Hines-Peralta Andrew, Sukhatme Vikas, Regan Meredith, Signoretti Sabina, Liu Zheng-jun, Goldberg S Nahum
Laboratory for Minimally Invasive Tumor Therapy, Department of Radiology, Beth Israel Deaconess Medical Center, 1 Deaconess Rd, WCC 308B, Boston, MA 02215, USA.
Radiology. 2006 Jul;240(1):82-9. doi: 10.1148/radiol.2401050788. Epub 2006 May 23.
To assess the extent of tumor blood flow reduction that is achievable with arsenic trioxide (As2O3) and the effect of As2O3 on radiofrequency (RF)-induced coagulation.
All animal protocols and experiments were approved by an institutional animal care and use committee before the start of the study. Experiments were conducted in three tumor models: intrarenal VX2 sarcoma in 27 rabbits, RCC 786-0 human renal cell carcinoma in 24 nude mice, and R3230 mammary adenocarcinoma in 40 rats. One dose (0-7.5 mg per kilogram of body weight) of As2O3 was administered (intraperitoneally in rodents, intravenously in rabbits) 1, 6, or 24 hours before standardized RF ablation, which was performed by using a 1-cm active tip, with mean temperatures of 70 degrees C +/- 2 (standard deviation) for 5 minutes in rodents and 90 degrees C +/- 2 for 6 minutes in rabbits. Laser Doppler flowmetry was used to quantify changes in blood flow, which were compared with diameters of induced tumor coagulation. Comparisons between groups were performed by using Student t tests or analysis of variance. The strengths of correlations between As2O3, tumor blood flow, and RF-induced coagulation were assessed by using linear and higher-order regression models and reported as R2 computations.
Administration of As2O3 significantly (P < .05) reduced blood flow and increased tumor destruction in all tumor models. In VX2 sarcoma tumors, 1 mg/kg As2O3 reduced mean tumor blood flow to 46% +/- 13 of the normal value. The mean resultant coagulation (1.1 cm +/- 0.1) was significantly greater than that achieved with RF ablation alone (0.6 cm +/- 0.1, P < .01). In RCC 786-0 and R3230 tumors, 5 mg/kg As2O3 reduced mean tumor blood flow to 57% +/- 6 and 46% +/- 6 of normal, respectively, increasing mean ablation extent to 0.8 cm +/- 0.1 for both models, compared with those achieved with the control treatment (0.6 cm +/- 0.1 and 0.5 cm +/- 0.1, respectively; P < .05 for both comparisons). Dose studies revealed correlations between drug dose, tumor blood flow, and RF-induced coagulation in all three tumor models (R2 = 0.60-0.79). Maximal RF synergy was observed 1 hour after As2O3 administration.
As2O3 administration represents a transient noninvasive method of reducing tumor blood flow during RF ablation, enabling larger zones of tumor destruction in multiple tumor models.
评估三氧化二砷(As2O3)可实现的肿瘤血流减少程度以及As2O3对射频(RF)诱导凝固的影响。
所有动物实验方案和实验在研究开始前均经机构动物护理和使用委员会批准。实验在三种肿瘤模型中进行:27只兔的肾内VX2肉瘤、24只裸鼠的人肾细胞癌RCC 786 - 0以及40只大鼠的R3230乳腺腺癌。在标准化RF消融前1、6或24小时给予一剂(0 - 7.5毫克/千克体重)As2O3(在啮齿动物中腹腔注射,在兔中静脉注射),使用1厘米的活性尖端进行RF消融,在啮齿动物中平均温度为70℃±2(标准差)持续5分钟,在兔中为90℃±2持续6分钟。使用激光多普勒血流仪量化血流变化,并与诱导的肿瘤凝固直径进行比较。组间比较采用Student t检验或方差分析。使用线性和高阶回归模型评估As2O3、肿瘤血流和RF诱导凝固之间的相关性强度,并以R2计算结果报告。
在所有肿瘤模型中,给予As2O3均显著(P <.05)降低了血流并增加了肿瘤破坏。在VX2肉瘤肿瘤中,1毫克/千克As2O3将平均肿瘤血流降低至正常值的46%±13。平均产生的凝固(1.1厘米±0.1)显著大于单独RF消融所达到的(0.6厘米±0.1,P <.01)。在RCC 786 - 0和R3230肿瘤中,5毫克/千克As2O3分别将平均肿瘤血流降低至正常的57%±6和46%±6,与对照治疗相比,两种模型的平均消融范围均增加至0.8厘米±0.1(分别为0.6厘米±0.1和0.5厘米±0.1;两次比较P均<.05)。剂量研究揭示了在所有三种肿瘤模型中药物剂量、肿瘤血流和RF诱导凝固之间存在相关性(R2 = 0.60 - 0.79)。在给予As2O3后1小时观察到最大的RF协同作用。
给予As2O3是一种在RF消融期间减少肿瘤血流的短暂非侵入性方法,可在多种肿瘤模型中实现更大区域的肿瘤破坏。