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首页> 外文期刊>Journal of Neuro-Oncology >Progress Report of a Phase I Study of the Intracerebral Microinfusion of a Recombinant Chimeric Protein Composed of Transforming Growth Factor (TGF)-α and a Mutated form of the Pseudomonas Exotoxin Termed PE-38 (TP-38) for the Treatment of Malignant Brain Tumors
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Progress Report of a Phase I Study of the Intracerebral Microinfusion of a Recombinant Chimeric Protein Composed of Transforming Growth Factor (TGF)-α and a Mutated form of the Pseudomonas Exotoxin Termed PE-38 (TP-38) for the Treatment of Malignant Brain Tumors

机译:脑内微输注由转化生长因子(TGF)-α和突变形式的假单胞菌外毒素称为PE-38(TP-38)组成的重组嵌合蛋白在脑内微输注的研究进展报告

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摘要

TP-38 is a recombinant chimeric targeted toxin composed of the EGFR binding ligand TGF-α and a genetically engineered form of the Pseudomonas exotoxin, PE-38. After in vitro and in vivo animal studies that showed specific activity and defined the maximum tolerated dose (MTD), we investigated this agent in a Phase I trial. The primary objective of this study was to define the MTD and dose limiting toxicity of TP-38 delivered by convection-enhanced delivery in patients with recurrent malignant brain tumors. Twenty patients were enrolled in the study and doses were escalated from 25ng/mL to 100 with a 40mL infusion volume delivered by two catheters. One patient developed Grade IV fatigue at the 100ng/mL dose, but the MTD has not been established. The overall median survival after TP-38 for all patients was 23 weeks whereas for those without radiographic evidence of residual disease at the time of therapy, the median survival was 31.9 weeks. Overall, 3 of 15 patients, with residual disease at the time of therapy, have demonstrated radiographic responses and one patient with a complete response and has survived greater than 83 weeks.
机译:TP-38是一种重组嵌合靶向毒素,由EGFR结合配体TGF-α和假单胞菌外毒素PE-38的基因工程形式组成。在进行了显示特定活性并确定最大耐受剂量(MTD)的体外和体内动物研究后,我们在I期试验中研究了该药物。这项研究的主要目的是确定对流性增强分娩对复发性脑肿瘤患者的TP-38的MTD和剂量限制毒性。该研究招募了20名患者,剂量从25ng / mL逐步增加至100,并通过两个导管输注40mL输液量。一名患者以100ng / mL的剂量出现IV级疲劳,但尚未确定MTD。在所有患者中,TP-38治疗后的总中位生存期为23周,而对于那些没有影像学证据证明存在残留疾病的患者,其中位生存期为31.9周。总体而言,每15例患者中有3例在治疗时出现残留疾病,表现出射线照相反应,而1例患者表现出完全反应,并且存活超过83周。

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