Hall Walter A, Sherr Gregory T
Department of Neurosurgery, University of Minnesota Medical School, MMC 96, 420 Delaware Street SE, Minneapolis, MN 55455, USA.
Expert Opin Drug Deliv. 2006 May;3(3):371-7. doi: 10.1517/17425247.3.3.371.
Malignant gliomas represent a difficult treatment challenge for the neuro-oncologist and the neurosurgeon. These tumours continue to be refractory to standard therapies, such as surgery, radiotherapy and conventional chemotherapy, and new therapeutic options are clearly needed. Therefore, investigators have recently taken a new direction and started to engineer compounds such as recombinant cytotoxins, antiangiogenesis factors and genetic delivery vectors. However, these promising new agents are all dependent on an effective distribution method in order to bypass the blood-brain barrier. Convection-enhanced delivery (CED) allows for the administration of targeted toxins and other agents directly into the brain at the site of a tumour via catheters placed with the aid of stereotactic or image-guided surgery. The use of this technique is gaining momentum as a newly accepted treatment modality where little else has produced durable results in the fight against gliomas. Direct intratumoural infusion was first performed in nude mouse flank tumour models of human malignant glioma. After significant testing in preclinical animal studies, this method of delivery was followed by the successful demonstration of in vivo efficacy in Phase I and II clinical trials. Currently, this technique is being used in the investigational setting at academic medical centres where investigators are starting to define the best practice for CED. Fundamental issues in this method of delivery such as rate of infusion, cannula size, infusate concentration and tissue-cannula sealing time shape the current discussion in the literature. Targeted toxin therapy represents one of the newest and most promising treatments for this unfortunate patient population, with proven clinical efficacy administered through CED, which is a novel approach to drug delivery.
恶性胶质瘤对神经肿瘤学家和神经外科医生来说是一个棘手的治疗难题。这些肿瘤对手术、放疗和传统化疗等标准疗法仍然具有抗性,显然需要新的治疗选择。因此,研究人员最近转向了一个新方向,开始研发重组细胞毒素、抗血管生成因子和基因传递载体等化合物。然而,这些有前景的新药物都依赖于一种有效的给药方法,以绕过血脑屏障。对流增强给药(CED)可通过在立体定向或影像引导手术辅助下放置的导管,将靶向毒素和其他药物直接注入肿瘤部位的大脑中。作为一种新被认可的治疗方式,这项技术的应用正在兴起,因为在对抗胶质瘤方面几乎没有其他方法能产生持久的效果。直接瘤内注射最初是在人恶性胶质瘤的裸鼠侧腹肿瘤模型中进行的。在临床前动物研究中经过大量测试后,这种给药方法在I期和II期临床试验中成功证明了其体内疗效。目前,这项技术正在学术医学中心的研究环境中使用,研究人员开始确定CED的最佳实践方法。这种给药方法的一些基本问题,如输注速率、套管尺寸、输注液浓度和组织-套管密封时间,构成了当前文献中的讨论内容。靶向毒素疗法是针对这一不幸患者群体的最新且最有前景的治疗方法之一,通过CED给药已证明具有临床疗效,这是一种新颖的药物递送方法。