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临床试验/NCT00115453
NCT00115453终止1 期

Boron Neutron Capture Therapy in the Treatment of Glioblastoma Multiforme

Boneca Corporation2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 1999年5月1日最近更新:
适应症

试验速览

阶段
1 期
状态
终止
发起方
入组人数
50
试验地点
2
主要终点
safety

研究概览

简要总结

Boron Neutron Capture Therapy (BNCT) is an experimental radiation therapy technique that is based on the principle of irradiating boron atoms with neutrons. When neutrons have relatively low energy, boron atoms that have been targeted to cancerous tissue using a suitable boron carrier (an amino acid derivative called BPA, boronophenylalanine) will capture the neutrons. As a result from the neutron capture the boron atoms will split into two, producing helium and lithium ions. The helium and lithium ions, in turn, have only a short pathlength in tissue (about 5 micrometers) and will deposit their cell damaging effect mainly within the tumor provided that the boron carrier (BPA) has accumulated in the tumor. In practice, the study participants will receive BPA as an approximately 2-hour intravenous infusion, following which the tumor is irradiated with low energy (epithermal) neutrons obtained from a nuclear reactor at the BNCT facility. BNCT requires careful radiation dose planning, but neutron irradiation will last approximately only for one hour. In this study BNCT is given only once. The study hypothesis is that glioblastoma tissue may accumulate the boron carrier compound, and glioblastoma might respond to BNCT.

详细描述

This is a single BNCT-facility, non-randomized, non-comparative, prospective, open-label, phase I/II trial to determine the value of BNCT in the treatment of subjects who have undergone surgery for glioblastoma, but glioblastoma has not been treated with radiation therapy or chemotherapy. The neutron irradiation site is the FiR 1 reactor site, located at Otaniemi, Espoo, Finland, about 6 kilometers from the Helsinki University Central Hospital, Helsinki, where patient evaluation and post-irradiation care will take place.

BPA is infused as a fructose complex (BPA-F) into a peripheral vein over 2 hours prior to neutron irradiation. Blood samples will be taken before starting the BPA infusion, and thereafter at 20 to 40 minute intervals during the infusion, following infusion, and after delivering neutron irradiation to monitor the blood boron concentration. The blood samples will be analyzed for boron to estimate the average blood boron level during neutron irradiation. The first 12 patients are treated using a BPA dose of 290 mg/kg, following which the dose of BPA is increased stepwise to 500 mg/kg, provided that unacceptable toxicity will not occur.

All patients will be evaluated for response using CT or magnetic resonance imaging (MRI).

研究设计

研究类型
Interventional
分配方式
Non Randomized
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 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Histologically confirmed glioblastoma multiforme
  • Supratentorial location
  • At least 30% of the tumor volume has been removed at craniotomy as judged from a pre/perioperative MRI
  • Ability to understand the concept of investigational therapy
  • Tolerates dexamethasone treatment
  • Adequate anti-epileptic medication
  • BNCT can be delivered within 6 weeks from the date of brain surgery
  • A written informed consent

排除标准

  • Age less than 18 or greater than 75
  • The tumor infiltrates into the optic chiasm or into the deep parts of the brain prohibiting delivery of an adequate radiation dose with BNCT
  • Prior radiation therapy to the brain
  • Prior chemotherapy, immunotherapy, or gene therapy
  • Karnofsky performance score <70
  • Severe cardiac, liver, or kidney failure
  • Severe infection
  • A cardiac pace-maker, or a metal implant in the head and neck region that will prohibit MRI examination
  • Pregnancy or lactation
  • Phenylketonuria

结局指标

主要结局

safety

时间窗: 3 years

次要结局

  • tumor response(one year)
  • effect on brain tissue(3 years)

研究者

发起方
Boneca Corporation
申办方类型
Industry

研究点 (2)

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