Impact of margin thermal ablation after endoscopic mucosal resection of large (≥20 mm) non-pedunculated colonic polyps on long-term recurrence

医学 粘膜切除术 边距(机器学习) 热烧蚀 外科 期限(时间) 胃肠病学 切除缘 内科学 烧蚀 切除术 计算机科学 量子力学 机器学习 物理
作者
Timothy O’Sullivan,Francesco Vito Mandarino,Julia Gauci,Anthony Whitfield,Clarence Kerrison,James Elhindi,Catarina Neto do Nascimento,Sunil Gupta,Oliver Cronin,Anthony Sakiris,Juan Francisco Prieto Aparicio,Sophie Arndtz,Gregor J. Brown,Spiro Raftopoulos,David J. Tate,Eric Y. Lee,Stephen J. Williams,Nicholas G. Burgess,Michael J. Bourke
出处
期刊:Gut [BMJ]
卷期号:74 (1): 67-74 被引量:9
标识
DOI:10.1136/gutjnl-2024-332907
摘要

Background and aims The efficacy of colorectal endoscopic mucosal resection (EMR) is limited by recurrence and the necessity for conservative surveillance. Margin thermal ablation (MTA) after EMR has reduced the incidence of recurrence at the first surveillance colonoscopy at 6 months (SC1). Whether this effect is durable to second surveillance colonoscopy (SC2) is unknown. We evaluated long-term surveillance outcomes in a cohort of LNPCPs that have undergone MTA. Methods LNPCPs undergoing EMR and MTA from four academic endoscopy centres were prospectively recruited. EMR scars were evaluated at SC1 and in the absence of recurrence, SC2 colonoscopy was conducted in a further 12 months. A historical control arm was generated from LNPCPs that underwent EMR without MTA. The primary outcome was recurrence at SC2 in all LNPCPs with a recurrence-free scar at SC1. Results 1152 LNPCPs underwent EMR with complete MTA over 90 months until October 2022. 854 LNPCPs underwent SC1 with 29/854 (3.4%) LNPCPs demonstrating recurrence. 472 LNPCPs free of recurrence at SC1 underwent SC2. 260 LNPCPs with complete SC2 follow-up formed the control arm from January 2012 to May 2016. Recurrence at SC2 was significantly less in the MTA arm versus controls (1/472 (0.2%) vs 9/260 (3.5%); p<0.001)). Conclusion LNPCPs that have undergone successful EMR with MTA and are free of recurrence at SC1 are unlikely to develop recurrence in subsequent surveillance out to 2 years. Provided the colon is cleared of synchronous neoplasia, the next surveillance can be potentially extended to 3–5 years. Such an approach would reduce costs and enhance patient compliance.
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