Rocconi Rodney P, Numnum Michael T, Zhu Zeng B, Lu Baogen, Wang Minghui, Rivera Angel A, Stoff-Khalili Mariam, Alvarez Ronald D, Curiel David T, Makhija Sharmila
Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, University of Alabama at Birmingham, 618 20th Street South, Old Hillman Building-Room 538, Birmingham, AL 35249-7333, USA.
Gynecol Oncol. 2006 Dec;103(3):985-9. doi: 10.1016/j.ygyno.2006.06.005. Epub 2006 Jul 20.
Icodextrin, a novel glucose polymer solution utilized for peritoneal dialysis, has been demonstrated to have prolonged intraperitoneal (IP) instillation volumes in comparison to standard PBS solutions. In an animal model of ovarian cancer, we explored whether a survival advantage exists utilizing icodextrin rather than PBS as a delivery solution for an infectivity enhanced virotherapy approach.
Initial experiments evaluated whether icodextrin would adversely affect replication of a clinical grade infectivity enhanced conditionally replicative adenovirus (Delta24-RGD). Virus was added to prepared blinded solutions of PBS or icodextrin (20%) and then evaluated in vitro in various human ovarian cancer cell lines (SKOV3.ip1, PA-1, and Hey) and in vivo in a SKOV3.ip1 human ovarian cancer IP murine model. Viral replication was measured by detecting adenovirus E4 gene levels utilizing QRT-PCR. Survival was subsequently evaluated in a separate SKOV3.ip1 ovarian cancer IP murine model. Cohorts of mice were treated in blinded fashion with PBS alone, icodextrin alone, PBS+Delta24-RGD, or icodextrin+Delta24-RGD. Survival data were plotted on Kaplan-Meier curve and statistical calculations performed using the log-rank test.
There was no adverse affect of icodextrin on vector replication in the ovarian cancer cell lines nor murine model tumor samples evaluated. Median survival in the IP treated animal cohorts was 23 days for the PBS group, 40 days for the icodextrin group, 65 days for the PBS+Delta24-RGD group, and 105 days for icodextrin+Delta24-RGD (p=0.023). Of note, 5 of the 10 mice in the icodextrin+Delta24-RGD group were alive at the end of the study period, all without evidence of tumor (120 days).
These experiments suggest that the use of dialysates such as icodextrin may further enhance the therapeutic effects of novel IP virotherapy and other gene therapy strategies for ovarian cancer. Phase I studies utilizing icodextrin-based virotherapy for ovarian cancer are currently in development.
艾考糊精是一种用于腹膜透析的新型葡萄糖聚合物溶液,与标准的磷酸盐缓冲盐水(PBS)溶液相比,已被证明具有更长的腹腔内(IP)灌注量。在卵巢癌动物模型中,我们探究了在感染性增强的病毒疗法中,使用艾考糊精而非PBS作为递送溶液是否存在生存优势。
初始实验评估了艾考糊精是否会对临床级感染性增强的条件性复制腺病毒(Delta24-RGD)的复制产生不利影响。将病毒添加到制备好的PBS或艾考糊精(20%)的盲法溶液中,然后在各种人卵巢癌细胞系(SKOV3.ip1、PA-1和Hey)中进行体外评估,并在SKOV3.ip1人卵巢癌IP小鼠模型中进行体内评估。通过使用实时定量聚合酶链反应(QRT-PCR)检测腺病毒E4基因水平来测量病毒复制。随后在另一个SKOV3.ip1卵巢癌IP小鼠模型中评估生存情况。将小鼠队列以盲法分别用单独的PBS、单独的艾考糊精、PBS+Delta24-RGD或艾考糊精+Delta24-RGD进行治疗。将生存数据绘制在Kaplan-Meier曲线上,并使用对数秩检验进行统计计算。
在所评估的卵巢癌细胞系和小鼠模型肿瘤样本中,艾考糊精对载体复制没有不利影响。IP治疗动物队列中,PBS组的中位生存期为23天,艾考糊精组为40天,PBS+Delta24-RGD组为65天,艾考糊精+Delta24-RGD组为105天(p=0.023)。值得注意的是,在研究期结束时,艾考糊精+Delta24-RGD组的10只小鼠中有5只存活,均无肿瘤证据(120天)。
这些实验表明,使用诸如艾考糊精之类的透析液可能会进一步增强新型IP病毒疗法及其他卵巢癌基因治疗策略的治疗效果。目前正在开展利用基于艾考糊精的病毒疗法治疗卵巢癌的I期研究。