z-logo
Premium
Scan‐rescan variability in perfusion assessment of tumors in MRI using both model and data‐derived arterial input functions
Author(s) -
Ashton Edward,
Raunig David,
Ng Chaan,
Kelcz Fredrick,
McShane Teresa,
Evelhoch Jeffrey
Publication year - 2008
Publication title -
journal of magnetic resonance imaging
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.563
H-Index - 160
eISSN - 1522-2586
pISSN - 1053-1807
DOI - 10.1002/jmri.21472
Subject(s) - perfusion , medicine , radiology , nuclear medicine
Purpose To evaluate the contribution to scan‐rescan coefficient of variation (CV) of patient‐specific arterial input function (AIF) measurement in dynamic contrast‐enhanced MRI (DCE‐MRI) data, and to determine whether any advantage or disadvantage to using a data‐derived arterial input function is related to the anatomical location of the target lesion. Materials and Methods Two methods are presented for the calculation of perfusion parameters from DCE‐MRI data using a two‐compartment model. The first method makes use of a single‐model AIF across all study data sets, while the second uses an automated process to derive an AIF specific to each data set. Both methods are applied to the analysis of a 25‐subject scan‐rescan study of patients with advanced solid tumors located in either the lungs or the liver. The parameters of interest in this study are the volume transfer constant between arterial plasma and extracellular extravascular space ( K trans ) and the blood‐normalized initial area under the tumor enhancement curve over the first 90 seconds postinjection ( IAUCBN 90 ). Results The use of a data‐derived AIF reduces the visit‐to‐visit CV in both parameters for liver lesions by approximately 70% while the improvement is less than 20% for lung lesions. Conclusion The use of a data‐derived AIF in the analysis of DCE‐MRI data provides a substantial reduction in scan‐rescan CV in the measurement of vascular parameters such as K trans and IAUCBN 90 . These results show a much larger advantage in the liver than in the lungs. However, this difference is largely driven by a small number of outliers, and may be spurious. J. Magn. Reson. Imaging 2008;28:791–796. © 2008 Wiley‐Liss, Inc.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here