Program Information
Early Prediction of Radiotherapy Induced Skin Reactions Using Dynamic Infrared Imaging
N Biswal1*, G Cifter2 , J Sun3 , N Sen4 , D Wang5 , A Diaz6 , K Griem7 , J Chu8 , (1) Rutgers Cancer Institute of New Jersey, New Brunswick, NJ, (2) ,Boston, MA, (3) Argonne National Laboratory, Lemont, IL, (4) Rush University Medical Center, Chicago, IL, (5) Rush University Medical Center, Chicago, IL, (6) Rush University Medical Center, Chicago, IL, (7) Rush University Medical Center, Chicago, IL, (8) Rush University Medical Center, Oak Brook, IL
Presentations
WE-FG-202-1 (Wednesday, August 3, 2016) 1:45 PM - 3:45 PM Room: 202
Purpose:To predict radiotherapy induced skin reactions using dynamic infrared imaging.
Methods:Thermal images were captured by our homebuilt system consisting of two flash lamps and an infrared (IR) camera. The surface temperature of the skin was first raised by ~ 6 oC from ~1 ms flashes. The camera then captured a series of IR images for 10 seconds. For each image, a baseline skin temperature was recorded for 0.5sec before heat impulse. The temporal temperature gradients were calculated between a reference point (immediately after the flash) and at a time point 9sec after that. Thermal effusivity, an intrinsic thermal property of a material, was calculated from the surface temperature decay of skin. We present experimental data in five patients undergoing radiation therapy, of which 2 were Head & Neck, 1 was Sarcoma and 2 were Breast cancer patients. The prescribed doses were 45 – 60 Gy in 25 - 30 fractions. Each patient was imaged before treatment and after every fifth fraction until end of the treatment course. An area on the skin, outside the radiation field, was imaged as control region. During imaging, each patient’s irradiated skins were scored based on RTOG skin morbidity scoring criteria.
Results:Temperature gradient, which is the temperature recovery rate, depends on the thermal properties of underlying tissue. It was observed that, the skin temperature and temporal temperature gradient increases with delivered radiation dose and skin RTOG score. The treatment does not change effusivity of superficial skin layer, however there was a significant difference in effusivity between treated and control areas at depth of ~ 1.5 - 1.8 mm, increases with dose.
Conclusion:The higher temporal temperature gradient and effusivity from irradiated areas suggest that there is more fluid under the irradiated skin, which causes faster temperature recovery. The mentioned effects may be predictors of Moist Desquamation.
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