Clinical Trial

MRD-Adapted Low-Dose Radiation Therapy During Frontline Chemoimmunotherapy for Diffuse Large B-Cell Lymphoma

Not Yet Recruiting Phase 2
View on ClinicalTrials.gov →
Summary
This prospective feasibility study evaluates a minimal residual disease (MRD)-adapted treatment strategy in patients with diffuse large B-cell lymphoma (DLBCL) receiving frontline chemoimmunotherapy. Circulating tumor DNA (ctDNA)-based MRD testing and interim positron emission tomography (PET) imaging after two cycles of therapy are used to guide treatment decisions. Patients with detectable MRD may receive low-dose radiation therapy (LDRT) to residual PET-avid disease sites in addition to standard systemic therapy, while patients with undetectable MRD continue standard frontline chemoimmunotherapy. The study aims to assess the feasibility and safety of integrating MRD-guided radiation therapy into frontline treatment of DLBCL.
Protocol Amendment History 2 changes
critical Phase changed: not applicable -> Phase 2 2026-05-14
critical Primary endpoint(s) modified 2026-05-14
Trial Details
NCT Number NCT07517705
Lead Sponsor University of Nebraska
Conditions Diffuse Large B-Cell Lymphoma
Enrollment 50 participants
Start Date 2026-06-12
Primary Completion 2030-11-12 (estimated)
Study Completion 2032-11-12 (estimated)
Updated on ClinicalTrials.gov 2026-05-13