Literature DB >> 8951358

Boron neutron capture therapy of brain tumors: past history, current status, and future potential.

R F Barth1, A H Soloway, R M Brugger.   

Abstract

Boron neutron capture therapy (BNCT) is based on the nuclear reaction that occurs when boron-10 is irradiated with low-energy thermal neutrons to yield alpha particles and recoiling lithium-7 nuclei. High-grade astrocytomas, glioblastoma multiforme, and metastatic brain tumors constitute a major group of neoplasms for which there is no effective treatment. There is growing interest in using BNCT in combination with surgery to treat patients with primary, and possibly metastatic brain tumors. For BNCT to be successful, a large number of 10B atoms must be localized on or preferably within neoplastic cells, and a sufficient number of thermal neutrons must reach and be absorbed by the 10B atoms to sustain a lethal 10B(n, alpha)7 Li reaction. Two major questions will be addressed in this review. First, how can a large number of 10B atoms be delivered selectively to cancer cells? Second, how can a high fluence of neutrons be delivered to the tumor? Two boron compounds currently are being used clinically, sodium borocaptate (BSH) and boronophenylalanine (BPA), and a number of new delivery agents are under investigation, including boronated porphyrins, nucleosides, amino acids, polyamines, monoclonal and bispecific antibodies, liposomes, and epidermal growth factor. These will be discussed, and potential problems associated with their use as boron delivery agents will be considered. Nuclear reactors, currently, are the only source of neutrons for BNCT, and the fission process within the core produces a mixture of lower-energy thermal and epithermal neutrons, fast or high (> 10,000 eV) energy neutrons, and gamma rays. Although thermal neutron beams have been used clinically in Japan to treat patients with brain tumors and cutaneous melanomas, epithermal neutron beams should be more useful because of their superior tissue-penetrating properties. Beam sources and characteristics will be discussed in the context of current and future BNCT trials. Finally, the past and present clinical trials on BNCT for brain tumors will be reviewed and the future potential of BNCT will be assessed.

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Year:  1996        PMID: 8951358     DOI: 10.3109/07357909609076899

Source DB:  PubMed          Journal:  Cancer Invest        ISSN: 0735-7907            Impact factor:   2.176


  10 in total

1.  Tolerance of the normal canine brain to epithermal neutron irradiation in the presence of p-boronophenylalanine.

Authors:  J A Coderre; P R Gavin; J Capala; R Ma; G M Morris; T M Button; T Aziz; N S Peress
Journal:  J Neurooncol       Date:  2000-05       Impact factor: 4.130

Review 2.  Common challenges and problems in clinical trials of boron neutron capture therapy of brain tumors.

Authors:  N Gupta; R A Gahbauer; T E Blue; B Albertson
Journal:  J Neurooncol       Date:  2003 Mar-Apr       Impact factor: 4.130

3.  Effect of dose and infusion time on the delivery of p-boronophenylalanine for neutron capture therapy.

Authors:  D D Joel; J A Coderre; P L Micca; M M Nawrocky
Journal:  J Neurooncol       Date:  1999-02       Impact factor: 4.130

4.  Enhanced survival of glioma bearing rats following boron neutron capture therapy with blood-brain barrier disruption and intracarotid injection of boronophenylalanine.

Authors:  W Yang; R F Barth; J H Rotaru; M L Moeschberger; D D Joel; M M Nawrocky; J H Goodman
Journal:  J Neurooncol       Date:  1997-05       Impact factor: 4.130

Review 5.  Ligand liposomes and boron neutron capture therapy.

Authors:  Jörgen Carlsson; Erika Bohl Kullberg; Jacek Capala; Stefan Sjöberg; Katarina Edwards; Lars Gedda
Journal:  J Neurooncol       Date:  2003 Mar-Apr       Impact factor: 4.130

6.  Tumor-cell targeted epiderimal growth factor liposomes loaded with boronated acridine: uptake and processing.

Authors:  Erika Bohl Kullberg; Marika Nestor; Lars Gedda
Journal:  Pharm Res       Date:  2003-02       Impact factor: 4.200

7.  Potential dual imaging nanoparticle: Gd2O3 nanoparticle.

Authors:  Md Wasi Ahmad; Wenlong Xu; Sung June Kim; Jong Su Baeck; Yongmin Chang; Ji Eun Bae; Kwon Seok Chae; Ji Ae Park; Tae Jeong Kim; Gang Ho Lee
Journal:  Sci Rep       Date:  2015-02-24       Impact factor: 4.379

8.  Responses of total and quiescent cell populations in solid tumors to boron and gadolinium neutron capture reaction using neutrons with two different energy spectra.

Authors:  S Masunaga; K Ono; Y Sakurai; M Suzuki; M Takagaki; T Kobayashi; Y Kinashi; M Akaboshi
Journal:  Jpn J Cancer Res       Date:  1998-01

9.  Applicability of combination with tirapazamine in boron neutron capture therapy.

Authors:  S Masunaga; K Ono; Y Sakurai; H Hori; T Kobayashi; M Takagaki; M Suzuki; Y Kinashi; M Akaboshi
Journal:  Jpn J Cancer Res       Date:  1998-07

10.  Pharmacokinetics of BPA in gliomas with ultrasound induced blood-brain barrier disruption as measured by microdialysis.

Authors:  Feng-Yi Yang; Yi-Li Lin; Fong-In Chou; Yu-Chuan Lin; Yen-Wan Hsueh Liu; Lun-Wei Chang; Yu-Ling Hsieh
Journal:  PLoS One       Date:  2014-06-17       Impact factor: 3.240

  10 in total

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