Esophageal cancer and Barrett's esophagus. The Barrett's Esophagus Genomic Study Group includes 154 physicians from diverse practice settings who collaborate to identify families with three or more members affected by classic long-segment Barrett's esophagus, a premalignant condition, with or without esophageal cancer. Blood specimens from these families are collected for genetic linkage analysis.
The Mayo Clinic Esophageal Adenocarcinoma and Barrett's Esophagus Registry is a unique resource that integrates phenotype, genotype and environmental risk factor analysis. This collaborative effort involves 48 Mayo Clinic physicians representing specialties such as gastroenterology and hepatology, genetic epidemiology, biostatistics, medical oncology, molecular biology, genetics, pathology, pulmonary medicine, psychology, radiation oncology, thoracic surgery and Mayo Clinic Comprehensive Cancer Center.
The aims of the Mayo Clinic Esophageal Adenocarcinoma and Barrett's Esophagus Registry include identifying candidate loci associated with gastroesophageal reflux disease symptoms and related complications, as well as contributing to the scientific literature on the genomic steps involved in the progression from Barrett's esophagus to invasive cancer. The registry is already being used for gene discovery projects. In addition, it may enable identification of genomic polymorphisms linked to distant metastasis or improved survival outcomes.