Chemoradiotherapy With Targeted Immunotherapy in Pediatric Lymphoma

This study is looking at new ways to treat non-Hodgkin lymphoma and Hodgkin lymphoma in children, adolescents, and young adults (ages 3 to 39). Researchers want to see if adding targeted immunotherapy drugs like polatuzumab vedotin or nivolumab to standard chemotherapy can be safe and help reduce the amount of anthracycline (a type of chemotherapy) needed, while still controlling the lymphoma. The study will enroll about 80 participants and will measure serious side effects related to polatuzumab vedotin and nivolumab over one year to see if these new combinations are safe. The goal is to find treatments that are effective with fewer side effects for these types of lymphoma.

Study design
This is an interventional study with an unclear phase, planning to enroll about 80 participants. It is exploring different combinations of chemotherapy and immunotherapy drugs.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed for Grade 3 and 4 Adverse Events related to polatuzumab vedotin and nivolumab for one year.

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NCT05253495

Chemoradiotherapy With Targeted Immunotherapy in Pediatric Lymphoma

Recruiting
PHASE2Ages 3–39InterventionalTreatment
New York Medical College
~80 participants
Updated 2025-06-13 on ClinicalTrials.gov
What's tested:DOC Group BPv-COMRAD 1 and 2 Group BPv-R-CYM 1 and 2 Group BDOC Group CMAD CPR 1 and 2Pv-R CYVE 1 and 2

At a glance

Recruiting sites
2 of 3 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Grade 3 and 4 Adverse Events related to polatuzumab vedotin
Measured over 1 year
+1 more outcome measured
Non-hodgkin Lymphoma
Hodgkin Lymphoma
3 sites across 3 states
Alabama1
Florida1
New York1
  • Mitchell Cairo, MD · PRINCIPAL_INVESTIGATOR · New York Medical Center

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Eligibility criteria

Inclusion

Newly diagnosed patients with histologically or cytologically proven newly diagnosed MB-NHL or cHL according to WHO Classification who meet the following criteria are eligible:
Adequate organ function

Exclusion

Primary mediastinal B-cell lymphoma (PMBL)
T-cell/histiocyte-rich large B-cell lymphoma
Gray zone lymphoma
Follicular lymphoma
Nodular lymphocyte-predominant Hodgkin lymphoma (NLPHL)
Posttransplant lymphoproliferative lymphoma (PTLD)
  • Grade 3 and 4 Adverse Events related to polatuzumab vedotin1 year

    to evaluate the DLTs of polatuzumab vedotin (Pv) in combination with rituximab (RTX) containing French-American-British (FAB) chemoimmunotherapy, with reduced dose anthracycline to MB-NHL

  • Grade 3 and 4 Adverse events related to nivolumab1 year

    To evaluate the DLTs of nivolumab to the backbone of reduced toxicity chemoimmunotherapy with brentuximab vedotin (Bv), vinblastine, dacarbazine and rituximab, with reduced dose anthracycline in intermediate and high risk cHL