## Abstract ## Background and Objectives Interstitial photodynamic therapy (PDT) is an emerging modality for the treatment of solid organ disease. Our group at the University of Pennsylvania has performed extensive studies that demonstrate the feasibility of interstitial PDT for prostate cancer. O
In vivo light dosimetry for motexafin lutetium-mediated PDT of recurrent breast cancer
✍ Scribed by Andreea Dimofte; Timothy C. Zhu; Stephen M. Hahn; Robert A. Lustig
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 365 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0196-8092
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Background and Objectives
To measure the fluence at tissue surface for patients in our Phase II clinical trial of motexafin lutetium (MLu)‐mediated chest wall photodynamic therapy for recurrent breast carcinoma and to compare it to the calculated irradiance.
Study Design/Materials and Methods
The spatial and time dependence of light fluence (rate) was monitored in vivo on the chest wall surface using isotropic detectors in five patients. Patients were given MLu either 4 mg/kg with light at 18 hours or 5 mg/kg with light at 24 hours using an irradiance of 150 J/cm^2^ at 730 nm, with an incident fluence rate of 75 mW/cm^2^. The ratio of fluence rate to the incident fluence rate was determined at the center of the treatment field. This ratio was used to estimate the effective attenuation coefficient, μ~eff~.
Results
The mean and standard deviation of the ratio for all patients was 1.6 ± 0.2. The corresponding range of μ~eff~ was between 0.87 and 2.1 cm^−1^, assuming reduced scattering coefficient, μ′~s~ = 4 cm^−1^.
Conclusions
A conversion factor was determined to convert the irradiance to fluence rate on the tissue surface. However, the fluence (or the ratio) on patient surface varied by 70% due to the heterogeneity of optical properties. This supports the use of real‐time in vivo dosimetry during photodynamic therapy. Lasers Surg. Med. 31:305–312, 2002. © 2002 Wiley‐Liss, Inc.
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