Leen E, Angerson W J, Warren H W, Goldberg J A, Sutherland G R, Cooke T G, McArdle C S
University Department of Surgery, Royal Infirmary, Glasgow, Scotland, UK.
Br J Cancer. 1993 Jun;67(6):1381-4. doi: 10.1038/bjc.1993.255.
Angiotensin II (AT-II) has been used to target regionally-administered cytotoxic microspheres in patients with intrahepatic tumours. The optimisation of vasoconstrictor targeting requires a knowledge of the blood flow changes induced by agents such as AT-II. We therefore assessed duplex/colour Doppler sonography (DCDS) as a means of evaluating the effects of AT-II infusion on hepatic arterial blood flow (HABF) and arterial resistance in patients with intrahepatic tumours. HABF was measured continuously in nine patients using DCDS before, during and after an infusion of AT-II (15 micrograms in 3 ml of saline over 90 s) via a hepatic artery catheter. In seven patients with less than 30% hepatic replacement by tumour, the baseline level of HABF was 331 +/- 85 ml min-1 (mean +/- s.d.), and this was reduced by 75-80% within 30 s of the start of AT-II infusion. HABF recovered rapidly from the end of the infusion, and increased by up to 20% above the baseline for approximately 2 min. In two patients with greater than 50% hepatic replacement, HABF showed no reduction but rose continuously from the start of AT-II infusion, increasing by a factor of 2-2.5 after 3-4 min. Arterial resistance showed reciprocal changes in all cases. We conclude that DCDS is effective in assessing the temporal changes in hepatic arterial blood flow caused by AT-II. In order to optimise tumour targeting, the injection of microspheres loaded with cytotoxic drugs should be completed before the end of the AT-II infusion. The targeting advantage of AT-II in patients with a high percentage hepatic replacement by tumour should be re-assessed.
血管紧张素II(AT-II)已被用于将局部给药的细胞毒性微球靶向肝内肿瘤患者。优化血管收缩剂靶向需要了解AT-II等药物引起的血流变化。因此,我们评估了双功/彩色多普勒超声(DCDS)作为评估AT-II输注对肝内肿瘤患者肝动脉血流(HABF)和动脉阻力影响的一种方法。通过肝动脉导管在9名患者中于输注AT-II(15微克溶于3毫升盐水中,在90秒内输注)之前、期间和之后使用DCDS连续测量HABF。在7名肿瘤肝替代率低于30%的患者中,HABF的基线水平为331±85毫升/分钟(平均值±标准差),在AT-II输注开始后30秒内降低了75 - 80%。HABF在输注结束后迅速恢复,并在约2分钟内比基线水平增加高达20%。在2名肿瘤肝替代率高于50%的患者中,HABF没有降低,而是从AT-II输注开始后持续上升,在3 - 4分钟后增加了2 - 2.5倍。在所有病例中动脉阻力都有相反的变化。我们得出结论,DCDS可有效评估AT-II引起的肝动脉血流的时间变化。为了优化肿瘤靶向,装载细胞毒性药物的微球注射应在AT-II输注结束前完成。AT-II在肿瘤肝替代率高的患者中的靶向优势应重新评估。