首页> 外文期刊>Neuro-Oncology >Convection-enhanced delivery of a topoisomerase Ⅰ inhibitor (nanoliposomal topotecan) and a topoisomerase Ⅱ inhibitor (pegylated liposomal doxorubicin) in intracranial brain tumor xenografts
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Convection-enhanced delivery of a topoisomerase Ⅰ inhibitor (nanoliposomal topotecan) and a topoisomerase Ⅱ inhibitor (pegylated liposomal doxorubicin) in intracranial brain tumor xenografts

机译:对流增强颅内肿瘤异种移植中拓扑异构酶Ⅰ抑制剂(纳米脂质体拓扑替康)和拓扑异构酶Ⅱ抑制剂(聚乙二醇化脂质体阿霉素)的对流传递

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摘要

Despite multimodal treatment options, the response and survival rates for patients with malignant gliomas remain dismal. Clinical trials with convection-enhanced delivery (CED) have recently opened a new window in neuro-oncology to the direct delivery of chemotherapeu-tics to the CNS, circumventing the blood-brain barrier and reducing systemic side effects. Our previous CED studies with liposomal chemotherapeutics have shown promising antitumor activity in rodent brain tumor models. In this study, we evaluated a combination of nanoliposomal topotecan (nLs-TPT) and pegylated liposomal doxorubicin (PLD) to enhance efficacy in our brain tumor models, and to establish a CED treatment capable of improving survival from malignant brain tumors. Both liposomal drugs decreased key enzymes involved in tumor cell replication in vitro. Synergistic effects of nLs-TPT and PLD on U87MG cell death were found. The combination displayed excellent efficacy in a CED-based survival study 10 days after tumor cell implantation. Animals in the control group and those in single-agent groups had a median survival of less than 30 days, whereas the combination group experienced a median survival of more than 90 days. We conclude that CED of two liposomal chemotherapeutics (nLs-TPT and PLD) may be an effective treatment option for malignant glio-mas.
机译:尽管有多种模式的治疗选择,恶性神经胶质瘤患者的反应和生存率仍然令人沮丧。对流增强递送(CED)的临床试验最近在神经肿瘤学领域打开了一个新的窗口,可以将化学治疗药物直接递送至CNS,从而规避了血脑屏障并减少了全身性副作用。我们之前使用脂质体化学治疗剂进行的CED研究表明,在啮齿动物脑肿瘤模型中,抗肿瘤活性很有希望。在这项研究中,我们评估了纳米脂质体拓扑替康(nLs-TPT)和聚乙二醇化脂质体阿霉素(PLD)的组合,以增强我们在脑肿瘤模型中的功效,并建立了能够改善恶性脑肿瘤生存的CED治疗。两种脂质体药物均降低了体外参与肿瘤细胞复制的关键酶。发现nLs-TPT和PLD对U87MG细胞死亡具有协同作用。肿瘤细胞植入后10天,该组合在基于CED的生存研究中显示出优异的疗效。对照组和单药组动物的中位生存期少于30天,而联合组动物的中位生存期则超过90天。我们得出结论,两种脂质体化学疗法(nLs-TPT和PLD)的CED可能是恶性神经胶质瘤的有效治疗选择。

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