Fatemeh Zabihollahy1, Steven S. Raman1, Pornphan Wibulpolprasert2, Robert Reiter3, Holden Wu1, and Kyung Hyun Sung1
1Radiology, University of California, Los Angeles, Los Angeles, CA, United States, 22Department of Diagnostic and Therapeutic Radiology, Ramathibodi Hospital, Bangkok, Thailand, 3Urology, University of California, Los Angeles, Los Angeles, CA, United States
Synopsis
Multiparametric magnetic resonance imaging (mpMRI) has a significant
impact on prostate cancer (PCa) diagnosis. However, it is important to realize
its accuracy for PCa detection. In this study, we compare mpMRI with
whole-mount histopathology (WMHP) images as a reference to discover the
limitation of mpMRI for PCa lesion localization. The results are presented as a
spatial probability map, corresponding to the prostate sector map
used in Prostate Imaging Reporting and Data System
version 2.1 (PI-RADSv2.1), to highlight the regions on the prostate glands that
require further attention from clinicians for a more accurate diagnosis of PCa
and its treatment planning.
Introduction
Multiparametric MRI (mpMRI) has been shown to be
accurate for the diagnosis of clinically significant prostate cancer (csPCa)
that requires treatment [1-3]. Previously, several studies determined the
performance of mpMRI based on the tumor size, Gleason score (GS), index, etc.
[4], compared with whole-mount histopathology (WMHP) as an ideal reference
standard for correlating individual prostate lesions to mpMRI. Sector map is a
canonical model of the prostate, consisting of forty-one sectors, to enable
clinicians to easily localize MRI findings [5-6], described by the PI-RADS v2 [7]. The purpose of
this study is to illustrate the sector-based performance of mpMRI for PCa
detection as a form of spatially localized probabilities to provide a useful
roadmap for mpMRI-based PCa diagnosis and prognosis. In particular, we investigate the distribution
of false-negative (FN) mpMRI findings for csPCa and index lesions on the per
sector basis to provide a visual aide for clinicians, drawing their attention
to the areas where the probability of FN csPCa and index lesions is higher. Method
This
HIPAA compliant study was approved by the review board of our local institute.
A total of 776 consecutive men underwent 3T mpMRI prior to radical
prostatectomy at a single institution between 2010 and 2020. 3T mpMRI was
compared with thin-section WMHP prepared by experienced genitourinary (GU)
pathologists. Patient-specific 3D-printed molds were used to section prostate
specimens in the axial plane in 5-mm steps from the base to the apex
perpendicular to the urethral plane to approximate the acquired imaging plane.
The GU pathologists delineated all PCa lesions, where the largest diameter,
location, and primary and secondary GS of each lesion were recorded.
GU
radiologists and pathologists re-reviewed each previously detected and graded
lesion on WMHP and 3T mpMRI and collectively determined concordance in the
monthly match meetings. A lesion that appeared on mpMRI
was labeled as a true positive (TP) if it presents on the WMHP, and its sectors
were recorded based on the appearance on mpMRI. If PCa lesions shown on WMHP
were not detected on mpMRI, they were classified as FN lesions, and their
sectors were assigned based on their appearance on WMHP. The mpMRI lesions were
categorized as false positives (FP) if there is no corresponding lesion on
WMHP. Clinically significant PCa was defined as a lesion with a GS of 7 or
greater [8]. The index lesion was defined as the PCa lesion with the highest GS
or the largest size or both.
To
calculate spatial probability, the number of TP, FP, and FN lesions in each
region of the sector map was counted and divided by the total number of PCa
lesions at the corresponding level. To illustrate the probability on the sector
map, three different colors, including red, orange, and yellow, were used to
display probability values of larger than 10%, less than 10% and larger than 5%,
and less than 5%, respectively. Results
In
776 patients, there existed 1,465 PCa lesions at WMHP including TP and FN
lesions, and of 1,465 PCa lesions, the detection rate of overall PCa lesions
was 52% including 72% of the csPCa tumors and 78% of the index lesions. Table
1 summarizes both the patient and lesion characteristics of the TP and FN
tumors on mpMRI. 76% of FN tumors were small (tumor diameter of < 1.5 cm).
At all anatomical levels, most FN csPCa and index lesions were located at the
left posterior of peripheral zone (PZ). Figure 1 shows the spatial
probability map for FN csPCa and index lesions. On multivariate analysis, the
majority of FN large (tumor diameter of > 1 cm), clinically significant,
index lesions with PSA>4 was in the posterior of PZ. Conclusion and Discussion
We characterized
the spatial localization of the PCa detection on mpMRI in terms of spatial probability corresponding to the sector map. Compared
to previous works on population spatial probability maps [4-6], using a sector map is easier for data
management/processing and directly relates to PI-RADS v2 reporting
guidelines. The spatial probability map of FNs may improve the diagnosis of PCa
using mpMRI as it highlights the areas with the highest probability of undiagnosed
tumors, where a careful review of the image by clinicians is required to assure
of the subject being cancer-free. Also, the results may reduce the need for systematic
prostate biopsy as it helps obtain samples from areas with the highest probability
of PCa lesion existence instead of removing samples from random areas of the
prostate gland. The outcomes facilitate the characterization of disease
appearance relative to anatomic levels and zones, which in turn may obviate the
necessity of MR-based prostate atlas. Moreover, incorporating our results into
the computer-aided diagnosis tools designed for automated detection of PCa is important, may lead to better performance as prior information and
hints given to the learner is a substantial ingredient to obtain a good
generalization error [9-10].
Our
localization scheme showed that using 3T mpMRI csPCa tumors in the left
posterior part of PZ at the mid and apex levels were mostly missed with a total
probability of 23%. Overall, mpMRI performance for sectoral localization of csPCa and index lesions was moderate in the posterior of PZ. Acknowledgements
This work was supported in part by the National
Institutes of Health R01-CA248506 and funds from the Integrated Diagnostics
Program, Departments of Radiological Sciences and Pathology, David Geffen
School of Medicine, UCLA. FZ would like to thank Heather Wilber at UCLA for her
help with creating figures.References
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