Department of Medical and Health Sciences, Faculty of Health Sciences, Linköping University, Sweden.
Eur J Cancer. 2013 Jan;49(1):115-20. doi: 10.1016/j.ejca.2012.07.032. Epub 2012 Aug 27.
The primary purpose of this study is to investigate if pretreatment plasma levels of vascular endothelial growth factor (VEGF) are predictive of the effect of celecoxib on survival in advanced non-small cell lung cancer (NSCLC) treated with palliative chemotherapy. A secondary objective is to describe the course of plasma VEGF levels during and after treatment with cytotoxic chemotherapy combined with celecoxib or placebo.
In a previously published double-blind multicenter phase III trial, 316 patients with NSCLC stage IIIB or IV and World Health Organisation (WHO) performance status 0-2 were randomised to receive celecoxib 400mg b.i.d. or placebo in combination with two-drug platinum-based chemotherapy. Chemotherapy cycle length was three weeks and planned duration of chemotherapy was four cycles. Celecoxib was given for a maximum of one year but was stopped earlier in case of disease progression or prohibitive toxicity. In a subset of patients, plasma VEGF levels were examined at onset of treatment and at 6, 12 and 20 weeks.
VEGF levels at start of treatment were obtained in 107 patients at four study sites. The median value was 70 pg/ml. Mean values declined during the first 12 weeks and then increased at 20 weeks. A subpopulation treatment effect pattern plot (STEPP) analysis showed an inverse relationship between initial plasma VEGF and the impact of celecoxib on survival with zero effect at 200 pg/ml. The effect on survival by celecoxib in the whole subset of patients was positive (hazard ratio (HR)=0.64 [confidence interval (CI) 0.43-0.95], p=0.028).
Low pretreatment plasma levels of VEGF appear to be predictive of a positive effect of celecoxib on survival.
本研究的主要目的是探讨血管内皮生长因子(VEGF)的预处理血浆水平是否可预测塞来昔布对姑息化疗治疗的晚期非小细胞肺癌(NSCLC)患者生存的影响。次要目的是描述联合使用细胞毒化疗药物和塞来昔布或安慰剂治疗期间和之后的血浆 VEGF 水平变化过程。
在一项先前发表的双盲多中心 III 期临床试验中,316 名 IIIB 或 IV 期 NSCLC 且世界卫生组织(WHO)体力状态 0-2 分的患者被随机分配接受塞来昔布 400mg,每日两次(b.i.d.)或安慰剂联合两药铂类为基础的化疗。化疗周期为 3 周,计划化疗 4 个周期。塞来昔布的使用最长为 1 年,但如果疾病进展或毒性不可耐受,会提前停药。在部分患者中,在治疗开始时以及治疗 6、12 和 20 周时检测血浆 VEGF 水平。
在 4 个研究地点,107 名患者获得了治疗开始时的 VEGF 水平。中位值为 70pg/ml。在最初的 12 周内,平均值下降,然后在 20 周时升高。亚组治疗效果模式图(STEPP)分析显示初始血浆 VEGF 与塞来昔布对生存的影响之间呈负相关,在 200pg/ml 时无影响。塞来昔布对整个患者亚组的生存影响为阳性(危险比(HR)=0.64[95%置信区间(CI)0.43-0.95],p=0.028)。
低预处理血浆 VEGF 水平似乎可预测塞来昔布对生存的积极影响。