Overview

This trial is active, not recruiting.

Condition lymphoma
Treatments anti-thymocyte globulin, busulfan, carboplatin, carmustine, cyclosporine, cytarabine, dexamethasone, etoposide phosphate, idarubicin, ifosfamide, leucovorin calcium, lomustine, melphalan, methotrexate, mitoxantrone hydrochloride, prednisolone, thiotepa, vinblastine sulfate, vindesine, allogeneic hematopoietic stem cell transplantation, autologous hematopoietic stem cell transplantation, peripheral blood stem cell transplantation, total-body irradiation
Sponsor European Inter-Group Co-operation on Childhood Non-Hodgkin Lymphoma
Start date April 2004
End date February 2014
Trial size 96 participants
Trial identifier NCT00317408, AIEOP-EICNHL-ALCL-RELAPSE, BFM-EICNHL-ALCL-RELAPSE, BSPHO-EICNHL-ALCL-RELAPSE, CCLG-NHL-2006-01, CDR0000466639, DCOG-EICNHL-ALCL-RELAPSE, EICNHL-ALCL-RELAPSE, EU-205118, EU-20618, EUDRACT-2005-003321-57, NOPHO-EICNHL-ALCL-RELAPSE, PPLLSG-EICNHL-ALCL-RELAPSE, SFCE-EICNHL-ALCL-RELAPSE, SHOP-EICNHL-ALCL-RELAPSE

Summary

RATIONALE: Giving combination chemotherapy and total-body irradiation before a peripheral stem cell transplant that uses the patient's or a donor's stem cells, helps stop both the growth of cancer cells and the patient's immune system from rejecting the stem cells. When the stem cells are infused into the patient they may help the patient's bone marrow make stem cells, red blood cells, white blood cells, and platelets. Giving combination chemotherapy and total-body irradiation followed by a stem cell transplant may be an effective treatment for anaplastic large cell lymphoma.

PURPOSE: This clinical trial is studying how well combination chemotherapy followed by stem cell transplant works in treating young patients with progressive or relapsed anaplastic large cell lymphoma.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Allocation non-randomized
Primary purpose treatment

Primary Outcomes

Measure
Event-free survival as measured by the Kaplan-Meier method
time frame:

Secondary Outcomes

Measure
Proportion of patients who are treated on protocol among all patients who meet the inclusion criteria
time frame:
Overall survival
time frame:
Acute and long term toxicity
time frame:
Rate of acute and chronic graft-vs-host disease in patients with allogeneic stem cell transplantation
time frame:
Treatment related mortality
time frame:

Eligibility Criteria

Male or female participants up to 21 years old.

DISEASE CHARACTERISTICS: - Histologically or cytologically confirmed anaplastic large cell lymphoma (ALCL) - Progressive disease OR first relapse - No second or subsequent relapse of ALCL - Slides available for national central pathology review - Availability of 1 of the following (for allogeneic stem cell transplantation only): - HLA-identical matched sibling donor - 10/10 HLA-matched nonsibling donor (related or unrelated) - 9/10 HLA-matched nonsibling donor (1-antigen-mismatched related or unrelated donor) - < 9/10 HLA-mismatched donor (related or unrelated) - Stem cells may be obtained from unmanipulated bone marrow or peripheral blood stem cells after filgrastim (G-CSF) stimulation PATIENT CHARACTERISTICS: - Not pregnant or nursing - Negative pregnancy test - Fertile patients must use effective contraception - Adequate hepatic, renal, and cardiac function - No HIV infection or AIDS - No severe immunodeficiency - No other prior malignancy - No pre-existing disease or condition prohibiting study treatment PRIOR CONCURRENT THERAPY: - At least 2 months since prior chemotherapy or radiotherapy - No significant pretreatment for first relapse - No prior organ transplantation - No concurrent participation in another clinical trial

