{"classes":[{"categories":[{"measurements":[{"groupId":"OG000","value":"18"}]}]}],"denoms":[{"counts":[{"groupId":"OG000","value":"48"}],"units":"Participants"}],"description":"Response Assessment included physical exam and evaluation of peripheral blood and bone marrow. There's no widely accepted criteria for response other than complete response (CR).\n\nCR for malignant hematologic diseases is met if all the following are met for \\>/= 1 month:\n\n1. absence of pathologic lymphadenopathy by physical and radiographic exam\n2. absence of constitutional symptoms due to disease\n3. Polymorphonuclear leukocyte count \\> 1,500/uL; platelet count \\>50,000/uL; and hemoglobin \\>10.0 g/dL\n4. bone marrow aspirate/biopsy done after (a) through (c) have been met, \\>/= 30% cellularity and an absence of abnormal lymphoid nodules or cells by flow cytometry, cytogenetics, etc.\n5. molecular markers of disease must be negative by polymerase chain reaction, Fluorescence in situ hybridization, cytogenetics etc.\n\nCR for solid tumors requires complete resolution of disease on physical exam and radiographs. CR for marrow failure is normal white cell, platelet and hematocrit values.","groups":[{"description":"Campath Purged Non-myeloablative Allo Stem Cell Transplant (ASCT) in lymphoma, myeloma, or marrow failure: leukemia or myelodysplasia; and solid tumors\n\nDonor will receive Granulocyte colony-stimulating factor (G-CSF) 8 mcg/kg/d subcutaneously twice daily (dose will be rounded to the nearest whole vial size), Granulocyte-macrophage colony-stimulating factor (GM-CSF) 15 mcg/kg/d subcutaneous or similar growth factor for donor mobilization. Donors will receive at least 3-6 doses of daily growth factor until adequate cells are mobilized.\n\nPreparative regimen: Begins on day -5 and consist of 4 days of daily fludarabine at 30 mg/m2/d infused over 30 minutes, cyclophosphamide 500 mg/m2/d infused over 1 hour, 5 days of Campath-1H at 20 mg/d in 250 ml of D5 normal saline or normal saline infused over 3 hours.\n\nSubject Evaluation will occur 2-3 times per week by physical exam for toxicity through day 45.","id":"OG000","title":"Campath Purged Non-myeloablative ASCT"}],"paramType":"NUMBER","populationDescription":"Cohort of subjects on the study who actually received \\>/=1 donor lymphocyte infusion (DLI). DLI doses ranged from 1×104 CD3+ cells/kg to 3.27 ×108 CD3+ cells/kg. Subjects were considered for a second and third DLI 8 weeks apart if they did not have \\>grade 2 toxicity from the initial DLI, donor availability, and insurance approved the infusion.","reportingStatus":"POSTED","timeFrame":"1 year","title":"Response","type":"SECONDARY","unitOfMeasure":"participants"}