David Geffen School of Medicine at UCLA, Santa Monica, CA 90404, USA.
Clin Colorectal Cancer. 2010 Apr;9(2):95-101. doi: 10.3816/CCC.2010.n.013.
Adding irinotecan and/or oxaliplatin to every-2-week 5-fluorouracil (5-FU)/leucovorin (LV) prolongs survival in patients with colorectal cancer (CRC) but increases neutropenia frequency. Pegfilgrastim is indicated to decrease infection as manifested by febrile neutropenia (FN) in patients receiving chemotherapy at > 14-day intervals. This randomized, placebo-controlled phase II study examined pegfilgrastim efficacy and safety in patients with CRC receiving every-2-week chemotherapy.
Patients with CRC were randomized 1:1 to pegfilgrastim 6 mg or placebo administered per-cycle on day 4. Randomization was stratified by chemotherapy regimen (patients received every-2-week FOLFOX4 [5-FU/LV/oxaliplatin], FOLFIRI [5-FU/LV/irinotecan], or FOIL [5-FU/LV/oxaliplatin/irinotecan] at physician discretion). The primary endpoint was incidence of grade 3/4 neutropenia. Secondary endpoints included incidence of grade 3/4 FN and adverse events. After 4 cycles of study treatment, progression-free survival (PFS) and overall survival (OS) were followed for <or= 2 years in long-term follow-up.
Of 241 eligible patients analyzed, 118 were in the placebo and 123 in the pegfilgrastim group. In the treatment period, the odds ratio for grade 3/4 neutropenia for pegfilgrastim versus placebo was 0.19 (95% CI, 0.10-0.37; P < .001); grade 3/4 FN incidence was also significantly lower in pegfilgrastim-treated patients (2%) compared with placebo-treated patients (8%; P = .04). Pegfilgrastim was well tolerated, with leukocyte counts remaining stable during cycles 2-4. In long-term follow-up, both treatment groups had similar PFS and OS.
Pegfilgrastim was well tolerated in patients with CRC receiving every-2-week chemotherapy and significantly reduced neutropenia and FN compared with placebo, though FN was uncommon in both treatment groups. Results suggest that pegfilgrastim administration is feasible in CRC patients receiving every-2-week chemotherapy.
在每 2 周接受氟尿嘧啶(5-FU)/亚叶酸钙(LV)治疗的基础上添加伊立替康和/或奥沙利铂可延长结直肠癌(CRC)患者的生存时间,但会增加中性粒细胞减少症的频率。培非格司亭被批准用于降低接受化疗间隔> 14 天的患者因发热性中性粒细胞减少症(FN)而表现出的感染。这项随机、安慰剂对照的 II 期研究检查了培非格司亭在每 2 周接受化疗的 CRC 患者中的疗效和安全性。
CRC 患者以 1:1 的比例随机分配至培非格司亭 6mg 或安慰剂,每周期在第 4 天给药。随机化按化疗方案分层(患者根据医生的判断接受每 2 周的 FOLFOX4[5-FU/LV/奥沙利铂]、FOLFIRI[5-FU/LV/伊立替康]或 FOIL[5-FU/LV/奥沙利铂/伊立替康])。主要终点是 3/4 级中性粒细胞减少症的发生率。次要终点包括 3/4 级 FN 的发生率和不良事件。在研究治疗的 4 个周期后,在长期随访中对无进展生存期(PFS)和总生存期(OS)进行了<或=2 年的随访。
在分析的 241 名合格患者中,118 名患者接受安慰剂治疗,123 名患者接受培非格司亭治疗。在治疗期间,培非格司亭与安慰剂相比,3/4 级中性粒细胞减少症的优势比为 0.19(95%CI,0.10-0.37;P<0.001);培非格司亭治疗组 3/4 级 FN 的发生率也明显低于安慰剂治疗组(2%比 8%;P=0.04)。培非格司亭耐受性良好,白细胞计数在第 2-4 周期保持稳定。在长期随访中,两组的 PFS 和 OS 相似。
培非格司亭在接受每 2 周化疗的 CRC 患者中耐受良好,与安慰剂相比,显著降低了中性粒细胞减少症和 FN 的发生率,但两组的 FN 均不常见。结果表明,培非格司亭在接受每 2 周化疗的 CRC 患者中是可行的。