High-Resolution Computed Tomography of Single Breast Cancer Microcalcifications in Vivo

Microcalcification is a hallmark of breast cancer and a key diagnostic feature for mammography. We recently described the first robust animal model of breast cancer microcalcification. In this study, we hypothesized that high-resolution computed tomography (CT) could potentially detect the genesis o...

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Main Authors: Kazumasa Inoue, Fangbing Liu, Jack Hoppin, Elaine P. Lunsford, Christian Lackas, Jacob Hesterman, Robert E. Lenkinski, Hirofumi Fujii, John V. Frangioni
Format: Article
Language:English
Published: SAGE Publishing 2011-07-01
Series:Molecular Imaging
Online Access:https://doi.org/10.2310/7290.2010.00050
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author Kazumasa Inoue
Fangbing Liu
Jack Hoppin
Elaine P. Lunsford
Christian Lackas
Jacob Hesterman
Robert E. Lenkinski
Hirofumi Fujii
John V. Frangioni
author_facet Kazumasa Inoue
Fangbing Liu
Jack Hoppin
Elaine P. Lunsford
Christian Lackas
Jacob Hesterman
Robert E. Lenkinski
Hirofumi Fujii
John V. Frangioni
author_sort Kazumasa Inoue
collection DOAJ
description Microcalcification is a hallmark of breast cancer and a key diagnostic feature for mammography. We recently described the first robust animal model of breast cancer microcalcification. In this study, we hypothesized that high-resolution computed tomography (CT) could potentially detect the genesis of a single microcalcification in vivo and quantify its growth over time. Using a commercial CT scanner, we systematically optimized acquisition and reconstruction parameters. Two ray-tracing image reconstruction algorithms were tested: a voxel-driven “fast” cone beam algorithm (FCBA) and a detector-driven “exact” cone beam algorithm (ECBA). By optimizing acquisition and reconstruction parameters, we were able to achieve a resolution of 104 μm full width at half-maximum (FWHM). At an optimal detector sampling frequency, the ECBA provided a 28 μm (21%) FWHM improvement in resolution over the FCBA. In vitro, we were able to image a single 300 μm X 100 μm hydroxyapatite crystal. In a syngeneic rat model of breast cancer, we were able to detect the genesis of a single microcalcification in vivo and follow its growth longitudinally over weeks. Taken together, this study provides an in vivo “gold standard” for the development of calcification-specific contrast agents and a model system for studying the mechanism of breast cancer microcalcification.
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spelling doaj-art-8c862d8289c9413c83e0f75187fe38862025-01-02T21:31:26ZengSAGE PublishingMolecular Imaging1536-01212011-07-011010.2310/7290.2010.0005010.2310_7290.2010.00050High-Resolution Computed Tomography of Single Breast Cancer Microcalcifications in VivoKazumasa InoueFangbing LiuJack HoppinElaine P. LunsfordChristian LackasJacob HestermanRobert E. LenkinskiHirofumi FujiiJohn V. FrangioniMicrocalcification is a hallmark of breast cancer and a key diagnostic feature for mammography. We recently described the first robust animal model of breast cancer microcalcification. In this study, we hypothesized that high-resolution computed tomography (CT) could potentially detect the genesis of a single microcalcification in vivo and quantify its growth over time. Using a commercial CT scanner, we systematically optimized acquisition and reconstruction parameters. Two ray-tracing image reconstruction algorithms were tested: a voxel-driven “fast” cone beam algorithm (FCBA) and a detector-driven “exact” cone beam algorithm (ECBA). By optimizing acquisition and reconstruction parameters, we were able to achieve a resolution of 104 μm full width at half-maximum (FWHM). At an optimal detector sampling frequency, the ECBA provided a 28 μm (21%) FWHM improvement in resolution over the FCBA. In vitro, we were able to image a single 300 μm X 100 μm hydroxyapatite crystal. In a syngeneic rat model of breast cancer, we were able to detect the genesis of a single microcalcification in vivo and follow its growth longitudinally over weeks. Taken together, this study provides an in vivo “gold standard” for the development of calcification-specific contrast agents and a model system for studying the mechanism of breast cancer microcalcification.https://doi.org/10.2310/7290.2010.00050
spellingShingle Kazumasa Inoue
Fangbing Liu
Jack Hoppin
Elaine P. Lunsford
Christian Lackas
Jacob Hesterman
Robert E. Lenkinski
Hirofumi Fujii
John V. Frangioni
High-Resolution Computed Tomography of Single Breast Cancer Microcalcifications in Vivo
Molecular Imaging
title High-Resolution Computed Tomography of Single Breast Cancer Microcalcifications in Vivo
title_full High-Resolution Computed Tomography of Single Breast Cancer Microcalcifications in Vivo
title_fullStr High-Resolution Computed Tomography of Single Breast Cancer Microcalcifications in Vivo
title_full_unstemmed High-Resolution Computed Tomography of Single Breast Cancer Microcalcifications in Vivo
title_short High-Resolution Computed Tomography of Single Breast Cancer Microcalcifications in Vivo
title_sort high resolution computed tomography of single breast cancer microcalcifications in vivo
url https://doi.org/10.2310/7290.2010.00050
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