Skip to main content
Prostate Cancer logoLink to Prostate Cancer
. 2019 Mar 3;2019:6932572. doi: 10.1155/2019/6932572

How Accurately Can Prostate Gland Imaging Measure the Prostate Gland Volume? Results of a Systematic Review

David R H Christie 1,2,, Christopher F Sharpley 2
PMCID: PMC6420971  PMID: 30941221

Abstract

Aim

The measurement of the volume of the prostate gland can have an influence on many clinical decisions. Various imaging methods have been used to measure it. Our aim was to conduct the first systematic review of their accuracy.

Methods

The literature describing the accuracy of imaging methods for measuring the prostate gland volume was systematically reviewed. Articles were included if they compared volume measurements obtained by medical imaging with a reference volume measurement obtained after removal of the gland by radical prostatectomy. Correlation and concordance statistics were summarised.

Results

28 articles describing 7768 patients were identified. The imaging methods were ultrasound, computed tomography, and magnetic resonance imaging (US, CT, and MRI). Wide variations were noted but most articles about US and CT provided correlation coefficients that lay between 0.70 and 0.90, while those describing MRI seemed slightly more accurate at 0.80-0.96. When concordance was reported, it was similar; over- and underestimation of the prostate were variably reported. Most studies showed evidence of at least moderate bias and the quality of the studies was highly variable.

Discussion

The reported correlations were moderate to high in strength indicating that imaging is sufficiently accurate when quantitative measurements of prostate gland volume are required. MRI was slightly more accurate than the other methods.

1. Introduction

There are many clinical situations in in the management of prostate diseases in which the measurement of the prostate gland volume (PGV) has a role [13]. For some of these the measurement does not need a high level of accuracy and simply detecting that the prostate is enlarged can be sufficient. For example, if a general practitioner is considering the choice of medication when treating benign prostatic hyperplasia (BPH), more precise measurements of the PGV may be required in other situations, for example, to calculate prostate specific antigen (PSA) density. For radiation oncologists, the PGV is used to determine the suitability of prostate cancer patients for low dose rate brachytherapy and the number of brachytherapy seeds to order. In those situations, a more accurate measure of the PGV is required and is usually obtained by medical imaging methods.

A number of imaging methods have been used to estimate the PGV, including ultrasound (US), either transrectally or suprapubically (TRUS, SPUS), Computer Tomography (CT), and Magnetic Resonance Imaging (MRI). Although many publications have described their accuracy, these have never been systematically reviewed, making it difficult to compare them. Our aim was to review the literature in order to determine the accuracy of imaging as a measure of PGV in a future planned study of the effects of neoadjuvant androgen deprivation therapy (NADT).

2. Materials and Methods

The PRISMA, AMSTAR-2, and QUADAS-2 tools were adopted to ensure the quality of the review. However, in this case the imaging tests were not being used as diagnostic tests but as measuring tools, so not all of the criteria for these were relevant [46]. The proposal for the review was submitted for registration to PROSPERO [7], but the review was completed before a response was received. Ethics committee approval was not required and no funding was obtained for this study.

The patient populations studied were those men undergoing imaging of the prostate for any reason, including those attending health services for prostate conditions. The interventions to be reviewed were the US, CT, and MRI, recognising that variations existing in the way each of these can be used to measure PGV. All study designs were considered and the outcome was to be any quantitative measure of accuracy when compared against the reference standard, meaning in vitro measurement of the PGV after radical prostatectomy.

Multiple medical literature databases were accessed in August 2018, including CINAHL Plus, Embase, Medline, Pubmed, and ScienceDirect and were searched for abstracts containing the terms “prostate volume” and “imaging OR US OR CT OR MRI” and “prostatectomy”. No other review protocol or similar previous publication existed. Titles and abstracts were reviewed by both of the authors and relevant full text articles were obtained for further review. The results were then tabulated so that the range of results could be seen, including correlations, concordance, and tendencies to over- or underestimate. For each study the date of publication, the numbers of patients, and the average age of the patients were tabulated.

