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首页> 外文期刊>Journal of Clinical Oncology >Granulocyte-macrophage colony-stimulating factor in patients with neutropenic fever is potent after low-risk but not after high-risk neutropenic chemotherapy regimens: results of a randomized phase III trial (see comments)
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Granulocyte-macrophage colony-stimulating factor in patients with neutropenic fever is potent after low-risk but not after high-risk neutropenic chemotherapy regimens: results of a randomized phase III trial (see comments)

机译:中性粒细胞减少症患者的粒细胞巨噬细胞集落刺激因子在低风险后有效,但在高风险中性粒细胞减少化疗方案后无效:一项随机III期试验的结果(请参阅评论)

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PURPOSE: A randomized unblinded phase III trial was designed to determine the ability of granulocyte-macrophage colony-stimulating factor (GM-CSF) to accelerate recovery from febrile neutropenia induced by chemotherapy. PATIENTS AND METHODS: A total of 68 patients with febrile neutropenia following chemotherapy defined as axillary temperature greater than 38 degrees C and absolute neutrophil count (ANC) less than 1 x 10(9)/L were included. After stratification for high- and low-risk chemotherapy to induce febrile neutropenia, treatment was randomized between GM-CSF at 5 microg/kg/d or control, both being associated with antibiotics. RESULTS: GM-CSF significantly reduced the median duration of neutropenia from 6 to 3 days for ANC less than 1 x 10(9)/L(P < .001) and from 4 to 3 days for ANC less than 0.5 x 10(9)/L (P=.024), days of hospitalization required for febrile neutropenia, and duration of antibiotics during hospitalization. The greatest benefit with GM-CSF appeared for patients who had received low-risk chemotherapy, for which the median duration of ANC less than 1 x 10(9)/L was reduced from 7 to 2.5 days (P < .001) and from 4 to 2 days for ANC less than 0.5 x 10(9)/L (P=.0011), the duration of hospitalization during the study from 7 to 4 days (P=.003), and the duration on antibiotics during hospitalization from 7 to 3.5 days (P < .001). A multivariate analysis, using Cox regression, showed that variables predictive for recovery from neutropenia were GM-CSF (P=.0010) and time interval between the first day of chemotherapy and randomization (P=.030). There was no benefit for GM-CSF when high-risk chemotherapy was considered. CONCLUSION: GM-CSF significantly shortened duration of neutropenia, duration of neutropenic fever-related hospitalization, and duration on antibiotics during hospitalization when febrile neutropenia occurred after low-risk chemotherapy, but not high-risk chemotherapy.
机译:目的:设计一项随机无盲III期试验,以测定粒细胞-巨噬细胞集落刺激因子(GM-CSF)加速从化学疗法诱导的发热性中性粒细胞减少症中恢复的能力。患者和方法:总共68例化疗后的发热性中性粒细胞减少症患者定义为腋温高于38摄氏度且绝对中性粒细胞计数(ANC)低于1 x 10(9)/ L。分层诱导高热中性粒细胞减少症的高危和低危化疗后,将治疗随机分配于5 mg / kg / d的GM-CSF或对照组,两者均与抗生素有关。结果:GM-CSF将中性粒细胞减少症的中位数持续时间从ANC小于1 x 10(9)/ L(P <.001)减少到6天到3天,而ANC小于0.5 x 10(9)从4到3天减少/ L(P = .024),发热性中性粒细胞减少症需要住院的天数以及住院期间抗生素的使用时间。 GM-CSF的最大益处出现在接受低风险化疗的患者中,其中ANC的中位时间少于1 x 10(9)/ L从7天减少到2.5天(P <.001),而从ANC小于0.5 x 10(9)/ L时为4到2天(P = .0011),研究期间的住院时间为7到4天(P = .003),住院期间的抗生素疗程为7至3.5天(P <.001)。使用Cox回归进行的多变量分析显示,预测中性粒细胞减少的恢复变量为GM-CSF(P = .0010)和化疗第一天与随机分组之间的时间间隔(P = .030)。当考虑高危化疗时,GM-CSF没有益处。结论GM-CSF可显着缩短中性粒细胞减少症的持续时间,中性粒细胞减少症相关住院的时间以及低危化学疗法后发生发热性中性粒细胞减少症的住院期间抗生素的持续时间,但不缩短高危化学疗法的发生时间。

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