TY - JOUR
T1 - Comparison of residence time estimation methods for radioimmunotherapy dosimetry and treatment planning-Monte Carlo simulation studies
AU - He, Bin
AU - Wahl, Richard L.
AU - Du, Yong
AU - Sgouros, George
AU - Jacene, Heather
AU - Flinn, Ian
AU - Frey, Eric C.
N1 - Funding Information:
The reconstruction code used in this work has been licensed to GE Healthcare for inclusion in a commercial product. Under separate licensing agreements between the General Electric Corporation and the Johns Hopkins University and the University of North Carolina at Chapel Hill and GE Healthcare, E. C. Frey is entitled to a share of royalty received by the universities on sales of products described in this article. The terms of this arrangement are being managed by the Johns Hopkins University in accordance with its conflict of interest policies. R. L. Wahl has received speakers fee and research grant support from GE Healthcare. R. L. Wahl has licensed inventions regarding radioimmunotherapy through the University of Michigan to GlaxoSmithKline and Biogen-Idec related to RIT agents Bexxar and Zevalin. He receives royalties from the sale of these agents. These agreements are being managed by the Johns Hopkins University in accordance with its conflict of interest policies.
Funding Information:
Manuscript received May 8, 2007; revised August 28, 2007. This work was supported by the National Institutes of Health (NIH) under Grant R01-CA109234. The content of this work is solely the responsibility of the authors and does not necessarily represent the official view of the NIH or its various institutes. Asterisk indicates corresponding author. *B. He is with the Department of Radiology, The Johns Hopkins University, 601 North Caroline Street, Baltimore, MD 21287 USA (e-mail: binhe@jhmi. edu).
PY - 2008/4
Y1 - 2008/4
N2 - Estimating the residence times in tumor and normal organs is an essential part of treatment planning for radioimmunotherapy (RIT). This estimation is usually done using a conjugate view whole body scan time series and planar processing. This method has logistical and cost advantages compared to 3-D imaging methods such as Single photon emission computed tomography (SPECT), but, because it does not provide information about the 3-D distribution of activity, it is difficult to fully compensate for effects such as attenuation and background and overlapping activity. Incomplete compensation for these effects reduces the accuracy of the residence time estimates. In this work we compare residence times estimates obtained using planar methods to those from methods based on quantitative SPECT (QSPECT) reconstructions. We have previously developed QSPECT methods that provide compensation for attenuation, scatter, collimator-detector response, and partial volume effects. In this study we compared the use of residence time estimation methods using QSPECT to planar methods. The evaluation was done using the realistic NCAT phantom with organ time activities that model 111In ibritumomab tiuxetan. Projection data were obtained using Monte Carlo simulations (MCS) that realistically model the image formation process including penetration and scatter in the collimator-detector system. These projection data were used to evaluate the accuracy of residence time estimation using a time series of QSPECT studies, a single QSPECT study combined with planar scans and the planar scans alone. The errors in the residence time estimates were <3.8%, <15%, and 2%-107% for the QSPECT, hybrid planar/QSPECT, and planar methods, respectively. The quantitative accuracy was worst for pure planar processing and best for pure QSPECT processing. Hybrid planar/QSPECT methods, where a single QSPECT study was combined with a series of planar scans, provided a large and statistically significant improvement in quantitative accuracy for most organs compared to the planar scans alone, even without sophisticated attention to background subtraction or thickness corrections in planar processing. These results indicate that hybrid planar/QSPECT methods are generally superior to pure planar methods and may be an acceptable alternative to performing a time series of QSPECT studies.
AB - Estimating the residence times in tumor and normal organs is an essential part of treatment planning for radioimmunotherapy (RIT). This estimation is usually done using a conjugate view whole body scan time series and planar processing. This method has logistical and cost advantages compared to 3-D imaging methods such as Single photon emission computed tomography (SPECT), but, because it does not provide information about the 3-D distribution of activity, it is difficult to fully compensate for effects such as attenuation and background and overlapping activity. Incomplete compensation for these effects reduces the accuracy of the residence time estimates. In this work we compare residence times estimates obtained using planar methods to those from methods based on quantitative SPECT (QSPECT) reconstructions. We have previously developed QSPECT methods that provide compensation for attenuation, scatter, collimator-detector response, and partial volume effects. In this study we compared the use of residence time estimation methods using QSPECT to planar methods. The evaluation was done using the realistic NCAT phantom with organ time activities that model 111In ibritumomab tiuxetan. Projection data were obtained using Monte Carlo simulations (MCS) that realistically model the image formation process including penetration and scatter in the collimator-detector system. These projection data were used to evaluate the accuracy of residence time estimation using a time series of QSPECT studies, a single QSPECT study combined with planar scans and the planar scans alone. The errors in the residence time estimates were <3.8%, <15%, and 2%-107% for the QSPECT, hybrid planar/QSPECT, and planar methods, respectively. The quantitative accuracy was worst for pure planar processing and best for pure QSPECT processing. Hybrid planar/QSPECT methods, where a single QSPECT study was combined with a series of planar scans, provided a large and statistically significant improvement in quantitative accuracy for most organs compared to the planar scans alone, even without sophisticated attention to background subtraction or thickness corrections in planar processing. These results indicate that hybrid planar/QSPECT methods are generally superior to pure planar methods and may be an acceptable alternative to performing a time series of QSPECT studies.
KW - Absolute quantitation
KW - Quantitative SPECT
KW - Radioimmunotherapy
KW - Residence time
UR - http://www.scopus.com/inward/record.url?scp=41649099345&partnerID=8YFLogxK
U2 - 10.1109/TMI.2007.908131
DO - 10.1109/TMI.2007.908131
M3 - Article
C2 - 18390348
AN - SCOPUS:41649099345
SN - 0278-0062
VL - 27
SP - 521
EP - 530
JO - IEEE Transactions on Medical Imaging
JF - IEEE Transactions on Medical Imaging
IS - 4
M1 - 4359074
ER -