Actively Recruiting

Phase 2
Age: 3Years - 39Years
All Genders
NCT05253495

Chemoradiotherapy With Targeted Immunotherapy in Pediatric Lymphoma

Led by New York Medical College · Updated on 2025-06-13

80

Participants Needed

3

Research Sites

334 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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).

CONDITIONS

Official Title

Chemoradiotherapy With Targeted Immunotherapy in Pediatric Lymphoma

Who Can Participate

Age: 3Years - 39Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Newly diagnosed patients with histologically or cytologically confirmed mature B-cell non-Hodgkin lymphoma or classical Hodgkin lymphoma according to WHO Classification
  • For MB-NHL: Burkitt lymphoma, Burkitt-like lymphoma with 11q aberration, diffuse large B-cell lymphoma NOS, or high grade B-cell lymphoma
  • For MB-NHL Cohort Ia: stage III with LDH ≥ 2 times upper limit normal or stage IV with 5-24% bone marrow lymphoma infiltration
  • For MB-NHL Cohort Ib: any CNS involvement and/or bone marrow involvement with ≥ 25% lymphoma cells or less than 20% tumor size reduction after DOC chemotherapy
  • For cHL Cohort IIa: stage I-IIA with bulky ± E, I-IIB no bulky ± E, IIIA ± E (intermediate risk)
  • For cHL Cohort IIb: stage IIB with bulky ± E, IIIA with bulky ± E, IIIB, IV (high risk)
  • Adequate organ function
Not Eligible

You will not qualify if you...

  • Primary mediastinal B-cell lymphoma
  • T-cell/histiocyte-rich large B-cell lymphoma
  • Gray zone lymphoma
  • Follicular lymphoma
  • Nodular lymphocyte-predominant Hodgkin lymphoma
  • Posttransplant lymphoproliferative lymphoma

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 3 locations

1

University of Alabama

Birmingham, Alabama, United States, 35233

Not Yet Recruiting

2

University of Flordia

Gainsville, Florida, United States, 32610

Actively Recruiting

3

New York Medical College

Vallhala, New York, United States, 10595

Actively Recruiting

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Research Team

M

Mitchell Cairo, MD

CONTACT

L

Lauren Harrison, RN

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

4

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