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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Chemoradiotherapy With Targeted Immunotherapy in Pediatric Lymphoma
At a glance
Conditions
Where it's being run
3 sites across 3 statesStudy leadership
- Mitchell Cairo, MD · PRINCIPAL_INVESTIGATOR · New York Medical Center
Who to contact
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Inclusion
Exclusion
What this trial measures
- 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