Cell-free DNA Study for Lymphoma Patients

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

Recruiting N/A Interventional Study
Lymphoma
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Diagnostic
Participants needed
517 (estimated)
Sponsor
M.D. Anderson Cancer Center · Other
Who this trial is looking for

This trial is looking for patients with diffuse large B-cell lymphoma who need treatment. Participants will provide blood samples before and after their treatment to help researchers understand the DNA found in the blood.

Are You a Good Fit for This Trial?

You may be able to join if

  • I am at least 18 years old
  • I have been diagnosed with diffuse large B-cell lymphoma
  • I can provide written consent to participate

You may not be able to join if

  • I am pregnant
  • I have cognitive impairments

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.

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About This Trial

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.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Male/female patients who are at least 18 years of age on the day of informed consent signing. 2. Patients must have a histologically documented diffuse large B-cell lymphoma requiring therapy. 3. Provision of written informed consent for the study. 4. Pregnant women not inclu…
Contacts

Chijioke Nze, MD

832-729-1752

CCNze@mdanderson.org

CONTACT