N. Piccirillo et al., Optimal timing of G-CSF administration after CD34(+) immunoselected peripheral blood progenitor cell transplantation, BONE MAR TR, 23(12), 1999, pp. 1245-1250
Citations number
20
Categorie Soggetti
Hematology,"Medical Research Diagnosis & Treatment
G-CSF accelerates neutrophil recovery after autologous peripheral blood pro
genitor cell transplantation (aPBPCT), although the optimal timing for its
administration is currently unknown. In order to establish the role and the
optimal timing of administration of G-CSF after immunoselected CD34(+) aPB
PCT, we analyzed the data from 21 consecutive patients affected by haematol
ogical malignancies. Patients were randomized into three groups according t
o G-CSF administration after transplantation: day +1 (group B); day +7 (gro
up C) or no G-CSF (group A). Serum G-CSF level was evaluated until engraftm
ent, The CD34+ cell dose reinfused was similar (P = 0.48), G-CSF significan
tly reduced time to recovery of PMN >0.5 x 10(9)/l (11 vs 14 vs 20.5 days)
(P = 0.00046); >1.0 x 10(9)/l (12 vs 15 vs 22) (P = 0.001), No difference w
as observed in the number of days with PMN <0.1 x 10(9)/l (5.5 vs 7 vs 8 da
ys), Platelet count >50 x 10(9)/l and >100 x 10(9)/l, reticulocytes >1%, le
ngth of hospitalization, non-prophylactic antibiotic therapy, fever, incide
nce of sepsis and transfusion support did not differ, Early or delayed G-CS
F after immunoselected CD34(+) aPBPCT significantly accelerated PMN recover
y but did not reduce the amount of supportive treatment or the duration of
hospitalization. Delaying the initiation of G-CSF did not reduce the length
of treatment (11.5 vs 12 days). Early or delayed G-CSF administration resu
lted in G-CSF peak serum levels 7 (early)-12 (delayed)-fold greater than an
endogenous response to neutropenia.