We evaluated the use of granulocyte CSF (G‐CSF) after both allogeneic BMT (allo‐BMT) and autologous BMT (ABMT) in children. After allo‐BMT, G‐CSF was used in 15 children who were compared with 20 historical controls. The ABMT patients were two sequential groups: the G‐CSF group of 13 children and 11 historical controls. The patients were conditioned with different high‐dose chemotherapy regimens with or without total body irradiation. G‐CSF was administered at 5 μg/kg/day s.c. and was continued until an absolute neutrophil count (ANC) of 1,000 × 106/l was reached. Following allo‐BMT, G‐CSF accelerated myeloid engraftment with a difference of 5 days at the ANC level of 500 × 106/l (P < 0.02) and 9 days at 1,000 × 106/l (P < 0.001). In the ABMT patients, G‐CSF also accelerated myeloid engraftment. The difference between the G‐CSF group and the control group was 6 days at ANC 200 (P < 0.05), 11 days at ANC 500 (P < 0.02), and 17 days at ANC 1,000 (P < 0.005). In the ABMT patients, benefit by G‐CSF was also observed in a smaller number of days with fever and days on antibiotics. We conclude that G‐CSG significantly accelerated myeloid engraftment, after both allogeneic and autologous BMT in children, and also decreased the duration of febrile illness in the ABMT patients. © 1996 Wiley‐Liss, Inc.