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临床试验/NCT01811498
NCT01811498已完成1 期

Phase I/II Trial of Repeated Super-Selective Intraarterial Cerebral Infusion of Bevacizumab (Avastin) for Treatment of Newly Diagnosed Glioblastoma Multiforme

Northwell Health1 个研究点 分布在 1 个国家目标入组 31 人开始时间: 2013年2月最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
已完成
入组人数
31
试验地点
1
主要终点
Progression-free Survival (PFS)

研究概览

简要总结

The high-grade malignant brain tumors, glioblastoma multiforme (GBM), comprise the majority of all primary brain tumors in adults. This group of tumors also exhibits the most aggressive behavior, resulting in median overall survival of only 9-12 months. Initial therapy consists of either surgical resection, external beam radiation, or both. All patients experience a recurrence after first-line therapy, so improvements in both first-line and salvage therapy are critical to enhancing quality-of-life and prolonging survival. It is unknown if currently used intravenous (IV) therapies even cross the blood brain barrier (BBB). We have shown in a previous phase I trial that a single Superselective Intraarterial Cerebral Infusion (SIACI) of Bevacizumab (up to 15mg/kg) is safe and effective in the treatment of recurrent GBM. Therefore, this phase I/II clinical research trial is an extension of that trial in that we seek to test the hypothesis that repeated dosing of intra-arterial Bevacizumab is safe and effective in the treatment of newly diagnosed malignant glioma. By achieving the aims of this study we will also determine if repeated intra-arterial Bevacizumab improves progression free and overall survival in newly diagnosed patients. We expect that this project will provide important information regarding the utility of repeated SIACI Bevacizumab therapy for malignant glioma, and may alter the way these drugs are delivered to our patients in the near future.

详细描述

The experimental aspects of this experimental plan will include:

  1. Subjects will first be treated with Mannitol prior to chemotherapy infusion (Mannitol 20%; delivered IA, 12.5 mL over 2 minutes) in order to disrupt the blood brain barrier. This technique has been used in several thousand subjects in previous studies for the IA delivery of chemotherapy for malignant glioma.
  2. Subjects will then be treated with repeated intraarterial delivery (SIACI) of Bevacizumab. Each subject will receive one dose of IA Bevacizumab on day 30, followed by chemoradiation. SIACI of Bevacizumab will be repeated every three months for a total of 3 infusions.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

SIACI of Bevacizumab

Experimental

Superselective Intraarterial Cerebral Infusion (SIACI) of Bevacizumab

干预措施: Bevacizumab (Drug)

结局指标

主要结局

Progression-free Survival (PFS)

时间窗: Percent of Participants with 6 Month Progression-Free Survival

PFS was defined from the date of the first dose of SIACI Bevacizumab until first documentation of disease pro- gression, or death from any cause, whichever occurred first.

Overall Survival (OS)

时间窗: 8 months, and until death of any cause, up to approximately 8 years

Overall Survival was defined from the date of the first dose of SIACI Bevacizumab until death from any cause.

次要结局

  • Number of Adverse Events(30 days post treatment)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

John Boockvar, MD Zucker SOM @Hofstra/Northwell

Professor

Feinstein Institute for Medical Research

研究点 (1)

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