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. Author manuscript; available in PMC: 2015 Dec 9.
Published in final edited form as: Clin Radiol. 2014 Jul 22;69(10):e398–e403. doi: 10.1016/j.crad.2014.06.012

Assessment of Change in Prostate Volume and Shape Following Surgical Resection Through Co-Registration of In Vivo MRI and Fresh Specimen Ex Vivo MRI

Clement Orczyk 1,3,4,5,6,7, Samir S Taneja 1,2, Henry Rusinek 1,2, Andrew B Rosenkrantz 2
PMCID: PMC4673982  NIHMSID: NIHMS611569  PMID: 25062923

Abstract

AIM

To compare the size and shape of the prostate between in-vivo and fresh ex-vivo magnetic resonance imaging (MRI), in order to quantify alterations in the prostate resulting from surgical resection.

MATERIAL AND METHOD

Ten patients who had undergone 3 T prostate MRI using a phased-array coil and who were scheduled for prostatectomy were included in this prospective study. The ex-vivo specimen underwent MRI prior to formalin fixation or any other histopathological processing. Prostate volume in vivo and ex vivo was assessed using planimetry. Prostate shape was assessed by calculating ratios between the diameters of the prostate in all three dimensions.

RESULTS

Mean prostate volume was significantly smaller ex vivo than in vivo (39.7±18.6 versus 50.8±26.8 cm3; p=0.008), with an average change in volume of −19.5%. The right-to-left (RL)/anteroposterior (AP) ratio of the prostate, representing the shape of the prostate within its axial plane, was significantly larger ex vivo than in vivo (1.33±0.14 versus 1.21±0.12; p=0.015), with an average percent change in RL/AP ratio of the prostate of +12.2%. There was no significant difference between in-vivo and ex-vivo acquisitions in terms of craniocaudal (CC)/AP (p=0.963, median change=−2.1%) or RL/CC (p=0.265, median change=+1.3%) ratios.

CONCLUSION

The observed volume and shape change following resection has not previously been assessed by comparison of in-vivo and fresh ex-vivo MRI and likely represents loss of vascularity and of connective tissue attachments in the ex-vivo state. These findings have implications for co-registration platforms under development to facilitate improved understanding of the accuracy of MRI in spatial localization of prostate tumours.

INTRODUCTION

Multiparametric magnetic resonance imaging (MRI) (mpMRI) of the prostate is increasingly being used for a broad array of clinical applications, including tumour detection and localization12, planning of targeted biopsies3, treatment selection4, preoperative planning4, and monitoring of active surveillance5. These applications rely upon accurate spatial localization of tumour on mpMRI. An understanding of the accuracy of such localization is important for proper incorporation of imaging findings on mpMRI into clinical practice. Such validation has been attempted in a large volume of previous studies via attempted correlation of in-vivo MRI images with histopathological findings observed following radical prostatectomy6. However, past studies have generally not considered or accounted for the potential impact of the surgical procedure itself upon the size and shape of the prostate. It is possible that alterations in prostate vascularity and elasticity resulting simply from the prostatectomy may significantly change prostate morphology7, thereby impairing the ability to reliably assess the accuracy of tumour localization at in-vivo MRI via correlation with histopathological slides, and adjustments to correct for such changes would be warranted in future research. Thus, in the present study, the size and shape of the prostate between in-vivo and ex-vivo prostate MRI images were compared, in an effort to quantify changes resulting from surgical resection. The ex-vivo prostate was imaged fresh, prior to formalin fixation or any other processing.

MATERIALS AND METHODS

Patients

This prospective study was HIPAA-compliant and approved by the institutional review board. All patients signed written informed consent prior to participation. Ten patients (mean age 65±5.94 years) with biopsy-proven prostate cancer scheduled to undergo radical prostatectomy were included. Mean preoperative prostate-specific antigen (PSA) level 6.17±0.43 ng/ml (median 6.2ng/ml). All patients had undergone a preoperative 3 T mpMRI of the prostate, which is routinely performed following a positive prostate biopsy at New York University Langone Medical Center. In addition, the fresh ex-vivo prostate specimen underwent MRI, as described below. No patient received therapy between MRI and surgery. Mean delay between MRI and surgery was 45.4±54 days (median 33 days). Final histopathological stages were: pT2c (n=3), pT3a (n=6), and pT3b (n=1). Final Gleason scores were 6 (3+3) in one case, 7 (3+4) in five cases, 7 (4+3) in four cases.

