Burkitt Lymphoma
Conditions
Keywords
Burkitt lymphoma, B-cell non Hodgkin lymphoma, B-cell ALL, Refractory, Relapse, Rituximab, Children
Brief summary
This is a multicentric phase II study of Mabthera (rituximab) in children and adolescents with relapsed and refractory B-cell NHL/L3ALL. The primary objective is to determine the response rate of Rituximab as single agent in relapsed or refractory Burkitt lymphoma, L3 acute leukemia, large B-cell lymphoma and non subclassified aggressive B-cell NHL
Detailed description
This is a multicentric phase II study of Mabthera (rituximab) in children and adolescents with relapsed and refractory B-cell NHL/L3ALL. The primary objective is to determine the response rate of Rituximab as single agent in relapsed or refractory Burkitt lymphoma, L3 acute leukemia, diffuse large B-cell lymphoma and non subclassified aggressive B-cell NHL. The secondary objectives are to assess the toxicity profile of Rituximab in children and adolescents as single agent, and when followed by chemotherapy, to study pharmacokinetics of Rituximab in serum and in CSF and to determine the overall duration of response, time to progression and survival in patients responders to antiCD20 initially alone and followed by chemotherapy. Patients will receive Rituximab (Mabthera) at 375 mg/m2, once a week during 4 weeks, administered in IV infusion starting at 50mg/h and increasing by steps of 50 mg/h every 30mn until the speed of 400 mg/h. Patients with combined CNS relapse will receive an intrathecal injection of MTX+HC+Ara-C 48 h after each injection of rituximab First assessment will be done prior to receiving the 3rd course of rituximab. Responding patients (CR, PR) and patients with objective effect (OE) will receive the 3rd and 4th injections of rituximab before starting the salvage chemotherapy (COPADM, CYVE/CC course or ICE, depending on previous chemotherapy regimen received by the patient, followed by HDCT+ hematopoietic stem cell rescue). A second evaluation will be done after the 4th course if performed.
Interventions
DRUGRituximab
Sponsors
Hoffmann-La Roche
Gustave Roussy, Cancer Campus, Grand Paris
Study design
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
6 Months to 20 Years
Healthy volunteers
No
Inclusion criteria
* Histologically or cytologically proven B-cell malignancies, either Burkitt NHL or L3 ALL or large B-cell lymphoma or aggressive B-cell NHL, with the exception of diffuse large B-cell lymphoma arising in the mediastinum. * Immunohistochemistry showing CD20 positivity * Measurable (at least one bi-dimensionally measurable lesion) or evaluable (bone marrow, bone involvement) disease in progression since the last evaluation * First relapsed or refractory disease after LMB or BFM protocol, except the isolated CNS relapses * Life expectancy \> 4 weeks * Performance status (Karnofsky) \> 30 * Adequate hepatic, renal and cardiac functions * Wash out of 3 weeks in case of recent chemotherapy * Complete initial work-up within 8 days prior to treatment * Able to comply with scheduled follow-up and with management of toxicity * Written inform consent form from adult patients and from parents and legal guardians for minor children
Exclusion criteria
* Active viral infection, especially chronic hepatitis B * previous salvage therapy for relapse * Prior or current history of severe allergy * Primary large B-cell lymphoma of the mediastinum * Isolated CNS relapse
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Rate of patients achieving at least objective response after 2 courses of rituximab | — |
Secondary
| Measure | Time frame |
|---|---|
| Rate of objective response after 4 courses of rituximab | — |
| Rate of initially responding patients who progressed during the second phase of treatment | — |
| Toxicity | — |
| Pharmacokinetic evaluation in serum and CSF | — |
Countries
France
Outcome results
None listed