Browse EPPT > MDA2013-02-02
Effect of Aspirin on Biomarkers of Barrett’s Esophagus After Successful Eradication of Barrett’s Esophagus with Radiofrequency Ablation

The following datasets contain the data available for EPPT MDA2013-02-02. The description and documentation for each file is listed below. SAS7bdat and CSV versions of the actual data will be available to CDAS projects approved to use this study's data.

Analysis Datasets

Files	Description
Data Dictionary (PDF - 1.3 MB)	1. The Enhanced Person dataset is created for analyses and contains all relevant information from most of the raw datasets received. Each record represents one participant and contains updated variable names, formats, and labels. All information coming from non-person-based datasets has been converted into a person-based format.
Data Dictionary (PDF - 50.3 KB)	2. The Adverse Event dataset contains adverse event information, including onset date, grade of severity, attribution to the study agent, and outcome. This version of the dataset includes updated variable names, formats, and labels.

Raw Datasets

These 51 datasets contain the raw form data received, excluding PII.

Show these datasets

Files	Description
Data Dictionary (PDF - 74.9 KB)	1. The Ablation History dataset contains ablation history
Data Dictionary (PDF - 41.4 KB)	2. The Admin Intervention dataset contains records date agent provided and start date
	3. The Adverse Event dataset contains adverse events that occurred during the study.
Data Dictionary (PDF - 42.7 KB)	4. The Adverse Events and Concomitant Medication Evaluation dataset contains records if there were any new or changes to adverse events or concomitant medications
Data Dictionary (PDF - 43.6 KB)	5. The Agent Interruption dataset contains details of interrupted or stopped agent administration
Data Dictionary (PDF - 48.6 KB)	6. The Alcohol History dataset contains alcohol use and history questionnaire
Data Dictionary (PDF - 89.9 KB)	7. The Baseline History Assessment dataset contains baseline history of other body system statues that aren’t in the standard list
Data Dictionary (PDF - 42.9 KB)	8. The Baseline Symptoms dataset contains symptoms at baseline
	9. The BE Merged456 dataset contains biomarker results from biopsy samples, cdx2, GAPDH values, and p65 values
Data Dictionary (PDF - 54.0 KB)	10. The Biopsy Specimen Research dataset contains biopsy and specimen details
Data Dictionary (PDF - 71.1 KB)	11. The Cancer History dataset contains cancer medical history
Data Dictionary (PDF - 46.0 KB)	12. The Cinical Lab: Other Labs dataset contains other lab test results
Data Dictionary (PDF - 42.9 KB)	13. The Clinical Lab: Blood Chemistry dataset contains lab blood chemistry results
Data Dictionary (PDF - 43.9 KB)	14. The Clinical Lab: Blood Hematology 1 dataset contains lab blood hematology results 1
Data Dictionary (PDF - 43.3 KB)	15. The Clinical Lab: Blood Hematology 2 dataset contains lab blood hematology results 2
Data Dictionary (PDF - 36.5 KB)	16. The Comments dataset contains general comments on any form data
Data Dictionary (PDF - 45.1 KB)	17. The Concomitant Medications dataset contains concomitant medications list covering the entire trial
Data Dictionary (PDF - 38.6 KB)	18. The Drug Labels Compliance dataset contains record of whether labels were affixed
Data Dictionary (PDF - 41.1 KB)	19. The Eligiblity Verification dataset contains eligibility status
Data Dictionary (PDF - 50.6 KB)	20. The Endoscopy Assessment dataset contains endoscopy assessment results and details
	21. The Exclusion Criteria Prev Version 7a2 dataset contains exclusion criteria details
Data Dictionary (PDF - 38.4 KB)	22. The Exclusion Criteria Version 7a2 dataset contains exclusion criteria details
Data Dictionary (PDF - 38.0 KB)	23. The Exclusion Criteria Version 9a4 dataset contains exclusion criteria details
Data Dictionary (PDF - 51.1 KB)	24. The Family Medical History dataset contains family relevant medical history
Data Dictionary (PDF - 38.8 KB)	25. The Inclusion Criteria Prev Version 8a3 dataset contains inclusion criteria details
Data Dictionary (PDF - 38.5 KB)	26. The Inclusion Criteria Version 8a3 dataset contains inclusion criteria details
Data Dictionary (PDF - 38.3 KB)	27. The Inclusion Criteria Version 9a4 dataset contains inclusion criteria details
Data Dictionary (PDF - 172.0 KB)	28. The Interval 1 Questionnaire dataset contains interval 1 questionnaire of participants various issues
Data Dictionary (PDF - 152.6 KB)	29. The Interval 2 Questionnaire dataset contains interval 2 questionnaire of participants various issues
Data Dictionary (PDF - 151.6 KB)	30. The Interval 3 Questionnaire dataset contains interval 3 questionnaire of participants various issues
Data Dictionary (PDF - 149.7 KB)	31. The Interval 4 Questionnaire dataset contains interval 4 questionnaire of participants various issues
Data Dictionary (PDF - 51.9 KB)	32. The Medical History dataset contains medical history
Data Dictionary (PDF - 49.2 KB)	33. The Off Study dataset contains off study date and reasons
Data Dictionary (PDF - 48.4 KB)	34. The Participant Contact Form dataset contains participant contact details
Data Dictionary (PDF - 59.5 KB)	35. The Physical Exam 1 dataset contains physical exam of body systems statuses
Data Dictionary (PDF - 57.9 KB)	36. The Physical Exam 2 dataset contains physical exam of anthropometry
Data Dictionary (PDF - 43.0 KB)	37. The Pregnancy Specimen Results dataset contains pregnancy test results
Data Dictionary (PDF - 41.7 KB)	38. The Randomization dataset contains randomization date and details
Data Dictionary (PDF - 54.7 KB)	39. The Registration Part 2a dataset contains registration details and some demographics
Data Dictionary (PDF - 54.3 KB)	40. The Registration Part 2b dataset contains basic registration details and some demographics
Data Dictionary (PDF - 45.3 KB)	41. The Screening Prev Version 8a3 dataset contains telephone screening results
	42. The Screening Version 8a3 dataset contains telephone screening results
Data Dictionary (PDF - 46.3 KB)	43. The Study Specimen Shipping Form dataset contains study specimen shipping details
Data Dictionary (PDF - 41.7 KB)	44. The Surgical History dataset contains surgical history
Data Dictionary (PDF - 48.8 KB)	45. The Symptom Assessment dataset contains participant symptom assessment
Data Dictionary (PDF - 49.3 KB)	46. The Tissue Histology dataset contains samples from biopsy or resection details
Data Dictionary (PDF - 43.1 KB)	47. The Tobacco History dataset contains tobacco use and history questionnaire
Data Dictionary (PDF - 50.9 KB)	48. The Trial Compliance dataset contains participant compliance
Data Dictionary (PDF - 36.8 KB)	49. The Unblinding Form dataset contains unblinding details
Data Dictionary (PDF - 36.0 KB)	50. The Verification dataset indicates that the investigator reviewed case report forms
Data Dictionary (PDF - 110.1 KB)	51. The Your Health And Wellbeing dataset contains your health and well being quality of life questionnaire

