Linot B, Augereau P, Breheret R, Laccourreye L, Capitain O
Oncopharmacology-Pharmacogenetics Department, Institut de Cancérologie de l'Ouest Nantes-Angers, 2 rue Moll, 49033, Angers Cedex, France,
Support Care Cancer. 2014 Oct;22(10):2831-7. doi: 10.1007/s00520-014-2270-8. Epub 2014 May 13.
Induction chemotherapy with docetaxel-cisplatin and 5-fluorouracil (DCF) for locally advanced head and neck cancers (HNC) is associated with a high risk of severe neutropenia or febrile neutropenia (FN). We conducted a retrospective study to evaluate the efficacy and safety of administering granulocyte colony-stimulating factor (G-CSF) on day 3 (D3) during chemotherapy (early G-CSF stimulation) versus after the end of chemotherapy, as per current guidelines (i.e., after the end of 5-FU perfusion; D7), and its impact on patient outcomes.
Patients ≥19 years old, with advanced HNC who received DCF induction chemotherapy (D and P 75 mg per meter squared (mg/m(2)) on day 1 and 5-FU 750 mg/m(2)/day from D1 to D5), were included in the analysis.
Data of 70 patients were analyzed from 01 January 2003 to 01 December 2010. Mean age was 56 years (range 45 to 77 years). Thirty-six patients (51.4 %) received pegfilgrastim on D7, and 28 (40 %) started G-CSF prophylaxis during chemotherapy; 12 (17.1 %) had daily filgrastim and 16 (22.9 %) pegfilgrastim on D3. Overall response rate (ORR) was 89.6 % (three early deaths due to infectious complications; 4.3 %). The 3-year overall survival (OS) rate was 72.8 %. FN rate was 14.3 % and chemotherapy delay was 12.9 %. In the D7 G-CSF arm, incidence of grade 3-4 neutropenia (p = 0.023), FN (p = 0.029), and cycle delays (p = 0.006) was statistically higher than the "early" G-CSF arm. A decrease of OS was observed at 2 years (from 85.1 to 63.5 %) of chemotherapy discontinuation or FN (p = 0.0348).
Early administration of G-CSF is safe and seems to be more effective than D7. Future prospective trials are required to confirm our results.
多西他赛-顺铂联合5-氟尿嘧啶(DCF)诱导化疗用于局部晚期头颈癌(HNC)时,严重中性粒细胞减少或发热性中性粒细胞减少(FN)风险较高。我们进行了一项回顾性研究,以评估在化疗第3天(D3)(早期G-CSF刺激)与按照当前指南在化疗结束后(即5-氟尿嘧啶灌注结束后;D7)给予粒细胞集落刺激因子(G-CSF)的疗效和安全性,及其对患者预后的影响。
纳入年龄≥19岁、接受DCF诱导化疗(第1天多西他赛和顺铂75毫克每平方米(mg/m²),第1天至第5天5-氟尿嘧啶750 mg/m²/天)的晚期HNC患者进行分析。
分析了2003年1月1日至2010年12月1日70例患者的数据。平均年龄56岁(范围45至77岁)。36例患者(51.4%)在D7接受培非格司亭治疗,28例(40%)在化疗期间开始G-CSF预防;12例(17.1%)在D3接受每日非格司亭治疗,16例(22.9%)在D3接受培非格司亭治疗。总体缓解率(ORR)为89.6%(3例因感染并发症早期死亡;4.3%)。3年总生存率(OS)为72.8%。FN发生率为14.3%,化疗延迟率为12.9%。在D7 G-CSF组,3-4级中性粒细胞减少(p = 0.023)、FN(p = 0.029)和周期延迟(p = 0.006)的发生率在统计学上高于“早期”G-CSF组。在化疗中断或FN发生2年时观察到OS下降(从85.1%降至63.5%)(p = 0.0348)。
早期给予G-CSF是安全的,且似乎比D7更有效。需要未来的前瞻性试验来证实我们的结果。