Endoscopic Resection or Ablation for Patients With Dysplasia or Intramucosal Cancer in Barrett's Esophagus
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Barrett's Esophagus
- Sponsor
- Midwest Biomedical Research Foundation
- Enrollment
- 12
- Locations
- 3
- Primary Endpoint
- Complete histological eradication of Barrett's esophagus
- Status
- Terminated
- Last Updated
- 8 years ago
Overview
Brief Summary
This clinical trial will evaluate a patient population with Barrett's esophagus(BE) containing high grade dysplasia or intramucosal cancer and compare the effects of endoscopically-guided radiofrequency ablation system(RFA) and endoscopically-guided stepwise endoscopic mucosal resection(S-EMR).
Detailed Description
This is a multi-center prospective, randomized controlled trial conducted at 4 centers. The patients with high grade dysplasia(HGD) and/or esophageal cancer(EC) who meet the study criteria will be enrolled, undergo a baseline diagnostic EMR and then be randomized in a 1:1 ratio to undergo treatment by either S-EMR or radiofrequency ablation(RFA). The initial staging EMR will not extend more than 50% of the esophageal circumference or more than 2 cm in longitudinal extent. Patients in the S-EMR group will undergo step-wise eradication of the BE segment using the Duette multi-band mucosectomy kit (Cook Medical, FDA approved) whereas those in the RFA group will undergo BE ablation using the endoscopically-guided HALO radiofrequency ablation system (Barrx Medical, FDA approved). Both treatment groups will undergo their respective treatment sessions every 2 months until either no Barrett's esophagus is seen or until a maximum of 4 treatment sessions. Once there is no visible Barrett's esophagus, patients will undergo surveillance biopsies (random 4 quadrant biopsies every 1 cm of the neo-squamous mucosa and random biopsies of the cardia) to evaluate for complete eradication of Barrett's esophagus. Regardless of whether there is visible Barrett's esophagus, all patients will undergo repeat endoscopy every 2 months for 1 year after enrollment. If no visible Barrett's esophagus is seen during the endoscopy, then surveillance biopsies to evaluate for dysplasia will be taken. Regardless of whether this is any visible Barrett's esophagus, all patients will undergo surveillance biopsies at 12 months after enrollment. The objective of this study is to compare the proportion of patients with complete eradication of Barrett's esophagus using S-EMR versus RFA at 12 months.
Investigators
PRATEEK SHARMA
Principal Investigator
Midwest Biomedical Research Foundation
Eligibility Criteria
Inclusion Criteria
- •Subjects shall be screened according to the following inclusion criteria. An answer of "no" to any inclusion criterion disqualifies a subject from participating in this study.
- •Patients age: \> 18 years
- •Subject has documented diagnosis of Barrett's esophagus, maximum endoscopic length of no more than C2M5 (i.e. no more than 2cm of circumferential extent and no more than 5cm of tongues) containing HGD/EC as follows:
- •HGD or EC documented on biopsy within previous 6 months from enrollment
- •Histology slides reviewed at central pathology service for ERADICATE Trial confirm HGD/EC.
- •Endoscopically visible lesion/area/pattern in a patient with HGD/EC either by high definition white light endoscopy, narrow band imaging, confocal laser endomicroscopy, or another enhanced imaging tool.
- •Ability to take oral proton pump inhibitor
- •For female subjects of childbearing potential, a negative urine pregnancy test within 2 weeks of enrollment and any subsequent endoscopy encounter
- •Subject is eligible for treatment and follow-up endoscopy and biopsy as required by the investigational plan
- •Ability to discontinue aspirin/NSAIDs/Clopidogrel 7 days before and after all ablation procedures
Exclusion Criteria
- •Subjects shall be screened according to the following exclusion criteria. An answer of "yes" to any exclusion criterion disqualifies a subject from participating in this study.
- •Extent of BE \>C2M5
- •The subject is pregnant or planning a pregnancy during the study period (12 months after treatment)
- •Esophageal stricture preventing passage of endoscope or catheter
- •Active erosive esophagitis
- •History of malignancy of the esophagus, esophageal varices or coagulopathy
- •Prior radiation therapy to the esophagus, except head and neck region radiation therapy.
- •Any previous ablation therapy within the esophagus (photodynamic therapy, multipolar electrocoagulation, argon plasma coagulation, laser treatment, or other)
- •Any previous EMR in the esophagus
- •Any previous esophageal surgery, including fundoplication
Outcomes
Primary Outcomes
Complete histological eradication of Barrett's esophagus
Time Frame: 12 months
Secondary Outcomes
- Complete histological clearance of dysplasia(12 months)
- Complication rates(12 months)