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OncoMatch/Clinical Trials/NCT06954805

Defining ctDNA Metrics in Posttransplant Lymphoproliferative Disorder (PTLD)

Is NCT06954805 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments for lymphoma.

Phase 2RecruitingJennifer AmengualNCT06954805Data as of May 2026

Treatment: Rituximab · Etoposide · Prednisone · Vincristine · Cyclophosphamide · Doxorubicin · CAPP-seqThe 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.

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Extracted eligibility criteria

Cancer type

Non-Hodgkin Lymphoma

Biomarker criteria

Required: CD20 overexpression (positive)

Histologically confirmed CD20+ PTLD

Prior therapy

Cannot have received: systemic chemotherapy

Exception: for PTLD

Patients who have received systemic chemotherapy for PTLD.

Cannot have received: chemotherapy

Exception: for other indications within 4 weeks (6 weeks for nitrosoureas or mitomycin C) prior to entering the study and must have recovered from adverse events due to agents administered more than 4 weeks earlier

Participants must not have had chemotherapy for other indications within 4 weeks (6 weeks for nitrosoureas or mitomycin C) prior to entering the study and must have recovered from adverse events due to agents administered more than 4 weeks earlier.

Cannot have received: anthracycline (doxorubicin, epirubicin)

Exception: must not have received more than a cumulative dose 250 mg/m2 of prior doxorubicin (or equivalent dose of another anthracycline, such as epirubicin) therapy (at any time prior to registration)

Participants must not have received more than a cumulative of dose 250 mg/m2 of prior doxorubicin (or equivalent dose of another anthracycline, such as epirubicin) therapy (at any time prior to registration).

Lab requirements

Blood counts

Organ function as assessed by laboratory testing is in appropriate range for receipt of rituximab and R-EPOCH per individual treating physician discretion.

Kidney function

Organ function as assessed by laboratory testing is in appropriate range for receipt of rituximab and R-EPOCH per individual treating physician discretion.

Liver function

Organ function as assessed by laboratory testing is in appropriate range for receipt of rituximab and R-EPOCH per individual treating physician discretion.

Cardiac function

Cardiac function testing is in appropriate range for receipt of rituximab and R-EPOCH per individual treating physician discretion.

Organ function as assessed by laboratory testing is in appropriate range for receipt of rituximab and R-EPOCH per individual treating physician discretion. Cardiac function testing is in appropriate range for receipt of rituximab and R-EPOCH per individual treating physician discretion.

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Stanford Medical Center · Stanford, California
  • Columbia University Irving Medical Center · New York, New York

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