The basis and advances in clinical application of boron neutron capture therapy

Boron neutron capture therapy (BNCT) was first proposed as early as 1936, and research on BNCT has progressed relatively slowly but steadily. BNCT is a potentially useful tool for cancer treatment that selectively damages cancer cells while sparing normal tissue. BNCT is based on the nuclear reactio...

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Published inRadiation oncology (London, England) Vol. 16; no. 1; pp. 216 - 8
Main Authors He, Huifang, Li, Jiyuan, Jiang, Ping, Tian, Suqing, Wang, Hao, Fan, Ruitai, Liu, Junqi, Yang, Yuyan, Liu, Zhibo, Wang, Junjie
Format Journal Article
LanguageEnglish
Published England BioMed Central Ltd 07.11.2021
BioMed Central
BMC
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Summary:Boron neutron capture therapy (BNCT) was first proposed as early as 1936, and research on BNCT has progressed relatively slowly but steadily. BNCT is a potentially useful tool for cancer treatment that selectively damages cancer cells while sparing normal tissue. BNCT is based on the nuclear reaction that occurs when B capture low-energy thermal neutrons to yield high-linear energy transfer (LET) α particles and recoiling Li nuclei. A large number of B atoms have to be localized within the tumor cells for BNCT to be effective, and an adequate number of thermal neutrons need to be absorbed by the B atoms to generate lethal B (n, α) Li reactions. Effective boron neutron capture therapy cannot be achieved without appropriate boron carriers. Improvement in boron delivery and the development of the best dosing paradigms for both boronophenylalanine (BPA) and sodium borocaptate (BSH) are of major importance, yet these still have not been optimized. Here, we present a review of this treatment modality from the perspectives of radiation oncology, biology, and physics. This manuscript provides a brief introduction of the mechanism of cancer-cell-selective killing by BNCT, radiobiological factors, and progress in the development of boron carriers and neutron sources as well as the results of clinical study.
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ISSN:1748-717X
1748-717X
DOI:10.1186/s13014-021-01939-7