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将血管紧张素II用作靶向肝内肿瘤患者细胞毒性微球的一种潜在方法。

The use of angiotensin II as a potential method of targeting cytotoxic microspheres in patients with intrahepatic tumour.

作者信息

Goldberg J A, Murray T, Kerr D J, Willmott N, Bessent R G, McKillop J H, McArdle C S

机构信息

University Department of Surgery, Royal Infirmary, Glasgow, UK.

出版信息

Br J Cancer. 1991 Feb;63(2):308-10. doi: 10.1038/bjc.1991.71.

Abstract

Cytotoxic microspheres have been developed for intra-arterial use in patients with liver metastases. Following injection, the distribution of microspheres reflects the pattern of hepatic arterial blood-flow. Vasoactive agents, such as angiotensin II, by producing vasoconstriction in normal liver, might divert arterial blood toward tumour and thereby enhance the delivery of drug-loaded particles. Using a double isotope technique, the distribution of radiolabelled microspheres to tumour and normal liver tissue was measured before and after angiotensin II infusion in nine patients with multiple liver metastases. The median increase in tumour: normal ratio following angiotensin II infusion was by a factor of 2.8 (range 0.8-11.7, P less than 0.05). This novel approach to regional chemotherapy, using a combination of angiotensin II infusion and cytotoxic microspheres, increases the exposure of tumour to cytotoxic agents and may, therefore, enhance tumour response rates.

摘要

细胞毒性微球已被开发用于肝转移患者的动脉内给药。注射后,微球的分布反映了肝动脉血流模式。血管活性药物,如血管紧张素II,通过在正常肝脏中引起血管收缩,可能会使动脉血流向肿瘤,从而增强载药颗粒的递送。采用双同位素技术,在9例多发肝转移患者中,测量了血管紧张素II输注前后放射性标记微球在肿瘤和正常肝组织中的分布。血管紧张素II输注后肿瘤与正常组织比值的中位数增加了2.8倍(范围为0.8 - 11.7,P < 0.05)。这种将血管紧张素II输注与细胞毒性微球相结合的新型区域化疗方法,增加了肿瘤对细胞毒性药物的暴露,因此可能提高肿瘤反应率。

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