A novel test developed by Johns Hopkins Kimmel Cancer Center investigators could give gastroenterologists insight into which patients with Barrett’s esophagus are likely to progress to esophageal cancer or an abnormal collection of cells called high-grade dysplasia.
This information could help physicians determine how to monitor or manage patients during clinical care.
The test, called Esopredict, is a PCR (polymerase chain reaction)-based laboratory test that, from biopsy samples, measures the level of DNA methylation changes in the genes RUNX3, p16, HPP1 and FBN1. Methylation changes often occur early during abnormal cell growth, before conditions can be detected clinically. By combining these results with patients’ age, physicians can gauge the likelihood that patients’ premalignant conditions will advance and help them determine how often to monitor or manage patients with potential neoplastic progression.
Using the tool in previously collected biopsies from 240 patients with Barrett’s esophagus from six medical centers, researchers determined that the overall risk for neoplastic progression was 5.1%. Patients in the highest risk group had a 21.7% risk of developing high-grade dysplasia or esophageal cancer, compared with a 6.87% risk among those in the high moderate group, a 3.25% risk for those in the low moderate group and just 1.27% among those in the lowest risk group. A description of the work was published online August 14 in The American Journal of Gastroenterology. The test is now commercially available.
Researchers ran the Esopredict test on 209 biopsy samples previously collected from patients with Barrett’s esophagus at Johns Hopkins and Allegheny Health Network, Capital Digestive Health, Mayo Clinic, University of Maryland and University of Connecticut healthcare sites. The first 99 patient samples served as a training set in which a model algorithm was designed, and the next 110 patient samples were analyzed as a validation set in which the algorithm was tested. Samples also were assayed from an additional group of 31 patients who went on to develop high-grade dysplasia or esophageal cancer and who had follow-up intervals longer than five years.
Some 78 of the 209 patients progressed to having high-grade dysplasia or esophageal cancer within five years of biopsy collection, while the remaining 131 had no progression over the next five years. Investigators ran several calculations with Esopredict to try to predict the likelihood of cancer or high-grade dysplasia developing. They stratified patients into two main groups: lower risk (further refined into low and low-moderate risk categories) or higher risk (further refined into high moderate or high-risk levels) of progressing to more serious conditions. Overall, they found that patients in the two higher risk groups to be 6.4 times more likely to progress to high-grade dysplasia or esophageal cancer within five years. Compared with patients considered lowest risk, the highest risk patients were 15.2 times more likely to progress to these more serious conditions.
