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对流增强递送IL13-PE38QQR治疗复发性恶性胶质瘤:正在进行的1期研究中期结果报告

Convection enhanced delivery of IL13-PE38QQR for treatment of recurrent malignant glioma: presentation of interim findings from ongoing phase 1 studies.

作者信息

Kunwar S

机构信息

Department of Neurological Surgery, University of California, San Francisco, CA 94143-0112, USA.

出版信息

Acta Neurochir Suppl. 2003;88:105-11. doi: 10.1007/978-3-7091-6090-9_16.

Abstract

IL13PE38QQR is a recombinant toxin composed of the enzymatically-active portion of Pseudomonas Exotoxin A conjugated with human IL13. Binding of IL13-PE38 to the IL13 receptor (IL13R) permits internalization of the recombinant toxin resulting in selective and potent cytoxicity at nanomolar concentrations. Normal brain tissue expresses little or no IL13R, but malignant gliomas overexpress IL13R conferring the selective cytotoxicity to the agent. Convection-enhanced delivery (CED), a novel direct drug delivery method to tumor and peritumoral region uses positive pressure infusion to generate a pressure gradient that optimizes distribution of macromolecules within the brain. Three phase I studies have been initiated to investigate IL13-PE38QQR as an anti-tumor agent for the treatment of patients with recurrent malignant gliomas. As of January 2003 a total of 46 patients have been treated. The presentation at the March 2003 EANS Local Therapy of Glioma meeting reflects adverse event findings through January 2003 and survival data through March 2003. Intratumoral infusion with or without resection is fairly well-tolerated with corticosteroids prophylaxis particularly for patients with raised intracranial pressure. Post-resection infusion into the peritumoral brain parenchyma also appears to be very well tolerated. Histopathological tumor effect was seen at drug concentrations of 0.5-2.0 microg/mL. Although phase I studies do not focus on efficacy evaluation, prolonged survival times have been observed in this select population of patients. The preclinical data and details and preliminary results of the three clinical trials are reviewed.

摘要

IL13PE38QQR是一种重组毒素,由与人类IL13结合的铜绿假单胞菌外毒素A的酶活性部分组成。IL13 - PE38与IL13受体(IL13R)结合可使重组毒素内化,从而在纳摩尔浓度下产生选择性和强效的细胞毒性。正常脑组织很少或不表达IL13R,但恶性胶质瘤过度表达IL13R,使该药物具有选择性细胞毒性。对流增强递送(CED)是一种向肿瘤和瘤周区域递送药物的新型直接给药方法,它利用正压输注产生压力梯度,以优化大分子在脑内的分布。已经启动了三项I期研究,以研究IL13 - PE38QQR作为治疗复发性恶性胶质瘤患者的抗肿瘤药物。截至2003年1月,共有46名患者接受了治疗。2003年3月欧洲神经肿瘤学会(EANS)胶质瘤局部治疗会议上的报告反映了截至2003年1月的不良事件发现以及截至2003年3月的生存数据。瘤内输注(无论有无切除)耐受性相当好,特别是对于颅内压升高的患者,预防性使用皮质类固醇。切除术后向瘤周脑实质内输注似乎也耐受性很好。在药物浓度为0.5 - 2.0微克/毫升时可观察到组织病理学肿瘤效应。虽然I期研究不侧重于疗效评估,但在这一特定患者群体中观察到了生存期延长。本文综述了临床前数据以及三项临床试验的细节和初步结果。

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