Esophageal Cancer, Precancerous Condition
Conditions
Keywords
esophageal cancer, adenocarcinoma of the esophagus, Barrett esophagus
Brief summary
RATIONALE: Screening tests may help doctors find cancer cells early and plan better treatment. It is not yet known whether endoscopy every 2 years is more effective than endoscopy only as needed in finding esophageal cancer in patients with Barrett esophagus. PURPOSE: This randomized phase III trial is studying endoscopy every 2 years to see how well it works compared with endoscopy only as needed in monitoring patients with Barrett esophagus.
Detailed description
OBJECTIVES: Primary * To establish whether endoscopic surveillance every 2 years or endoscopy at need only is superior in terms of overall survival and, if neither is superior, whether endoscopy at need only is non-inferior to surveillance every 2 years in patients with Barrett esophagus. Secondary * To estimate the cost-effectiveness of endoscopic surveillance every 2 years as compared to endoscopy at need only. * To establish whether there is a significant difference between endoscopic surveillance every 2 years or endoscopy at need only in terms of the incidence of esophageal cancer, gastric or esophageal cancer, or all cancers. * To establish whether there is a significant difference between endoscopic surveillance every 2 years or endoscopy at need only in terms of the time to diagnosis of esophageal adenocarcinoma. * To establish whether there is a significant difference between endoscopic surveillance every 2 years or endoscopy at need only in terms of the stage of esophageal adenocarcinoma at diagnosis using TNM staging. * To establish whether there is a significant difference between endoscopic surveillance every 2 years or endoscopy at need only in terms of morbidity and mortality related to endoscopy, esophageal surgery, and other endoscopy-related interventions (e.g., ablation). * To establish whether there is a significant difference between endoscopic surveillance every 2 years or endoscopy at need only in terms of the frequency of endoscopy. OUTLINE: This is a multicenter study. Patients are stratified according to age at diagnosis (\< 65 years vs ≥ 65 years), length of Barrett metaplasia segment including tongues (\< 2 cm vs ≥ 2 cm and ≤ 3 cm vs \> 3 cm and ≤ 8 cm vs \> 8 cm), and newly diagnosed disease (defined as the date of endoscopy confirming Barrett metaplasia was within the past 4 months) (yes vs no). Patients are randomized to 1 of 2 intervention arms. * Arm I: Patients undergo surveillance endoscopy with quadrantic biopsies taken every 2 cm. Patients undergo endoscopy every 2 years for a total of 6 endoscopies over 10 years. * Arm II: Patients undergo endoscopy as needed over 10 years. All patients may undergo urgent endoscopy if they develop dysphagia, unexplained weight loss of \> 7 lb, iron-deficiency anemia, recurrent vomiting, or worsening upper gastrointestinal symptoms. All patients complete a questionnaire that includes a quality-of-life measure and questions about medication at baseline, every 2 years, and following key events (e.g., diagnosis of any cancer or high-grade dysplasia).
Interventions
2 yearly endoscopy versus endoscopy at need
2 yearly endoscopy versus endoscopy at need
2 yearly endoscopy versus endoscopy at need
2 yearly endoscopy versus endoscopy at need
2 yearly endoscopy versus endoscopy at need
QOL aims to elicit any differences in QOL between 2 yearly endoscopy versus endoscopy at need
All Barretts patients to be screened
Sponsors
Study design
Eligibility
Inclusion criteria
DISEASE CHARACTERISTICS: * Histologically confirmed circumferential Barrett metaplasia meeting 1 of the following criteria: * At least 1 cm from the gastro-esophageal junction * At least a 2 cm non-circumferential tongue of Barrett metaplasia * Undergone endoscopy within the last 2 years to confirm Barrett metaplasia and exclude high-grade dysplasia and carcinoma * No known high-grade dysplasia or carcinoma PATIENT CHARACTERISTICS: * Resident of the United Kingdom * Informed of the risk of Barrett esophagus developing into esophageal cancer, either at the visit when the invitation letter is issued or on a documented previous occasion * Able to undergo endoscopy * No medical conditions that would make endoscopy difficult or hazardous PRIOR CONCURRENT THERAPY: * See Disease Characteristics
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Overall survival | — |
Secondary
| Measure | Time frame |
|---|---|
| Incidence of esophageal cancer, gastric or esophageal cancer, or all cancers | — |
| Time to diagnosis of esophageal adenocarcinoma | — |
| Cost-effectiveness | — |
| Morbidity and mortality related to endoscopy, esophageal surgery, and other endoscopy-related interventions | — |
| Frequency of endoscopy | — |
| Stage of esophageal adenocarcinoma at diagnosis using TNM staging | — |
Countries
United Kingdom