Plain-English translation of NCT07282912 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
Phase 2 — Testing in a bigger group (up to a few hundred people) to see if the treatment actually works and is still safe.
This trial is testing whether people with advanced cancers of the digestive system (including esophagus, stomach, pancreas, and bile ducts) benefit from surgery or radiation therapy added to standard chemotherapy. The study focuses on patients whose cancer has spread to only a few locations and whose cancer markers (called circulating tumor DNA) have become undetectable after initial chemotherapy—suggesting the cancer is responding well. The trial will compare two groups: one continuing standard chemotherapy alone, and another receiving additional surgery or radiation to remove or treat remaining cancer sites.
Some patients with limited spread of these aggressive cancers may benefit from surgery or radiation to treat remaining tumors, but it's not yet clear which patients benefit most or whether this approach improves long-term survival. This trial will help doctors understand whether adding these interventions to chemotherapy extends how long patients stay cancer-free.
You likely qualify if…
You likely don't qualify if…
After confirming your cancer markers are undetectable, you will be randomly assigned to one of two groups. If assigned to the standard care group, you will continue your current chemotherapy until your cancer progresses. If assigned to the intervention group, you will undergo surgery and/or radiation therapy over a three-month period to remove or treat remaining cancer sites, with follow-up blood tests to monitor your cancer markers. Both groups will have regular clinic visits and imaging scans to monitor your progress.
AI-generated summary from trial data · Aug 9, 2026 · Not medical advice
United States