RecruitingNot ApplicableNCT05676450

Feasibility and Clinical Utility of Cell-free DNA (cfDNA) in Identifying Actionable Alterations and Minimal Residual Disease for Lymphoma Patients Across Community Centers in Texas


Sponsor

M.D. Anderson Cancer Center

Enrollment

517 participants

Start Date

Feb 23, 2023

Study Type

INTERVENTIONAL

Conditions

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.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is examining whether a blood test that looks for cancer DNA (called cell-free DNA or liquid biopsy) can help find useful genetic information and detect minimal remaining disease in lymphoma patients treated at community cancer centers in Texas. The goal is to make advanced testing more accessible outside of major academic hospitals. **You may be eligible if...** - You are at least 18 years old - You have been diagnosed with a type of lymphoma called diffuse large B-cell lymphoma that requires treatment - You are willing to provide written consent **You may NOT be eligible if...** - You are pregnant - You have significant cognitive impairment Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DIAGNOSTIC_TESTcell-free DNA

Given by IV (vein)


Locations(2)

MD Anderson Cancer Center

Houston, Texas, United States

Cancer Therapy and Research Center at The UT Health Science Center at San Antonio

San Antonio, Texas, United States

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NCT05676450


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