Although there were relevant articles published over a period of more than 50 years, we arbitrarily adopted a time limit of 22 years (since 1995), as we assumed that the extensive developments in the technology of the imaging and reference methods would render articles published before that time less relevant. Titles that were published only published in abstract form or relating to animal studies were also excluded. Several articles have compared the accuracy of the other less invasive imaging methods with the TRUS including SPUS, transperineal US, CT, and MRI. However, unless these involved a comparison against an in vitro reference method they were not considered further here. For the same reason we excluded several articles that compared different formulae used to calculate the PGV from standard imaging measurements [810] and one study that compared in vivo and ex vivo MRI measurements (all showing high correlation) [11]. We excluded many articles describing other aspects of the measurement of PGV, such as interobserver variation, or the ability to detect diseases.

No source data extraction for meta-analysis was attempted. Assessment of publication bias was not considered to be necessary. However, the tools for reporting reviews and particularly the QUADAS-2 tool encourage review authors to develop review-specific bias and quality assessments [6]. We considered that the authors of each study might report more favourable results if they were performing most of the imaging themselves, or if those undertaking the reference measurement were not blinded to the results of the imaging. Thus, a bias score was derived with a total score 0-2, a higher score indicating greater potential for bias. The quality of each study was also assessed by considering the imaging measurement (using either a planimetric calculation or autosegmentation method), the reference measurement (using a fresh specimen that had the seminal vesicles removed), the number of patients (more than 50), and whether both concordance and correlation were considered (total score 0 to 4, a higher score indicating higher quality).

3. Results

The search strategy initially generated 758 titles. Selected abstracts were reviewed by both authors blindly, but only 57 were considered relevant. Complete text versions of those articles were obtained, but only 11 had usable data. Secondary searching through 43 titles generated a further 17 articles, identifying a total of 28 articles. Some of these reported imaging measurements from more than one imaging method, describing a total of 33 comparisons between the PGV measured by an imaging method and by the reference method. The search strategy is described in Figure 1.

Figure 1.

Figure 1

Results of the search strategy.

The 28 articles described studies with a wide variety of sample sizes (5 to 1844 patients) but had a combined total of 7768 patients. The patients were from countries all over the world, mostly USA and Korea but also five different European countries and Australia. The dates of publication were well spread across the range of dates, from 1995 to 2018. The results were tabulated depending on the imaging method used, as shown in Tables 1 (US), 2 (CT), and 3 (MRI). Ages, weights, and volumes were rounded up or down to the nearest whole numbers.

Table 1.

Summary of articles measuring the PGV by TRUS in chronological order.

First author,
Year of publication,
Country
Number of patients,
Age
TRUS Imaging details,
Mean volume
Reference method,
Mean volume
Reference method details Correlation
data
Concordance
Data and over/under estimation
Other
comments
Scores for Bias (0-2)
and
Quality (0-4)
Wolff [12] 1995
Germany
25 pts, age NS EC, Mean NS Specimen weight, SGF applied, mean 36gm SV weight subtracted Linear regression R=0.83
P<0.0001
NS Two methods of EC compared, NSD B2
Q0

Tewari [13] 1996
USA
48 pts
Age NS
EC
mean 60gm
Weighed after fixation, SGF applied, mean 65 gm SV removed NS Students t-test p=0.04
PGV was underestimated by about 10%
Also used MRI but not compared with reference. B2
Q1

Matthews [14] 1996 USA 100 pts
Age NS
EC
Mean 36mL
Mean 45 mL
EC from measurements
Within 1 hr of excision NS Students t-test
P<0.01
PGV was underestimated if <30mL and overestimated if >30mL
B2
Q1

Zlotta [15] 1999
Belgium and Austria
36 pts
Age NS
EC
Mean 29 mL
Weighed
Mean 34 mL
Details NS Pearson's R=0.78
P<0.001
Students t-test p=0.004 TZ volume measurement was more accurate than whole prostate B2
Q0

Park [16] 2000
South Korea
16 pts
Mean 62 yrs
EC, mean 30 mL transaxial and 33 mL midsagittal EC from specimen, mean 32 mL Within 1 hr of excision 0.71 Midsagittal
0.83 Transaxial
Method NS
Student's t-test NSD AP measured in two planes, NSD B2
Q1

Freedland [17] 2005 USA 753 pts
Age NS
Details NS Weight, otherwise details NS Included SV and vasa tips Spearman r=0.71
P<0.001
NS From a larger study of 1602 RP pts in the SEARCH database, mean age 63 yrs, mean specimen weight 44gm B1
Q1