Trial Summary

This randomized placebo-controlled phase II trial studies the safety of and how well aspirin works in preventing Barrett’s esophagus from returning after it has been successfully eliminated by radiofrequency ablation. Studying samples of tissue from patients with Barrett’s esophagus for the levels of a specific protein that is linked to developing Barrett’s esophagus may help doctors learn whether aspirin can prevent it from returning after it has been successfully treated.

Patients are randomized to 1 of 2 treatment arms.

• ARM I: Patients receive aspirin orally (PO) once daily (QD) for 12 months.
• ARM II: Patients receive placebo PO QD for 12 months.

Enrollment Statistics

Target Enrollment: 40

Actual Registration: 33

• 21 people randomized (21 of 33 registered)
  • 10 in Arm I: Aspirin
    • 7 Completed study
    • 1 Lost to follow-up
    • 1 Refused follow-up
    • 1 Withdrew
  • 11 in Arm II: Placebo
    • 5 Completed study
    • 1 Dropped due to adverse event
    • 1 Lost to follow-up
    • 3 Refused follow-up
    • 1 Withdrew
• 12 people not randomized (12 of 33 registered)
  • 11 Ineligible
  • 1 Other

Eligibility Criteria

Inclusion Criteria

• Known diagnosis of histologically-confirmed BE with or without dysplasia (as defined by the presence of specialized columnar epithelium anywhere in the tubular esophagus with ≥ 1 cm of circumferential involvement or non-circumferential involvement of specialized columnar epithelium) requiring radiofrequency ablation
• Documentation of complete ablation of BE after radiofrequency ablation on two endoscopic examinations at least 3 months apart (including no evidence of BE on surveillance biopsies) as determined by the pathologist at each site; completion of ablation should have occurred no greater than 36 months prior to randomization
• The effects of the candidate chemoprevention agents on the developing human fetus remain incompletely defined; for this reason, persons of childbearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for the duration of study participation; should a participant become pregnant or suspect she is pregnant while participating in this trial, she should inform the research personnel and her clinical care provider immediately
• Willingness to provide tissue samples for research purposes
• No chronic use of aspirin or nonsteroidal anti-inflammatory drugs (NSAIDs) or selective cyclooxygenase-2 (COX-2) inhibitors during one month prior to randomization; chronic use is defined as any aspirin or NSAID use on ≥ 7 days during one month preceding the beginning of randomization
• Hemoglobin ≥ 10 g/dL or hematocrit ≥ 30% (obtained ≤ 45 days prior to randomization)
• Leukocyte count ≥ 3,000/microliter (obtained ≤ 45 days prior to randomization)
• Platelet count ≥ 100,000/microliter (obtained ≤ 45 days prior to randomization)
• Absolute neutrophil count ≥ 1,500/microliter (obtained ≤ 45 days prior to randomization)
• Creatinine ≤ 2.5 × institutional upper limit of normal (ULN) (obtained ≤ 45 days prior to randomization)
• OR glomerular filtration rate (GFR) > 30 ml/min/1.73 m^2 (obtained ≤ 45 days prior to randomization)
• Total bilirubin ≤ 2 × institutional ULN (obtained ≤ 45 days prior to randomization)
• Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase [SGOT]) ≤ 2.5 × institutional ULN (obtained ≤ 45 days prior to randomization)
• Alanine aminotransferase (ALT) (serum glutamate pyruvate transaminase [SGPT]) ≤ 2.5 × institutional ULN (obtained ≤ 45 days prior to randomization)
• A negative serum pregnancy test at baseline, but within 21 days of randomization, for persons of childbearing potential only
• Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2
• Ability to understand and the willingness to sign a written informed consent document; a legally authorized representative (LAR) may sign informed consent for persons who do not have the capacity to legally consent to take part in the study

