Home › Non-Hodgkin Lymphoma › NCT05253495
Chemoradiotherapy With Targeted Immunotherapy in Pediatric Lymphoma
Reducing the Burden of Oncologic Chemoradiotherapy And Radiation Exposure From Diagnostic Imaging by Utilizing Targeted Immunotherapy in Children, Adolescents and Young Adults With Lymphoma
Who can join
Ages 3 to 39 · All sexes
Full eligibility criteria
Inclusion Criteria: * 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: COHORT I: Burkitt lymphoma (ICD-O 9687/3) Burkitt-like lymphoma with 11q aberration (ICD-O 9687/3) Diffuse large B-cell lymphoma, NOS (ICD-O 9680/3) High grade B-cell lymphoma (ICD-O 9680/3) COHORT Ia: stage III with LDH ≥ 2 ULN OR stage IV (5-24% bone marrow lymphoma infiltration) (GROUP B)61 COHORT Ib: any CNS involvement and/or BM involvement (≥ 25% lymphoma cells) (GROUP C)61 OR patients with less than 20% tumor size reduction post chemotherapy with cyclophosphamide, dexamethasone, vincristine (DOC Reduction for Cohort Ia). COHORT II Classical Hodgkin lymphoma (ICD-O 9650/3, 9663/3, 9651/3, 9652/3, 9653/3) COHORT IIa: stage I-IIA with bulky ± E, I-IIB no bulky ± E, IIIA ± E (INTERMEDIATE RISK) COHORT IIb: stage IIB with bulky ± E, IIIA with bulky ± E, IIIB, IV (HIGH RISK) * Adequate organ function Exclusion Criteria: * 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)
About the study
The addition of targeted immunotherapy will be safe and well tolerated and facilitate the reduction of anthracycline exposure while preserving lymphoma disease control in children, adolescents and young adults (CAYA) with mature B-cell non-Hodgkin lymphoma (MB-NHL) and classical Hodgkin lymphoma (cHL).
What is being tested
- DOC Group B (drug)
- Pv-COMRAD 1 and 2 Group B (drug)
- Pv-R-CYM 1 and 2 Group B (drug)
- DOC Group C (drug)
- MAD CPR 1 and 2 (drug)
- Pv-R CYVE 1 and 2 (drug)
Sponsor: New York Medical College · Participants: 80 · Started: Feb 1, 2022
Contact the study team
- Mitchell Cairo, MD · Phone: 9145942150
- Lauren Harrison, RN · Phone: 617-285-7844
Official record on ClinicalTrials.gov — NCT05253495
Locations in the U.S.
| Alabama | University of Alabama, Birmingham (Not yet recruiting) |
| Florida | University of Flordia, Gainsville |
| New York | New York Medical College, Vallhala |
Conditions
From ClinicalTrials.gov, data retrieved Oct 3, 2026. Each study sets its own eligibility; the study team decides who can join.