Monte Carlo simulations for optimal light delivery in photodynamic therapy of non-melanoma skin cancer

R. M. Valentine*, K. Wood, C. T. A. Brown, S. H. Ibbotson, H. Moseley

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

The choice of light source is important for the efficacy of photodynamic therapy (PDT) of non-melanoma skin cancer. We simulated the photodynamic dose (PDD) delivered to a tumour during PDT using theoretical radiation transfer simulations performed via our 3D Monte Carlo radiation transfer (MCRT) model for a range of light sources with light doses up to 75 J cm(-2). The PDD delivered following superficial irradiation from (A) non-laser light sources, (B) monochromatic light, (C) alternate beam diameters and (D) re-positioning of the tumour within the tissue was computed. (A) The final PDD deposited to the tumour at a depth of 2 mm by the Paterson light source was 2.75, 2.50 and 1.04 times greater than the Waldmann 1200, Photocure and Aktilite, respectively. (B) Tumour necrosis occurred at a depth of 2.23 mm and increased to 3.81 mm for wavelengths 405 and 630 nm, respectively. (C) Increasing the beam diameter from 10 to 50 mm had very little effect on depth of necrosis. (D) As expected, necrosis depths were reduced when the tumour was re-positioned deeper into the tissue. These MCRT simulations show clearly the importance of choosing the correct light source to ensure optimal light delivery to achieve tumour necrosis.

Original languageEnglish
Pages (from-to)6327-6345
Number of pages19
JournalPhysics in Medicine and Biology
Volume57
Issue number20
DOIs
Publication statusPublished - 21 Oct 2012

Keywords

  • BASAL-CELL CARCINOMAS
  • AXISYMMETRICAL CIRCUMSTELLAR ENVELOPES
  • DELTA-AMINOLEVULINIC-ACID
  • PHOTOSENSITIZER FLUORESCENCE
  • INTRINSIC FLUORESCENCE
  • 5-AMINOLEVULINIC ACID
  • MULTIPLE-SCATTERING
  • THOMSON SCATTERING
  • SINGLET OXYGEN
  • BOWENS-DISEASE

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