Boron neutron capture therapy (BNCT): Implications of neutron beam and boron compound characteristics

Citation
Fj. Wheeler et al., Boron neutron capture therapy (BNCT): Implications of neutron beam and boron compound characteristics, MED PHYS, 26(7), 1999, pp. 1237-1244
Citations number
21
Categorie Soggetti
Radiology ,Nuclear Medicine & Imaging","Medical Research Diagnosis & Treatment
Journal title
MEDICAL PHYSICS
ISSN journal
00942405 → ACNP
Volume
26
Issue
7
Year of publication
1999
Pages
1237 - 1244
Database
ISI
SICI code
0094-2405(199907)26:7<1237:BNCT(I>2.0.ZU;2-O
Abstract
The potential efficacy of boron neutron capture therapy (BNCT) for malignan t glioma is a significant function of epithermal-neutron beam biophysical c haracteristics as well as boron compound biodistribution characteristics. M onte Carlo analyses were performed to evaluate the relative significance of these factors on theoretical tumor control using a standard model. The exi sting, well-characterized epithermal-neutron sources at the Brookhaven Medi cal Research Reactor (BMRR), the Petten High Flux Reactor (HFR), and the Fi nnish Research Reactor (FiR-1) were compared. Results for a realistic accel erator design by the E. O. Lawrence Berkeley National Laboratory (LBL) are also compared. Also the characteristics of the compound p-Boronophenylaline Fructose (BPA-F) and a hypothetical next-generation compound were used in a comparison of the BMRR and a hypothetical improved reactor. All component s of dose induced by an external epithermal-neutron beam fall off quite rap idly with depth in tissue. Delivery of dose to greater depths is limited by the healthy-tissue tolerance and a reduction in the hydrogen-recoil and in cident gamma dose allow for longer irradiation and greater dose at a depth. Dose at depth can also be increased with a beam that has higher neutron en ergy (without too high a recoil dose) and a more forward peaked angular dis tribution. Of the existing facilities, the FiR-1 beam has the better qualit y (lower hydrogen-recoil and incident gamma dose) and a penetrating neutron spectrum and was found to deliver a higher value of Tumor Control Probabil ity (TCP) than other existing beams at shallow depth. The greater forwardne ss and penetration of the HFR the FiR-1 at greater depths. The hypothetical reactor and accelerator beams outperform at both shallow and greater depth s. In all cases, the hypothetical compound provides a significant improveme nt in efficacy but it is shown that the full benefit of improved compound i s not realized until the neutron beam is fully optimized. (C) 1999 American Association of Physicists in Medicine. [S0094-2405(99)01907-0].