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Pharmacokinetic modeling of a novel hypoxia PET tracer [18F]HX4 in patients with non-small cell lung cancer

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2016

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Springer International Publishing
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Verwer, E. E., C. M. L. Zegers, W. van Elmpt, R. Wierts, A. D. Windhorst, F. M. Mottaghy, P. Lambin, and R. Boellaard. 2016. “Pharmacokinetic modeling of a novel hypoxia PET tracer [18F]HX4 in patients with non-small cell lung cancer.” EJNMMI Physics 3 (1): 30. doi:10.1186/s40658-016-0167-y. http://dx.doi.org/10.1186/s40658-016-0167-y.

Abstract

Background: [18F]HX4 is a promising new PET tracer developed to identify hypoxic areas in tumor tissue. This study analyzes [18F]HX4 kinetics and assesses the performance of simplified methods for quantification of [18F]HX4 uptake. To this end, eight patients with non-small cell lung cancer received dynamic PET scans at three different time points (0, 120, and 240 min) after injection of 426 ± 72 MBq [18F]HX4, each lasting 30 min. Several compartment models were fitted to time activity curves (TAC) derived from various areas within tumor tissue using image-derived input functions. Results: Best fits were obtained using the reversible two-tissue compartment model with blood volume parameter (2T4k+VB). Simplified measures correlated well with VT estimates (tumor-to-blood ratio (TBr) R 2 = 0.96, tumor-to-muscle ratio R 2 = 0.94, standardized uptake value R 2 = 0.89). Conclusions: [18F]HX4 shows reversible kinetics in tumor tissue: 2T4k+VB. TBr based on static imaging at 2 or 4 h can be used for quantification of [18F]HX4 uptake. Electronic supplementary material The online version of this article (doi:10.1186/s40658-016-0167-y) contains supplementary material, which is available to authorized users.

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Hypoxia, Molecular imaging, Positron emission tomography (PET), Non-small cell lung cancer (NSCLC), Tracer kinetic modeling, Standardized uptake value (SUV), Tumor-to-blood ratio, Image-derived input function (IDIF)

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