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Magnetic resonance imaging assessment of a convective therapy delivery paradigm in a canine prostate model
Author(s) -
Shetty Anil M.,
Stafford R. Jason,
Elliott Andrew M.,
Kassouf Wassim,
Brown Gordon A.,
Stephens L. Clifton,
Tinkey Peggy T.,
Bidaut Luc,
Pisters Louis L.,
Hazle John D.
Publication year - 2007
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.21206
Subject(s) - ex vivo , in vivo , magnetic resonance imaging , nuclear medicine , medicine , prostate , pathology , biomedical engineering , radiology , biology , microbiology and biotechnology , cancer
Purpose To quantitatively investigate the feasibility of MRI as a tool for assessing the spatial distribution of a convectively delivered agent using a canine prostate model. Materials and Methods Canine prostates (ex vivo, n = 3; in vivo, n = 12) were injected under several injection paradigms with a solution of gadolinium‐DTPA for MR contrast and methylene blue as a grossly visible surrogate drug marker. Ex vivo and in vivo distributions were assessed at 1.5T and quantitatively compared. Results Measured distributions using MRI and methylene blue pathology photographs were analyzed using a Bland–Altman method. The fractional percentage volume covered (V frac ) compared the measurements grossly: Pearson's correlation coefficients were R = 0.99 for ex vivo and R = 0.77 for in vivo ( P < 0.05). The fractional percentage of area covered (A frac ) demonstrated the high degree of spatial correlation between individual slices: R = 0.93 for ex vivo and R = 0.98 for in vivo ( P < 0.05). There was no statistically observable bias in scale or offset between the measurements. Conclusion Measured distributions using MRI and pathology were highly correlated and unbiased, indicating the potential of MRI as a tool for quantitative assessment of interstitial delivery of injected therapies in vivo. J. Magn. Reson. Imaging 2007. © 2007 Wiley‐Liss, Inc.