Management Guidelines for Barrett's Esophagus
The management of Barrett's esophagus should follow a structured approach based on the 2024 NICE guidelines, including regular endoscopic surveillance with high-resolution white light endoscopy and Seattle protocol biopsies, with surveillance intervals determined by the presence and grade of dysplasia. 1
Diagnosis and Initial Management
- Barrett's esophagus is defined as a length of at least 1 cm of columnar epithelium in the esophagus, confirmed by histopathology 1
- For newly diagnosed patients:
Endoscopic Surveillance Protocol
Technique
- Use high-resolution white light endoscopy with Seattle biopsy protocol 1
- Take 4-quadrant biopsies every 2 cm in non-dysplastic Barrett's 1
- Take 4-quadrant biopsies every 1 cm in patients with known/suspected dysplasia 1
- Separately submit biopsies of any mucosal irregularities 1
- Document findings using Prague classification and Paris classification (for visible lesions) 2
- Allow minimum 1-minute inspection time per cm of Barrett's length 2
Surveillance Intervals
Based on the most recent NICE guidelines 1:
Non-dysplastic Barrett's esophagus:
Indefinite for dysplasia:
- Optimize acid-suppressant medication
- Repeat endoscopy in 6 months
- If no definite dysplasia found, follow non-dysplastic surveillance protocol 1
Low-grade dysplasia (LGD):
High-grade dysplasia (HGD):
Management of Dysplasia and Early Cancer
Low-grade Dysplasia
- Offer radiofrequency ablation for confirmed LGD on two separate endoscopies, confirmed by a second pathologist 2
- If not treated with ablation, perform surveillance every 6 months initially 1
High-grade Dysplasia
- Offer endoscopic resection for visible lesions 1
- Offer ablation for flat HGD and residual Barrett's after resection 1, 2
- Consider p53 immunostain as an adjunct to improve diagnostic reproducibility 1
Stage 1 Esophageal Adenocarcinoma
- Offer endoscopic resection for staging 1
- For T1a adenocarcinoma:
- For T1b adenocarcinoma:
- Low-risk (invasion ≤500μm, no lymphovascular invasion, well/moderate differentiation): consider endoscopic resection 2
- High-risk (deeper invasion, lymphovascular invasion, poor differentiation): offer oesophagectomy if fit for surgery 1
- Consider radiotherapy (alone or with chemotherapy) for high-risk patients not suitable for surgery 1
Post-treatment Follow-up
After endoscopic eradication therapy:
- First follow-up should be performed in an expert center 2
- Careful inspection of neo-squamocolumnar junction using high-definition white-light endoscopy 2
- Targeted biopsies of any suspicious areas 2
- For baseline HGD/EAC: follow-up at 1,2,3,4,5,7, and 10 years 2
- For baseline LGD: follow-up at 1,3, and 5 years 2
Prevention Strategies
- Do NOT offer aspirin to prevent progression to dysplasia/cancer 1
- Screen for cardiovascular risk factors for which aspirin therapy might be indicated 1
- Antireflux surgery is not more effective than medical therapy for cancer prevention 1
Important Caveats
- Visible lesions should always be considered malignant until proven otherwise 1
- Diagnosis of dysplasia should be confirmed by two gastrointestinal pathologists 1
- Endoscopic surveillance has limitations with sampling error exceeding 95% using standard protocols 3
- The incidence of adenocarcinoma in Barrett's esophagus is relatively low (1/220 patient-years) 4, but surveillance improves outcomes in patients with dysplasia 5
- All patients with dysplasia or early cancer should be discussed at a specialist MDT including an interventional endoscopist, upper GI cancer surgeon, radiologist, and GI pathologist 1