| Literature DB >> 30315644 |
Valentin Demidov1, Xiao Zhao2, Olga Demidova3, Hilary Y M Pang1, Costel Flueraru4, Fei-Fei Liu1,2,5, I Alex Vitkin1,5,6.
Abstract
Radiation therapy (RT) is widely and effectively used for cancer treatment but can also cause deleterious side effects, such as a late-toxicity complication called radiation-induced fibrosis (RIF). Accurate diagnosis of RIF requires analysis of histological sections to assess extracellular matrix infiltration. This is invasive, prone to sampling limitations, and thus rarely used; instead, current practice relies on subjective clinical surrogates, including visual observation, palpation, and patient symptomatology questionnaires. This preclinical study demonstrates that functional optical coherence tomography (OCT) is a useful tool for objective noninvasive in-vivo assessment and quantification of fibrosis-associated microvascular changes in tissue. Data were collected from murine hind limbs 6 months after 40-Gy single-dose irradiation and compared with nonirradiated contralateral tissues of the same animals. OCT-derived vascular density and average vessel diameter metrics were compared to quantitative vascular analysis of stained histological slides. Results indicate that RIF manifests significant microvascular changes at this time point posttreatment. Abnormal microvascular changes visualized by OCT in this preclinical setting suggest the potential of this label-free high-resolution noninvasive functional imaging methodology for RIF diagnosis and assessment in the context of clinical RT. (2018) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE).Entities:
Keywords: cancer treatment; microcirculation; optical coherence tomography; radiation-induced fibrosis; radiotherapy; speckle variance optical coherence tomography
Mesh:
Year: 2018 PMID: 30315644 DOI: 10.1117/1.JBO.23.10.106003
Source DB: PubMed Journal: J Biomed Opt ISSN: 1083-3668 Impact factor: 3.170