Phase I/II trial of neutrophil transfusions from donors stimulated with G-CSF and dexamethasone for treatment of patients with infections in hematopoietic stem cell transplantation
Th. Price et al., Phase I/II trial of neutrophil transfusions from donors stimulated with G-CSF and dexamethasone for treatment of patients with infections in hematopoietic stem cell transplantation, BLOOD, 95(11), 2000, pp. 3302-3309
We examined the feasibility of a community blood bank granulocyte transfusi
on program utilizing community donors stimulated with a single-dose regimen
of subcutaneous granulocyte colony-stimulating factor (G-CSF) plus oral de
xamethasone, The recipients of these transfusions were neutropenic stem cel
l transplantation patients with severe bacterial or fungal infection. Ninet
een patients received 165 transfusions (mean 8.6 transfusions/patient, rang
e 1-25). Community donors provided 94% of the transfusions; relatives accou
nted for only 6% of the transfusions. Sixty percent of the community donors
initially contacted agreed to participate, and 98% of these individuals in
dicated willingness to participate again. Transfusion of 81.9 +/- 2.3 x 10(
9) neutrophils (mean +/- SD) resulted in a mean 1-hour posttransfusion neut
rophil increment of 2.6 +/- 2.6 x 10(3)/mu L and restored the peripheral ne
utrophil count to the normal range in 17 of the 19 patients. The buccal neu
trophil response, a measure of the capacity of neutrophils to migrate to ti
ssue sites in vivo, was restored to normal in most patients following the t
ransfusion. Chills, fever, and arterial oxygen desaturation of greater than
or equal to 3% occurred in 7% of the transfusions, but these changes were
not sufficient to limit therapy. Infection resolved in 8 of 11 patients wit
h invasive bacterial infections or candidemia, These studies indicate that
transfusion of neutrophils from donors stimulated with G-CSF plus dexametha
sone can restore a severely neutropenic patient's blood neutrophil supply a
nd neutrophil inflammation response. Further studies are needed to evaluate
the clinical efficacy of this therapy. (Blood, 2000; 95:3302-3309) (C) 200
0 by The American Society of Hematology.