Premium
Systematic review with meta‐analysis: the long‐term efficacy of Barrett's endoscopic therapy—stringent selection criteria and a proposal for definitions
Author(s) -
Desai Madhav,
Rösch Thomas,
Sundaram Suneha,
Chandrasekar Viveksandeep Thoguluva,
Kohli Divyanshoo,
Spadaccini Marco,
Hassan Cesare,
Repici Alessandro,
Sharma Prateek
Publication year - 2021
Publication title -
alimentary pharmacology and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.308
H-Index - 177
eISSN - 1365-2036
pISSN - 0269-2813
DOI - 10.1111/apt.16473
Subject(s) - medicine , dysplasia , barrett's oesophagus , meta analysis , intestinal metaplasia , barrett's esophagus , gastroenterology , adenocarcinoma , surgery , cancer
Summary Background Barrett's endoscopic therapy (BET) is well established for neoplasia in Barrett's oesophagus using a concept of complete eradication of all Barrett's. However, long‐term efficacy is not known. Aims To perform a systematic review and meta‐analysis to examine long‐term efficacy of BET for Barrett's neoplasia. Methods Electronic databases were searched for studies meeting stringent criteria: (a) subjects with high‐grade dysplasia and/or superficial adenocarcinoma who underwent BET (ablation ± endoscopic mucosal resection); (b) BET completion by confirmation of complete eradication of neoplasia (CE‐N) and intestinal metaplasia (CE‐IM) with systematic sampling and (c) clearly defined follow‐up (endoscopy and biopsy) protocol of ≥2 years thereafter for detection of recurrence. Pooled estimates of CE‐N and CE‐IM after BET completion and follow‐up were analysed. Results Eight studies met the stringent criteria (n = 794, males 89%, age 64.6 years). Despite high efficacy of BET at therapy completion (CE‐N: 95.9 [91.7‐98.7]%; CE‐IM: 90.9 [83‐96.6]%), this declined (CE‐N: 89 [73.4‐98.2]%; CE‐IM: 77.8 [65.6‐88]%) over 3.4 years of follow‐up. There was considerable heterogeneity. Only two studies reported a post‐BET follow‐up of >5 years (CE‐IM 50 [41.5%‐58.5]%). Higher person years of follow‐up seem to correlate with decrease in BET efficacy. Conclusion Using stringent criteria for appropriate study selection with sufficient follow‐up, a lack of high‐quality controlled intervention trials becomes evident for assessment of long‐term durable remission rates of BET despite initial high success rates. We plea for a uniform documentation of study details which could be used in future trials.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom