L. Madero et al., G-CSF AFTER AUTOLOGOUS BONE-MARROW TRANSPLANTATION FOR MALIGNANT DISEASES IN CHILDREN, Bone marrow transplantation, 15(3), 1995, pp. 349-351
The use of recombinant human granulocyte-stimulating factor (G-CSF) ha
s been shown to effectively accelerate granulocytic recovery after aut
ologous bone marrow transplantation (BMT) in adults, The experience, h
owever, is limited in children, We evaluated the hematopoietic reconst
itution in 41 consecutive children undergoing autologous BMT for hemat
ologic malignancies (21 acute lymphoblastic leukemia, five non-Hodgkin
's lymphoma) and solid tumours (seven neuroblastoma, two brain tumor,
three Ewing's sarcoma, two Wilms' tumor, one rhabdomyosarcoma), Their
ages ranged from 2 to 16 years (mean 7.2 years), rhG-CSF was given at
a dose of 10 mu g/kg/day i.v. in a 2h infusion from day +1 until day 28 or until the absolute neutrophil count (ANC) was >1 x 10(9)/L, Thes
e patients were compared with a similar historical control group of 38
children who did not receive rhG-CSF after autologous BMT, The number
of cells infused was similar in both groups, At the dose and schedule
used in the present study, rhG-CSF was well tolerated and no side-eff
ects were observed, Our data show that rhG-CSF accelerates engraftment
and reduces the number of febrile days and antibiotic use, Furthermor
e, patients who were treated had less infections.