Skip to main content
Log in

Boron neutron capture therapy (BNCT) for malignant melanoma with special reference to absorbed doses to the normal skin and tumor

  • Scientific Papers
  • Published:
Australasian Physics & Engineering Sciences in Medicine Aims and scope Submit manuscript

Abstract

Twenty-two patients with malignant melanoma were treated with boron neutron capture therapy (BNCT) using10B-p-boronophenylalanine (BPA). The estimation of absorbed dose and optimization of treatment dose based on the pharmacokinetics of BPA in melanoma patients is described. The doses of γ-rays were measured using small TLDs of Mg2SiO4 (Tb) and thermal neutron fluence was measured using gold foil and wire. The total absorbed dose to the tissue from BNCT was obtained by summing the primary and capture γ-ray doses and the high LET radiation doses from10B(n,α)7Li and14N(n,p)14C reactions. The key point of the dose optimization is that the skin surrounding the tumour is always irradiated to 18 Gy−Eq, which is the maximum tolerable dose to the skin, regardless of the10B-concentration in the tumor. The neutron fluence was optimized as follows. (1) The10B concentration in the blood was measured 15−40 min after the start of neutron irradiation. (2) The10B-concentration in the skin was estimated by multiplying the blood10B value by a factor of 1.3. (3) The neutron fluence was calculated. Absorbed doses to the skin ranged from 15.7 to 37.1 Gy−Eq. Among the patients, 16 out of 22 patients exhibited tolerable skin damage. Although six patients showed skin damage that exceeded the tolerance level, three of them could be cured within a few months after BNCT and the remaining three developed severe skin damage requiring skin grafts. The absorbed doses to the tumor ranged from 15.7 to 68.5 Gy−Eq and the percentage of complete response was 73% (16/22). When BNCT is used in the treatment of malignant melanoma, based on the pharmacokinetics of BPA and radiobiological considerations, promising clinical results have been obtained, although many problems and issues remain to be solved.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Hawthorne, M. F.The role of chemistry in the development of boron neutron capoture therapy of cancer, Angew Chem Int Ed Engl 32:950–984, 1993.

    Article  Google Scholar 

  2. Misihma, Y.Neutron capture treatment of malignant melanoma using 10 B-chlorpromazine, Pigment Cell Res 1:215–221, 1973.

    Google Scholar 

  3. Mishima, Y., Honda, C., Ichihashi, M., et al.Treatment of malignant melanoma by single thermal neutron capture therapy with melanoma-seeking 10 B-compound, Lancet 12:383–389, 1989.

    Google Scholar 

  4. Mishima, Y.Selective thermal neutron capture therapy of cancer cells using their specific metabolic activitiesmelanoma as prototype, In: Mishima Y, ed. Cancer Neutron Capture Therapy, New York, London, Plenum Press, 1–26, 1996.

    Google Scholar 

  5. Yoshino, K., Suzuki, K., Mori, Y., et al.Improvement of solubility of p-boronophenylalanine by complex formation with monosaccharides.Strahlenther Oncol, 165:127–129, 1989.

    CAS  Google Scholar 

  6. Kobayashi, T. and Kanda, K.Microanalysis of ppm-order 10 B concentration in tissue for neutron capture therapy by prompt gamma-ray spectrometry, Nucl Inst Method 204:525–531, 1982.

    Article  Google Scholar 

  7. Overgaard, J.The role of radiotherapy in recurrent and metastatic malignant melanomas: A clinical radiobiological study, Int J Radiat Oncol Biol Phys 12, 867–872, 1986.

    CAS  PubMed  Google Scholar 

  8. Douglas, B. G.Implication of the quadratic cell survival curve and human skin radiation “tolerance dose” on fractionation and superfractionation dose selection, Int J Radiat Oncol Biol Phys 8, 1135–1142, 1982.

    CAS  PubMed  Google Scholar 

  9. Fukuda, H., Hiratsuka, J., Honda, C., et al.Boron neutron capture therapy of malignant melanoma using 10 B-paraboronophenylalanine with special reference to evaluation of radiation dose and damage to the normal skin, Radiat Res 138:435–442, 1994.

    Article  CAS  PubMed  Google Scholar 

  10. Fukuda H, Mishima Y, Hiratsuka J, et al.BNCT of malignant melanoma — radiobiological analysis and data comparison with conventional radiotherapy. In: Mishima Y, ed.Cancer Neutron Capture Therapy, New York, London: Plenum Press: 663–671, 1996

    Google Scholar 

  11. Fukuda, H., Honda, C., Wadabayashi, N., et al.Pharmacokinetics of 10 B-p-boronophenyl-alanine in tumours, skin and blood of melanoma patients: a study of boron neutron capture therapy for malignant melanoma, Melanoma Res 9:75–83, 1999.

    Article  CAS  PubMed  Google Scholar 

  12. Hornsey, S.The relationship between total dose, number of fractions and fraction size in the response of malignant melanoma in patients, Br J Radiol 51:905–909, 1977

    Article  Google Scholar 

  13. Overgaard, J.Radiation therapy of malignant melanoma, Int J Radiat Oncol Phys 6:41–44, 1980.

    CAS  Google Scholar 

  14. Overgaad, J., Overgaard, M., Hansen, P. V., et al.Some factors of importance in the radiation treatment of malignant melanoma, Radiother Oncol 5:183–192, 1986.

    Article  Google Scholar 

  15. Hebermalz, H. J., Fisher, J. J.Radiation therapy of malignant melanoma: Experience with high individual treatment doses, Cancer 38:2258–2262, 1976.

    Article  Google Scholar 

  16. Konefal, J. B., Emami, B., Pilepich, M. V.Malignant melanoma: Analysis of dose fractionation in radiation therapy, Radiology 164:607–610, 1987.

    CAS  PubMed  Google Scholar 

  17. Mackie, R. M., Young, D.Human malignant melanoma, Int J Dermatol 23: 433- 443, 1984.

    CAS  PubMed  Google Scholar 

  18. Bradley, P. D., Rosenfeld, A. B.Tissue equivalence correction for silicon microdosimetry detectors in boron neutron capture therapy, Medical Physics 25:2220–2225, 1998.

    Article  CAS  PubMed  Google Scholar 

  19. Imahori, Y., Ueda, S., Ohmori, Y., et al.Fluorine-18-labeled fluoroboronophenylalanine PET in patients with glioma. J Nucl Med 39:325–333, 1998.

    CAS  PubMed  Google Scholar 

  20. Kabalka, G. W., Smith, G. T., Reid, W. S., et al.Evaluation of fluorine-18-BPA-fructose for boron neutron capture treatment planning, J Nucl Med 38: 1762–1767, 1997.

    CAS  PubMed  Google Scholar 

  21. Kobayashi, T., Sakurai, Y. and Ichikawa, M.A non-invasive dose estimation system for clinical BNCT based on PGSPECT — Conceptual study and fundamental experiments using HPGe and CdTe semiconductor detectors, Medical Phys 27:2124–2132, 2000.

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to H. Fukuda.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Fukuda, H., Hiratsuka, J., Kobayashi, T. et al. Boron neutron capture therapy (BNCT) for malignant melanoma with special reference to absorbed doses to the normal skin and tumor. Australas. Phys. Eng. Sci. Med. 26, 97–103 (2003). https://doi.org/10.1007/BF03178777

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF03178777

Key words

Navigation