Vincenzi Bruno, Santini Daniele, Russo Antonio, Gavasci Michele, Battistoni Fabrizio, Dicuonzo Giordano, Rocci Laura, Rosaria Valerio Maria, Gebbia Nicola, Tonini Giuseppe
University Campus Bio-Medico, Medical Oncology, Via Emilio Longoni, 69, 00155, Rome, Italy.
Pharmacogenomics. 2007 Apr;8(4):319-27. doi: 10.2217/14622416.8.4.319.
We designed this trial to investigate if modifications in levels of circulating vascular endothelial growth factor (VEGF) may be related to clinical response and outcome in advanced colorectal cancer patients during treatment with a weekly combination of cetuximab plus irinotecan.
A total of 45 heavily pretreated metastatic colorectal cancer patients were prospectively evaluated for circulating levels of VEGF during the treatment with cetuximab plus weekly irinotecan. VEGF circulating levels were assessed at the following time points: just before and at 1, 21, 50 and 92 days after the start of cetuximab plus irinotecan treatment.
Basal VEGF median levels were significantly decreased just 1 day after the first anticancer infusion (p = 0.016) and reached the highest statistical significance 92 days after the first infusion (p < 0.0001). A total of 22 patients showed a reduction in median VEGF circulating levels of at least 50% 92 days after the first infusion with respect to the basal time point. For patients with at least a 50% reduction in VEGF levels, the response rate was 45.5% compared with 8.7% in the nonreduced VEGF group (p = 0.014). The median time to progression was 6 months in the reduced VEGF group versus 3.9 months in the other patients (p < 0.0001). In addition, overall survival was longer in patients with VEGF reduction (11.0 months) than in patients without (9.6 months; p = 0.01).
These data represent the first evidence that suggests a role of VEGF reduction in the prediction of efficacy of treatment with cetuximab plus weekly irinotecan in heavily pretreated advanced colorectal cancer patients.
我们设计了这项试验,以研究循环血管内皮生长因子(VEGF)水平的变化是否可能与晚期结直肠癌患者在接受西妥昔单抗联合伊立替康每周治疗期间的临床反应及预后相关。
共有45例经过多次预处理的转移性结直肠癌患者在接受西妥昔单抗联合每周一次伊立替康治疗期间,对其VEGF的循环水平进行了前瞻性评估。在以下时间点评估VEGF的循环水平:在开始西妥昔单抗联合伊立替康治疗前、治疗开始后1天、21天、50天和92天。
首次抗癌输注后仅1天,基础VEGF中位水平即显著下降(p = 0.016),并在首次输注后92天达到最高统计学显著性(p < 0.0001)。共有22例患者在首次输注后92天,其VEGF循环中位水平相对于基础时间点至少降低了50%。对于VEGF水平至少降低50%的患者,缓解率为45.5%,而VEGF水平未降低组为8.7%(p = 0.014)。VEGF水平降低组的中位疾病进展时间为6个月,而其他患者为3.9个月(p < 0.0001)。此外,VEGF水平降低的患者总生存期(11.0个月)比未降低的患者(9.6个月;p = 0.01)更长。
这些数据首次表明,VEGF水平降低在预测西妥昔单抗联合每周一次伊立替康治疗重度预处理晚期结直肠癌患者的疗效中具有一定作用。