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Clinical Trial Summary

To test the feasibility of collecting cell-free DNA (cfDNA) samples from DLBCL patients before and after treatment. cfDNA is DNA traveling in your blood outside of a cell and is easily collected from blood samples drawn using the vein puncture method.


Clinical Trial Description

Primary Objective: • To determine the feasibility and clinical utility of ctDNA in identifying actionable alterations and minimal residual disease for lymphoma patients across community centers in Texas. Secondary Objectives: - To provide useful prognostic information before treatment, assess molecular response at interim time points and residual disease at the end of therapy, and identify tumor-specific mutations - Levels of cfDNA and its association with both EFS and OS in patients receiving therapy ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05676450
Study type Interventional
Source M.D. Anderson Cancer Center
Contact Christopher Flowers, MD
Phone (713) 745-6095
Email crflowers@mdanderson.org
Status Recruiting
Phase N/A
Start date February 23, 2023
Completion date August 31, 2026

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