Treatment-Induced Changes in Tumor Oxygenation Predict Photodynamic Therapy Outcome
- 15 October 2004
- journal article
- Published by American Association for Cancer Research (AACR) in Cancer Research
- Vol. 64 (20) , 7553-7561
- https://doi.org/10.1158/0008-5472.can-03-3632
Abstract
Photodynamic therapy (PDT) requires oxygen to cause tumor damage, yet therapy itself can deplete or enhance tumor oxygenation. In the present work we measured the PDT-induced change in tumor oxygenation and explored its utility for predicting long-term response to treatment. The tissue hemoglobin oxygen saturation (SO2) of murine tumors was noninvasively measured by broadband diffuse reflectance spectroscopy. In initial validation studies, the oxyhemoglobin dissociation curve for mouse blood was accurately recreated based on measurements during deoxygenation of a tissue phantom of mouse erythrocytes. In vivo studies exhibited excellent correlation between carbogen-induced changes in SO2 and pO2 of radiation-induced fibrosarcoma tumors measured by reflectance spectroscopy and the Eppendorf pO2 histograph, respectively. In PDT studies radiation-induced fibrosarcoma tumor SO2 was measured immediately before and after Photofrin-PDT (135 J/cm2, 38 mW/cm2). Animals were subsequently followed for tumor growth to a volume of 400 mm3 (time-to-400 mm3) or the presence of tumor cure (no tumor growth at 90 days after treatment). In animals that recurred, the PDT-induced change in tumor SO2, i.e., relative-SO2 (SO2 after PDT/SO2 before PDT) was positively correlated with treatment durability (time-to-400 mm3). The predictive value of relative-SO2 was confirmed in a second group of animals with enhanced pre-PDT oxygenation due to carbogen breathing. Furthermore, when all of the animals were considered (those that recurred and those that were cured) a highly significant association was found between increasing relative-SO2 and increasing probability of survival, i.e., absence of recurrence. As independent variables, the SO2 after PDT, the pre-PDT tumor volume, and light penetration depth all failed to predict response. As an independent variable, the SO2 before PDT demonstrated a weak negative association with treatment durability; this association was driven by a correlation between decreasing pre-PDT SO2 and increasing relative-SO2. These data suggest that monitoring of PDT-induced changes in tumor oxygenation may be a valuable prognostic indicator.Keywords
This publication has 50 references indexed in Scilit:
- Diffuse Optical Tomography of Cerebral Blood Flow, Oxygenation, and Metabolism in Rat during Focal IschemiaJournal of Cerebral Blood Flow & Metabolism, 2003
- Correlation of in vivo photosensitizer fluorescence and photodynamic-therapy-induced depth of necrosis in a murine tumor modelJournal of Biomedical Optics, 2003
- In Vivo NADH Fluorescence Monitoring as an Assay for Cellular Damage in Photodynamic Therapy¶Photochemistry and Photobiology, 2001
- Oxygen monitoring during 5-aminolaevulinic acid induced photodynamic therapy in normal rat colon: Comparison of continuous and fractionated light regimesJournal of Photochemistry and Photobiology B: Biology, 2000
- Predictions and measurements of scattering and absorption over broad wavelength ranges in tissue phantomsApplied Optics, 1997
- Improved solutions of the steady-state and the time-resolved diffusion equations for reflectance from a semi-infinite turbid mediumJournal of the Optical Society of America A, 1997
- R: A Language for Data Analysis and GraphicsJournal of Computational and Graphical Statistics, 1996
- Influence of Fractionation and Fluence Rate in Photodynamic Therapy with Photofrin or mTHPCRadiation Research, 1996
- Nuclear Magnetic Resonance Spectroscopy and Sensitizer-Adduct Measurements of Photodynamic Therapy-Induced Ischemia in Solid TumorsJNCI Journal of the National Cancer Institute, 1991
- Triplet excited states and semiquinone radicals of 1,4-disubstituted anthraquinonesJournal of Photochemistry and Photobiology A: Chemistry, 1990