Non Hodgkin Lymphoma Clinical Trial

Blood Stem Cell Transplant in Treating Patients With Hematologic Cancer

Summary

RATIONALE: Giving chemotherapy drugs and total-body irradiation before a donor peripheral blood stem cell transplant helps stop the growth of cancer cells. It also helps stop the patient's immune system from rejecting the donor's stem cells. When the healthy stem cells from a donor are infused into the patient they may help the patient's bone marrow make stem cells, red blood cells, white blood cells, and platelets.

PURPOSE: This phase II trial is studying the effectiveness of donor peripheral blood stem cell transplant in treating patients with hematologic cancer.

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Full Description

OBJECTIVES:

Determine the efficacy and safety of allogeneic peripheral blood stem cell transplantation in achieving engraftment in patients with hematologic malignancy.
Determine the hematopoietic recovery, incidence of chemoradiotherapeutic toxicity, relapse, graft-versus-host disease, and survival of patients treated with this regimen.

OUTLINE: Patients receive a preparative chemoradiotherapeutic regimen and graft-versus-host disease prophylaxis prior to transplantation. Patients undergo allogeneic peripheral blood stem cell transplantation on day 0.

Patients are followed every 1-2 weeks for 6 months and at 9, 12, 24, and 36 months.

PROJECTED ACCRUAL: A total of 62 patients will be accrued for this study within 4 years.

View Eligibility Criteria

Eligibility Criteria

DISEASE CHARACTERISTICS:

Diagnosis of one of the following:

Chronic myelogenous leukemia

Philadelphia chromosome-positive OR
Molecular evidence of bcr/abl gene rearrangement

Acute myeloid leukemia, acute lymphocytic leukemia, lymphoma, histiocytoses, myelodysplasia, juvenile chronic myelomonocytic leukemia, aplastic anemia, paroxysmal nocturnal hemoglobinuria, or Fanconi's anemia

Confirmed by cytochemistry, immunophenotyping, and/or chromosomal abnormalities
Multiple myeloma

Hereditary immunodeficiency disorders

Confirmed by immunologic determination

Sickle cell anemia or beta-thalassemia

Confirmed by hemoglobin electrophoresis

Storage disorders (e.g., Gaucher's disease, Hurler's disease, or metachromatic leukodystrophy)

Confirmed by metabolic testing
Other non-malignant conditions
Eligible for allogeneic peripheral blood stem cell or bone marrow transplantation

PATIENT CHARACTERISTICS:

Age:

65 and under

Performance status:

Not specified

Life expectancy:

Not specified

Hematopoietic:

Not specified

Hepatic:

Not specified

Renal:

Not specified

PRIOR CONCURRENT THERAPY:

Biologic therapy

Not specified

Chemotherapy

Not specified

Endocrine therapy

Not specified

Radiotherapy

Not specified

Surgery

Not specified

Study is for people with:

Non Hodgkin Lymphoma

Estimated Enrollment:

48

Study ID:

NCT00008216

Recruitment Status:

Terminated

Sponsor:

Columbia University

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There is 1 Location for this study

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Herbert Irving Comprehensive Cancer Center at Columbia University Medical Center
New York New York, 10032, United States

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Study is for people with:

Non Hodgkin Lymphoma

Estimated Enrollment:

48

Study ID:

NCT00008216

Recruitment Status:

Terminated

Sponsor:


Columbia University

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