Laboratory for Minimally Invasive Tumor Therapies, Department of Radiology, Beth Israel Deaconess Medical Center/Harvard Medical School, Boston, MA 02215, USA.
J Control Release. 2012 Jun 10;160(2):239-44. doi: 10.1016/j.jconrel.2011.12.031. Epub 2011 Dec 30.
To investigate the effect of IV liposomal quercetin (a known down-regulator of heat shock proteins) alone and with liposomal doxorubicin on tumor growth and end-point survival when combined with radiofrequency (RF) tumor ablation in a rat tumor model.
Solitary subcutaneous R3230 mammary adenocarcinoma tumors (1.3-1.5 cm) were implanted in 48 female Fischer rats. Initially, 32 tumors (n=8, each group) were randomized into four experimental groups: (a) conventional monopolar RF alone (70°C for 5 min), (b) IV liposomal quercetin alone (1 mg/kg), (c) IV liposomal quercetin followed 24hr later with RF, and (d) no treatment. Next, 16 additional tumors were randomized into two groups (n=8, each) that received a combined RF and liposomal doxorubicin (15 min post-RF, 8 mg/kg) either with or without liposomal quercetin. Kaplan-Meier survival analysis was performed using a tumor diameter of 3.0 cm as the defined survival endpoint.
Differences in endpoint survival and tumor doubling time among the groups were highly significant (P<0.001). Endpoint survivals were 12.5±2.2 days for the control group, 16.6±2.9 days for tumors treated with RF alone, 15.5±2.1 days for tumors treated with liposomal quercetin alone, and 22.0±3.9 days with combined RF and quercetin. Additionally, combination quercetin/RF/doxorubicin therapy resulted in the longest survival (48.3±20.4 days), followed by RF/doxorubicin (29.9±3.8 days).
IV liposomal quercetin in combination with RF ablation reduces tumor growth rates and improves animal endpoint survival. Further increases in endpoint survival can be seen by adding an additional anti-tumor adjuvant agent liposomal doxorubicin. This suggests that targeting several post-ablation processes with multi-drug nanotherapies can increase overall ablation efficacy.
为了研究 IV 脂质体槲皮素(一种已知的热休克蛋白下调剂)单独使用以及与脂质体阿霉素联合应用于射频(RF)肿瘤消融治疗大鼠肿瘤模型时对肿瘤生长和终点生存的影响。
在 48 只雌性 Fischer 大鼠中植入 1.3-1.5cm 的单一皮下 R3230 乳腺腺癌肿瘤。最初,32 个肿瘤(n=8,每组)随机分为四个实验组:(a)单独使用传统的单极 RF(70°C 持续 5 分钟),(b)IV 脂质体槲皮素(1mg/kg),(c)IV 脂质体槲皮素后 24 小时后加用 RF,(d)无治疗。然后,另外 16 个肿瘤随机分为两组(n=8,每组),在 RF 后 15 分钟给予 RF 和脂质体阿霉素(8mg/kg),并分别给予或不给予脂质体槲皮素。使用肿瘤直径为 3.0cm 作为定义的生存终点进行 Kaplan-Meier 生存分析。
各组终点生存和肿瘤倍增时间的差异具有高度显著性(P<0.001)。对照组的终点生存率为 12.5±2.2 天,单独使用 RF 治疗的肿瘤为 16.6±2.9 天,单独使用脂质体槲皮素治疗的肿瘤为 15.5±2.1 天,联合使用 RF 和槲皮素的肿瘤为 22.0±3.9 天。此外,联合使用槲皮素/RF/阿霉素治疗的肿瘤生存时间最长(48.3±20.4 天),其次是 RF/阿霉素(29.9±3.8 天)。
IV 脂质体槲皮素联合 RF 消融可降低肿瘤生长速度并提高动物终点生存率。通过添加额外的抗肿瘤佐剂脂质体阿霉素,可以进一步提高终点生存率。这表明,使用多药物纳米疗法靶向多个消融后过程可以提高整体消融效果。