In-vivo MRI acquisition

Patients underwent preoperative MRI of the prostate using a 3 T system (Magnetom Trio, Siemens Healthcare, Erlangen, Germany) using a pelvic phased-array coil. The protocol included an axial turbo-spin echo (TSE) T2-weighted imaging (T2WI) sequence of the prostate and seminal vesicle [3600 ms repetition time (TR)/123 ms echo time (TE); 3 mm section thickness; 160 × 160 mm field of view (FOV); 256 × 256 matrix; parallel imaging factor of 2; three signals averaged]. Dynamic contrast-enhanced (DCE) imaging and diffusion-weighted imaging (DWI) were also performed, but not assessed as part of this study.

Surgical resection and ex-vivo MRI

All 10 patients underwent robotic-assisted radical prostatectomy, performed by a single surgeon with 15 years of experience (SST). The fresh surgical specimen was prepared by sewing a segment of urethral catheter into the prostatic urethra for preservation of urethral elongation. Within 12 h of resection and prior to formalin fixation, sectioning, or any other histopathological processing, the fresh specimen underwent ex-vivo MRI using the same 3 T system as for in-vivo imaging and comprising T2WI with sequence parameters matching in-vivo MRI aside from use of a rectangular FOV of 40% given the lack of surrounding pelvic tissues. During this delay, the specimen was maintained at 4°C to minimi ze tissue changes.

Assessment of prostate volume and shape

Analysis of the images was performed by a research fellow (C.O.), under supervision of a fellowship-trained abdominal radiologist (A.B.R.), with 5 years of experience in prostate MRI interpretation. The image analysis was performed using locally-developed in-house software (Firevoxel), which has previously been used to assess volume of other tissues 8.

Volume measurements of the in-vivo and ex-vivo prostate was achieved via planimetry, which has been previously shown to be an accurate method for this purpose 9. First, the prostate was manually delineated on in-vivo and ex-vivo T2WI, excluding of surrounding peri-prostatic fat, the neurovascular bundles (if present ex vivo), the bladder neck, and the seminal vesicles. Subsequently, volume was computed on a voxel basis.

The shape of the prostate was assessed by initially measuring the largest diameter of the prostate in the anteroposterior (AP), right-to-left (RL), and craniocaudal (CC) dimensions. Then, the AP/RL, AP/CC, and RL/CC ratios were calculated in vivo and ex vivo.

Statistical assessment

Paired t-tests were used to compare prostate volume, the three linear dimensions of the prostate, and the three ratios between these linear dimensions representing prostate shape, between in-vivo and ex-vivo images for each case. The mean, standard deviation, and median percent changes in volume and in terms of the three ratios were computed between the in-vivo and ex-vivo images. All p-values are two-sided and considered statistically significant at p<0.05. Statistical analysis was performed using software (R, version 2.14.0, CRAN, Vienna, Austria) and Excel (version 2011, Microsoft, Redmond, WA, USA).

RESULTS

In-vivo and ex-vivo MRI acquisitions, as well as the described volume and shape measurements, were successfully performed in all 10 patients. The obtained volume and shape measurements are summarized in Table 1. Mean prostate volume was significantly smaller ex vivo than in vivo (39.7±18.6 versus 50.8±26.8 cm3, respectively; p=0.008), with an average percent change in size of the prostate of −19.5%, equivalent to a 23% greater volume of the prostate on in-vivo, compared with ex-vivo, MRI (Figure 1). In addition, there was a decrease in size of the prostate in all three dimensions between ex-vivo and in-vivo scans: RL dimension, 4.82±0.77 cm versus 5.05±0.92 cm, p=0.015; AP dimension, 3.62±0.56 cm versus 4.01±0.78 cm, p=0.002; CC dimension, 3.9±0.82 cm versus 4.09±1.40 cm, p=0.087.

Table 1.

