This study investigates the value of monitoring molecular residual disease (MRD) based on circulating tumor DNA (ctDNA) in resected pancreatic cancer.
The study evaluates the prognostic value of baseline MRD and the role of MRD dynamic changes after treatment in guiding further treatment decisions.
- Who can participate: Adults aged 18 and older with pancreatic cancer who have undergone curative-intent surgery and have an ECOG performance status score of 2 or less can participate. Participants should have an expected survival time of at least 3 months.
- Study details: Participants will provide peripheral blood samples for MRD testing before starting adjuvant chemotherapy and at the first imaging assessment after chemotherapy.