Parisa Movahedi1, Hanne Hakkarainen2, Harri Merisaari1, Heidi Liljenbäck1, Helena Virtanen1, Hannu Juhani Aronen1, Heikki Minn1, Matti Poutanen1, Anne Roivainen1, Timo Liimatainen2, and Ivan Jambor1
Tumor growth in mice
preclinical prostate cancer model (human prostate cancer cells, PC-3) was
followed for 4 weeks by weekly DWI in control
group (n=10) and treatment group (n=9) receiving Docetaxel. DWI data sets were acquired using 15 b-values
in the range of 0-500s/mm2 and 12 b-values the range of 0-2000 s/mm2. The DWI
signal decays were fitted using monoexponential, biexponential, kurtosis and
stretched exponential models/functions. Bayesian shrinkage prior method and independent
least squares fitting have been applied and fitting quality evaluated by corrected
Akaike Information Criteria. Bayesian modeling improved quality of DWI
parametric maps derived using high b-value DWI data sets. Our result does not
support the use of biexponential, kurtosis and stretched exponential
models/functions for low b value DWI data sets of PC-3 mice
preclinical prostate cancer model.