| Literature DB >> 25146878 |
Jing Dong1, Hui Jin Toh2, Patricia S P Thong2, Chuan Sia Tee2, Renzhe Bi1, Khee-Chee Soo2, Kijoon Lee3.
Abstract
Tumor response during photodynamic therapy (PDT) is heavily dependent on treatment parameters such as light dose, photosensitizer concentration, and tissue oxygenation. Therefore, it is desirable to have a real-time hemodynamic monitoring device in order to fine-tune the parameters and improve PDT efficacy. In this paper, such a tumor response monitoring system was built incorporating both frequency domain diffuse optical spectroscopy (FD-DOS) and diffuse correlation spectroscopy (DCS), which enables concurrent monitoring of tissue oxygenation (StO₂), total hemoglobin concentration (THC) and relative blood flow (rBF). The tumor metabolic rate of oxygen (TMRO₂) was calculated by using the hemodynamic parameters. Mouse models bearing xenograft tumors were subjected to chlorin e6 (Ce6)-mediated PDT, and the four parameters were monitored with varying treatment conditions. The results show (1) At 3 h post-PDT, rStO₂, rBF and rTMRO₂ exhibited sharp PDT-induced decreases in responders (>40% reduction in tumor volume). Statistically significant difference between responders and non-responders were observed in rStO₂ and rBF, but not in rTMRO₂. (2) Non-responders show gradual recovery of rStO₂, rBF and rTMRO₂ from ∼24 h post-PDT, while responder group did not show recovery up until 48 h post-PDT. Long-term study results up to 2 weeks are also shown. It suggests the hybrid diffuse optical system is not only capable of real-time treatment monitoring, but also able to extract tumor metabolic rate of oxygen to provide more insights about therapy mechanism. Translation of this technique to the clinic will make a quick prognosis feasible and help with treatment optimization.Entities:
Keywords: Diffuse correlation spectroscopy (DCS); Diffuse optical spectroscopy (DOS); Photodynamic therapy (PDT); Relative blood flow (rBF); Tissue oxygenation (StO(2)); Tumor metabolic rate of oxygen (TMRO(2))
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Year: 2014 PMID: 25146878 DOI: 10.1016/j.jphotobiol.2014.07.020
Source DB: PubMed Journal: J Photochem Photobiol B ISSN: 1011-1344 Impact factor: 6.252