Comparison of volume and shape assessments between in vivo and ex vivo MRI

In-vivo MRI Ex-vivo MRI
Volume
Mean±SD (cc) 50.8±26.8 39.7±18.6
p-Valuea 0.008
Average percent changeb −19.5
Median percent changeb −22.3%
RL/AP ratio
Mean±SD 1.21±0.12 1.33±0.14
p-Valuea 0.015
Average percent changeb 12.2%
Median percent changeb 11.3%
CC/AP ratio
Mean±SD 1.09±0.22 1.10±0.18
p-Valuea 0.963
Average percent changeb 0.34%
Median percent changeb −2.1%
RL/CC ratio
Mean±SD 1.15±0.29 1.24±0.22
p-Valuea 0.265
Average percent changeb 8.8%
Median percent changeb 1.3%
a

Listed in bold when statistically significant at p<0.05.

b

Change from in-vivo to ex-vivo measurements.

RL/AP ratio, right-to-left/anteroposterior ratio; CC/AP ratio, craniocaudal/anteroposterior ratio; RL/CC ratio, right-to-left/craniocaudal ratio.

Figure 1.

Figure 1

Comparison of in-vivo and ex-vivo prostate volumes in 10 patients. p-Value represents result of paired t-test comparing the two sets of data.

The ratios between the three linear dimensions of the prostate were compared to assess for a tendency for the shape of the prostate to change between in-vivo and ex-vivo scans in a particular orientation (Fig. 2). The RL/AP ratio of the prostate, thus representing the shape of the prostate within its axial plane, was significantly larger ex vivo than in vivo (1.33±0.14 versus 1.21±0.12, respectively; p=0.015), with an average percent change in RL/AP ratio of the prostate of +11.3%. There was no significant difference between scans in terms of CC/AP ratio (p=0.963, average percent change=−2.1%) or RL/CC ratio (p=0.265, average percent change = +1.3%). Images from a representative case are shown in Fig. 3.

Figure 2.

Figure 2

Comparison of in-vivo and ex-vivo ratios of linear prostate dimensions in 10 patients. p-Value represents result of paired t-test comparing the two sets of data.

Figure 3.

Figure 3

Change in volume and shape between in-vivo and ex-vivo MRI. Axial T2WI images at the level of the verumontanum are shown for (a) in-vivo and (b) ex-vivo acquisitions for a single patient. (c–d) Images depict an identical red contour reflecting the external contour of the (c) in-vivo prostate, although superimposed on the prostate in both images and demonstrating the smaller size of the (d) ex-vivo prostate. (e–f) Images depict identical dotted green lines reflecting the RL and AP dimensions of the (e) in-vivo prostate, although superimposed on the prostate in both images and demonstrating the change in relation between these lines in the (f) ex-vivo prostate. (g–h) Images depict a three-dimensional, rendered, shaded surface display of the (g) in-vivo and (h) ex-vivo prostate, generated from the two sets of T2WI images, demonstrating a difference in prostate shape between the two scans; the prostate exhibits its typical pyramidal shape in the in-vivo scan and a relatively spherical shape in the ex-vivo scan.

DISCUSSION

In the present study, a significant difference was observed in volume of the prostate following surgical resection, with an average loss of 19.5% of the gland’s volume. To the authors’ knowledge, this finding has not been previously assessed by comparison of in-vivo and ex-vivo prostate MRI. The use of MRI for this purpose facilitated the determination of prostate dimensions and volume. Furthermore, via careful evaluation of ex-vivo T2WI, it was possible to include within the ex-vivo volume measurement only the prostate gland itself, while excluding all surrounding tissues. This is important because the resected prostate is intimately associated with surrounding tissue such as fat, pelvic fascia, or the neurovascular bundles, depending of the operative technique. These adjacent structures can confound accurate specimen measurements of the specimen, but cannot be removed physically; doing so may negatively impact evaluation of the surgical margin status 10 and lead to improper staging. Thus, the present approach to evaluating the ex-vivo prostate via MRI allowed for accurate measurements after image-based exclusion of peri-prostatic structures, while preserving the integrity of the specimen for further histopathological evaluation.

An additional key aspect of the present method was that the in-vivo MRI was performed without use of an endorectal coil, which potentially could compress and deform the prostate, thereby confounding the comparison with the ex-vivo prostate. For instance, Heijmink et al.11 reported an approximately 18% difference in volume of the prostate evaluated by MRI between examinations performed with and without an endorectal coil. Thus, in the present study, the only difference between the two acquisitions was the interval surgical procedure itself.