Loeb [18] 2005
USA
1844 pts
Mean 65 yrs
EC
Mean 40gm
Mean wt 50 gm Included SV Spearman's
R=0.65
PGV was generally underestimated, more accurate with smaller PGV TRUS better than DRE B1
Q2

Cabello-Benevente [19] 2006 Spain 33 pts
Age NS
EC
Mean 39cc
Weight
54 gm
Details NS Pearson r=0.79 Student's t-test
P=0.001
Underestimated by 29%
B2
Q1

Lee [20] 2006 Korea 73 pts, age NS EC
Mean 39cc
Fresh weight within 1 hr, SGF applied, mean 37cc SV removed Pearson r=0.88
P< 0.001
Overestimated if <35cc, underestimated if >35cc Also tested MRI, which was more accurate B2
Q4

Sajadi [21] 2007 USA 497 pts
Mean 60yrs
EC
Mean 37.4cc
Specimen weight mean 45 gm Fresh Weight included SV Spearman's
R=0.692, p<0.001
Usually underestimated VA study B1
Q3

Jeong [22] 2008 Korea 21 pts, mean 66 yrs EC, Means 42-51 mL Fresh specimen within 1 hr, displacement method, mean 40mL SV removed Linear regression, R=0.90-94 Students t-test
P=0.1-<0.001
Axial and midsagittal measurements of AP were compared, axial better for TRUS
Also used MRI with both EC and PC, where Midsagittal and PC most accurate B2
Q3

Rodriguez [23] 2008 USA 124 pts
Age NS
EC
Mean NS
Displacement method and weight (together correlated 0.997). Defatted but SV attached. Correlations not given but only 24% within +/- 10% Underestimated wt in all size categories No mean values given B1
Q2

Acer [24] 2010
Turkey
5 pts
Mean 60 yrs
EC Mean vol 43 cc Fluid displacement
Mean 53 cc
SV removed Kruskal Wallis
P = 0.677 (NSD)
21% underestimation B2
Q2

Hong [25] 2012
Australia
236 pts
Mean 61 yrs
EC 37 mL Weight post Formalin fixation
46 mL
SV removed Spearman r=0.74 Concordance coefficients also provided 0.31-0.46, considered poor Also performed EC on specimens, median 32 mL, concluded weight more useful B1
Q3

Varkarakis [26] 2013 Greece 60 pts mean 64 yrs Both TRUS and SPUS Both EC, means 45-50 cc resp Displacement of fresh specimen, mean 45 cc SV and vas removed NS SPUS overestimated PGV, TRUS NSD Also used CT B2
Q2

Bienz [27] 2014
Canada and USA
440 pts
Age NS
EC
4 Volume categories
Weighed before fixation Details NS Pearson improved with volume r = 0.17-0.84
P= 0.056-<0.01
ANOVA
PGV was underestimated <30 and overestimated >80cc, avg absolute error 39%
Median lobe made no difference B2
Q3

Kilic [28] 2014 Turkey 163 pts, mean age 64 yrs EC
TRUS and SPUS, means 51 and 50 mL respectively
Fresh weights, Mean 55 gm SV included
SGF applied
ICC 0.84-0.90 Both TRUS and SPUS underestimated the PGV
TRUS slightly better than SPUS (NSD)
Also used CT, TRUS and SPUS more accurate B2
Q2

Paterson [29] 2016 Canada 318 pts
Mean 63 yrs
EC
Mean 39cc
Fluid displacement method. Mean 37cc Prostate weight also used (ICC=0.96) ICC 0.74 Underestimated on average by 3cc MRI slightly more accurate B1
Q3

Pts: patients, Yrs: years of age, TRUS: transrectal ultrasound, SPUS: suprapubic ultrasound, EC: ellipsoid calculation, PC: planimetric calculation, NS: not stated, VA: Veterans Affairs, SV: seminal vesicles, TZ: transitional zone, MRI: magnetic resonance imaging, CT: computer tomography, AP: anteroposterior, ICC: intraclass correlation coefficient, SGF: specific gravity factor (1.05 g/mL), and SEARCH: shared equal access regional cancer hospital.

Table 2.

Summary of articles measuring the PGV by CT.