Additional Information

Official title Treatment Protocol for Relapsed Anaplastic Large Cell Lymphoma of Childhood and Adolescence
Description OBJECTIVES: Primary - Improve the probability of event-free survival in children and adolescents with early progression of anaplastic large cell lymphoma (ALCL) and/or relapse of ALCL with CD3-positive immunophenotype treated with reinduction combination chemotherapy followed by allogeneic or autologous stem cell transplantation. - Determine whether a conditioning regimen comprising carmustine, etoposide phosphate, cytarabine, and melphalan (BEAM) (without total body irradiation) for autologous stem cell transplantation is an effective treatment for patients with relapsed CD3-negative ALCL occurring after the intensive phase of treatment. - Determine the impact of vinblastine in patients with late relapse of CD3-negative ALCL who have not received vinblastine during frontline therapy. Secondary - Determine overall survival and treatment-related mortality in patients treated with these regimens. - Determine acute and long-term toxicity in patients treated with these regimens. - Determine the rate of acute and chronic graft-vs-host disease in patients treated with allogeneic stem cell transplantation. OUTLINE: This is a multicenter, prospective, nonrandomized study. Patients are stratified according to time from initial diagnosis to progression/relapse, immunophenotype of lymphoma cells (CD3-positive + vs CD3-negative), stem cell donor availability (matched sibling donor vs 9/10 or 10/10 matched unrelated donor), and vinblastine during frontline therapy (yes vs no). - Group 1 (early progression): Patients receive 1 course of ICM chemotherapy followed by 1 course of ICI chemotherapy. - ICM chemotherapy: Patients receive methotrexate, cytarabine, and prednisolone intrathecally (IT) on day 1, mitoxantrone hydrochloride IV over 5 hours on days 1 and 2, carboplatin IV continuously on days 2-5 and ifosfamide IV continuously on days 2-6. - ICI chemotherapy: Patients receive methotrexate, cytarabine, and prednisolone intrathecally on day 1, idarubicin IV over 4 hours on days 1 and 2, carboplatin IV continuously on days 2-5, and ifosfamide IV continuously on days 2-6. Patients then proceed to allogeneic stem cell transplantation. - Group 2 (relapsed disease and CD3-positive lymphoma cells): Patients are stratified according to stem cell donor availability (yes vs no). - Available donor: Patients receive 2 courses of CC chemotherapy and then proceed to allogeneic stem cell transplantation. - Unavailable donor : Patients receive 2 courses of CC chemotherapy comprising dexamethasone orally or IV on days 1-5, vindesine IV on day 1, cytarabine IV over 3 hours on days 1 and 2, etoposide phosphate IV over 2 hours on days 3-5, and methotrexate, cytarabine, and prednisolone IT on day 5. Patients then receive 1 course of CVA chemotherapy comprising oral lomustine on day 1, vinblastine IV on days 1, 8, 15, and 22, and cytarabine IV over 1 hour on days 1-5. Patients undergo leukapheresis for collection of autologous peripheral blood stem cells after the first and/or second course of CC chemotherapy. Patients then proceed to autologous stem cell transplantation. - Group 3 (relapsed disease, CD3-negative immunophenotype, and received vinblastine during frontline therapy): Patients receive 2 courses of CC chemotherapy and 1 course of CVA chemotherapy as described above. Patients undergo leukapheresis for collection of autologous peripheral blood stem cells (PBSC) after the first and/or second course of CC chemotherapy. Patients then proceed to autologous stem cell transplantation. - Group 4 (late relapse, CD3-negative immunophenotype, and did not receive vinblastine during frontline therapy): Patients receive vinblastine IV once weekly for 24 months. Patients with disease progression during or relapsed disease after vinblastine therapy undergo treatment as in group 3. - Autologous stem cell transplantation (SCT): Patients receive a conditioning regimen comprising carmustine IV over 1 hour on day -7, etoposide phosphate IV over 1 hour and cytarabine IV over 30 minutes on days -6 to -3, and melphalan IV over 15 minutes on day -2. Patients undergo autologous SCT on day 0. - Allogeneic SCT: Beginning 4-6 weeks after the start of the last chemotherapy course, patients receive 1 of the following conditioning regimens based on age: - Patients > 2 years of age undergo total body irradiation on days -7 to -5 and receive thiotepa IV over 1 hour on day -4 and etoposide IV over 4 hours on day -3. Patients undergo allogeneic SCT on day 0. - Patients ≤ 2 years of age receive oral busulfan 4 times daily on days -8 to -5, thiotepa IV over 1 hour twice on day -4, and etoposide phosphate IV over 4 hours on day -3. Patients undergo allogeneic SCT on day 0. Patients undergoing SCT from an unrelated donor also receive antithymocyte globulin IV over 4 hours on days -3 to -1. All patients receive graft-versus-host (GVHD) prophylaxis as described below. - GVHD prophylaxis: GVHD prophylaxis is administered as per donor status. - Matched sibling donor: Patients receive cyclosporine IV over 2 hours or orally on day -1 to 60 followed by a taper. - 10/10 or 9/10 matched unrelated donor: Patients receive cyclosporine IV over 2 hours or orally on days -1 to 100 followed by a taper, methotrexate IV on days 1, 3, and 6, and leucovorin calcium IV on days 2, 4, and 7. - Mismatched donor: Patients do not receive GVHD prophylaxis, however, CD3-positive lymphocytes are extracted from donor stem cells. After completion of study treatment, patients are followed periodically for 10 years. PROJECTED ACCRUAL: A total of 96 patients will be accrued for this study.
Trial information was received from ClinicalTrials.gov and was last updated in September 2015.
Information provided to ClinicalTrials.gov by National Cancer Institute (NCI).