Cancer Institute (Key Laboratory of Cancer Prevention and Intervention, China National Ministry of Education), The Second Affiliated Hospital, School of Medicine, Zhejiang University, 88 Jiefang Road, Hangzhou, Zhejiang Province 310009, China.
Cancer Lett. 2011 Dec 15;312(1):109-16. doi: 10.1016/j.canlet.2011.08.008. Epub 2011 Aug 16.
Vascular-targeting agents (VTAs) can be divided into two groups: anti-angiogenesis agents and vascular disrupting agents (VDAs). The purpose of this study was to evaluate the antineoplastic activity of a combination of the anti-angiogenesis agent, Endostar, and the VDA combretastatin, A4 phosphate (CA4P). This study is the first to evaluate the activity of this combination against tumors and the first to investigate the activity of the combination against osteosarcoma. Endostar combined with CA4P had a good anti-tumor effect with no significant toxicity, and was at least not inferior to adriamycin, which is the main drug for osteosarcoma. The use of VDAs combined with anti-angiogenic drugs can result in significantly enhanced anti-tumor effects, providing a novel approach to cancer treatment, which could effectively complement standard treatments. It is believed that this exciting new treatment has the potential to transform the management of cancer.
血管靶向药物(VTAs)可分为两类:抗血管生成药物和血管破坏药物(VDAs)。本研究旨在评估血管生成抑制剂恩度与 VDA 康普瑞丁磷酸二钠(CA4P)联合的抗肿瘤活性。本研究首次评估了该联合方案对肿瘤的活性,也是首次研究该联合方案对骨肉瘤的活性。恩度联合 CA4P 具有良好的抗肿瘤作用,且毒性不明显,至少不逊于骨肉瘤的主要药物阿霉素。VDAs 联合抗血管生成药物的使用可显著增强抗肿瘤作用,为癌症治疗提供了一种新方法,可有效补充标准治疗。人们相信,这种令人兴奋的新疗法有可能改变癌症的治疗管理。