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Evaluation of limited blood sampling population input approaches for kinetic quantification of [(18)F]fluorothymidine PET data

BACKGROUND: Quantification of kinetic parameters of positron emission tomography (PET) imaging agents normally requires collecting arterial blood samples which is inconvenient for patients and difficult to implement in routine clinical practice. The aim of this study was to investigate whether a pop...

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Autores principales: Contractor, Kaiyumars B, Kenny, Laura M, Coombes, Charles R, Turkheimer, Federico E, Aboagye, Eric O, Rosso, Lula
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3340309/
https://www.ncbi.nlm.nih.gov/pubmed/22444834
http://dx.doi.org/10.1186/2191-219X-2-11
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author Contractor, Kaiyumars B
Kenny, Laura M
Coombes, Charles R
Turkheimer, Federico E
Aboagye, Eric O
Rosso, Lula
author_facet Contractor, Kaiyumars B
Kenny, Laura M
Coombes, Charles R
Turkheimer, Federico E
Aboagye, Eric O
Rosso, Lula
author_sort Contractor, Kaiyumars B
collection PubMed
description BACKGROUND: Quantification of kinetic parameters of positron emission tomography (PET) imaging agents normally requires collecting arterial blood samples which is inconvenient for patients and difficult to implement in routine clinical practice. The aim of this study was to investigate whether a population-based input function (POP-IF) reliant on only a few individual discrete samples allows accurate estimates of tumour proliferation using [(18)F]fluorothymidine (FLT). METHODS: Thirty-six historical FLT-PET data with concurrent arterial sampling were available for this study. A population average of baseline scans blood data was constructed using leave-one-out cross-validation for each scan and used in conjunction with individual blood samples. Three limited sampling protocols were investigated including, respectively, only seven (POP-IF7), five (POP-IF5) and three (POP-IF3) discrete samples of the historical dataset. Additionally, using the three-point protocol, we derived a POP-IF3M, the only input function which was not corrected for the fraction of radiolabelled metabolites present in blood. The kinetic parameter for net FLT retention at steady state, K(i), was derived using the modified Patlak plot and compared with the original full arterial set for validation. RESULTS: Small percentage differences in the area under the curve between all the POP-IFs and full arterial sampling IF was found over 60 min (4.2%-5.7%), while there were, as expected, larger differences in the peak position and peak height. A high correlation between K(i )values calculated using the original arterial input function and all the population-derived IFs was observed (R(2 )= 0.85-0.98). The population-based input showed good intra-subject reproducibility of K(i )values (R(2 )= 0.81-0.94) and good correlation (R(2 )= 0.60-0.85) with Ki-67. CONCLUSIONS: Input functions generated using these simplified protocols over scan duration of 60 min estimate net PET-FLT retention with reasonable accuracy.
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spelling pubmed-33403092012-05-01 Evaluation of limited blood sampling population input approaches for kinetic quantification of [(18)F]fluorothymidine PET data Contractor, Kaiyumars B Kenny, Laura M Coombes, Charles R Turkheimer, Federico E Aboagye, Eric O Rosso, Lula EJNMMI Res Original Research BACKGROUND: Quantification of kinetic parameters of positron emission tomography (PET) imaging agents normally requires collecting arterial blood samples which is inconvenient for patients and difficult to implement in routine clinical practice. The aim of this study was to investigate whether a population-based input function (POP-IF) reliant on only a few individual discrete samples allows accurate estimates of tumour proliferation using [(18)F]fluorothymidine (FLT). METHODS: Thirty-six historical FLT-PET data with concurrent arterial sampling were available for this study. A population average of baseline scans blood data was constructed using leave-one-out cross-validation for each scan and used in conjunction with individual blood samples. Three limited sampling protocols were investigated including, respectively, only seven (POP-IF7), five (POP-IF5) and three (POP-IF3) discrete samples of the historical dataset. Additionally, using the three-point protocol, we derived a POP-IF3M, the only input function which was not corrected for the fraction of radiolabelled metabolites present in blood. The kinetic parameter for net FLT retention at steady state, K(i), was derived using the modified Patlak plot and compared with the original full arterial set for validation. RESULTS: Small percentage differences in the area under the curve between all the POP-IFs and full arterial sampling IF was found over 60 min (4.2%-5.7%), while there were, as expected, larger differences in the peak position and peak height. A high correlation between K(i )values calculated using the original arterial input function and all the population-derived IFs was observed (R(2 )= 0.85-0.98). The population-based input showed good intra-subject reproducibility of K(i )values (R(2 )= 0.81-0.94) and good correlation (R(2 )= 0.60-0.85) with Ki-67. CONCLUSIONS: Input functions generated using these simplified protocols over scan duration of 60 min estimate net PET-FLT retention with reasonable accuracy. Springer 2012-03-24 /pmc/articles/PMC3340309/ /pubmed/22444834 http://dx.doi.org/10.1186/2191-219X-2-11 Text en Copyright ©2012 Contractor 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 Original Research
Contractor, Kaiyumars B
Kenny, Laura M
Coombes, Charles R
Turkheimer, Federico E
Aboagye, Eric O
Rosso, Lula
Evaluation of limited blood sampling population input approaches for kinetic quantification of [(18)F]fluorothymidine PET data
title Evaluation of limited blood sampling population input approaches for kinetic quantification of [(18)F]fluorothymidine PET data
title_full Evaluation of limited blood sampling population input approaches for kinetic quantification of [(18)F]fluorothymidine PET data
title_fullStr Evaluation of limited blood sampling population input approaches for kinetic quantification of [(18)F]fluorothymidine PET data
title_full_unstemmed Evaluation of limited blood sampling population input approaches for kinetic quantification of [(18)F]fluorothymidine PET data
title_short Evaluation of limited blood sampling population input approaches for kinetic quantification of [(18)F]fluorothymidine PET data
title_sort evaluation of limited blood sampling population input approaches for kinetic quantification of [(18)f]fluorothymidine pet data
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3340309/
https://www.ncbi.nlm.nih.gov/pubmed/22444834
http://dx.doi.org/10.1186/2191-219X-2-11
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