Stem Cell Augmented, Elutriated Grafts for Allogeneic Bone Marrow Transplantation
graft versus host disease prophylaxis/therapy
+ allogeneic bone marrow transplantation
Lymphadenopathy+109
+ Urogenital Diseases
+ Genital Diseases
Supportive Care Study
Summary
Study start date: March 1, 1997
Actual date on which the first participant was enrolled.OBJECTIVES: Determine whether stem cell augmented, elutriated grafts prevent graft versus host disease in patients undergoing allogeneic bone marrow transplantation. OUTLINE: Patients receive elutriated CD34+ augmented donor bone marrow on day 0. Bone marrow samples are obtained before day 100, around 6 months, and 1 year after transplant. PROJECTED ACCRUAL: Not specified
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.Supportive Care Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Until 65 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
DISEASE CHARACTERISTICS: Histologically confirmed diagnosis of one the following: Acute myelogenous leukemia in CR1, ER1, CR2, ER2, CR3 Acute lymphocytic leukemia in CR1, ER1, CR2, ER2, CR3 Non-Hodgkin's lymphoma Hodgkin's lymphoma Multiple myeloma with no more than 12 months of prior alkylator based chemotherapy Myelodysplastic syndrome (MDS) Acute leukemia arising out of MDS Primary resistant acute leukemia Chronic myelomonocytic leukemia Aplastic anemia (40 years of age and over) Solid tumor malignancy (germ cell, sarcoma, breast, etc.) Genetic disorders or inborn errors of metabolism as defined by preparative regimen protocol Chronic myelogenous leukemia Must meet all inclusion criteria specified by the respective preparative regimen protocol No aplastic anemia under 40 years of age or myelofibrosis PATIENT CHARACTERISTICS: Age: 0.5 to 65 Performance status: Not specified Life expectancy: Not specified Hematopoietic: Not specified Hepatic: Not specified Renal: Not specified PRIOR CONCURRENT THERAPY: Biologic therapy: No prior red blood cell or platelet transfusions from a sibling donor Chemotherapy: Not specified Endocrine therapy: Not specified Radiotherapy: Not specified Surgery: Not specified
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Baltimore, United StatesOpen Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins in Google Maps