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Early neutropenia on day 8 treated with adjuvant Docetaxel-based chemotherapy in early breast cancer patients: Putative mechanisms within the neutrophil pool system

机译:早期乳腺癌患者在第8天接受以多西他赛为基础的辅助化疗治疗的早期中性粒细胞减少:中性粒细胞池系统内的推定机制

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摘要

Most chemotherapy regimens cause neutropenic nadirs between days 10 and 14, and administration of granulocyte colony-stimulating factor (G-CSF) support relies on this timing. In docetaxel (DOC)-based chemotherapy, the frequency of febrile neutropenia (FN) and the G-CSF dose administered varied greatly between studies. Our study goal was to forecast the necessary dose of G-CSF by comparing day 8 neutropenia with putative changes within the neutrophil pool. We conducted a retrospective observational analysis of 242 early breast cancer patients who had received adjuvant DOC-based chemotherapy (DOC group) compared with 43 patients who had received FEC chemotherapy (FEC group). Patients who were given a standard dose and had a blood test on day 8 in the 1st cycle were eligible. In the DOC group, patients routinely received prophylactic administration of G-CSF (150 μg/body) on day 3 and received additional G-CSF based on a blood test on day 8. Results of the day 8 blood test showed that severe neutropenia (<500/mm3, average 494/mm3) was observed in 152 out of 242 (62.8%) patients in the DOC group, while in the FEC group (n = 43), neutropenia was ambiguous (average 1,741/mm3). In the FEC group, 9 out of 43 patients (20.9%) and in the DOC group, 27 out of 242 patients (11.1%) experienced FN. In the DOC group, day 8 neutropenia was predictive for FN in a logistic regression model (OR 0.79 [95% CI: 0.655–0.952], p = 0.013). Among 214 patients under 70 years old, the planned chemotherapy cycle was completed in 190 (88.8%) patients who also received the maximum dose of G-CSF (150 μg/body) four times, while 23 patients could not complete the planned chemotherapy cycle, but only five because of FN-related complications. Patients treated with DOC should be treated for primary prophylaxis with G-CSF support at an earlier time starting with a relatively small dose.
机译:大多数化疗方案会在10到14天之间导致中性粒细胞减少,并且粒细胞集落刺激因子(G-CSF)支持的给药依赖于这一时机。在基于多西紫杉醇(DOC)的化疗中,研究之间的发热性中性粒细胞减少症(FN)的频率和G-CSF的剂量差异很大。我们的研究目标是通过比较第8天的嗜中性白血球减少症和嗜中性白血球池内的假定变化来预测G-CSF的必要剂量。我们对242例接受DOC辅助化疗的早期乳腺癌患者(DOC组)进行了回顾性观察分析,而43例接受了FEC化疗的患者则进行了回顾性分析。接受标准剂量并在1 st 周期的第8天接受血液检查的患者符合条件。在DOC组中,患者常规在第3天接受预防性给予G-CSF(150微克/体),并在第8天接受血液检查时接受额外的G-CSF。第8天血液检查结果显示严重中性粒细胞减少( DOC组242例患者中有152例(62.8%)观察到<500 / mm 3 ,平均494 / mm 3 ),而FEC组(n = 43),中性粒细胞减少症是模棱两可的(平均1,741 / mm 3 )。在FEC组中,43名患者中有9名(20.9%),在DOC组中,242名患者中有27名(11.1%)经历了FN。在DOC组中,在逻辑回归模型中,第8天的中性粒细胞减少可预测FN(OR 0.79 [95%CI:0.655–0.952],p = 0.013)。在214名70岁以下的患者中,有190例(88.8%)患者完成了计划的化疗周期,并且四次接受最大剂量的G-CSF(150μg/人),而23名患者无法完成计划的化疗周期,但由于FN相关并发症而仅有5个。接受DOC治疗的患者应从相对较小的剂量开始,在较早的时间就接受G-CSF支持进行一级预防。

著录项

  • 期刊名称 PLoS Clinical Trials
  • 作者

    Yoshihiko Furuya;

  • 作者单位
  • 年(卷),期 2012(14),4
  • 年度 2012
  • 页码 e0215576
  • 总页数 12
  • 原文格式 PDF
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