Low-Intensity Preparation and Allogeneic Transplant in Patients With Cancers of the Blood

NCT ID: NCT00146055

Last Updated: 2012-08-09

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 60 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2000-03-31
• Study Completion Date: 2007-10-31

Brief Summary

The purpose of this study is to determine whether a less-intensive preparative therapy followed by an allogeneic peripheral stem cell transplantation will provide an effective treatment for your disease and whether it will be associated with fewer side effects.

Detailed Description

Combinations of high-dose chemotherapy and radiation therapy (preparative regimen) followed with allogeneic bone marrow or stem cell transplantation from an unrelated donor is a current treatment approach. Chemotherapeutic drugs and radiation are given in higher doses to increase their effectiveness. High-dose chemotherapy and radiation therapy generally affect cells that are dividing. They are used to treat cancer because cancer cells divide more often than most other cells. High-dose treatment severely damages the patient's bone marrow so that the patient no longer is able to produce needed blood cells. Peripheral stem cell transplantation allows stem cells that were damaged by treatment to be replaced with healthy stem cells that can produce the blood cells the patient needs. Patients experience a number of complications after transplantation. Some are temporary and relatively minor; yet others can be life threatening. Many doctors consider high-dose chemotherapy, by itself or with radiation, and bone marrow or stem cell transplantation as the best available treatment option for diseases under specific circumstances. However, this study will explore whether a less-intensive preparative therapy before the peripheral stem cell transplantation will prove to be safer, have less side effects, and be an effective treatment for certain diseases.

Conditions

Myeloma, Plasma-Cell; Lymphoma, Malignant; Myeloproliferative Disorders; Myelodysplastic Syndromes; Waldenstrom's Macroglobulinemia

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Interventions

Reduced intensity conditioning with allogeneic transplant

Intervention Type: PROCEDURE

Eligibility Criteria

Inclusion Criteria

Patients must be a candidate for unrelated donor stem cell transplantation and the donor and recipient must be 5/6 or 6/6 matched. In addition, patients must have one of the following histologically confirmed diagnosis :

1. Patients with previously treated AML (M0 - M7 by FAB classification)

• who are in not in complete remission (CR).
• who are in second or later CR.
• who have 5-30% persistent blasts in bone marrow following induction or salvage chemotherapy.
• who have high-risk feature in first complete remission e.g. presence of Philadelphia chromosome or non-core-binding factor type of chromosomal abnormalities.

2. Patients with myelodysplastic syndromes and IPS int-1, int-2 or high-risk scores who are transfusion-dependent.

3. Patients with chronic myeloid leukemia who are in accelerated, blastic, or or chronic phase

4. Patients with acute lymphoblastic leukemia

• who are in first complete remission and have high risk disease [Ph' or t (4; 11) , WBC> 30,000, > 4 weeks to achieve CR].
• who are in second or greater CR.
• who did not achieve a CR following induction or salvage therapy.

5. Patients with Hodgkin's or non-Hodgkin's lymphoma who are not curable with conventional chemotherapy and do not have any tumor larger than 5 centimeters in diameter.

6. Patients with myeloma or plasma cell neoplasms who are :

• stage III at presentation.
• stage I-II at presentation but were not responding or progressed after first line therapy.

7. Patient with chronic lymphocytic leukemia or Waldenström's macroglobulinemia who progressed after first-line therapy.

8. Patients with MDS or myeloproliferative disorders who had history of life-threatening complications related to thrombosis, hemorrhagic diathesis or intractable hypercatabolic state (fever cachexia).

Exclusion Criteria

1. Cardiac disease of symptomatic nature; < 25% ejection fraction.

2. Severe renal disease; creatinine > 2.O mg/dl or creatinine clearance < 40 ml/min. (Corrected for age)

3. Severe pulmonary disease < 60% normal (FEV1 & FVC).

4. Severe hepatic disease; bilirubin >2.0, and/or transaminase > 3 x normal corrected for age.

5. Karnofsky performance status of < 60%.

6. Patients with evidence of HIV infection by western blot.

7. Any conditions, in the opinion of the transplant team such as substance abuse, or severe personality disorder that would keep the patients from complying with the needs of the protocol and would markedly increase the morbidity and mortality from the procedure.

• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Michigan Rogel Cancer Center

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

John E. Levine, MS MD

Role: PRINCIPAL_INVESTIGATOR

The Univeristy of Michigan

Locations

The University of Michigan

Ann Arbor, Michigan, United States

Countries

United States

Other Identifiers

UMCC 9970

Identifier Type: -

Identifier Source: org_study_id