TRANSFUSIONS OF GRANULOCYTE-COLONY-STIMULATING FACTOR-MOBILIZED GRANULOCYTE COMPONENTS TO ALLOGENEIC TRANSPLANT RECIPIENTS - ANALYSIS OF KINETICS AND FACTORS DETERMINING POSTTRANSFUSION NEUTROPHIL AND PLATELETCOUNTS
D. Adkins et al., TRANSFUSIONS OF GRANULOCYTE-COLONY-STIMULATING FACTOR-MOBILIZED GRANULOCYTE COMPONENTS TO ALLOGENEIC TRANSPLANT RECIPIENTS - ANALYSIS OF KINETICS AND FACTORS DETERMINING POSTTRANSFUSION NEUTROPHIL AND PLATELETCOUNTS, Transfusion, 37(7), 1997, pp. 737-748
BACKGROUND: Granulocyte-colony-stimulating factor (G-CSF) is a safe an
d effective agent for mobilization of neutrophils in normal donors, co
nsistently resulting in cell yields per leukapheresis (LA) procedure t
hat are superior to those with other agents. LA components also contai
n platelets, whose clinical relevance is unknown. STUDY DESIGN AND MET
HODS: This study describes the kinetics of and analyzes the factors de
termining the ANC and platelet count increments seen with each of thre
e transfusions of granulocytes collected from HLA-matched sibling dono
rs receiving G-CSF (n = 10; maximum of 3 LA procedures/donor). The tra
nsfusions were given to recipients (n = 10) on alternate days beginnin
g Day 1 after allogeneic bone marrow transplant (BMT). RESULTS: Signif
icant, sustained increments in the recipient ANCs were observed after
the transfusion of G-CSF-mobilized LA components. The mean peak posttr
ansfusion increments in the ANCs were 1195, 729, and 631 per mu L with
transfusion of donor LA components on Days 1, 3, and 5, respectively.
The length of time that the mean posttransfusion ANG was at or above
the baseline (pretransfusion) value was 25 to 37 hours, depending on t
he post-BMT day when the component was administered. No consistent rel
ationship was observed between LA component granulocyte dose, baseline
recipient ANC, or temperature elevation and posttransfusion ANC incre
ments. Large numbers of platelets (mean, 2.55 x 10(11)) were present i
n LA components, and this resulted in significant increments from base
line in the mean platelet count 1 hour after LA component transfusions
. Between Days 1 and 7, the duration of severe neutropenia was shorter
and the percentage of patients requiring nondonor platelet transfusio
ns was less in study patients who received LA component transfusions t
han in a similar historical control group who did not. CONCLUSION: The
transfusion of G-CSF-mobilized, HLA-matched LA components to allogene
ic BMT recipients resulted in significant and sustained increments in
the ANC and the platelet count. Within the range examined, a relations
hip between neutrophil dose and an increment in the ANC was not demons
trated.