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在临床肿瘤学中,用于血管生成和抗血管生成药物的生物标志物。

Biomarkers for angiogenesis and antiangiogenic drugs in clinical oncology.

机构信息

Laboratory of Hematology-Oncology, European Institute of Oncology, via Ripamonti 435, Milan, Italy.

出版信息

Breast. 2009 Oct;18 Suppl 3:S48-50. doi: 10.1016/S0960-9776(09)70272-3.

Abstract

AIMS

The clinical use of anti-angiogenic drugs, alone or in combination with other drugs, is increasing in medical oncology. However, identifying the best suited drug and the optimal dosage and schedule for treatment of patients remain challenging.

METHODS AND RESULTS

We reviewed data about surrogate biomarkers of angiogenesis and anti-angiogenic drug activity currently available in the literature. Circulating endothelial cells (CECs) and circulating endothelial progenitors (CEPs) have been found to have some predictive potential in some clinical trials involving advanced breast cancer patients. Molecular surrogate markers, on the other hand, are more scanty at the present time, because the identification of truly endothelial-cell-restricted genes and/or antigens has been so far more elusive.

CONCLUSION

The search and validation of new biomarkers for angiogenesis and anti-angiogenic drug activity have many biological, technical and clinical facets which render this task particularly complex. An accurate planning of biomarker search and validation throughout future clinical studies is highly warranted.

摘要

目的

抗血管生成药物在肿瘤医学中的临床应用正在增加,无论是单独使用还是与其他药物联合使用。然而,确定最适合的药物以及治疗患者的最佳剂量和方案仍然具有挑战性。

方法和结果

我们回顾了目前文献中关于血管生成和抗血管生成药物活性的替代生物标志物的数据。循环内皮细胞(CEC)和循环内皮祖细胞(CEP)在一些涉及晚期乳腺癌患者的临床试验中具有一定的预测潜力。另一方面,分子替代标志物目前还比较匮乏,因为迄今为止,真正的内皮细胞特异性基因和/或抗原的鉴定更加困难。

结论

对血管生成和抗血管生成药物活性的新生物标志物的研究和验证具有许多生物学、技术和临床方面,这使得这项任务特别复杂。在未来的临床研究中,非常有必要对生物标志物的研究和验证进行精确的规划。

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