Skip to content

Blood Transplantation for Patients With Hematologic Malignancies or Bone Marrow Failure States

Megadose T-cell Depleted HLA-nonidentical Blood Progenitor Cell Transplantation for Patients With Hematologic Malignancies or Bone Marrow Failure States

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00038779
Enrollment
7
Registered
2002-06-07
Start date
1996-08-14
Completion date
2004-09-20
Last updated
2018-10-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aplastic Anemia, Leukemia, Non Hodgkin's Lymphoma

Keywords

Lymphoma, CML, CLL, AML, ALL, MDS, AA

Brief summary

The purpose of this study is to assess early treatment failure within 100 days and to assess the effect of this regimen on engraftment, GVHD, immune recovery, relapse of malignancy and survival.

Interventions

PROCEDUREMegadose T-cell Depleted HLA-nonidentical Blood Progenitor Cell Transplantation

Sponsors

M.D. Anderson Cancer Center
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
No minimum to 49 Years
Healthy volunteers
No

Inclusion criteria

* Patients with acute leukemia, lymphoma that failed to respond or relapsed after chemotherapy or CML beyond first chronic phase. * Patients with aplastic anemia or myelodysplasia which failed to respond to primary therapy are eligible. * Patients with low grade lymphoma or CLL will only be eligible if they failed two chemotherapy regimens and have stage IV disease. * Patients must be \<age 50 with a related haploidentical donor (phenotypically one, two or three HLA A, B and DR antigen mismatched) donor. * Patients should have adequate hepatic and renal function with a bilirubin of less than or equal to 1.5mg%, SGPT less than or equal to 3x the upper limits of normal, and creatine less than or equal to 1.5mg%. * Patients with serious intercurrent medical illness are not eligible. * Patients and their donors must provide written informed consent.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026