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      A Quantitative Diffuse Reflectance Imaging (QDRI) System for Comprehensive Surveillance of the Morphological Landscape in Breast Tumor Margins

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          Abstract

          In an ongoing effort to address the clear clinical unmet needs surrounding breast conserving surgery (BCS), our group has developed a next-generation multiplexed optical-fiber-based tool to assess breast tumor margin status during initial surgeries. Specifically detailed in this work is the performance and clinical validation of a research-grade intra-operative tool for margin assessment based on diffuse optical spectroscopy. Previous work published by our group has illustrated the proof-of-concept generations of this device; here we incorporate a highly optimized quantitative diffuse reflectance imaging (QDRI) system utilizing a wide-field (imaging area = 17cm 2) 49-channel multiplexed fiber optic probe, a custom raster-scanning imaging platform, a custom dual-channel white LED source, and an astronomy grade imaging CCD and spectrograph. The system signal to noise ratio (SNR) was found to be greater than 40dB for all channels. Optical property estimation error was found to be less than 10%, on average, over a wide range of absorption (μ a = 0–8.9cm -1) and scattering (μ s’ = 7.0–9.7cm -1) coefficients. Very low inter-channel and CCD crosstalk was observed (2% max) when used on turbid media (including breast tissue). A raster-scanning mechanism was developed to achieve sub-pixel resolution and was found to be optimally performed at an upsample factor of 8, affording 0.75mm spatially resolved diffuse reflectance images (λ = 450–600nm) of an entire margin (area = 17cm 2) in 13.8 minutes (1.23cm 2/min). Moreover, controlled pressure application at the probe-tissue interface afforded by the imaging platform reduces repeated scan variability, providing <1% variation across repeated scans of clinical specimens. We demonstrate the clinical utility of this device through a pilot 20-patient study of high-resolution optical parameter maps of the ratio of the β-carotene concentration to the reduced scattering coefficient. An empirical cumulative distribution function (eCDF) analysis is used to reduce optical property maps to quantitative distributions representing the morphological landscape of breast tumor margins. The optimizations presented in this work provide an avenue to rapidly survey large tissue areas on intra-operative time scales with improved sensitivity to regions of focal disease that may otherwise be overlooked.

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          Diffuse reflectance spectroscopy of human adenomatous colon polyps in vivo.

          Diffuse reflectance spectra were collected from adenomatous colon polyps (cancer precursors) and normal colonic mucosa of patients undergoing colonoscopy. We analyzed the data by using an analytical light diffusion model, which was tested and validated on a physical tissue model composed of polystyrene beads and hemoglobin. Four parameters were obtained: hemoglobin concentration, hemoglobin oxygen saturation, effective scatterer density, and effective scatterer size. Normal and adenomatous tissue sites exhibited differences in hemoglobin concentration and, on average, in effective scatterer size, which were in general agreement with other studies that employ standard methods. These results suggest that diffuse reflectance can be used to obtain tissue information about tissue structure and composition in vivo.
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            MCML--Monte Carlo modeling of light transport in multi-layered tissues.

            A Monte Carlo model of steady-state light transport in multi-layered tissues (MCML) has been coded in ANSI Standard C; therefore, the program can be used on various computers. Dynamic data allocation is used for MCML, hence the number of tissue layers and grid elements of the grid system can be varied by users at run time. The coordinates of the simulated data for each grid element in the radial and angular directions are optimized. Some of the MCML computational results have been verified with those of other theories or other investigators. The program, including the source code, has been in the public domain since 1992.
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              Factors predicting the use of breast-conserving therapy in stage I and II breast carcinoma.