First author,
Year of publication,
Country
Number of patients,
Age
CT Imaging details
Mean volume
Reference method
Mean volume
Reference details Correlation
data
Concordance
Data and over/under estimation
Other
comments
Scores for Bias (0-2)
and
Quality (0-4)
Varkarakis [26] 2013
Greece
60 pts, Mean 64 yrs EC,
Mean 54 cc
Displacement of fresh specimen, Mean 45 cc SV and vas removed NS Overestimated PGV Also used TRUS and SPUS, CT larger and less accurate B2  
Q2

Kilic [28]
2014 Turkey
163 pts, Mean age 64 yrs EC,
Mean 63 mL
Fresh weights, Mean 55 gm SV included  
SGF applied
ICC 0.78 Overestimated on average by 15%, better agreement for larger PGV Also used TRUS and SPUS, CT larger than both p<0.001 B2  
Q2

Pts: patients, Yrs: years of age, TRUS: transrectal ultrasound, SPUS: suprapubic ultrasound, EC: ellipsoid calculation, PC: planimetric calculation, NS: not stated, SV: seminal vesicles, ICC: intraclass correlation coefficient, and SGF: specific gravity factor (1.05 g/mL).

Table 3.

Summary of articles measuring the PGV by MRI in chronological order.

First author,
Year of publication,
Country
Number of patients,
Age
MRI Imaging details,
Median volume
Reference method,
Median volume
Reference details Correlation
data
Concordance
Data and over/under estimation
Other
comments
Scores for Bias (0-2) and
Quality (0-4)
Sosna [30] 2003
USA
11 pts, Mean 59 yrs EC, PC, and ex vivo PC
Mean volumes 26-31 EC, 37 PC, 34 mL ex vivo,3T MRI,
no ERC
Fresh specimen weighed, SGF applied, Mean 40mL SV removed Linear regression
R=0.32-0.75 for EC, 0.65 for PC in vivo, 0.86 for PC ex vivo
6 combinations of various axes used for EC, best was sagittal for AP and SI, axial for RL B2
Q2

Lee [20]
2006
Korea
73 pts, age NS EC, Mean 38cc
3T or ERC NS
Fresh weight within 1 hr, SGF applied, Mean 37cc SV removed Pearson R=0.96
P< 0.001
Overestimated if < 35cc, underestimated if >35cc Also tested TRUS, but MRI more accurate B2
Q4

Jeong [22] 2008 Korea 21 pts, Mean 66 yrs EC and PC, Means 41-51 mL,
ERC used,
3T NS
displacement method, Mean 40mL Fresh specimen within 1 hr, SV removed Linear regression, R=0.84-92 Students t-test
P=0.03-0.70
PC most accurate B2
Q3

Kwon [31] 2010 Korea 579, Mean 64 yrs EC,
Mean 32 mL, 1.5T MRI,
ERC NS
Fresh weight, Mean NS SV removed Pearson R=0.69
P< 0.001
NS B2
Q2

Bulman [32]
2012
USA
91 pts, Mean 59 yrs mpMRI EC, PC (manual and MFA).
ERC, 3T, Mean 41-45 mL
Freshly weighed, Mean 50 mL Average weight of SVs subtracted Wilcoxon signed rank test and linear regression 0.78-0.90 Bland-Altman plots, 92-97% within limits of agreement. All of the MRI methods underestimated the volume by around 15% Multiple readers used, MFA similar in accuracy to manual planimetry, both more accurate than EC B2
Q4

Turkbey [33]
2012
USA
98 pts, Median 61 yrs EC, PC and automated PC, Means 29-48 cc
3T, ERC
Fresh specimen weight, Mean 52 cc Included SVs Pearson r=0.86-0.91
P<0.0001
Partial and full Dice similarity coefficient 0.85-0.92 Autosegmentation faster than manual PC B2
Q3

Karademir [34] 2013,
USA
61 pts, Median 64 yrs Automated volume calculation,
Mean 46 cc,
1.5T mpMRI, ERC
Weight from pathology reports, mean 50cc Standard SV weight subtracted Pearson r=0.94
P<0.0001
Underestimated by 10% on average B2
Q2

Hong [35],
2014,
USA
1756 pts, Median 59 yrs EC,
Median 31mL
3T NS,
ERC NS
Weight from pathology report,
Mean NS
Details NS Pearson R=0.82,
p< 0.0001
NS Higher grade cancer associated with smaller volume B2
Q1

Le Nobin [36], 2014,
USA
37 pts, Mean 60 yrs PC
Mean 47 mL
3T mpMRI,
ERC NS
Post fixation,
Mean 47 mL
Details NS NS Bland Altman 95% limits -7 to +8 mL B2
Q2

