Author/Authors :
Jan J. Cornelissen، نويسنده , , Bronno van der Holt، نويسنده , , Eefke J. Petersen، نويسنده , , Lars Vindelov، نويسنده , , Charlotte A. Russel، نويسنده , , Martin H?glund، نويسنده , , Johan Maertens، نويسنده , , Harry C. Schouten، نويسنده , , Eric Braakman، نويسنده , , Monique M. C. Steijaert، نويسنده , , J. Mark J. M. Zijlmans، نويسنده , , Ineke Slaper-Cortenbach، نويسنده , , Marc A. Boogaerts، نويسنده , , Bob L?wenberg، نويسنده , , Leo F. Verdonck، نويسنده ,
Abstract :
Objective. Peripheral blood progenitor cells (PBPC) have been established as an alternative source of hematopoietic stem cells for allogeneic transplantation, but an increased incidence of both acute and chronic graft-vs-host disease (GVHD) has become apparent. We performed a prospective randomized trial comparing bone marrow transplantation (BMT) vs PBPC transplantation (PBPCT) using CD34+ selection for T-cell depletion (TCD) in both study arms.
Patients and Methods. Between January 1996 and October 2000, 120 patients with a diagnosis of acute leukemia, myelodysplasia, multiple myeloma, or lymphoma were randomized to receive either filgrastim-mobilized PBPC or BM from HLA-identical sibling donors after standard high-dose chemoradiotherapy. Patient characteristics did not differ between study arms.
Results. Recipients of PBPC received more CD3+ T cells (median: 3.0 vs 2.0×105/kg, p<0.0001) and more CD34+ cells (median: 3.6 vs 0.9×106/kg, p<0.0001). Neutrophil and platelet recoveries occurred significantly faster after PBPCT. The cumulative incidence of acute GVHD grades II–IV was 37% after BMT vs 52% after PBPCT and was most significantly (p = 0.007) affected by the number of CD3+ T cells in the graft. Acute GVHD appeared strongly associated with increased treatment-related mortality (TRM) in a time-dependent analysis. Higher numbers of CD34+ cells were associated with less TRM. With a median follow-up of 37 months (range: 12–75), overall survival at 4 years from transplantation was 60% after BMT and 34% for recipients of PBPCT (p = 0.04), which difference was largely due to increased GVHD and TRM in PBPC recipients receiving T-cell dosages greater than 2×105/kg.
Conclusion. Outcome following T cell–depleted PBPCT critically depends on the number of CD3+ T cells, whereby high T-cell numbers may blunt a favorable effect of higher CD34+ cell numbers.