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评估生物抗血管生成疗法的体内疗效。

Assessing the in vivo efficacy of biologic antiangiogenic therapies.

机构信息

Norris Comprehensive Cancer Center, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.

出版信息

Cancer Chemother Pharmacol. 2013 Jan;71(1):1-12. doi: 10.1007/s00280-012-1978-8. Epub 2012 Oct 9.

Abstract

PURPOSE

To review key clinical issues underlying the assessment of in vivo efficacy when using antiangiogenic therapies for cancer treatment.

METHODS

Literature relevant to use of antiangiogenic therapies in cancer was reviewed, with particular emphasis on the assessment of in vivo efficacy of these agents, as well as additional angiogenic factors that could play a role in escape from angiogenesis inhibition.

RESULTS

In order to grow and metastasize, tumors need to continually acquire new blood supplies; therefore, therapeutic inhibition of angiogenesis has become a component of anticancer treatment for many tumor types. Bevacizumab, a humanized monoclonal antibody directed at vascular endothelial growth factor A (VEGF-A), has shown activity in combination with chemotherapy in metastatic colorectal cancer. Nevertheless, the use of antiangiogenic therapies remains suboptimal; specifically, optimal dose, duration of therapy, and combination of agents remain unknown. Also, at present, it is not possible to determine which patients are most likely to respond to a given form of antiangiogenic therapy. There has been increased recognition of alternative pathways possibly associated with disease progression in patients undergoing antiangiogenic therapy targeted at VEGF-A. Multiligand-targeted antiangiogenic therapies, such as ziv-aflibercept (formerly known as aflibercept, VEGF Trap), are currently undergoing clinical evaluation. Ziv-aflibercept forms monomeric complexes with VEGF-A, VEGF-B, and PlGF, which have a long half-life, allowing optimization of ziv-aflibercept doses and angiogenic blockage.

CONCLUSIONS

Although antiangiogenic therapies have increased treatment options for cancer patients, their use is limited by a lack of established and standardized methodology to evaluate their efficacy in vivo. Circulating endothelial cells, hypertension, and several molecular and imaging-based markers have potential for use as biomarkers in these patients and may better define appropriate patient populations.

摘要

目的

综述癌症抗血管生成治疗中体内疗效评估所涉及的关键临床问题。

方法

对癌症抗血管生成治疗的相关文献进行了回顾,特别强调了这些药物体内疗效评估,以及可能在抗血管生成抑制作用中发挥作用的其他血管生成因子。

结果

为了生长和转移,肿瘤需要不断获得新的血液供应;因此,治疗性抑制血管生成已成为许多肿瘤类型抗癌治疗的一部分。贝伐单抗是一种针对血管内皮生长因子 A(VEGF-A)的人源化单克隆抗体,已显示与化疗联合应用于转移性结直肠癌的疗效。然而,抗血管生成治疗的应用仍不理想;具体来说,最佳剂量、治疗持续时间和联合用药仍不清楚。此外,目前尚无法确定哪些患者最有可能对某种形式的抗血管生成治疗有反应。人们越来越认识到,在接受针对 VEGF-A 的抗血管生成治疗的患者中,可能存在与疾病进展相关的替代途径。多配体靶向抗血管生成治疗,如 ziv-aflibercept(以前称为 aflibercept,VEGF Trap),目前正在进行临床评估。Ziv-aflibercept 与 VEGF-A、VEGF-B 和 PlGF 形成单体复合物,半衰期长,可优化 ziv-aflibercept 剂量和血管生成阻断。

结论

尽管抗血管生成治疗为癌症患者提供了更多的治疗选择,但由于缺乏评估其体内疗效的既定和标准化方法,其应用受到限制。循环内皮细胞、高血压和几种分子和基于成像的标志物有可能作为这些患者的生物标志物,并且可以更好地定义合适的患者人群。

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