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Autologous Blood and Marrow Transplantation for Hematologic Malignancies and Selected Solid Tumors
This pilot trial studies different high-dose chemotherapy regimens with or without total-body irradiation (TBI) to compare how well they work when given before autologous stem cell transplant (ASCT) in treating patients with hematologic cancer or solid tumors. Giving high-dose chemotherapy with or without TBI before ASCT stops the growth of cancer cells by stopping them from dividing or killing them. After treatment, stem cells are collected from the patient's blood or bone marrow and stored. More chemotherapy may be given to prepare for the stem cell transplant. The stem cells are then returned to the patient to replace the blood forming cells that were destroyed by the chemotherapy.
PRIMARY OBJECTIVES: I. Estimate the progression free survival (PFS) distribution for Hodgkin lymphoma (HL), non-Hodgkin lymphoma (NHL) and multiple myeloma (MM) for each disease-specific high dose therapy regimen. SECONDARY OBJECTIVES: I. Estimate the PFS distribution for amyloidosis, acute leukemia and selected solid tumors for each disease-specific high dose therapy regimen. II. Explore the role of risk factors in the outcome of all treated patients. III. Examine the high dose therapy regimen-related toxicity (RRT) and overall survival after bone marrow transplant (BMT). OUTLINE: Patients are assigned to conditioning regimens based on disease, age, and co-morbidities.
Age
4 - No limit years
Sex
ALL
Healthy Volunteers
No
Roswell Park Cancer Institute
Buffalo, New York, United States
Start Date
June 29, 2006
Primary Completion Date
July 9, 2018
Completion Date
July 9, 2018
Last Updated
April 22, 2021
174
ACTUAL participants
etoposide
DRUG
cyclophosphamide
DRUG
carmustine
DRUG
melphalan
DRUG
busulfan
DRUG
carboplatin
DRUG
thiotepa
DRUG
total-body irradiation
RADIATION
autologous hematopoietic stem cell transplantation
PROCEDURE
autologous-autologous tandem hematopoietic stem cell transplantation
PROCEDURE
Lead Sponsor
Roswell Park Cancer Institute
Collaborators
NCT02159495
NCT02122081
Data Source & Attribution
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