Management of Barrett's Esophagus
For Barrett's esophagus without dysplasia, provide proton pump inhibitors for symptom control and perform surveillance endoscopy every 3-5 years; for confirmed low-grade dysplasia, offer radiofrequency ablation; for high-grade dysplasia or T1a adenocarcinoma, perform endoscopic resection followed by ablation of residual Barrett's tissue. 1, 2, 3
Initial Assessment and Patient Education
- Offer a clinical consultation immediately after diagnosis to discuss the annual cancer progression risk of approximately 0.2-0.5% and establish a surveillance plan 1, 4, 5
- Provide both verbal and written information about the diagnosis, treatment options, and patient support groups 3, 4
- Ensure patients understand that Barrett's esophagus is a premalignant condition requiring long-term monitoring but has a relatively low cancer risk 5
Symptom Control and Medical Management
- Use proton pump inhibitors as first-line therapy for gastroesophageal reflux symptom control 3, 4, 5
- Do not offer anti-reflux surgery specifically to prevent progression to dysplasia or cancer, as it is not more effective than medical therapy for cancer prevention 1, 3, 4
- Do not prescribe aspirin specifically to prevent progression to esophageal dysplasia and cancer 3, 4
Endoscopic Surveillance Protocol
Technique Standards
- Use high-resolution white light endoscopy with the Seattle biopsy protocol: four-quadrant biopsies every 2 cm throughout the Barrett's segment 1, 3, 4, 6
- Maintain a minimum of 1-minute inspection time per cm of Barrett's esophagus length during surveillance 6
- Document landmarks, the Barrett's segment (one picture per cm of length), and the esophagogastric junction in retroflexed position 6
- Use the Prague classification for Barrett's length and Paris classification for visible lesions 6
Surveillance Intervals Based on Dysplasia Status
Non-dysplastic Barrett's esophagus:
- Perform surveillance endoscopy every 3-5 years 1, 4, 7
- For Barrett's segments ≥1 cm and <3 cm: surveillance every 5 years 6
- For Barrett's segments ≥3 cm and <10 cm: surveillance every 3 years 6
- For Barrett's segments ≥10 cm: refer to a Barrett's esophagus expert center 6
- For irregular Z-line or columnar-lined esophagus <1 cm: no routine biopsies or surveillance needed 6
Indefinite for dysplasia:
- Perform endoscopic surveillance at 6-month intervals with dose optimization of acid-suppressant medication 1, 3, 4
Low-grade dysplasia:
- Confirm the diagnosis with biopsy samples from two separate endoscopic examinations, verified by at least two expert gastrointestinal pathologists 1, 2, 3, 4
- This confirmation step is critical because low-grade dysplasia is frequently overcalled by community pathologists, particularly when esophageal inflammation is present 2
- Offer radiofrequency ablation as primary treatment once diagnosis is confirmed 1, 2, 3, 4, 6
- For patients who decline or defer ablation: perform surveillance at 6-12 month intervals 2
High-grade dysplasia:
- Offer endoscopic resection of visible esophageal lesions as first-line treatment 1, 3, 4, 6
- Offer endoscopic ablation of any residual Barrett's esophagus after endoscopic resection 1, 3, 4, 6
- For high-grade dysplasia without visible lesions: offer endoscopic ablation treatment to prevent progression to invasive cancer 6
When to Discontinue Surveillance
- Consider discontinuing surveillance if the patient has reached 75 years of age at the time of the last surveillance endoscopy and/or life expectancy is less than 5 years 6
Management of Stage 1 Esophageal Adenocarcinoma
T1a Adenocarcinoma
- Offer endoscopic resection as first-line treatment 1, 3, 4, 6
- Endoscopic resection is curative for T1a Barrett's cancer with well/moderate differentiation and no signs of lymphovascular invasion 6
- Offer endoscopic ablation of any residual Barrett's esophagus after endoscopic resection 1, 3, 4, 6
- Offer endoscopic follow-up to monitor for recurrence 1, 3
T1b Adenocarcinoma
- For patients fit for surgery with high-risk features (incomplete endoscopic resection, lymphovascular invasion, or deep submucosal invasion >500 μm): offer oesophagectomy 1, 3, 4
- Low-risk submucosal T1b adenocarcinoma (submucosal invasion ≤500 μm AND no lymphovascular invasion AND no poor tumor differentiation) can be treated by endoscopic resection with adequate follow-up including gastroscopy, endoscopic ultrasound, and CT/PET-CT in expert centers 6
- For patients unfit for oesophagectomy but at high risk of cancer progression: consider radiotherapy alone or combined with chemotherapy 1, 3, 4
- High-risk T1b adenocarcinoma (invasion >500 μm, lymphovascular invasion, or poor differentiation) requires complete staging and multidisciplinary discussion for additional treatments 6
- Offer endoscopic follow-up after radiotherapy 1
Staging Considerations
- Do not use CT before endoscopic resection for staging suspected T1 oesophageal adenocarcinoma 3, 4
- Do not use endoscopic ultrasonography before endoscopic resection for staging suspected T1a oesophageal adenocarcinoma 1, 4
- Consider endoscopic ultrasound for nodal staging in patients with suspected T1b oesophageal adenocarcinoma based on endoscopic appearances or histological examination 1, 3, 4
Post-Eradication Therapy Surveillance
First Follow-up
- Perform the first endoscopic follow-up after successful endoscopic eradication therapy in an expert center 6
- Use high-definition white-light endoscopy and virtual chromoendoscopy to carefully inspect the neo-squamocolumnar junction and neo-squamous epithelium for recurrent dysplasia 6
Biopsy Protocol After Eradication
- Do not perform routine four-quadrant biopsies of neo-squamous epithelium after successful endoscopic eradication therapy 6
- Obtain four-quadrant random biopsies just distal to a normal-appearing neo-squamocolumnar junction to detect dysplasia in the absence of visible lesions 6
- Obtain targeted biopsies where there is suspicion of recurrent Barrett's esophagus in the tubular esophagus or visible lesions suspicious for dysplasia 6
Surveillance Intervals After Successful Eradication
For baseline diagnosis of high-grade dysplasia or adenocarcinoma:
- Surveillance at 1,2,3,4,5,7, and 10 years after last treatment, after which surveillance may be stopped 6
For baseline diagnosis of low-grade dysplasia:
- Surveillance at 1,3, and 5 years after last treatment, after which surveillance may be stopped 6
Critical Pitfalls to Avoid
- Never proceed with ablation based on a single pathologist's diagnosis or single endoscopy for low-grade dysplasia, as the false-positive rate is extremely high in community practice 2
- Do not offer anti-reflux surgery or aspirin specifically for cancer prevention, as evidence does not support these interventions 1, 2, 3, 4
- Ensure all dysplasia diagnoses are confirmed by at least two expert gastrointestinal pathologists to avoid unnecessary interventions 2, 4
- Optimize acid suppression before repeat biopsies in cases of indefinite dysplasia to minimize inflammation that can confound dysplasia diagnosis 2