Literature DB >> 7782854

Performance of sulfhydryl boron hydride in patients with grade III and IV astrocytoma: a basis for boron neutron capture therapy.

C P Ceberg1, A Persson, A Brun, R Huiskamp, A S Fyhr, B R Persson, L G Salford.   

Abstract

This study investigated the rationale of boron neutron capture therapy (BNCT) for the treatment of Grade III and IV astrocytoma. The European Community joint research program on BNCT plans to use sulfhydryl boron hydride (BSH) in clinical trials. The work presented here, examines the performance of BSH in eight patients with Grade III and IV astrocytoma using a measurement technique which precisely correlates the boron uptake with the histology of the tumor and the peritumoral brain. Astrocytomas are exceptionally heterogeneous and spread migrating tumor cells into the surrounding brain. The patients were infused with 50 mg BSH per kilogram of body weight at 12, 18, 24 or 48 hours before surgery. At the time of operation, specimens were obtained of the tumor, skin, muscle, dura, blood, urine, and, when surgically possible, the brain adjacent to tumor. In three patients the intracellular boron distribution was investigated by subcellular fractionation. The blood clearance was biphasic with half-lives of 0.6 and 8.2 hours. After 3 days, approximately 70% of the dose injected was excreted in the urine. The maximum boron concentration in the tumor was 20 ppm, 12 hours after the infusion. The tumor-to-blood ratios ranged between 0.2 and 1.4, with the highest values after 18 to 24 hours. In the brain specimens the boron concentration never exceeded 1 ppm. This work confirms a selective uptake of boron in the tumor compared to the surrounding brain and that boron, to some extent, is incorporated in the tumor cells.

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Year:  1995        PMID: 7782854     DOI: 10.3171/jns.1995.83.1.0079

Source DB:  PubMed          Journal:  J Neurosurg        ISSN: 0022-3085            Impact factor:   5.115


  6 in total

Review 1.  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

2.  Postoperative treatment of glioblastoma with BNCT at the petten irradiation facility (EORTC protocol 11,961).

Authors:  K Hideghéty; W Sauerwein; K Haselsberger; F Grochulla; H Fankhauser; R Moss; R Huiskamp; D Gabel; M de Vries
Journal:  Strahlenther Onkol       Date:  1999-06       Impact factor: 3.621

3.  Binding and distribution of Na2B12H11SH on cellular and subcellular level in tumor tissue of glioma patients in boron neutron capture therapy.

Authors:  B Otersen; D Haritz; F Grochulla; M Bergmann; W Sierralta; D Gabel
Journal:  J Neurooncol       Date:  1997-05       Impact factor: 4.130

4.  Determination of the subcellular distribution of mercaptoundecahydro-closo-dodecaborate (BSH) in human glioblastoma multiforme by electron microscopy.

Authors:  Michael Neumann; Ulrike Kunz; Heiner Lehmann; Detlef Gabel
Journal:  J Neurooncol       Date:  2002-04       Impact factor: 4.130

5.  Subcellular biodistribution of sodium borocaptate (BSH: Na2B12H11SH) in a rat glioma model in boron neutron capture therapy.

Authors:  Teruyoshi Kageji; Shinji Nagahiro; Birte Otersen; Detlef Gabel; Manekazu Nakaichi; Yoshinobu Nakagawa
Journal:  J Neurooncol       Date:  2002-09       Impact factor: 4.130

6.  Tissue uptake of BSH in patients with glioblastoma in the EORTC 11961 phase I BNCT trial.

Authors:  Katalin Hideghéty; Wolfgang Sauerwein; Andrea Wittig; Claudia Götz; Philippe Paquis; Frank Grochulla; Klaus Haselsberger; John Wolbers; Ray Moss; Rene Huiskamp; Heinz Fankhauser; Martin de Vries; Detlef Gabel
Journal:  J Neurooncol       Date:  2003 Mar-Apr       Impact factor: 4.130

  6 in total

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