Chernyak [37], 2015,
USA
49 pts, Mean 59 yrs EC, either 1.5T or 3T
With and without ERC, Means 46 and 51 cc
Weight retrospectively collected from report, Mean 55 gm Included SV ICC improved with ERC 0.90-0.96, mainly due to AP measurement MRI underestimated weight, more so with ERC (9 vs 4 gm) B1
Q2

Mazaheri [38], 2015,
USA
195 pts, Median 62 yrs EC and PC, Median 42 cc for both,
3T MRI, ERC
Fresh weight from pathology report, Median 52 cc Standard SV weight subtracted, applied SGF Lin CCC used to assess correlation and concordance Lin CCC = 0.85 (EC) and 0.87 (PC), both underestimated by approx. 10mL B2
Q3

Paterson [29], 2016,
Canada
318 pts
Mean 63 yrs
EC
Mean 39cc
Fluid displacement method. Mean vol 37cc Also prostate weight
(ICC=0.96)
ICC 0.83 Overestimation more common when a median lobe was present Also used TRUS, MRI slightly more accurate, B1
Q3

Bezinque [39], 2018,
USA
99 pts, Median 63 yrs Various EC and PC methods, Medians 35 to 49,
3T mpMRI,
No ERC
Specimen wt and volume, Medians 37-54 mL Details NS ICC 0.66-0.73 NS MRI with segmentation was considered the reference B1
Q2

Pts: patients, Yrs: years of age, TRUS: transrectal ultrasound, EC: ellipsoid calculation, PC: planimetric calculation, NS: not stated, SVs: seminal vesicles, TZ: transitional zone, mpMRI: multiparametric magnetic resonance imaging, MFA: multifeature active shape model, ERC: endorectal coil, 3T: 3-tesla, AP: anteroposterior, ICC: intraclass correlation coefficient, SGF: specific gravity factor (1.05 g/mL), CC: craniocaudal, SP: specific gravity, SEARCH: shared equal access regional cancer hospital, and Lin CCC: Lin's concordance correlation coefficient.

Two articles included both US and CT imaging methods, and these appear in both Tables 1 and 2 [26, 28]. Four articles included both US and MRI imaging methods, in three of these articles both imaging methods were compared with the reference standard, so all three articles appear in both Tables 1 and 3 [20, 22, 29]. In the fourth article, the TRUS measurements were not compared with a reference standard so the results only appear in the table relating to MRI scans, Table 3 [39].

The 18 articles that related to the use of US are shown in Table 1. They were published between 1995 and 2016 and included a total of 4792 patients. All of these used TRUS, but two also used SPUS [26, 28]. The correlation coefficients most commonly fell in the range of 0.70-0.90, indicating high levels of correlation.

Only two articles were related to the use of CT [26, 28]. They involved 223 patients in total and were published in 2013 and 2014. Both of these also included results about TRUS, as shown in Table 2. Only one of these [28] recorded a correlation coefficient at 0.78. Both indicated that the CT volumes were generally larger than TRUS and less accurate. Both also assessed SPUS and found little difference between SPUS and TRUS.

There were 13 articles that related to the use of MRI as shown in Table 3. They included 3388 patients and were published between 2003 and 2018. Correlation coefficients commonly lay between 0.8 and 0.96, a slightly higher range than TRUS and CT. Four articles that described both MRI and TRUS all indicated slightly better results for MRI [13, 20, 22, 29].

While reviewing the articles we made various observations about the methods that were used. The articles often applied geometric terms to describe the shape of the prostate in order to calculate the PGV using each imaging method. The term “ellipsoid” was often used, which is a 3-dimensional volume with three perpendicular axes. The term “spheroid” was sometimes used, meaning that two of the axes are identical. The term “prolate spheroid” was also sometimes used, meaning that these two axes are shorter than the lengthened third axis (rugby ball shape). To convert the measurements of the three axes to a volume, the ellipsoid calculation (EC) was often made by applying the standard formula (height × length × width × π/6). A wide variety of modifications to this were used. Other articles often used a planimetric calculation (PC or volumetry), which involves contouring the periphery of the gland on consecutive 3-5 mm slices, either axial or sagittal, and summating the series of volumes.

