| Literature DB >> 31304678 |
Yifeng Zeng1, Sreyankar Nandy1, Bin Rao1, Shuying Li1, Andrea R Hagemann2, Lindsay K Kuroki2, Carolyn McCourt2, David G Mutch2, Matthew A Powell2, Ian S Hagemann3,2, Quing Zhu1,4.
Abstract
Ovarian cancer is a heterogeneous disease at the molecular and histologic level. Optical coherence tomography (OCT) is able to map ovarian tissue optical properties and heterogeneity, which has been proposed as a feature to aid in diagnosis of ovarian cancer. In this manuscript, depth-resolved en face scattering maps of malignant ovaries, benign ovaries, and benign fallopian tubes obtained from 20 patients are provided to visualize the heterogeneity of ovarian tissues. Six features are extracted from histograms of scattering maps. All features are able to statistically distinguish benign from malignant ovaries. Two prediction models were constructed based on these features: a logistic regression model (LR) and a support vector machine (SVM). The optimal set of features is mean scattering coefficient and scattering map entropy. The LR achieved a sensitivity and specificity of 97.0% and 97.8%, and SVM demonstrated a sensitivity and specificity of 99.6% and 96.4%. Our initial results demonstrate the feasibility of using OCT as an "optical biopsy tool" for detecting the microscopic scattering changes associated with neoplasia in human ovarian tissue.Entities:
Keywords: cancer prediction; optical coherence tomography; ovarian cancer; scattering coefficient map
Mesh:
Year: 2019 PMID: 31304678 PMCID: PMC7982142 DOI: 10.1002/jbio.201900115
Source DB: PubMed Journal: J Biophotonics ISSN: 1864-063X Impact factor: 3.207