Exclusion Criteria

• Inability to abstain from, NSAID (including aspirin), and selective COX-2 inhibitor therapy at the time of randomization through the completion of the study (the study period is defined as baseline to exit endoscopy at 18 months after randomization which defines the completion of the study); participants may take Tylenol and non-NSAID pain relievers
• Current or planned use of anticoagulant drugs such as: warfarin, heparin, low molecular weight heparin, Plavix, or Aggrenox throughout the course of the study
• Individuals taking the drugs listed below may not be randomized unless they are willing to stop the medications (and possibly change to alternative non-excluded medications to treat the same conditions) no less than 1 month prior to starting aspirin or placebo on this study; consultation with the participant's primary care provider will be obtained prior to stopping any agent; the use of the following drugs or drug classes is prohibited during aspirin/placebo treatment:
  • NSAIDs: such as aspirin, Naprosyn, ketorolac and others NSAIDs
  • COX-2 inhibitors: such as celecoxib, rofecoxib
  • Valproic acid
  • Sulfinpyrazone
  • Probenecid
  • Corticosteroids (other than short-term use defined as less than 2 weeks or pro re nata [prn (when necessary)] use of an inhaler less than twice per month)
  • Platelet aggregation inhibitors, except in a monitored antithrombotic regimen
  • Methotrexate (MTX)
  • Vaccines containing live viruses
  • Gingko
• Individuals with uncontrolled renal insufficiency or renal failure
• Participants with fundoplication within the past year, bariatric surgery or any other major upper gastrointestinal (GI) surgery; fundoplication more than one year ago will not be grounds for exclusion; cholecystectomy will not be grounds for exclusion
• History of invasive cancer diagnosis ≤ 12 months prior to randomization, excepting nonmelanoma skin cancer; patients with T1a adenocarcinoma of the esophagus arising in the setting of Barrett's esophagus are eligible for enrollment in the trial
• History of cancer treatment ≤ 12 months prior to randomization, excepting hormonal therapy (except treatment for non-melanoma skin cancer or carcinoma-in-situ of the cervix)
• Receipt of any other investigational agents ≤ 3 months prior to randomization, except innocuous agents with no known interaction with the study agents (e.g., standard dose multivitamins or topical agents for limited skin conditions), at the discretion of the protocol lead investigator at each participating site
• History of allergic reactions attributed to aspirin or compounds of similar chemical or biologic composition to the study agent
• History of endoscopically or radiographically diagnosed peptic ulcer disease with upper GI bleeding during the past 5 years or history of endoscopically or radiographically diagnosed peptic ulcer disease with upper GI bleeding any time while taking aspirin
• Uncontrolled intercurrent illness including, but not limited to: ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, bleeding disorder, vitamin K deficiency, alcohol abuse (defined as ingestion of 3 or more drinks per day) or psychiatric illness/social situations that would limit compliance with study requirements
• Pregnant women
• Breast feeding women
• Surveillance biopsies demonstrating residual BE at qualifying exam
• Presence of an esophageal stricture defined as "any recognizable change in esophageal luminal caliber that is accompanied by symptoms of dysphagia, or any asymptomatic narrowing that either will not allow any adult endoscope to pass or allows passage with resistance"
• Patients with human immunodeficiency virus (HIV) infection

Schema

The Schema is a timeline of the study. It indicates start/end points, visits expected, major testing to be done, and any other information that is crucial to understanding how the study was completed.

Results/Findings:

Objectives/Methods

Placebo-controlled phase II study evaluated aspirin’s effect on CDX2 mRNA and prostanoid production in native and neosquamous epithelium after successful radiofrequency ablation (RFA) in Barrett’s esophagus.

Results

At 12 months TXB2, PGF2α, PGD2, PGE2, PGE1, and α13PGE2 increased in native squamous but not neosquamous epithelium in individuals randomized to placebo. Aspirin use significantly reduced CDX2 mRNA in native squamous epithelium, and was associated with decreases in PGE1, PGE2 and 13PGE2 in neosquamous epithelium.

Conclusions

After RFA, native squamous and neosquamous epithelium exhibit different molecular markers and responses to aspirin suggesting that different sources of squamous progenitors contribute to esophageal re-epithelization.