The reference tests were laboratory (in vitro) assessments of prostatectomy specimens which could be analysed by either weighing the specimen or measuring displacement. Weighing was done either by weighing the fresh specimen or after fixation with formalin. In some articles, the specimen was weighed after removal of fat, seminal vesicles or remnants of the vasa deferentia. Some articles subtracted a standard weight for the seminal vesicles from the prostate weight, which might be expected to be more inaccurate in prostates that were unusually large or small. Also in some articles, the weight of the prostate was converted to a volume by applying standard values for the specific gravity of prostate tissue (1.05 g/mL). In some articles, the volumes were identified by displacement of fluid or by measuring the maximum dimensions and using these to calculate an ellipsoid. These variations in the imaging and reference tests were recorded in the tables. These variations in methodology appeared to make little or no difference to the accuracy measures.

The bias and quality scores revealed that no articles were completely free of bias as in nearly all of the articles the authors conducted the imaging assessment themselves and it was rarely stated that those undertaking the reference measurement were blinded to the results of the imaging measurement. Quality scores generally improved with the date of publication. There was no indication that bias or quality played a major role in influencing the reported accuracy of the imaging methods used for PGV measurement.

4. Discussion

We found that no previous review of this topic had been performed and that the accuracy of imaging as a method of measuring the PGV was most commonly defined by correlation statistics that were generally moderate to high, most commonly between 0.70 and 0.96. Overall these results suggest that imaging is an accurate test for quantitatively measuring PGV and could be used in a study of the effects of NADT. Of the various imaging methods, TRUS was the most commonly studied. It had been studied long before our cut-off date of 1995, but the accuracy could be expected to depend on technical factors such as the image acquisition time and the resolution of the image, which have improved over time. Immobilisation of the patient may also have improved, especially if the lithotomy position is used rather than the lateral decubitus position. There were only two CT articles, both of which suggested that the scan overestimated the PGV. MRI articles only appeared after 2003, but MRI appeared slightly more accurate, including all three articles that directly compared TRUS and MRI. TRUS could be expected to be more operator dependant than MRI and TRUS measurements are likely to be affected more by pressure on the prostate from the balloon than by an endorectal coil (ERC), although the ERC also involves a balloon that can affect the volume [40]. MRI software may include multifeature active shape models (MFA's) which provide an accurate, automated method of planimetric measurement [32]. The software may also include sophisticated mechanisms for aligning the prostate images ex vivo with in vivo images, providing an additional means of assessing the PGV [41].

For those articles that described the EC method of volume measurement, there were inconsistent findings about which planes or axes to use. Some showed that the dimensions of the prostate measured on a midsagittal plane were more accurate than an axial plane on TRUS [22] and MRI [30] although an earlier TRUS study had found no difference [16]. Several articles showed that the PC method was more accurate than EC for TRUS and MRI [22, 30, 32, 38]. When PC was done by automated methods, these were just as accurate and could be recorded faster than by manual methods [32, 33, 39].

Regarding the tendency to over or underestimate the PGV, seven articles described this tendency without dividing the patients into those with larger or smaller prostates and found mixed results. For TRUS, four were underestimated while one was overestimated. With CT both were overestimated, while with MRI four were underestimated. There were four articles that divided patients into those either above or below their median values and three found the imaging tended to overestimate smaller glands and tended to underestimate larger glands, while in the remaining one it was the reverse. The underestimation of larger PGVs was the most consistent finding. The optimal way to assess the over and underestimation with volume is with Bland-Altman statistical methods, as these can show how the pattern changes across the range of volumes [42, 43]. There were few articles in this review that used this method [32, 36].

Our review had some limitations. Firstly, the methods used to perform the imaging, to calculate the volume, and to compare it with the reference methods all varied widely, making it difficult to combine them. Secondly, there were variations in the reference test methods used, with many using specimen weight rather than volume. Thirdly, none of the articles were completely free of bias, and none achieved maximum potential quality. However, none of these limitations seem likely to affect the conclusions we have drawn.

