A randomized, multicenter study of G-CSF starting on day+1 vs day+5 after autologous peripheral blood progenitor cell transplantation

被引:26
作者
de Azevedo, AM
Nucci, M
Maiolino, A
Vigorito, AC
Simoes, BP
Aranha, FJP
Tabak, DG
Voltarelli, J
de Souza, C
机构
[1] Univ Fed Rio de Janeiro, Univ Hosp, Rio De Janeiro, Brazil
[2] Univ Estadual Campinas, Campinas, SP, Brazil
[3] Univ Sao Paulo, BR-14049 Ribeirao Preto, SP, Brazil
[4] CEMO, Inst Nacl Canc, Rio De Janeiro, Brazil
关键词
G-CSF; autologous; bone marrow transplants; randomized; clinical trial;
D O I
10.1038/sj.bmt.1703538
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
In order to assess the effect of delaying G-CSF administration after autologous peripheral blood progenitor cell (PBPC) transplantation on the duration of neutropenia, 87 patients were randomized to receive G-CSF 5 mug/kg/day starting on day +1 (n = 45) or +5 (n = 42) following PBPC transplantation, until recovery of the neutrophils. The duration of neutropenia (<0.5 x 10(9)/1) was shorter in the day +1 group (7 vs 8 days; P = 0.02), especially in patients receiving melphalan 200 mg/m(2) and CD34(+) cell doses >3.0 X 10(6)/kg. These patients had a later onset of neutropenia after transplant. There were no differences in time to neutrophil and platelet engraftment, or in the incidence of fever and documentation of infection. Although the duration of antibiotic therapy (7 vs 10.5 days; P = 0.01) and time to hospital discharge (13 vs 15 days; P = 0.02) were shorter in the day +1 group, these differences could not be predicted by the day of G-CSF initiation in multivariate analysis. Starting G-CSF on day +1 does not result in faster neutrophil engraftment but in later onset and consequently, slightly shorter duration of neutropenia in patients who receive melphalan 200 mg/m2 and CD34(+) cell doses >3.0 x 10(6)/kg.
引用
收藏
页码:745 / 751
页数:7
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