Barrett's Esophagus Unit, Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, USA.
Division of Gastroenterology and Hepatology, Mayo Clinic, Scottsdale, Arizona, USA.
Gut. 2019 Aug;68(8):1379-1385. doi: 10.1136/gutjnl-2018-317513. Epub 2019 Jan 11.
Surveillance interval protocols after complete remission of intestinal metaplasia (CRIM) post radiofrequency ablation (RFA) in Barrett's oesophagus (BE) are currently empiric and not based on substantial evidence. We aimed to assess the timeline, location and patterns of recurrence following CRIM to inform these guidelines.
Data on patients undergoing RFA for BE were obtained from prospectively maintained databases of five (three USA and two UK) tertiary referral centres. RFA was performed until CRIM was confirmed on two consecutive endoscopies.
594 patients achieved CRIM as of 1 May 2017. 151 subjects developed recurrent BE over a median (IQR) follow-up of 2.8 (1.4-4.4) years. There was 19% cumulative recurrence risk of any BE within 2 years and an additional 49% risk over the next 8.6 years. There was no evidence of a clinically meaningful change in the recurrence hazard rate of any BE, dysplastic BE or high-grade dysplasia/cancer over the duration of follow-up, with an estimated 2% (95% CI -7% to 12%) change in recurrence rate of any BE in a doubling of follow-up time. 74% of BE recurrences developed at the gastro-oesophageal junction (GOJ) (24.1% were dysplastic) and 26% in the tubular oesophagus. The yield of random biopsies from the tubular oesophagus, in the absence of visible lesions, was 1% (BE) and 0.2% (dysplasia).
BE recurrence risk following CRIM remained constant over time, suggesting that lengthening of follow-up intervals, at least in the first 5 years after CRIM, may not be advisable. Sampling the GOJ is critical to detecting recurrence. The requirement for random biopsies of the neosquamous epithelium in the absence of visible lesions may need to be re-evaluated.
在 Barrett 食管(BE)射频消融(RFA)后完全缓解肠上皮化生(CRIM)的监测间隔方案目前是经验性的,而不是基于大量证据。我们旨在评估 CRIM 后复发的时间、位置和模式,为制定这些指南提供信息。
从五个三级转诊中心的前瞻性维护数据库中获得接受 RFA 治疗 BE 的患者数据。进行 RFA,直到在连续两次内镜检查中确认 CRIM。
截至 2017 年 5 月 1 日,594 例患者达到 CRIM。中位(IQR)随访 2.8(1.4-4.4)年后,151 例患者出现复发性 BE。在 2 年内,任何 BE 的累积复发风险为 19%,在接下来的 8.6 年内,风险增加 49%。在整个随访期间,任何 BE、异型增生 BE 或高级别异型增生/癌症的复发危险率均无明显变化,任何 BE 的复发率估计在随访时间加倍时仅变化 2%(95%CI -7%至 12%)。74%的 BE 复发发生在胃食管交界处(GOJ)(24.1%为异型增生),26%发生在管状食管。在没有可见病变的情况下,管状食管随机活检的阳性率为 1%(BE)和 0.2%(异型增生)。
CRIM 后 BE 复发风险随时间保持不变,表明至少在 CRIM 后 5 年内,延长随访间隔时间可能不是明智之举。对 GOJ 进行采样对于检测复发至关重要。需要重新评估在没有可见病变的情况下对新生鳞状上皮进行随机活检的要求。