Donor Umbilical Cord Blood Transplant By Injection Into the Bone Marrow in Treating Patients With Hematologic Cancer
Myeloproliferative Disorders, Leukemia, Lymphoma
About this trial
This is an interventional treatment trial for Myeloproliferative Disorders focused on measuring adult acute myeloid leukemia in remission, adult acute myeloid leukemia, childhood acute myeloid leukemia in remission, secondary acute myeloid leukemia, accelerated phase chronic myelogenous leukemia, childhood chronic myelogenous leukemia, chronic phase chronic myelogenous leukemia, relapsing chronic myelogenous leukemia, refractory anemia with excess blasts, de novo myelodysplastic syndromes, myelodysplastic syndromes, adult diffuse large cell lymphoma, adult diffuse mixed cell lymphoma, adult diffuse small cleaved cell lymphoma, adult lymphoblastic lymphoma, grade 3 follicular lymphoma, mantle cell lymphoma, childhood large cell lymphoma, childhood lymphoblastic lymphoma, adult acute lymphoblastic leukemia, acute lymphoblastic leukemia, refractory anemia, refractory cytopenia, childhood acute myeloid leukemia, adult immunoblastic large cell lymphoma, blastic phase chronic myelogenous leukemia, chronic eosinophilic leukemia, chronic neutrophilic leukemia, childhood small noncleaved cell lymphoma, childhood myelodysplastic syndromes
Eligibility Criteria
Inclusion Criteria: Acute myeloid leukemia (AML): high risk CR1 Acute lymphocytic leukemia (ALL): high risk CR1 [t(9;22), t (1:19), t(4;11) or other MLL rearrangements] or > 1 cycle to obtain CR; CR2+. All patients must be in CR as defined by hematological recovery, AND <5% blasts by light microscopy within the bone marrow with a cellularity of ≥15%. Chronic myelogenous leukemia (CML) excluding refractory blast crisis. To be eligible in first chronic phase (CP1) patient must have failed or be intolerant to imatinib mesylate. Myelodysplasia (MDS) IPSS Int-2 or High risk (i.e. RAEB, RAEBt) or refractory anemia with severe pancytopenia or high risk cytogenetics. Chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL), marginal zone B-cell lymphoma or follicular lymphoma that have progressed after at least two prior therapies. Patients with bulky disease (nodal mass greater than 5 cm). Lymphoplasmacytic lymphoma, mantle-cell lymphoma, prolymphocytic leukemia are eligible after initial therapy in CR1+ or PR1+. Large cell NHL > CR2/> PR2. Patients in CR2/PR2 with initial short remission (<6 months) are eligible. Lymphoblastic lymphoma. Multiple myeloma beyond PR2. Karnofsky performance status (PS) 90-100% (adults) Lansky PS 50-100% (children) Acceptable organ function Exclusion Criteria: Active infection at time of transplantation History of HIV infection Pregnant or breast feeding. Chemotherapy refractory large cell and high grade NHL (ie progressive disease after > 2 salvage regimens) Extensive prior therapy including > 12 months alkylator therapy or > 6 months alkylator therapy with extensive radiation. Diffuse myelofibrosis of BM (bone marrow) (any severity) regardless of primary diagnosis (focal fibrosis acceptable provided it involves < 20% of BM volume). History of pelvic irradiation.
Sites / Locations
Arms of the Study
Arm 1
Experimental
Transplant Patients
Patients receiving umbilical cord blood transplantation.