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An algorithm for longitudinal registration of PET/CT images acquired during neoadjuvant chemotherapy in breast cancer: preliminary results
BACKGROUND: By providing estimates of tumor glucose metabolism, (18)F-fluorodeoxyglucose positron emission tomography (FDG-PET) can potentially characterize the response of breast tumors to treatment. To assess therapy response, serial measurements of FDG-PET parameters (derived from static and/or d...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3520720/ https://www.ncbi.nlm.nih.gov/pubmed/23157877 http://dx.doi.org/10.1186/2191-219X-2-62 |
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author | Li, Xia Abramson, Richard G Arlinghaus, Lori R Chakravarthy, Anuradha Bapsi Abramson, Vandana Mayer, Ingrid Farley, Jaime Delbeke, Dominique Yankeelov, Thomas E |
author_facet | Li, Xia Abramson, Richard G Arlinghaus, Lori R Chakravarthy, Anuradha Bapsi Abramson, Vandana Mayer, Ingrid Farley, Jaime Delbeke, Dominique Yankeelov, Thomas E |
author_sort | Li, Xia |
collection | PubMed |
description | BACKGROUND: By providing estimates of tumor glucose metabolism, (18)F-fluorodeoxyglucose positron emission tomography (FDG-PET) can potentially characterize the response of breast tumors to treatment. To assess therapy response, serial measurements of FDG-PET parameters (derived from static and/or dynamic images) can be obtained at different time points during the course of treatment. However, most studies track the changes in average parameter values obtained from the whole tumor, thereby discarding all spatial information manifested in tumor heterogeneity. Here, we propose a method whereby serially acquired FDG-PET breast data sets can be spatially co-registered to enable the spatial comparison of parameter maps at the voxel level. METHODS: The goal is to optimally register normal tissues while simultaneously preventing tumor distortion. In order to accomplish this, we constructed a PET support device to enable PET/CT imaging of the breasts of ten patients in the prone position and applied a mutual information-based rigid body registration followed by a non-rigid registration. The non-rigid registration algorithm extended the adaptive bases algorithm (ABA) by incorporating a tumor volume-preserving constraint, which computed the Jacobian determinant over the tumor regions as outlined on the PET/CT images, into the cost function. We tested this approach on ten breast cancer patients undergoing neoadjuvant chemotherapy. RESULTS: By both qualitative and quantitative evaluation, our constrained algorithm yielded significantly less tumor distortion than the unconstrained algorithm: considering the tumor volume determined from standard uptake value maps, the post-registration median tumor volume changes, and the 25th and 75th quantiles were 3.42% (0%, 13.39%) and 16.93% (9.21%, 49.93%) for the constrained and unconstrained algorithms, respectively (p = 0.002), while the bending energy (a measure of the smoothness of the deformation) was 0.0015 (0.0005, 0.012) and 0.017 (0.005, 0.044), respectively (p = 0.005). CONCLUSION: The results indicate that the constrained ABA algorithm can accurately align prone breast FDG-PET images acquired at different time points while keeping the tumor from being substantially compressed or distorted. TRIAL REGISTRATION: NCT00474604 |
format | Online Article Text |
id | pubmed-3520720 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Springer |
record_format | MEDLINE/PubMed |
spelling | pubmed-35207202012-12-13 An algorithm for longitudinal registration of PET/CT images acquired during neoadjuvant chemotherapy in breast cancer: preliminary results Li, Xia Abramson, Richard G Arlinghaus, Lori R Chakravarthy, Anuradha Bapsi Abramson, Vandana Mayer, Ingrid Farley, Jaime Delbeke, Dominique Yankeelov, Thomas E EJNMMI Res Preliminary Research BACKGROUND: By providing estimates of tumor glucose metabolism, (18)F-fluorodeoxyglucose positron emission tomography (FDG-PET) can potentially characterize the response of breast tumors to treatment. To assess therapy response, serial measurements of FDG-PET parameters (derived from static and/or dynamic images) can be obtained at different time points during the course of treatment. However, most studies track the changes in average parameter values obtained from the whole tumor, thereby discarding all spatial information manifested in tumor heterogeneity. Here, we propose a method whereby serially acquired FDG-PET breast data sets can be spatially co-registered to enable the spatial comparison of parameter maps at the voxel level. METHODS: The goal is to optimally register normal tissues while simultaneously preventing tumor distortion. In order to accomplish this, we constructed a PET support device to enable PET/CT imaging of the breasts of ten patients in the prone position and applied a mutual information-based rigid body registration followed by a non-rigid registration. The non-rigid registration algorithm extended the adaptive bases algorithm (ABA) by incorporating a tumor volume-preserving constraint, which computed the Jacobian determinant over the tumor regions as outlined on the PET/CT images, into the cost function. We tested this approach on ten breast cancer patients undergoing neoadjuvant chemotherapy. RESULTS: By both qualitative and quantitative evaluation, our constrained algorithm yielded significantly less tumor distortion than the unconstrained algorithm: considering the tumor volume determined from standard uptake value maps, the post-registration median tumor volume changes, and the 25th and 75th quantiles were 3.42% (0%, 13.39%) and 16.93% (9.21%, 49.93%) for the constrained and unconstrained algorithms, respectively (p = 0.002), while the bending energy (a measure of the smoothness of the deformation) was 0.0015 (0.0005, 0.012) and 0.017 (0.005, 0.044), respectively (p = 0.005). CONCLUSION: The results indicate that the constrained ABA algorithm can accurately align prone breast FDG-PET images acquired at different time points while keeping the tumor from being substantially compressed or distorted. TRIAL REGISTRATION: NCT00474604 Springer 2012-11-16 /pmc/articles/PMC3520720/ /pubmed/23157877 http://dx.doi.org/10.1186/2191-219X-2-62 Text en Copyright ©2012 Li et al.; licensee Springer. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Preliminary Research Li, Xia Abramson, Richard G Arlinghaus, Lori R Chakravarthy, Anuradha Bapsi Abramson, Vandana Mayer, Ingrid Farley, Jaime Delbeke, Dominique Yankeelov, Thomas E An algorithm for longitudinal registration of PET/CT images acquired during neoadjuvant chemotherapy in breast cancer: preliminary results |
title | An algorithm for longitudinal registration of PET/CT images acquired during neoadjuvant chemotherapy in breast cancer: preliminary results |
title_full | An algorithm for longitudinal registration of PET/CT images acquired during neoadjuvant chemotherapy in breast cancer: preliminary results |
title_fullStr | An algorithm for longitudinal registration of PET/CT images acquired during neoadjuvant chemotherapy in breast cancer: preliminary results |
title_full_unstemmed | An algorithm for longitudinal registration of PET/CT images acquired during neoadjuvant chemotherapy in breast cancer: preliminary results |
title_short | An algorithm for longitudinal registration of PET/CT images acquired during neoadjuvant chemotherapy in breast cancer: preliminary results |
title_sort | algorithm for longitudinal registration of pet/ct images acquired during neoadjuvant chemotherapy in breast cancer: preliminary results |
topic | Preliminary Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3520720/ https://www.ncbi.nlm.nih.gov/pubmed/23157877 http://dx.doi.org/10.1186/2191-219X-2-62 |
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