RecruitingPhase 2NCT06954805

Defining ctDNA Metrics in Posttransplant Lymphoproliferative Disorder (PTLD)

Defining the Role of ctDNA Monitoring in a Risk Stratified Clinical Trial for Posttransplant Lymphoproliferative Disorder (PTLD)


Sponsor

Jennifer Amengual

Enrollment

30 participants

Start Date

Apr 14, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to find out if there is a benefit to giving rituximab with etoposide, prednisone, vincristine, cyclophosphamide and doxorubicin (R-EPOCH) in participants who have high-risk B-cell PTLD in their 2nd phase of treatment (consolidation) while those with low-risk disease will be spared of chemotherapy and treated with rituximab consolidation alone. This study is also being done to find out about the usefulness of circulating tumor DNA (ctDNA), a novel blood test which, has been shown to help guide treatment decisions in other types of lymphoma. The goal is to answer the question if ctDNA is a viable and informative tool in treating PTLD with the hope that in the future it may be used to individualize study treatment for participants with PTLD in a way that limits study treatment toxicity without losing the effectiveness of the treatment plan.


Eligibility

Min Age: 15 Years

Plain Language Summary

Simplified for easier understanding

This study investigates whether a blood test that detects fragments of tumor DNA (called ctDNA) can be used to monitor and predict outcomes in patients with a condition called post-transplant lymphoproliferative disorder (PTLD) — a type of lymphoma that can develop in people who have had an organ transplant due to immune suppression. Researchers want to see if ctDNA levels in the blood correspond with how patients respond to treatment. **You may be eligible if...** - You are 15 or older with a confirmed diagnosis of CD20-positive PTLD (a specific subtype of lymphoma after organ transplant) - You have at least one measurable area of disease (a lymph node 1.5 cm or larger) - You have had a CT or PET-CT scan within the past 28 days - Any hepatitis B or C infection is being properly managed and viral load is undetectable **You may NOT be eligible if...** - You have active hepatitis B (viral load above 500 IU/mL) that is not being treated - You have HIV that is not being controlled with antiviral medication 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

DRUGRituximab

Rituximab is a genetically engineered chimeric murine/human monoclonal IgG1 kappa antibody directed against the CD20 antigen. The Fab domain of rituximab binds to the CD20 antigen on B lymphocytes, and the Fc domain recruits immune effector functions to mediate B cell lysis. 375 mg/m2 Rituximab will be administered to participants by IV.

DRUGEtoposide

Etoposide is a topoisomerase II inhibitor and appears to cause DNA strand breaks. It has been shown to delay transit of cells through S phase and arrest cells in late S or early G2 phase. 50 mg/m2 Etoposide will be administered to participants by IV.

DRUGPrednisone

Prednisone can prevent or suppress inflammation and immune responses. Prednisone's action may include the inhibition of leukocyte infiltration at the site of inflammation, interference in the function of mediators of inflammatory response, and suppression of humoral immune responses. 60 mg/m2 Prednisone will be administered to participants by PO.

DRUGVincristine

Vincristine is a vinca alkaloid. The mechanism of action of vincristine is thought to be due to inhibition of microtubule formation in the mitotic spindle. This leads to arrest of dividing cells during the metaphase stage. 0.4 mg/m2 Vincristine will be administered to participants by IV.

DRUGCyclophosphamide

The mechanism of action is thought to involve cross-linking of tumor cell DNA. Cyclophosphamide is biotransformed principally in the liver to active alkylating metabolites which are thought to cross-link to tumor cell DNA. These metabolites interfere with the growth of rapidly proliferating susceptible malignant cells. 375 mg/m2 Cyclophosphamide will be administered to participants by IV.

DRUGDoxorubicin

Doxorubicin is an anthracycline, topoisomerase II inhibitor. It is isolated from cultures of Streptomyces peucetius var. caesius. The cytotoxic effect of doxorubicin is related to nucleotide base intercalation and cell membrane lipid binding activities. It blocks nucleotide replication and the action of DNA and RNA polymerases. The interaction between doxorubicin and topoisomerase II to form DNA-cleavable complexes appears to be an important mechanism of its cytocidal activity. 10 mg/m2 Doxorubicin will be administered to participants by IV.

DEVICECAPP-seq

Next generation sequencing (NGS) tool used to detect tiny amounts of cancer DNA in the blood, allowing for early diagnosis and monitoring of cancer in a non-invasive way.


Locations(2)

Stanford Medical Center

Stanford, California, United States

Columbia University Irving Medical Center

New York, New York, United States

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NCT06954805


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