Peripheral Blood (PB) Versus Bone Marrow (BM) in Allogeneic Stem Cell Transplantation

European Society for Blood and Marrow Transplantation

Status and phase

Completed

Phase 3

Conditions

Acute Leukemia

Chronic Myelogenous Leukemia

Myelodysplastic Syndrome

Treatments

Procedure: Peripheral blood stem cell transplantation

Procedure: Bone marrow transplantation

Study type

Interventional

Funder types

NETWORK

Industry

Identifiers

NCT01020175

GCSF-940136

Details and patient eligibility

About

350 patients with early leukemias were assigned to receive peripheral blood or bone marrow transplantation; the occurrence of acute and chronic graft versus host disease, survival, transplantation-related mortality, and relapse rates were compared.

Full description

The trial was designed to investigate the safety and outcome of allogeneic filgrastim-mobilized PBPCT compared with allogeneic BMT in patients with standard-risk leukemia. A total of 350 patients between 18 and 55 years of age with acute leukemias in remission or chronic myelogenous leukemia in first chronic phase were randomized to receive either filgrastim-mobilized peripheral blood progenitor cells or bone marrow cells from HLA-identical sibling donors after standard high-dose chemoradiotherapy. The study was approved by the ethics committees of all participating centers, and all patients and donors gave informed consent before any study-related procedure was performed. Donor-recipient pairs were randomized to undergo either BMT or PBPCT. Randomization was carried out centrally at the International Institute for Drug Development (id2), Brussels, Belgium, and used the minimization method to allocate donor and recipient to allogeneic BMT or PBPCT. The randomization strata were as follows: diagnosis (chronic myeloid leukemia [CML] vs other diseases), sex mismatch of donor and recipient, and whether the donor was female and nulliparous. Follow-up visits were scheduled for 6, 12, 24, and 36 months after the date of transplantation.

Neutrophil and platelet recovery occurred significantly faster after transplantation of peripheral blood progenitor cells than after bone marrow transplantation. Acute graft versus host disease of grades II-IV was significantly more frequent in recipients of peripheral blood progenitor cells than in recipients of marrow cells The cumulative incidence of chronic graft versus host disease was higher with peripheral blood progenitor cells than with bone marrow cells

Enrollment

350 patients

Sex

All

Ages

18 to 55 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients with either diagnosis of AML in first or second remission, in first untreated relapse (blast count in marrow < 30%); ALL in first or second remission, in first untreated relapse (blast count in marrow < 30%); CML in first chronic phase, in first accelerated phase (total blast and promyelocytes in marrow and or peripheral blood < 30%) or MDS (excluding RAEB-t).
Age between 18 and 55 years.
ECOG performance status between 0,1 or 2.
HLA-identical sibling donor.
Written informed consent.

Exclusion criteria

Serum creatinine more than 10% above the normal range for the centre.
Left ventricular size and function abnormal.
DLCO < 50%.
Bilirubin > 2mg/dL (34.2 µmol/L).
Splenectomised or splenic irradiation.
Psychiatric, addictive, or any other disorder, which compromises ability to give truly informed consent for participation in this study.
Currently receiving non-licensed drugs which may affect GVHD or engraftment.
Pregnant or lactating women.
Known sensitivity to E.coli derived products.
HIV positive.
Previously received BM/PBPC transplant.