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一项在卵巢癌化疗期间使用粒细胞巨噬细胞集落刺激因子的双盲安慰剂对照研究。

A double-blind placebo-controlled study with granulocyte-macrophage colony-stimulating factor during chemotherapy for ovarian carcinoma.

作者信息

de Vries E G, Biesma B, Willemse P H, Mulder N H, Stern A C, Aalders J G, Vellenga E

机构信息

Department of Internal Medicine, University Hospital Groningen, The Netherlands.

出版信息

Cancer Res. 1991 Jan 1;51(1):116-22.

PMID:1988077
Abstract

In a placebo-controlled double-blind dose-finding trial, 15 patients with ovarian cancer stage III or IV received daily s.c. 1.5, 3, or 6 micrograms/kg recombinant human granulocyte-macrophage colony-stimulating factor (GM-CSF). At each dose step three patients received recombinant human GM-CSF, and two received placebo. Chemotherapy comprised 6 cycles of carboplatin, 300 mg/m2, and cyclophosphamide, 750 mg/m2, by i.v. bolus on day 1 every 4 weeks. GM-CSF, given on days 6-12 on an outpatient basis, raised the mean leukocyte count on days 7, 10, and 15 and the mean neutrophil count on days 7 and 10 at all dose levels as compared with the control group. Neutrophil counts of less than 0.5 x 10(9)/liter occurred in 20 of 22 cycles in the control group and in 5 of 17 cycles at the 6-micrograms/kg/day GM-CSF dose level (P less than 0.0005). In comparison with the control group, the mean eosinophil count was higher on days 10 and 15 at all GM-CSF doses, as was the mean monocyte count on day 15. The mean platelet count was raised at the 3- and 6-micrograms GM-CSF doses on days 15 and 22. Chemotherapy dose reduction or postponement due to myelotoxicity occurred in 9 of 28 cycles in the placebo groups versus 5 of 44 cycles in the GM-CSF group (not significant). Local skin infiltrates at the GM-CSF injection sites occurred in 8/9 patients, leading to premature removal of two patients from the study. Capillary leakage of 131I-albumin was increased in all patients 5 days after the first chemotherapy course but was not significantly affected by 4 days of GM-CSF treatment. Tumor necrosis factor alpha and C-reactive protein serum levels increased during GM-CSF administration at the 6-micrograms dose level, but interleukin 6 serum levels were not affected. We conclude that a dose of 3 and 6 micrograms/kg/day GM-CSF reduces the severity of neutropenia and thrombocytopenia after carboplatin-cyclophosphamide. This GM-CSF dose does not induce additional capillary leakage.

摘要

在一项安慰剂对照的双盲剂量探索试验中,15例III期或IV期卵巢癌患者每日皮下注射1.5、3或6微克/千克重组人粒细胞巨噬细胞集落刺激因子(GM-CSF)。在每个剂量组,3例患者接受重组人GM-CSF,2例接受安慰剂。化疗方案为每4周一次,第1天静脉推注卡铂300毫克/平方米和环磷酰胺750毫克/平方米,共6个周期。GM-CSF在第6至12天门诊给药,与对照组相比,所有剂量水平下,第7、10和15天的平均白细胞计数以及第7和10天的平均中性粒细胞计数均有所升高。对照组22个周期中有20个周期中性粒细胞计数低于0.5×10⁹/升,GM-CSF剂量为6微克/千克/天时,17个周期中有5个周期出现这种情况(P<0.0005)。与对照组相比,所有GM-CSF剂量下第10和15天的平均嗜酸性粒细胞计数均较高,第15天的平均单核细胞计数也较高。GM-CSF剂量为3和6微克时,第15和22天平均血小板计数升高。安慰剂组28个周期中有9个周期因骨髓毒性而减少或推迟化疗剂量,GM-CSF组44个周期中有5个周期出现这种情况(无显著差异)。GM-CSF注射部位局部皮肤浸润在9例患者中出现8例,导致2例患者提前退出研究。首次化疗疗程后5天,所有患者131I-白蛋白的毛细血管渗漏均增加,但GM-CSF治疗4天对此无显著影响。GM-CSF剂量为6微克时,给药期间肿瘤坏死因子α和C反应蛋白血清水平升高,但白细胞介素6血清水平未受影响。我们得出结论,GM-CSF剂量为3和6微克/千克/天可降低卡铂-环磷酰胺治疗后中性粒细胞减少和血小板减少的严重程度。该GM-CSF剂量不会引起额外的毛细血管渗漏。

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