Peripheral Stem Cell Transplant in Treating Patients With High-Risk Leukemia

NCT00066417 · Status: TERMINATED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 51

Last updated 2013-05-01

No results posted yet for this study

Summary

RATIONALE: Giving chemotherapy and total-body irradiation before a donor peripheral stem cell transplant helps stop the growth of cancer and abnormal cells and helps stop the patient's immune system from rejecting the donor's stem cells. When the stem cells from a related donor, that do not exactly match the patient's blood, 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 how well peripheral stem cell transplant works in treating patients with high-risk leukemia.

Conditions

  • Chronic Myeloproliferative Disorders
  • Leukemia
  • Myelodysplastic/Myeloproliferative Diseases

Interventions

DRUG

cyclosporine

DRUG

fludarabine phosphate

DRUG

methylprednisolone

DRUG

therapeutic allogeneic lymphocytes

DRUG

thiotepa

PROCEDURE

allogeneic bone marrow transplantation

PROCEDURE

biological therapy

PROCEDURE

bone marrow ablation with stem cell support

PROCEDURE

bone marrow transplantation

PROCEDURE

chemotherapy

PROCEDURE

leukocyte therapy

PROCEDURE

non-specific immune-modulator therapy

PROCEDURE

peripheral blood lymphocyte therapy

PROCEDURE

peripheral blood stem cell transplantation

PROCEDURE

radiation therapy

Sponsors & Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)

    lead NIH

Principal Investigators

  • Bipin N. Savani, MD · National Heart, Lung, and Blood Institute (NHLBI)

Study Design

Purpose
TREATMENT
Masking
NONE

Eligibility

Min Age
10 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Completion
2007-01-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00066417 on ClinicalTrials.gov