抗血管内皮生长因子治疗损害结肠癌患者视网膜微循环内皮功能-一项观察性研究。

Manja Reimann, Gunnar Folprecht, Rocco Haase, Karolin Trautmann, Gerhard Ehninger, Heinz Reichmann, Focke Ziemssen, Tjalf Ziemssen
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引用次数: 15

摘要

背景:评估贝伐单抗(抗vegf治疗)对脑微血管和全身心血管调节的急性作用。设计和研究对象:连续20例结直肠癌患者(中位年龄:60.4岁,范围45.5-73.9岁)接受贝伐单抗静脉注射(5mg /kg)不耦合化疗。在贝伐单抗输注前和输注后24小时内,研究患者的视网膜内皮功能。进行了一系列3次24小时动态血压测量。视网膜内皮功能测定为闪烁光诱导的血管舒张。通过刺激运动检查了压力反射弧的完整性和自主心血管控制。结果:贝伐单抗治疗显著降低视网膜小动脉对闪烁光的血管扩张能力。贝伐单抗输注后观察到舒张压和心率略有下降,但这与视网膜功能的变化无关。贝伐单抗输注后,硝酸甘油的压力反应在很大程度上得以保留。在抗血管生成治疗下,夜间血压调节异常的患者比例增加。自主血压控制不受贝伐单抗治疗的影响。结论:贝伐单抗急性损害微血管功能独立于血压变化。视网膜微循环成像似乎是监测贝伐单抗药效学效果的宝贵工具。试验注册:NCT ID: NCT00740168。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Anti-Vascular endothelial growth factor therapy impairs endothelial function of retinal microcirculation in colon cancer patients - an observational study.

Anti-Vascular endothelial growth factor therapy impairs endothelial function of retinal microcirculation in colon cancer patients - an observational study.

Anti-Vascular endothelial growth factor therapy impairs endothelial function of retinal microcirculation in colon cancer patients - an observational study.

Anti-Vascular endothelial growth factor therapy impairs endothelial function of retinal microcirculation in colon cancer patients - an observational study.

Background: To assess acute effects of bevacizumab (anti-VEGF therapy) on cerebral microvessels and systemic cardiovascular regulation.

Design and subjects: 20 consecutive patients with colorectal cancer (median age: 60.4 years, range 45.5-73.9 years) received bevacizumab intravenously (5 mg/kg) uncoupled of chemotherapy. Prior to and within the first 24 hours after bevacizumab infusion, patients were investigated for retinal endothelial function. A series of a triple 24-hour ambulatory blood pressure measurement was conducted. Retinal endothelial function was determined as flicker light-induced vasodilation. The integrity of baroreflex arc and autonomic cardiovascular control was examined by stimulatory manoeuvres.

Results: Bevacizumab therapy significantly reduced the vasodilatory capacity of retinal arterioles in response to flicker light. A slight decrease in diastolic pressure and heart rate was observed after bevacizumab infusion but this was unrelated to changes in retinal function. The pressure response upon nitroglycerin was largely preserved after bevacizumab infusion. The proportion of patients with abnormal nocturnal blood pressure regulation increased under anti-angiogenic therapy. Autonomic blood pressure control was not affected by bevacizumab treatment.

Conclusions: Bevacizumab acutely impairs microvascular function independent of blood pressure changes. Imaging of the retinal microcirculation seems a valuable tool for monitoring pharmacodynamic effects of bevacizumab.

Trial registration: NCT ID: NCT00740168.

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