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首页> 外文期刊>Revista da Associao Médica Brasileira >The safety and clinical efficacy of recombinant human granulocyte colony stimulating factor injection for colon cancer patients undergoing chemotherapy
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The safety and clinical efficacy of recombinant human granulocyte colony stimulating factor injection for colon cancer patients undergoing chemotherapy

机译:重组人粒细胞集落刺激因子注射液对结肠癌化疗患者的安全性和临床疗效

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摘要

Summary Objective: The present study was designed to evaluate safety and efficacy of recombinant human granulocyte colony stimulating factor (G-CSF) injection and whether this regimen could reduce the incidence of adverse events caused by chemotherapy. Method: A total of 100 patients with colon cancer who were treated with chemotherapy in our hospital from January 2011 to December 2014 were randomly divided into two groups, with 50 patients in each group. The patients in the treatment group received G-CSF 24 hours after chemotherapy for consecutive three days; the patients in the control group received the same dose of normal saline. Routine blood tests were performed 7 days and 14 days after chemotherapy. Results: Compared with the control group, the incidences of febrile neutropenia and leukocytopenia in the treatment group were significantly lower (p<0.05). In addition, the incidence of liver dysfunction in the treatment group was lower than that of the control group, without statistical significance. The incidence of myalgia in the treatment was higher than that of the control group without statistical significance. Conclusion: The present study indicated that G-CSF injection after chemotherapy is safe and effective for preventing adverse events in colon cancer patients with chemotherapy.
机译:摘要目的:本研究旨在评估重组人粒细胞集落刺激因子(G-CSF)注射剂的安全性和有效性,以及该方案是否可以减少化疗引起的不良事件的发生。方法:将2011年1月至2014年12月在我院接受化疗的100例结肠癌患者随机分为两组,每组50例。治疗组患者化疗后24小时连续3天接受G-CSF治疗。对照组患者接受相同剂量的生理盐水。化疗后7天和14天进行常规血液检查。结果:与对照组相比,治疗组发热性中性粒细胞减少症和白细胞减少症的发生率显着降低(p <0.05)。此外,治疗组的肝功能障碍发生率低于对照组,无统计学意义。治疗中肌痛的发生率高于对照组,无统计学意义。结论:本研究表明,化疗后G-CSF注射液可有效预防结肠癌化疗患者的不良事件。

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