Optimal timing of G-CSF administration after CD34(+) immunoselected peripheral blood progenitor cell transplantation

Citation
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
Journal title
BONE MARROW TRANSPLANTATION
ISSN journal
02683369 → ACNP
Volume
23
Issue
12
Year of publication
1999
Pages
1245 - 1250
Database
ISI
SICI code
0268-3369(199906)23:12<1245:OTOGAA>2.0.ZU;2-F
Abstract
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.