Predicting Risk of Cancer in Barrett's Esophagus



Status:Enrolling by invitation
Conditions:Cancer, Gastroesophageal Reflux Disease , Gastrointestinal
Therapuetic Areas:Gastroenterology, Oncology
Healthy:No
Age Range:18 - 95
Updated:2/20/2019
Start Date:January 2002
End Date:June 2020

Use our guide to learn which trials are right for you!

Methylation in Cancer Progression of Barrett's Esophagus

The purpose of this study is to determine if there are any early changes in DNA markers of
blood and esophageal tissue in people with gastric reflux, Barrett's esophagus or esophageal
cancer that can warn of a progression to esophageal cancer.

Patients with Barrett's esophagus (BE) have an increased risk of esophageal adenocarcinoma
which is 40-125 fold higher than in the general population. However, the current techniques
of detecting dysplasia and observing abnormal p53 immunohistochemical staining are not
accurate or reliable methods for determining which BE patients will progress to cancer. DNA
hypermethylation is an epigenetic process that occurs in the promoter region of certain
genes, resulting in suppression of gene expression. Inactivation of specific genes via
hypermethylation has been highly associated with cancer.

The primary objective of this research is to determine whether DNA hypermethylation is a
biomarker that will predict which patients with BE are likely to progress to adenocarcinoma.
Patients with BE and/or esophageal adenocarcinoma who undergo endoscopy at the Johns Hopkins
Hospital will comprise the cohort of subjects. Gene hypermethylation will be assessed by
performing methylation-specific Polymerase Chain Reaction (PCR) on a panel of 8
cancer-related genes.

Specific Aim 1: To compare the prevalence of gene hypermethylation in BE patients with
different grades of dysplasia and/or adenocarcinoma, using archived specimens.

Specific Aim 2: To determine whether the presence of gene hypermethylation in initial
biopsies of BE patients is associated with progression to adenocarcinoma, using archived
specimens. To compare gene hypermethylation with currently available markers for neoplastic
progression.

Specific Aim 3: To determine whether methylated DNA from BE and/or adenocarcinoma can be
detected in the peripheral blood of patients, by comparing methylation profiles of esophageal
biopsy specimens with peripheral blood samples taken at the same time in prospectively
enrolled patients.

If hypermethylation of one or more genes is detected at an early stage in BE patients who
later progress to adenocarcinoma, hypermethylation could be used as an early predictor for
adenocarcinoma even before pathologic changes are evident. Furthermore, this research will
help determine the specific genetic events that occur in the neoplastic transformation from
BE to adenocarcinoma.

The long-term goal of this project is to determine whether hypermethylation can identify BE
patients who are at high risk for neoplastic progression, thus allowing for early
intervention in the form of more frequent endoscopic surveillance, chemoprevention, ablative
therapy, or surgery.

Inclusion Criteria:

- People who are undergoing upper endoscopy as part of their medical care with a history
of esophageal cancer, Barrett's esophagus, or upper gastrointestinal symptoms.

Exclusion Criteria:

- People who are are currently having chemotherapy, or who have completed chemotherapy
within the last 4 weeks.

- People who have ever had radiation treatments to their chest.
We found this trial at
2
sites
Columbia, Maryland 21044
Principal Investigator: Marcia I Canto, MD
Phone: 410-502-2893
?
mi
from
Columbia, MD
Click here to add this to my saved trials
1800 Orleans St.
Baltimore, Maryland 21287
410-955-5000
Principal Investigator: Marcia I. Canto, M.D.
Phone: 410-502-2893
Johns Hopkins Hospital Patients are the focus of everything we do at The Johns Hopkins...
?
mi
from
Baltimore, MD
Click here to add this to my saved trials