This finding in terms of volume reduction is important given the role of correlative studies between multiparametric and histology, which have often used radical prostatectomy specimens as the reference standard, in influencing the clinical integration of mpMRI 12,13. Numerous past studies have accounted for shrinkage of the prostate attributed to the process of histopathological processing 1416. This step accounts for change in volume due to tissue dehydration that results from formalin fixation and paraffin embedding, but does not correct for the loss of volume due to the surgery procedure, as per the current report. It is possible that a greater degree of volume correction may be needed than in past studies given the additional observed contribution of the surgical procedure to volume changes.

Although the decrease in volume of the ex-vivo prostate was due to a reduction in size in all dimensions, this size reduction was not homogeneous between the three dimensions, as indicated by the significant difference in the AP/RL ratio between the two acquisitions. Thus, the surgical procedure is associated with a change in the shape of the prostate in the axial plane. This spatial deformation may relate to a loss of connective tissue attachments, for instance to the dorsal venous complex or lateral pelvic fascia17, that maintain the shape of the in-vivo prostate, thereby releasing the prostate in the ex-vivo state and resulting in a change in shape given the prostate’s viscoelastic properties18. Therefore, magnification alone of histopathological images, in order to account for the volume reduction, is not likely to be sufficient to achieve optimal co-registration of in-vivo prostate MRI and histopathological images; rather, as correlation of lesions is predominantly performed within the axial plane, measures are needed to correct for the deformation within this plane resulting from the surgery.

Numerous reports describe co-registration platforms currently in development from a variety of centres 19,20,21. The present findings support the need for such platforms to employ a three-dimensional deformable approach in order to achieve optimal correlation. The resulting improved compensation for changes in volume and shape will be of much value when performing co-localization of small tumours between MRI and histology.

Limitations of the present study include the small sample size, lack of assessment of reproducibility of the volume metrics, and lack of confirmation of suggested reasons for the change in prostate volume following prostatectomy.

In conclusion, via performance of MRI of fresh ex-vivo prostatectomy specimens, a significant decrease of approximately 19% was demonstrated in the volume of the prostate resulting from this surgical procedure. In addition, the surgery resulted in a significant change in shape of the prostate in the axial plane. It is, therefore, advised that co-registration platforms employ three-dimensional deformable transformation to compensate for this volume loss and change in orientation in the axial plane, in order to achieve reasonable accuracy in correlation. More accurate co-registration incorporating the present findings will facilitate improved understanding of the accuracy of mpMRI in the spatial localization of tumours within the prostate.

Highlights.

  • Preresection prostates to freshly resected prostates were compared for volume and shape.

  • Volume and shape were quantified using in vivo and ex vivo T2w MRI at 3T.

  • A −19.5% statistically significant volume decrease was reported after resection.

  • Significant change in shape is observed on the axial slices.

  • Findings impact MRI-histology correlation studies and further clinical deductions.

ACKNOWLEDGEMENTS

The authors acknowledge The Joseph and Diane Steinberg Charitable Trust and the Grant 1UL1RR029893 from the National Center for Research Resources, National Institutes of Health for support. C.O., H.R. and A.B.R. have nothing to disclose. S.S.T. is consultant for Eigen, consultant and scientific investigator for GTX, scientific investigator for Steba Biotech, speaker for Janssen, has royalties from Elsevier.

Footnotes

Publisher's Disclaimer: This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final citable form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.

Disclosure and financial interest:

Clement Orczyk, Henry Rusinek and Andrew B Rosenkrantz have nothing to disclose.

Samir S Taneja is consultant for Eigen, consultant and scientific investigator for GTX, scientific investigator for Steba Biotech, speaker for Janssen, has royalties from Elsevier. No direct financial conflict of interest is identified.

Author’s Contributions:

Clement Orczyk MD MSc, Samir S Taneja MD, Henry Rusinek PhD, Andrew B Rosenkrantz MD
  1. guarantor of integrity of the entire study C ORCZYK
  2. study concepts and design- C ORCZYK, SS TANEJA, H RUSINEK, AB ROSENKRANTZ
  3. literature research C ORCZYK, AB ROSENKRANTZ, H RUSINEK, SS TANEJA
  4. clinical studies SS TANEJA, AB ROSENKRANTZ
  5. experimental studies / data analysis C ORCZYK, H RUSINEK, AB ROSENKRANTZ
  6. statistical analysis C ORCZYK
  7. manuscript preparation C ORCZYK, AB ROSENKRANTZ
  8. manuscript editing. C ORCZYK, SS TANEJA, H RUSINEK, AB ROSENKRANTZ.

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