Chemoradiotherapy With Targeted Immunotherapy in Pediatric Lymphoma
Launched by NEW YORK MEDICAL COLLEGE · Feb 22, 2022
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
The clinical trial titled "Chemoradiotherapy With Targeted Immunotherapy in Pediatric Lymphoma" is studying a new approach to treating certain types of lymphoma, specifically non-Hodgkin lymphoma and Hodgkin lymphoma, in children, adolescents, and young adults. The goal is to see if adding a targeted immunotherapy (a type of treatment that helps the immune system fight cancer) to the standard treatment can safely reduce the amount of anthracycline (a chemotherapy drug) needed while still effectively controlling the disease.
To participate, patients must be newly diagnosed with specific types of lymphoma, such as Burkitt lymphoma or classical Hodgkin lymphoma, and meet certain health criteria. The trial is currently recruiting participants aged between 1 and 25 years, and it’s open to all genders. Those who join the study can expect to receive the new treatment alongside standard care, with close monitoring to ensure their safety and health. This trial offers a hopeful option for young patients facing these challenging cancers.
Gender
ALL
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 New York Medical College
New York Medical College (NYMC) is a distinguished institution dedicated to advancing medical education, research, and healthcare delivery. As a clinical trial sponsor, NYMC leverages its expertise in biomedical research and a commitment to innovative therapies to conduct rigorous and ethical clinical studies. The college fosters collaboration among a diverse team of researchers, clinicians, and healthcare professionals to translate scientific discoveries into tangible health solutions. With a focus on improving patient outcomes and addressing pressing medical challenges, NYMC is at the forefront of clinical research, contributing significantly to the advancement of medical knowledge and practice.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Valhalla, New York, United States
Birmingham, Alabama, United States
Vallhala, New York, United States
Gainesville, Florida, United States
Gainsville, Florida, United States
Patients applied
Trial Officials
Mitchell Cairo, MD
Principal Investigator
New York Medical Center
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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