To Determine the Role of Adding Campath-1H or ATG Given In-vivo in Addition to Fludarabine and Low Dose Busulfex on Outcome in Patients Treated With Reduced Intensity Conditioning

Hadassah Medical Center

Status and phase

Withdrawn

Phase 3

Conditions

Myelodysplastic Syndrome

Acute Myeloid Leukemia

Treatments

Drug: Campath-1H /ATG

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT00226512

230704-HMO-CTIL

Details and patient eligibility

About

Multi-institutional randomized phase III trial of a non-myeloablative preparative regimen with fludarabine and busulfex with or without anti-lymphocyte antibodies (monoclonal humanized Campath-1H administered s.c. or polyclonal rabbit anti-T lymphocyte antibodies (ATG), combined with low dose and short course cyclosporine A (CSA) and methotrexate (MTX) as the sole agent for prevention of graft-vs-host disease (GVHD) for patients with acute myelogenous leukemia or myelodysplastic syndrome undergoing allogeneic stem cell transplantation from an HLA compatible donor.

Enrollment

203 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Confirmed diagnosis of AML or MDS, with no lower or upper age limit:
a) Induction failure
b) First or subsequent remission
c) Untreated first relapse
Patients must have an HLA compatible donor willing and capable of donating peripheral blood stem cells (first choice) or bone marrow progenitor cells using conventional techniques and blood lymphocytes if indicated (HLA compatible defined as 5/6 or 6/6 matched related or 10/10 molecular matched unrelated donor (A,B,C,DR,DRB1).

Exclusion criteria

Donor contraindication (HIV seropositive confirmed by Western Blot, Hepatitis B antigenemia).
Evidence of bone marrow disease.
Unable to donate bone marrow or peripheral blood due to concurrent medical condition.