TY - GEN
T1 - Influence of three reconstruction algorithms on the estimation of the standardize uptake value in 18F-fluoride PET
AU - Grecchi, Elisabetta
AU - Thielemans, Kris
AU - Cook, Gary J.
AU - Tsoumpas, Charalampos
PY - 2013
Y1 - 2013
N2 - In clinical practice accurate and precise quantification of PET images is of crucial importance especially for tumor staging when comparing pre- and post- treatment scans. For example a change in the standardized uptake values (SUV) of 10-20% can discriminate whether a treatment is effective or not. However, several factors cause degradation of the accuracy and precision of quantitative information. Iterative reconstruction methods can help towards more accurate tumor delineation and potentially quantification. However, the most commonly used reconstruction technique (Ordered Subset Expectation Maximization, OSEM) has pitfalls that are critical for quantification: bias (e.g. at early iterations and at low count statistics) and noise (e.g. at late iterations). The aim of this work is to evaluate the quantitative performance of existing reconstruction algorithms with acquired phantom data and PET/CT ( 18F-fluoride and 11C-choline) scans of patients with metastatic prostate cancer. Data are reconstructed with three different ordered subset (OS) methods: OSEM, OS Maximum A Posteriori One Step Late (OSMAPOSL) with the Median Root Prior and OS Separable Paraboloidal Surrogate (OSSPS) with the Quadratic Prior. These three algorithms are available with the open source Software for Tomographic Image Reconstruction (STIR, http://stir.sf.net). We investigate the SUVmax and SUVmean for each of the three reconstruction methods and how they change over sub-iteration. Our findings show that the subset limit cycle behavior does not affect the comparison of the SUV estimates for identical acquisition. On the other hand fine parameter tuning is necessary to achieve better tradeoff between convergence, bias and noise.
AB - In clinical practice accurate and precise quantification of PET images is of crucial importance especially for tumor staging when comparing pre- and post- treatment scans. For example a change in the standardized uptake values (SUV) of 10-20% can discriminate whether a treatment is effective or not. However, several factors cause degradation of the accuracy and precision of quantitative information. Iterative reconstruction methods can help towards more accurate tumor delineation and potentially quantification. However, the most commonly used reconstruction technique (Ordered Subset Expectation Maximization, OSEM) has pitfalls that are critical for quantification: bias (e.g. at early iterations and at low count statistics) and noise (e.g. at late iterations). The aim of this work is to evaluate the quantitative performance of existing reconstruction algorithms with acquired phantom data and PET/CT ( 18F-fluoride and 11C-choline) scans of patients with metastatic prostate cancer. Data are reconstructed with three different ordered subset (OS) methods: OSEM, OS Maximum A Posteriori One Step Late (OSMAPOSL) with the Median Root Prior and OS Separable Paraboloidal Surrogate (OSSPS) with the Quadratic Prior. These three algorithms are available with the open source Software for Tomographic Image Reconstruction (STIR, http://stir.sf.net). We investigate the SUVmax and SUVmean for each of the three reconstruction methods and how they change over sub-iteration. Our findings show that the subset limit cycle behavior does not affect the comparison of the SUV estimates for identical acquisition. On the other hand fine parameter tuning is necessary to achieve better tradeoff between convergence, bias and noise.
U2 - 10.1109/NSSMIC.2013.6829363
DO - 10.1109/NSSMIC.2013.6829363
M3 - Conference contribution
AN - SCOPUS:84904184035
SN - 9781479905348
T3 - IEEE Nuclear Science Symposium Conference Record
BT - 2013 IEEE Nuclear Science Symposium and Medical Imaging Conference, NSS/MIC 2013
PB - Institute of Electrical and Electronics Engineers Inc.
T2 - 2013 60th IEEE Nuclear Science Symposium and Medical Imaging Conference, NSS/MIC 2013
Y2 - 27 October 2013 through 2 November 2013
ER -