Effects of glycosylated recombinant human granulocyte colony-stimulating factor after high-dose cytarabine-based induction chemotherapy for adult acute myeloid leukaemia

被引:31
作者
Bradstock, K [1 ]
Matthews, J
Young, G
Lowenthal, R
Baxter, H
Arthur, C
Bashford, J
Brighton, T
Cannell, P
Dunlop, L
Durrant, S
Enno, A
Eliadis, P
Gill, D
Gillett, A
Gottlieb, D
Januszewicz, H
Joshua, D
Leahy, M
Schwarer, A
Taylor, K
机构
[1] Westmead Hosp, Dept Haematol, Westmead, NSW 2145, Australia
[2] Peter MacCallum Canc Inst, Trial Ctr, Melbourne, Vic, Australia
[3] Royal Prince Alfred Hosp, Camperdown, NSW, Australia
[4] Royal Hobart Hosp, Hobart, Tas, Australia
[5] Royal N Shore Hosp, St Leonards, NSW 2065, Australia
[6] St George Hosp, Kogarah, NSW 2217, Australia
[7] Royal Perth Hosp, Perth, WA, Australia
[8] Liverpool Hosp, Liverpool, NSW, Australia
[9] Royal Brisbane Hosp, Herston, Qld, Australia
[10] Newcastle Mater Hosp, Waratah, NSW, Australia
[11] Wesley Med Ctr, Brisbane, Qld, Australia
[12] Princess Alexandra Hosp, Woolloongabba, Qld 4102, Australia
[13] Fremantle Hosp, Fremantle, WA, Australia
[14] Alfred Hosp, Prahran, Vic 3181, Australia
[15] Mater Misericordiae Univ Hosp, Brisbane, Qld, Australia
基金
英国医学研究理事会;
关键词
acute myeloid leukemia; lenograstim; granulocyte colony-stimulating factor; chemotherapy; dose intensity;
D O I
10.1038/sj.leu.2402218
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The Australian Leukaemia Study Group (ALSG) investigated whether G-CSF would accelerate haemopoietic recovery after induction treatment for acute myeloid leukaemia (AML) intensified with high-dose cytarabine, and therefore improve response rates and survival. Patients were randomised to receive lenograstim (glycosylated recombinant human G-CSF) 5 mug per kg body weight subcutaneously daily from day 8 after starting chemotherapy, or no cytokine, following chemotherapy with cytarabine 3 g/m(2) every 12 h on days 1, 3, 5, and 7, together with idaruibicin 9 or 12 mg/m(2) on days 1, 2, and 3, plus etoposide 75 mg/m(2) on days 1 to 7 inclusive. Patients had untreated AML, and were aged 16 to 60 years. Overall, 54 evaluable patients were randomised to receive lenograstim and 58 to no cytokine. Patients in the lenograstim arm had a significantly shorter duration of neutropenia <0.5x10(9)/l compared to patients in the no cytokine arm (median 18 vs 22 days; P=0.0005), and also shorter duration of total leucopenia <1.0 x 10(9)/l (17 vs 19 days; P=0.0002), as well as a reduction in duration of treatment with therapeutic intravenous antibiotics (20 vs 24 days; P=0.015) and a trend to reduced number of days with fever >38.0 degreesC (9 vs 12 days; P=0.18). There were no differences between the two groups in platelet recovery, red cell or platelet transfusions, or non-haematological toxicities. For patients achieving CR after their first induction course, a reduction in the time to the start of the next course of therapy was observed in the lenograstim arm, from a median of 40.5 days to a median of 36 days (P=0.082). The overall complete response rates to chemotherapy were similar, 81% in the lenograstim arm vs 75% for the no cytokine arm (P=0.5), and there was no significant difference in the survival durations. We conclude that the granulopoietic stimulating effect of G-CSF is observed after induction therapy for AML intensified by high-dose cytarabine, resulting in an improvement in a number of clinically important parameters with no major adverse effects.
引用
收藏
页码:1331 / 1338
页数:8
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