Boron Neutron Capture Therapy (BNCT) as Treatment of Glioblastoma
Information source: Boneca Corporation
Information obtained from ClinicalTrials.gov on August 08, 2008 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Glioblastoma
Intervention: irradiation (Radiation)
Phase: Phase 1/Phase 2
Status: Recruiting
Sponsored by: Boneca Corporation Official(s) and/or principal investigator(s): Heikki Joensuu, M.D., prof., Principal Investigator, Affiliation: Helsinki University
Overall contact: Mauri Kouri, M.D., Phone: +358-9-4711, Email: mauri.kouri@hus.fi
Summary
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.
Clinical Details
Official title: Boron Neutron Capture Therapy in the Treatment of Glioblastoma Multiforme
Study design: Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study
Primary outcome: safety
Secondary outcome: tumor responseeffect on brain tissue
Detailed description:
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).
Eligibility
Minimum age: 18 Years.
Maximum age: 75 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- 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
Exclusion Criteria:
- 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
Locations and Contacts
Mauri Kouri, M.D., Phone: +358-9-4711, Email: mauri.kouri@hus.fi
Department of Oncology, Helsinki University Central Hospital, Helsinki FIN-00029, Finland; Recruiting Heikki Joensuu, M.D., prof., Phone: +358-9-4711, Email: heikki.joensuu@hus.fi Mikael Kajanti, M.D., Phone: +358-9-4711, Email: mikael.kajanti@hus.fi Mauri Kouri, M.D., Sub-Investigator Leena Kankaanranta, M.D., Sub-Investigator Juhani Collan, M.D., Sub-Investigator
Additional Information
Boneca Corporation is a Finnish company that provides BNCT.
Related publications: Kouri M, Kankaanranta L, Seppala T, Tervo L, Rasilainen M, Minn H, Eskola O, Vahatalo J, Paetau A, Savolainen S, Auterinen I, Jaaskelainen J, Joensuu H. Undifferentiated sinonasal carcinoma may respond to single-fraction boron neutron capture therapy. Radiother Oncol. 2004 Jul;72(1):83-5.
Starting date: May 1999
Ending date: February 2009
Last updated: September 12, 2007
|