Skip to content
Study details
Enrolling now

Defining ctDNA Metrics in Posttransplant Lymphoproliferative Disorder (PTLD)

Jennifer Amengual
NCT IDNCT06954805ClinicalTrials.gov data as of Apr 2026
Phase

Phase 2

Target enrollment

30

Study length

about 3 years

Ages

15+

Locations

2 sites in CA, NY

What this study is about

This trial is testing if rituximab with etoposide, prednisone, vincristine, cyclophosphamide and doxorubicin (R-EPOCH) is beneficial for people with high-risk B-cell PTLD during their second phase of treatment. It's also evaluating the use of circulating tumor DNA (ctDNA), a blood test that may help guide treatment decisions in lymphoma patients, to see if it can be used to personalize treatment and reduce side effects without losing effectiveness.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take Cyclophosphamide
  • 2.Take Doxorubicin
  • 3.Take Etoposide
  • +3 more

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Injection / IVInjection / IV

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

cyclophosphamide (Alkylating chemotherapy; crosslinks DNA strands), doxorubicin (Anthracycline chemotherapy; intercalates DNA and inhibits topoisomerase II), etoposide, prednisone, rituximab (Monoclonal antibody; targets CD20 on B-cells to destroy them), vincristine

Drug routes

infusion, injection, intravenous, oral

Endpoints

Primary: Number of participants with Complete Response (CR) rate of 60% or higher

Secondary: Duration of Overall Response (OR), Event Free Survival rate, Progression-Free Survival (PFS) rate

Body systems

Oncology