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首页> 外文期刊>Supportive care in cancer: official journal of the Multinational Association of Supportive Care in Cancer >Full-dose chemotherapy in early stage breast cancer regardless of absolute neutrophil count and without G-CSF does not increase chemotherapy-induced febrile neutropenia
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Full-dose chemotherapy in early stage breast cancer regardless of absolute neutrophil count and without G-CSF does not increase chemotherapy-induced febrile neutropenia

机译:早期乳腺癌中的全剂量化疗,无论绝对中性粒细胞计数如何,也没有G-CSF,都不会增加化疗引起的发热性中性粒细胞减少

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Purpose: Does giving full-dose adjuvant chemotherapy to patients with early stage breast cancer (ESBC) regardless of the day-before absolute neutrophil count (ANC) lead to an increased incidence of chemotherapy-induced febrile neutropenia (CIFN)? What factors may predispose patients to CIFN? Methods: This was a retrospective chart review conducted on all patients receiving adjuvant chemotherapy for ESBC at a mid-sized community hospital in Toronto, Ontario, Canada between September 2005 and August 2011. Day-before CBC data were collected along with other patient characteristics. CIFN was confirmed by hospital records. One hundred fifty-four patients met the inclusion criteria. Overall, 830 cycles of chemotherapy were analyzed. Univariate and multivariate logistic regression analyses were used to identify risk factors for CIFN. Results: Twenty-two episodes of CIFN were observed. There was no significant difference in day-before ANC between patients who developed CIFN relative to those who did not. The day-before ANC was 1.5 × 109/L for 88 cycles of chemotherapy. ANC analyzed as a continuous variable showed that the odds ratio (OR) for CIFN was 0.97 (95 % CI 0.82-1.13, p = NS). The pseudo R 2 statistic, which is a measure of variability accounted for by a regression model, was only 0.0008, indicating that ANC explained less than 1 % of the variability in the risk of CIFN. The most significant predictor of CIFN was the chemotherapy regimen, with docetaxel (Taxotere)/cyclophosphamide demonstrating the highest risk (OR 7.1, 95 % CI 1.4-34.9, p = 0.016). Conclusions: Full-dose adjuvant chemotherapy may be given to patients with ESBC regardless of the day-before ANC, without significantly increasing the risk of CIFN. The chemotherapy regimen is the most significant predictor for CIFN.
机译:目的:不管绝对嗜中性白血球计数(ANC)的前一天如何,对早期乳腺癌(ESBC)患者进行全剂量辅助化疗是否会导致化疗诱导的发热性中性粒细胞减少症(CIFN)发生率增加?哪些因素可能使患者容易接受CIFN?方法:这是一项回顾性图表回顾,回顾了2005年9月至2011年8月间在加拿大安大略省多伦多市的一家中型社区医院接受ESBC辅助化疗的所有患者。在收集CBC数据及其他患者特征之前的一天。医院记录证实了CIFN。 154名患者符合纳入标准。总体上分析了830个周期的化疗。单因素和多因素logistic回归分析用于确定CIFN的危险因素。结果:观察到22例CIFN。发生CIFN的患者与未发生CIFN的患者在ANC前一天没有显着差异。 88疗程的ANC前一天<1.5×109 / L。作为连续变量进行分析的ANC显示,CIFN的优势比(OR)为0.97(95%CI 0.82-1.13,p = NS)。伪R 2统计量(由回归模型解释的变异性度量)仅为0.0008,表明ANC解释的CIFN风险变异性不足1%。 CIFN的最重要预测指标是化疗方案,其中多西他赛(Taxotere)/环磷酰胺的风险最高(OR 7.1,95%CI 1.4-34.9,p = 0.016)。结论:无论ANC的前一天如何,ESBC患者均可进行全剂量辅助化疗,而不会显着增加CIFN的风险。化疗方案是CIFN最重要的预测指标。

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