              To define patterns of care for the local therapy of stage I and II breast cancer and to identify factors used to select patients for breast-conserving therapy (BCT). A convenience sample of 16,643 patients with stage I and II breast cancer treated in 1994 was obtained from hospital-based tumor registries. Histologic variables were determined from original pathology reports. BCT was performed in 42.6% of patients. Multivariate analysis demonstrated that living in the Northeast United States (odds ratio [OR], 2.48; 95% confidence interval [CI], 2.16 to 2.84), having a clinical T1 tumor (OR, 2.51; 95% CI, 2.27 to 2.78), and having a tumor without an extensive intraductal component (OR, 2.07; 95% CI, 1.81 to 2.37) were the strongest predictors of breast-conserving surgery. Radiation therapy was given to 86% of patients who had breast-conserving surgery. Age less than 70 years was the most significant predictor of receiving radiation (OR, 2.11; 95% CI, 1.77 to 2.25). Tumor variables did not correlate with the use of radiation, but favorable tumor characteristics were associated with the use of breast-conserving surgery. Despite strong evidence supporting the use of BCT, the majority of women continue to be treated with mastectomy. Predictors of the use of BCT do not correspond to those suggested in guidelines.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, CA USA )
                1932-6203
                15 June 2015
                2015
                : 10
                : 6
                : e0127525
                Affiliations
                [1 ]Department of Biomedical Engineering, Duke University, Durham, NC, United States of America
                [2 ]Department of Pathology, Duke University Medical Center, Durham, NC, United States of America
                [3 ]Department of Surgery, Duke University Medical Center, Durham, NC, United States of America
                [4 ]Department of Surgery, The University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, United States of America
                [5 ]Zenalux Biomedical, Research Triangle Park, NC, United States of America
                [6 ]Department of Biomedical Engineering, Tulane University, New Orleans, LA, United States of America
                [7 ]The Division of Environmental Sciences and Policy, Duke University, Durham, NC, United States of America
                Institute of Physics, University of Zurich, SWITZERLAND
                Author notes

                Competing Interests: Dr. Brown, Ms. Krieger, Dr. von Windheim, and Dr. Ramanujam own stock in, and have been employed by or provided consulting services for, Zenalux Biomedical, Inc., a company which developed portions of the technology described in this manuscript. Zenalux Biomedical has licenses, or options to license, intellectual property invented by Dr. Ramanujam and Dr. Brown. Zenalux Biomedical did not support any of the original work reported in this manuscript, either in cash or in kind. Zenalux, Inc. developed the 49-channel fiber-optic probe (trademark C49) and provided the imaging spectrograph described in this manuscript. All other components, including the light source, imaging platform, and acquisition software, were developed at Duke University. The Monte-Carlo inversion algorithm used as one component of the software is used under license to Zenalux, Inc., (US PATENT 7,570,988). This does not alter the authors’ adherence to all the PLOS ONE policies on sharing data and materials.

                Conceived and designed the experiments: BSN NR JQB MSK J. Geradts RG. Performed the experiments: BSN CES CM J. Gallagher. Analyzed the data: BSN CES NR CM JQB J. Geradts. Contributed reagents/materials/analysis tools: BSN NR JVW JQB. Wrote the paper: BSN CES JQB LGW CM MSK J. Gallagher J. Geradts RG JVW NR.

                Article
                PONE-D-15-00581
                10.1371/journal.pone.0127525
                4468201
                26076123
                b8734cbe-e74f-4661-af86-0a29eaf37c30
                Copyright @ 2015

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited

                History
                : 7 January 2015
                : 16 April 2015
                Page count
                Figures: 11, Tables: 2, Pages: 25
                Funding
                This project was supported by the Department of Defense (DOD) ( http://www.defense.gov/) Grant Number W81XWH-09-1-0410 and by the Small Business Technology Transfer (STTR) ( http://www.sbir.gov) phase II Grant Number 2R42CA128160-02 “Fast Spectral Imaging Device For Tumor Margin Mapping” awarded to Zenalux, Inc. and Duke University. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Zenalux, Inc. provided support in the form of salaries for authors JQB, MSK, JAvW, and NR, but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific roles of these authors are articulated in the 'author contributions' section.
                Categories
                Research Article
                Custom metadata
                All relevant non-clinical data are within the paper and its Supporting Information files. The clinical reflectance data can be found at: http://dukespace.lib.duke.edu/dspace/handle/10161/9504.

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