Ozkaynak M Fevzi, Krailo Mark, Chen Zhengjia, Feusner James
Section of Hematology/Oncology and Blood and Marrow Transplantation, Department of Pediatrics, New York Medical College, Valhalla, NY 10595, USA.
Pediatr Blood Cancer. 2005 Sep;45(3):274-80. doi: 10.1002/pbc.20366.
To determine if granulocyte colony-stimulating factor (G-CSF) with empirical antibiotics accelerates febrile neutropenia resolution compared with antibiotics without it.
Eligible children were treated without prophylactic G-CSF and presented with fever (temperature >38.3 degrees C) and neutropenia afterward. Patients with acute myelogenous leukemia and myelodysplastic syndrome were excluded. Assignments were randomized between G-CSF (5 microg/kg/day) or none beginning within 24 hr of antibiotics. Subcutaneous administration was recommended, but intravenous G-CSF was allowed. Patients remained on study until absolute neutrophil count (ANC) >500/microl and > or =48 hr without fever.
One of 67 patients enrolled was ineligible, 59 had acute lymphoblastic leukemia (ALL). Thirty-four were assigned to antibiotics, 32 to G-CSF plus antibiotics. Adding G-CSF significantly reduced neutropenia and febrile neutropenia recovery times. Median days to febrile neutropenia resolution was nine earlier with G-CSF (4 vs. 13 days) (P < 0.0001). However, there was no difference in the resolution of fever between arms. Hospitalization median was shorter by 1 day with G-CSF (4 vs. 5 days) (P = 0.04). There was no difference in the duration of IV and oral antibiotic treatment, addition of antifungal therapy, and shock incidence. A trend for decreased incidence of late fever with G-CSF was noted (6.3 vs. 23.5%) (P = 0.08).
Adding G-CSF to empiric antibiotic coverage accelerates chemotherapy-induced febrile neutropenia resolution by 9 days in pediatric patients, mainly with ALL, which results in a small but significant difference in the median length of hospitalization.
确定与单纯使用抗生素相比,联合经验性抗生素使用粒细胞集落刺激因子(G-CSF)是否能加速发热性中性粒细胞减少症的缓解。
符合条件的儿童未接受预防性G-CSF治疗,之后出现发热(体温>38.3摄氏度)及中性粒细胞减少。急性髓系白血病和骨髓增生异常综合征患者被排除。在开始使用抗生素的24小时内,随机分配使用G-CSF(5微克/千克/天)或不使用。建议皮下给药,但也允许静脉使用G-CSF。患者持续接受研究直至绝对中性粒细胞计数(ANC)>500/微升且无发热≥48小时。
67名入组患者中有1名不符合条件,59名患有急性淋巴细胞白血病(ALL)。34名被分配接受抗生素治疗,32名接受G-CSF加抗生素治疗。添加G-CSF显著缩短了中性粒细胞减少和发热性中性粒细胞减少的恢复时间。使用G-CSF时,发热性中性粒细胞减少症缓解的中位天数提前了9天(4天对13天)(P<0.0001)。然而,两组之间发热的缓解情况没有差异。使用G-CSF时住院中位时间缩短了1天(4天对5天)(P = 0.04)。静脉和口服抗生素治疗的持续时间、抗真菌治疗的添加以及休克发生率没有差异。注意到使用G-CSF有晚期发热发生率降低的趋势(6.3%对23.5%)(P = 0.08)。
在经验性抗生素治疗中添加G-CSF可使儿科患者(主要是ALL患者)化疗引起的发热性中性粒细胞减少症的缓解加速9天,这导致住院中位时长有微小但显著的差异。