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Search / Trial NCT00002547

Chemotherapy and Bone Marrow Transplantation in Treating Patients Acute Myeloid With Leukemia or Myelodysplastic Syndrome

Launched by BARBARA ANN KARMANOS CANCER INSTITUTE · May 21, 2004

Trial Information

Current as of March 19, 2025

Completed

Keywords

Recurrent Childhood Acute Myeloid Leukemia Recurrent Adult Acute Myeloid Leukemia Untreated Adult Acute Myeloid Leukemia Untreated Childhood Acute Myeloid Leukemia And Other Myeloid Malignancies Adult Acute Myeloid Leukemia In Remission Childhood Acute Myeloid Leukemia In Remission Adult Acute Erythroid Leukemia (M6) Adult Acute Myeloblastic Leukemia Without Maturation (M1) Adult Acute Myeloblastic Leukemia With Maturation (M2) Adult Acute Promyelocytic Leukemia (M3) Adult Acute Myelomonocytic Leukemia (M4) Adult Acute Monoblastic Leukemia (M5a) Adult Acute Megakaryoblastic Leukemia (M7) Childhood Acute Myeloblastic Leukemia Without Maturation (M1) Childhood Acute Myeloblastic Leukemia With Maturation (M2) Childhood Acute Promyelocytic Leukemia (M3) Childhood Acute Myelomonocytic Leukemia (M4) Childhood Acute Monoblastic Leukemia (M5a) Childhood Acute Monocytic Leukemia (M5b) Childhood Acute Erythroleukemia (M6) Childhood Acute Megakaryocytic Leukemia (M7) Refractory Anemia With Excess Blasts Refractory Anemia With Excess Blasts In Transformation Chronic Myelomonocytic Leukemia Secondary Acute Myeloid Leukemia Adult Acute Monocytic Leukemia (M5b) Previously Treated Myelodysplastic Syndromes Childhood Myelodysplastic Syndromes

ClinConnect Summary

OBJECTIVES: I. Determine overall and leukemia-free survival of patients with acute nonlymphocytic leukemia or myelodysplastic syndrome treated with busulfan and cyclophosphamide (low-risk patients) or cytarabine, busulfan, and cyclophosphamide (high-risk patients) followed by allogeneic or syngeneic bone marrow transplantation. II. Compare the therapeutic effects of these cytoreduction regimens with those reported in the literature for similar patients who undergo syngeneic or allogeneic marrow transplantation following cytoreduction that includes total-body irradiation. III. Determine the ...

Gender

ALL

Eligibility criteria

  • DISEASE CHARACTERISTICS: The following hematologic malignancies are eligible: Acute nonlymphocytic leukemia in one of the following categories: In complete remission In early relapse Newly diagnosed FAB types M6 and M7 Myelodysplastic syndromes including: Refractory anemia with excessive blasts Refractory anemia with excessive blasts in transformation Chronic myelomonocytic leukemia Secondary acute myeloid leukemia Transplantation priority given in decreasing order of: First remission Second remission Third remission Early relapse, with priority further reduced for: Refractory response to platelet transfusion Severe infection within 6 weeks prior to referral History of major organ pathology or insult (hepatitis, renal damage, pulmonary disease, cystitis, etc.) CNS disease allowed but priority status for transplantation lowered Donor Criteria: Sibling or matched related/unrelated donor required Donor priority as follows: Monozygotic twin Genotypical or phenotypical HLA-A, -B, -C, and -D match Match at any 2 loci (A, B, Dr) on the other haplotype ABO-compatible donor preferred Marrow processed to eliminate mismatched erythrocytes if ABO incompatible In case of multiple donors, priority is: ABO compatibility Age over 18 Same sex No physiologic, psychologic, or medical contraindication to donation procedure No increased anesthetic risk due to pre-existing illness HIV negative
  • PATIENT CHARACTERISTICS: Age: 6 months to 60 years Performance status: No preterminal or moribund patients Life expectancy: No severe limits on life expectancy due to diseases other than leukemia Hematopoietic: See Disease Characteristics Hepatic: Bilirubin no greater than 2.0 mg/dL Transaminases no greater than 3 times normal No severe hepatic disease Renal: Creatinine no greater than 1.5 mg/dL OR Creatinine clearance at least 60 mL/min No severe renal disease No history of severe cystitis with cyclophosphamide Cardiovascular: LVEF at least 50% No symptomatic cardiac disease Pulmonary: FEV1 and FVC at least 75% of normal No severe pulmonary disease Other: HIV negative No severe personality disorder or severe mental illness No condition (such as substance abuse) that would markedly increase the morbidity and mortality of transplantation Criteria of hepatic, renal, cardiac, and pulmonary function and mental illness are used only for initial screening of potential candidates; patients who do not meet these criteria may still be eligible at the discretion of the transplant team
  • PRIOR CONCURRENT THERAPY: See Disease Characteristics

Trial Officials

Esteban Abella, MD

Principal Investigator

Barbara Ann Karmanos Cancer Institute

About Barbara Ann Karmanos Cancer Institute

The Barbara Ann Karmanos Cancer Institute, a leading nonprofit cancer research and treatment center located in Detroit, Michigan, is dedicated to advancing innovative cancer therapies and improving patient outcomes through rigorous clinical trials. Affiliated with Wayne State University, the institute emphasizes a multidisciplinary approach, integrating cutting-edge research with compassionate patient care. With a commitment to translating laboratory discoveries into effective treatments, Karmanos plays a pivotal role in the national landscape of cancer research, focusing on personalized medicine and the development of novel therapeutic strategies to combat various forms of cancer.

Locations

Detroit, Michigan, United States

People applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Discussion 0

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