AJR:174, June 2000 1575
Initial Experience with
Contrast-Enhanced Sonography
of the Prostate
OBJECTIVE. We investigated the usefulness of contrast-enhanced sonography to depict
vascularity in the prostate and improve the detection of prostatic cancer.
SUBJECTS AND METHODS. Twenty-six patients with an elevated prostate-specific
antigen level (≥ 4 ng/ml) or an abnormal digital rectal examination were enrolled in a phase II
study of an IV injected sonographic contrast agent. Continuous gray-scale, intermittent gray-
scale, phase inversion gray-scale, and power Doppler sonography of the prostate were per-
formed. Sonographic findings were correlated with sextant biopsy results.
RESULTS. After the administration of contrast material, gray-scale and Doppler images
revealed visible enhancement ( p < 0.05). Using intermittent imaging, we found focal en-
hancement in two isoechoic tumors that were not visible on baseline images. No definite focal
area of enhancement was identified in any patient without cancer. Contrast-enhanced images
revealed transient hemorrhage in the biopsy tracts of three patients.
CONCLUSION. Enhancement of the prostate can be seen on gray-scale and Doppler
sonographic images after the administration of an IV contrast agent. Contrast-enhanced
intermittent sonography of the prostate may be useful for the selective enhancement of
malignant prostatic tissue.
n 1999, approximately 179,300
American men developed pros-
tatic cancer [1]. Because approxi-
mately one third of patients sent for biopsy
have cancer, we estimate that over 500,000
prostate biopsies are performed annually in
the United States. Although most clinicians
use sonography to guide needle placement
for prostate biopsy, a recent review of the
prostate sonography literature suggests that
imaging has little advantage for the detection
of malignant lesions [2]. Our own evaluation
of gray-scale, color, and power Doppler
sonography reveals that these techniques are
minimally superior to chance in the detection
of prostatic cancer [3]. An accurate noninva-
sive imaging study of prostatic cancer would
allow limited targeted biopsy of suspicious
sites and might reduce the number of pa-
tients subjected to biopsy of the prostate.
Increased microvessel density in prostatic
cancer is reported to correlate with the pres-
ence of metastases [4], the stage of disease [5–
7], and disease-specific survival [8, 9]. In other
words, microvessel density in prostatic cancer
is predictive of clinically significant disease.
Microbubble-based sonographic contrast
agents may reveal prostatic cancer based on in-
creased microvascularity. Although color Dop-
pler enhancement of the prostate has been
reported with contrast agents [10, 11], no pub-
lished study has revealed gray-scale parenchy-
mal enhancement of the prostate. We used
intermittent gray-scale imaging to evaluate
contrast-enhanced imaging of the prostate and
to selectively enhance the neovasculature asso-
ciated with prostatic cancer.
Subjects and Methods
Twenty-six patients with prior abnormal digital
rectal exams or elevated (≥4 ng/ml) prostate-specific
antigen levels were recruited for a phase II study of
the contrast agent Imagent (AF0150; Alliance Phar-
maceutical, San Diego, CA). Eligible patients were
18–80 years old and scheduled for transrectal sonog-
raphy of the prostate with biopsy. Patient age ranged
from 38 to 81 years (mean age, 64 years). The study
included 18 Caucasians, six African-Americans, one
Hispanic, and one Indian. The institutional review
board approved this study, and written informed
consent was obtained from each patient.
Study participants were prepared according to
standard operating procedure for patients undergoing
Ethan J. Halpern
1
Lev Verkh
2
Flemming Forsberg
1
Leonard G. Gomella
3
Robert F. Mattrey
4
Barry B. Goldberg
1
Received August 18, 1999; accepted after revision
November 3, 1999.
Supported in part by Alliance Pharmaceutical Corporation.
1
Department of Radiology, Jefferson Prostate Center,
Thomas Jefferson University, 132 S. 10th St., Philadelphia,
PA 19107-5244. Address correspondence to E. J. Halpern.
2
Alliance Pharmaceutical Corp., 3040 Science Park Rd.,
San Diego, CA 92121.
3
Department of Urology, Jefferson Prostate Center,
Thomas Jefferson University, Philadelphia, PA 19107-5244.
4
Department of Radiology, University of California at San
Diego, 200 N. Arbor Dr., San Diego, CA 92103.
AJR 2000;174:1575–1580
0361–803X/00/1746–1575
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