Trust, London, UK.
  • Lipman G; Research Department of Tissue and Energy, Division of Surgery and Interventional Science, University College London, London, UK.
  • Smart HL; Department of Gastroenterology and Hepatology, Royal Liverpool University Hospital, Liverpool, UK.
  • Bhandari P; Princess Alexandra Hospital, Portsmouth, UK.
  • Smith L; Bradford Teaching Hospitals NHS Foundation Trust, Bradford, UK.
  • Willert R; Central Manchester University Hospitals NHS Foundation Trust, Manchester,UK.
  • Fullarton G; Glasgow Royal Infirmary, Glasgow, UK.
  • Di Pietro M; Addenbrooke's Hospital, Cambridge, UK.
  • Gordon C; Royal Bournemouth Hospital, Bournemouth, UK.
  • Penman I; Royal Infirmary Edinburgh, Edinburgh, UK.
  • Barr H; Oesophagogastric Surgery, Gloucestershire Hospital NHS Trust, Birmingham, UK.
  • Patel P; Department of Gastroenterology, Southampton University Hospital, Southampton, UK.
  • Kapoor N; Digestive Diseases Centre, Aintree University Hospital, Liverpool, UK.
  • Hoare J; St Mary's Hospital NHS Trust, London, UK.
  • Narayanasamy R; St James Hospital, Dublin, Republic of Ireland.
  • Ang Y; Centre of Gastrointestinal Sciences, University of Manchester, Salford Royal Foundation NHS Trust, Salford, UK.
  • Veitch A; Department of Gastroenterology, Royal Wolverhampton Hospitals NHS Trust, Wolverhampton, UK.
  • Ragunath K; Department of Gastroenterology, Nottingham University Hospital NHS Trust, Nottingham, UK.
  • Novelli M; Department of Gastroenterology, University College Hospital NHS Foundation Trust, London, UK.
  • Lovat LB; Research Department of Tissue and Energy, Division of Surgery and Interventional Science, University College London, London, UK Department of Gastroenterology, University College Hospital NHS Foundation Trust, London, UK.
Gut ; 64(8): 1192-9, 2015 Aug.
Article in En | MEDLINE | ID: mdl-25539672
ABSTRACT

BACKGROUND:

Barrett's oesophagus (BE) is a pre-malignant condition leading to oesophageal adenocarcinoma (OAC). Treatment of neoplasia at an early stage is desirable. Combined endoscopic mucosal resection (EMR) followed by radiofrequency ablation (RFA) is an alternative to surgery for patients with BE-related neoplasia.

METHODS:

We examined prospective data from the UK registry of patients undergoing RFA/EMR for BE-related neoplasia from 2008 to 2013. Before RFA, visible lesions were removed by EMR. Thereafter, patients had RFA 3-monthly until all BE was ablated or cancer developed (endpoints). End of treatment biopsies were recommended at around 12 months from first RFA treatment or when endpoints were reached. Outcomes for clearance of dysplasia (CR-D) and BE (CR-IM) at end of treatment were assessed over two time periods (2008-2010 and 2011-2013). Durability of successful treatment and progression to OAC were also evaluated.

RESULTS:

508 patients have completed treatment. CR-D and CR-IM improved significantly between the former and later time periods, from 77% and 56% to 92% and 83%, respectively (p<0.0001). EMR for visible lesions prior to RFA increased from 48% to 60% (p=0.013). Rescue EMR after RFA decreased from 13% to 2% (p<0.0001). Progression to OAC at 12 months is not significantly different (3.6% vs 2.1%, p=0.51).

CONCLUSIONS:

Clinical outcomes for BE neoplasia have improved significantly over the past 6 years with improved lesion recognition and aggressive resection of visible lesions before RFA. Despite advances in technique, the rate of cancer progression remains 2-4% at 1 year in these high-risk patients. TRIAL REGISTRATION NUMBER ISRCTN93069556.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Precancerous Conditions / Barrett Esophagus / Esophageal Neoplasms / Adenocarcinoma / Registries / Esophagoscopy / Catheter Ablation Type of study: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: Gut Year: 2015 Document type: Article Affiliation country: Reino Unido

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Precancerous Conditions / Barrett Esophagus / Esophageal Neoplasms / Adenocarcinoma / Registries / Esophagoscopy / Catheter Ablation Type of study: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: Gut Year: 2015 Document type: Article Affiliation country: Reino Unido