西地尼布联合化疗治疗结直肠癌患者 207 种血清因子的预后/预测价值。

Prognostic/predictive value of 207 serum factors in colorectal cancer treated with cediranib and/or chemotherapy.

机构信息

Clinical Oncology, AstaZeneca, Macclesfield, UK.

出版信息

Br J Cancer. 2013 Nov 26;109(11):2765-73. doi: 10.1038/bjc.2013.649. Epub 2013 Oct 22.

Abstract

BACKGROUND

The prognostic and predictive value of multiple serum biomarkers was evaluated using samples from a randomised phase III study (HORIZON II) investigating chemotherapy with or without cediranib in metastatic colorectal cancer (mCRC).

METHODS

Baseline levels of 207 protein markers were measured in serum samples from 582 HORIZON II (FOLFOX/XELOX plus cediranib 20 mg (n=330) or placebo (n=252)) patients. Median baseline values of each biomarker were used to categorise patients as high or low. Markers were then assessed for their association with efficacy, defined by progression-free survival (PFS) and overall survival (OS). A generalised boosted regression model identified markers of particular interest.

RESULTS

Correlation of protein levels with PFS and OS suggested that multiple factors had a prognostic value, independent of treatment arm, including IL-6, IL-8, C-reactive protein (CRP), ICAM-1 and carcinoembryonic antigen (CEA). Among the angiogenesis regulators, low levels of vascular endothelial growth factor (VEGF), VEGF-D, VEGFR-1, VEGFR-3, NRP1 and Tie-2 correlated with better outcome.

CONCLUSION

This large data set generated using serum samples from mCRC patients treated with chemotherapy and VEGF inhibitors, defines baseline characteristics for 207 serum proteins. Multiple prognostic factors were identified that could be disease related or predict which patients derive most benefit from 5-fluorouracil (5-FU)-based chemotherapy, meriting further exploration in prospective studies.

摘要

背景

使用来自随机 III 期研究(HORIZON II)的样本评估了多种血清生物标志物的预后和预测价值,该研究调查了转移性结直肠癌(mCRC)中化疗联合或不联合 Cediranib 的效果。

方法

在 582 名 HORIZON II 患者(FOLFOX/XELOX 加 Cediranib 20 mg(n=330)或安慰剂(n=252))的血清样本中测量了 207 种蛋白质标志物的基线水平。每个生物标志物的中位数基线值用于将患者分为高或低。然后评估标志物与疗效的相关性,疗效定义为无进展生存期(PFS)和总生存期(OS)。广义增强回归模型确定了特别有意义的标志物。

结果

蛋白水平与 PFS 和 OS 的相关性表明,多种因素具有预后价值,与治疗臂无关,包括 IL-6、IL-8、C 反应蛋白(CRP)、ICAM-1 和癌胚抗原(CEA)。在血管生成调节剂中,低水平的血管内皮生长因子(VEGF)、VEGF-D、VEGFR-1、VEGFR-3、NRP1 和 Tie-2 与更好的结果相关。

结论

使用接受化疗和 VEGF 抑制剂治疗的 mCRC 患者的血清样本生成的这个大型数据集,定义了 207 种血清蛋白的基线特征。确定了多个预后因素,这些因素可能与疾病相关,或者预测哪些患者从基于 5-氟尿嘧啶(5-FU)的化疗中获益最大,值得在前瞻性研究中进一步探讨。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1bb/3844909/4f3d3261de21/bjc2013649f1.jpg

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