Dynamic contrast enhanced MRI of prostate cancer: correlation with morphology and tumour stage, histological grade and PSA.

AIM: To quantify MRI enhancement characteristics of normal and abnormal prostatic tissues and to correlate these with tumour stage, histological grade and tumour markers. MATERIALS AND METHODS: Quantitative gradient recalled echo MR images were obtained following bolus injection of gadopentetate dimeglumine in 48 patients with prostate cancer. Turbo spin-echo T2-weighted images at the same anatomical position were reviewed for the presence of tumours (45 regions), normal peripheral zone (33 regions), and normal appearing central gland (30 regions). Time-signal intensity parameters (onset time, mean gradient and maximal amplitude of enhancement and wash-out score) and modelling parameters (permeability surface area product, lesion leakage space and maximum gadolinium concentration) were correlated with tumour stage, histological grade (Gleason score) and serum prostatic specific antigen (PSA) levels. RESULTS: Significant differences were noted between peripheral zone and tumour with respect to signal intensity and modelling parameters (P = 0.0001), except onset time. No differences between central gland and tumour enhancement values were seen. There was weak correlation between MRI tumour stage and tumour vascular permeability (r(2) = 12%; P = 0.02) and maximum tumour gadolinium concentration (r(2) = 14%; P = 0.015). However, no significant correlations were seen with Gleason score or PSA levels. CONCLUSION: Quantification of MR contrast enhancement characteristics allows tissue discrimination in prostate cancer consistent with known variations in microvessel density estimates.

Comparative efficacy of and sequence choice for two oral contrast agents used during MR imaging.

OBJECTIVE: Our objective was to compare the efficacy of a positive and a negative oral contrast agent and to determine the optimal sequence choice for use in pelvic MR imaging. SUBJECTS AND METHODS: We undertook a prospective randomized trial of 57 patients with pelvic cancer who were examined with MR imaging after oral administration of a positive contrast agent (27 patients) or a negative contrast agent (30 patients). T1- and T2-weighted breath-hold and non-breath-hold gradient-recalled echo and turbo spin-echo sequences were obtained. Using the hard-copy images, we graded filling and distention of the small bowel, bowel wall conspicuity, delineation of normal and pathologic structures, and artifacts. RESULTS: Good or excellent small-bowel filling and distention was obtained in 17 patients (63%) receiving the positive agent and in 26 patients (87%) receiving the negative agent, and bowel wall conspicuity was graded good or excellent in 19 patients (70%) and 20 patients (67%), respectively. Normal and pathologic structures were better delineated with the negative agent (20 patients [74%] and 27 patients [90%], respectively; p = .02). Breath-hold gradient-recalled echo T1-weighted images were preferred for the positive agent (78%), and breath-hold T2-weighted images were preferred for the negative agent (93%). Contrast artifacts were more frequently seen with the negative agent (11% and 93%, respectively; p = .0001), and such artifacts were eliminated using T2-weighted sequences. CONCLUSION: Both contrast agents were effective in pelvic MR imaging, but delineation of normal and pathologic structures was better with the negative agent. Gradient-recalled echo T1-weighted sequences are recommended for positive contrast agents, and breath-hold T2-weighted sequences are recommended for negative contrast agents.

Probing tumor microvascularity by measurement, analysis and display of contrast agent uptake kinetics.

This paper describes a measurement protocol for acquiring quantitative dynamic MRI data and novel analysis and display software (Magnetic Resonance Imaging Workbench (MRIW)). Proton density-weighted and T1-weighted two-dimensional gradient echo images are used to quantify tissue contrast agent concentration. The dynamic studies last approximately 7 minutes, with 10-second temporal resolution. Analyses of signal and concentration changes with time are performed, allowing capillary permeability-surface area product, tissue leakage space, enhancement onset time, mean enhancement gradient and maximum enhancement level to be mapped as false-color parametric overlays registered with anatomic images. Quantification of permeability and leakage space provides a method for comparing physiology in patients between visits or for intersite comparisons.