drugset / Trial / NCT03311958

Molecular Monitoring With Circulating Tumor DNA and Nivolumab Maintenance

NCT03311958

Phase 0 Completed 15 enrolled Fox Chase Cancer Center
NaSingle-groupOpen-labelTreatment

Summary

Patients suffering from diffuse large B-cell lymphoma (DLBCL) who relapse within 12 months of chemotherapy usually undergo salvage therapies, followed by autologous transplant with a low success rate. These treatments for relapse have significant toxicities and may not be tolerated well by the patients. These patients need an effective means of identifying relapse at an early time point to be treated effectively. Detection of circulating tumor DNA (ctDNA) has been reported to be a sensitive and more specific method to detect relapse at an early stage compared to PET/ CT scans. Purpose of this trial is to monitor patients who have undergone successful chemotherapy for the presence of ctDNA. Patients who test positive for ctDNA would be treated with Nivolumab for a period of 2 years to avoid complete relapse.

Timeline

Start
2018-05-15
Primary completion
2024-01-26
Completion
2024-01-26

Drugs

EvaluationDrugModalityDoseRoute
Subject Nivolumab Monoclonal antibody 240 mg Intravenous