Literature DB >> 12749701

A critical assessment of boron target compounds for boron neutron capture therapy.

M Frederick Hawthorne1, Mark W Lee.   

Abstract

Boron neutron capture therapy (BNCT) has undergone dramatic developments since its inception by Locher in 1936 and the development of nuclear energy during World War II. The ensuing Cold War spawned the entirely new field of polyhedral borane chemistry, rapid advances in nuclear reactor technology and a corresponding increase in the number to reactors potentially available for BNCT. This effort has been largely oriented toward the eradication of glioblastoma multiforme (GBM) and melanoma with reduced interest in other types of malignancies. The design and synthesis of boron-10 target compounds needed for BNCT was not channeled to those types of compounds specifically required for GBM or melanoma. Consequently, a number of potentially useful boron agents are known which have not been biologically evaluated beyond a cursory examination and only three boron-10 enriched target species are approved for human use following their Investigational New Drug classification by the US Food and Drug Administration; BSH, BPA and GB-10. All ongoing clinical trials with GBM and melanoma are necessarily conducted with one of these three species and most often with BPA. The further development of BNCT is presently stalled by the absence of strong support for advanced compound evaluation and compound discovery driven by recent advances in biology and chemistry. A rigorous demonstration of BNCT efficacy surpassing that of currently available protocols has yet to be achieved. This article discusses the past history of compound development, contemporary problems such as compound classification and those problems which impede future advances. The latter include means for biological evaluation of new (and existing) boron target candidates at all stages of their development and the large-scale synthesis of boron target species for clinical trials and beyond. The future of BNCT is bright if latitude is given to the choice of clinical disease to be treated and if a recognized study demonstrating improved efficacy is completed. Eventually, BNCT in some form will be commercialized.

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Year:  2003        PMID: 12749701     DOI: 10.1007/bf02699932

Source DB:  PubMed          Journal:  J Neurooncol        ISSN: 0167-594X            Impact factor:   4.130


  40 in total

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Journal:  Adv Drug Deliv Rev       Date:  2000-03-15       Impact factor: 15.470

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Journal:  Bioconjug Chem       Date:  1992 May-Jun       Impact factor: 4.774

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Journal:  J Invest Dermatol       Date:  1982-03       Impact factor: 8.551

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Journal:  Proc Natl Acad Sci U S A       Date:  1992-10-01       Impact factor: 11.205

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Journal:  Br J Cancer       Date:  1991-04       Impact factor: 7.640

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  25 in total

1.  A novel method of boron delivery using sodium iodide symporter for boron neutron capture therapy.

Authors:  Sanath Kumar; Svend O Freytag; Kenneth N Barton; Jay Burmeister; Michael C Joiner; Bijan Sedghi; Benjamin Movsas; Peter J Binns; Jae Ho Kim; Stephen L Brown
Journal:  J Radiat Res       Date:  2010       Impact factor: 2.724

Review 2.  Advancements in Tumor Targeting Strategies for Boron Neutron Capture Therapy.

Authors:  Micah John Luderer; Pilar de la Puente; Abdel Kareem Azab
Journal:  Pharm Res       Date:  2015-06-02       Impact factor: 4.200

Review 3.  Physical, dosimetric and clinical aspects and delivery systems in neutron capture therapy.

Authors:  Bagher Farhood; Hadi Samadian; Mahdi Ghorbani; Seyed Salman Zakariaee; Courtney Knaup
Journal:  Rep Pract Oncol Radiother       Date:  2018-08-01

4.  A Hypoxia-Targeted Boron Neutron Capture Therapy Agent for the Treatment of Glioma.

Authors:  Micah John Luderer; Barbara Muz; Pilar de la Puente; Sanmathi Chavalmane; Vaishali Kapoor; Raymundo Marcelo; Pratim Biswas; Dinesh Thotala; Buck Rogers; Abdel Kareem Azab
Journal:  Pharm Res       Date:  2016-07-11       Impact factor: 4.200

5.  Therapeutic efficacy of boron neutron capture therapy mediated by boron-rich liposomes for oral cancer in the hamster cheek pouch model.

Authors:  Elisa M Heber; M Frederick Hawthorne; Peter J Kueffer; Marcela A Garabalino; Silvia I Thorp; Emiliano C C Pozzi; Andrea Monti Hughes; Charles A Maitz; Satish S Jalisatgi; David W Nigg; Paula Curotto; Verónica A Trivillin; Amanda E Schwint
Journal:  Proc Natl Acad Sci U S A       Date:  2014-10-27       Impact factor: 11.205

6.  Boron neutron capture therapy demonstrated in mice bearing EMT6 tumors following selective delivery of boron by rationally designed liposomes.

Authors:  Peter J Kueffer; Charles A Maitz; Aslam A Khan; Seth A Schuster; Natalia I Shlyakhtina; Satish S Jalisatgi; John D Brockman; David W Nigg; M Frederick Hawthorne
Journal:  Proc Natl Acad Sci U S A       Date:  2013-03-27       Impact factor: 11.205

7.  Carborane clusters in computational drug design: a comparative docking evaluation using AutoDock, FlexX, Glide, and Surflex.

Authors:  Rohit Tiwari; Kiran Mahasenan; Ryan Pavlovicz; Chenglong Li; Werner Tjarks
Journal:  J Chem Inf Model       Date:  2009-06       Impact factor: 4.956

Review 8.  Boron chemicals in diagnosis and therapeutics.

Authors:  Bhaskar C Das; Pritam Thapa; Radha Karki; Caroline Schinke; Sasmita Das; Suman Kambhampati; Sushanta K Banerjee; Peter Van Veldhuizen; Amit Verma; Louis M Weiss; Todd Evans
Journal:  Future Med Chem       Date:  2013-04       Impact factor: 3.808

9.  Folate Functionalized Boron Nitride Nanotubes and their Selective Uptake by Glioblastoma Multiforme Cells: Implications for their Use as Boron Carriers in Clinical Boron Neutron Capture Therapy.

Authors:  Gianni Ciofani; Vittoria Raffa; Arianna Menciassi; Alfred Cuschieri
Journal:  Nanoscale Res Lett       Date:  2008-11-25       Impact factor: 4.703

Review 10.  A critical assessment of boron neutron capture therapy: an overview.

Authors:  Rolf F Barth
Journal:  J Neurooncol       Date:  2003 Mar-Apr       Impact factor: 4.130

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