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Bone Marrow Transplantation in Treating Patients With Chronic Lymphocytic Leukemia

M.D. Anderson Cancer Center logo

M.D. Anderson Cancer Center

Status and phase

Completed
Phase 2

Conditions

Leukemia

Treatments

Radiation: Total Body Irradiation (TBI)
Procedure: Allogeneic Bone Marrow Transplantation
Procedure: Autologous Bone Marrow Transplantation
Drug: Cyclophosphamide

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT00002844
P30CA016672 (U.S. NIH Grant/Contract)
CDR0000065081 (Registry Identifier)
NCI-G96-1034
MDA-DM-90106 (Other Identifier)
DM90-106

Details and patient eligibility

About

RATIONALE: Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die. Combining chemotherapy with bone marrow transplantation may allow the doctor to give higher doses of chemotherapy drugs and kill more cancer cells.

PURPOSE: Phase II trial to study the effectiveness of bone marrow transplantation in treating patients with chronic lymphocytic leukemia.

Full description

OBJECTIVES: Examine the potential role for high dose cyclophosphamide, total body irradiation and bone marrow transplantation for patients with chronic lymphocytic leukemia who are at high risk for disease progression.

OUTLINE: Patients receive daily intravenous infusions of cyclophosphamide for two days, followed by total body irradiation in four daily exposures. After completion of the total body irradiation, allogeneic or autologous bone marrow is infused intravenously.

PROJECTED ACCRUAL: 50 patients are expected to be accrued.

Enrollment

49 patients

Sex

All

Ages

16 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

DISEASE CHARACTERISTICS: Chronic lymphocytic leukemia (CLL) patients after initial relapse who have achieved a complete or partial remission with fludarabine therapy or after initial relapse or progression Prolymphocytic leukemia in first remission or after relapse Patients 15-65 years old who lack an HLA-identical sibling are eligible for autologous BM transplantation Patients 16-50 years old with an HLA identical or one antigen mismatched related donor are eligible for allogeneic BM transplantation

PATIENT CHARACTERISTICS: Age: 15-65 (See Disease Characteristics) Performance status: Zubrod no more than 2 Hematopoietic: Not specified Hepatic: Bilirubin no greater than 1.5 mg/dL Renal: Creatinine no greater than 1.5 mg/dL Cardiovascular: Cardiac ejection fraction at least 50% Pulmonary: DLCO at least 50% of predicted Other: No severe concomitant medical or psychiatric illnesses

PRIOR CONCURRENT THERAPY: No extensive prior radiotherapy which would prevent administration of total body radiation Patients may also participate in study MDA-DM-92082 for retroviral gene marking of the autologous marrow and blood cells

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

49 participants in 1 patient group

Cyclophosphamide + TBI + BMT
Experimental group
Description:
TBI = Total Body Irradiation and BMT = Bone Marrow Transplantation (allogeneic or autologous bone marrow)
Treatment:
Drug: Cyclophosphamide
Procedure: Autologous Bone Marrow Transplantation
Procedure: Allogeneic Bone Marrow Transplantation
Radiation: Total Body Irradiation (TBI)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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