Department of Surgery, Saiseikai Osaka Nakatsu Hospital, Osaka, Japan.
PLoS One. 2019 Apr 18;14(4):e0215576. doi: 10.1371/journal.pone.0215576. eCollection 2019.
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.
大多数化疗方案会导致中性粒细胞减少症的最低点出现在第 10 天至第 14 天之间,而粒细胞集落刺激因子(G-CSF)的给药依赖于这个时间点。在多西紫杉醇(DOC)为基础的化疗中,发热性中性粒细胞减少症(FN)的频率和给予的 G-CSF 剂量在研究之间差异很大。我们的研究目标是通过比较第 8 天的中性粒细胞减少症与中性粒细胞池内的潜在变化,预测 G-CSF 的必要剂量。我们对 242 名接受辅助性 DOC 为基础的化疗的早期乳腺癌患者(DOC 组)和 43 名接受 FEC 化疗的患者(FEC 组)进行了回顾性观察分析。符合条件的患者为第 1 周期接受标准剂量且在第 8 天进行血液检查的患者。在 DOC 组中,患者常规在第 3 天给予预防性 G-CSF(150μg/体)给药,并根据第 8 天的血液检查结果给予额外的 G-CSF。第 8 天的血液检查结果显示,242 名患者中有 152 名(62.8%)患者出现严重中性粒细胞减少症(<500/mm3,平均 494/mm3),而在 FEC 组(n=43)中,中性粒细胞减少症不明确(平均 1741/mm3)。在 FEC 组中,9 名患者(20.9%)和在 DOC 组中,27 名患者(11.1%)发生 FN。在 logistic 回归模型中,DOC 组第 8 天的中性粒细胞减少症是 FN 的预测因素(OR 0.79[95%CI:0.655-0.952],p=0.013)。在 214 名年龄在 70 岁以下的患者中,190 名(88.8%)患者完成了计划的化疗周期,同时接受了最大剂量的 G-CSF(150μg/体)四次,而 23 名患者无法完成计划的化疗周期,但只有 5 名患者因 FN 相关并发症而无法完成。接受 DOC 治疗的患者应在更早的时间开始用相对较小的剂量进行 G-CSF 支持的一级预防治疗。