Future studies into the measurement of the PGV should use the MRI when the highest level of accuracy is needed using planimetric methods of calculation. Ideally a 3-tesla machine would be used to achieve optimal image quality and without an ERC as that can distort the PGV. The assessment of the volume of individual zones within the prostate could be studied as these can be affected differently by different diseases and treatments. When assessing a method of measurement of the PGV, multiple operators and blinding should be incorporated to avoid bias. The reference method would ideally involve assessment of the PGV by displacement as soon as the prostate is removed, avoiding the effects of shrinkage during fixation and avoiding the need for a volume conversion factor when weight is used. Extraneous tissue should be removed, including the seminal vesicles and remnants of the vasa deferentia. Measures of correlation and concordance should be included, and Bland-Altman plots should be presented to graphically demonstrate agreement, including under and overestimation.

5. Conclusions

Our study suggests that the use of imaging to measure the PGV is still a topic of significant interest and that no previous systematic reviews have been undertaken. The correlation of the PGV measured by imaging with the reference methods was in the range of a distribution from 0.70 to 0.96, which is accurate enough for some of the purposes that require quantitative PGV measurements. MRI was slightly more accurate than the other methods.

Acknowledgments

Thanks are due to Ipsen for assistance in obtaining the references.

Conflicts of Interest

The authors have no conflicts of interest and no funding to declare.

Authors' Contributions

Both authors were involved in the conception of the study, searching the literature, reviewing the papers, and preparing the manuscript.

References

  • 1.Harris M. R. E., Harding E. J., Bates T. S., Speakman M. J. Gland volume in the assessment of prostatic disease: Does size matter? BJU International. 2007;100(3):506–508. doi: 10.1111/j.1464-410X.2007.06939.x. [DOI] [PubMed] [Google Scholar]
  • 2.Olsson C. A., Lavery H. J., Sebrow D., et al. Does size matter? The significance of prostate size on pathologic and functional outcomes in patients undergoing robotic prostatectomy. Arab Journal of Urology. 2011;9(3):159–164. doi: 10.1016/j.aju.2011.10.002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Mandel P., Weinhold P., Michl U., Huland H., Graefen M., Tilki D. Impact of prostate volume on oncologic, perioperative, and functional outcomes after radical prostatectomy. The Prostate. 2015;75(13):1436–1446. doi: 10.1002/pros.23023. [DOI] [PubMed] [Google Scholar]
  • 4.Moher D., Liberati A., Tetzlaff J., Altman D. G. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. BMJ. 2009;339 doi: 10.1136/bmj.b2535.b2535 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Shea B. J., Reeves B. C., Wells G., et al. AMSTAR 2: a critical appraisal tool for systematic reviews that include randomised or non-randomised studies of healthcare interventions, or both. BMJ. 2017;21:p. 358. doi: 10.1136/bmj.j4008.j4008 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Whiting P. F., Rutjes A. W. S., Westwood M. E., et al. QUADAS-2: A revised tool for the quality assessment of diagnostic imaging studies. Annals of Internal Medicine. 2011;155(8):529–536. doi: 10.7326/0003-4819-155-8-201110180-00009. [DOI] [PubMed] [Google Scholar]
  • 7.PROSPERO: International prospective register of systematic reviews. 2011, http://www.crd.york.ac.uk/CRDWeb/ShowRecord.asp?ID=42011100485. [DOI] [PMC free article] [PubMed]
  • 8.Bangma C. H., Qais A., Niemer H. J., Grobbee D. E., Schröder F. H. Transrectal ultrasonic volumetry of the prostate: In vivo comparison of different methods. The Prostate. 1996;28(2):107–110. doi: 10.1002/(SICI)1097-0045(199602)28:2&#x0003c;107::AID-PROS5&#x0003e;3.0.CO;2-D. [DOI] [PubMed] [Google Scholar]
  • 9.Eri L. M., Thomassen H., Brennhovd B., Haheim L. L. Accuracy and repeatability of prostate volume measurements by transrectal ultrasound. Prostate Cancer and Prostatic Diseases. 2002;5(4):273–278. doi: 10.1038/sj.pcan.4500568. [DOI] [PubMed] [Google Scholar]
  • 10.Nathan M. S., Seenivasagam K., Mei Q., Wickham J. E. A., Miller R. A. Transrectal ultrasonography: Why are estimates of prostate volume and dimension so inaccurate? British Journal of Urology. 1996;77(3):401–407. doi: 10.1046/j.1464-410X.1996.90214.x. [DOI] [PubMed] [Google Scholar]
  • 11.Orczyk C., Taneja S. S., Rusinek H., Rosenkrantz A. B. Assessment of change in prostate volume and shape following surgical resection through co-registration of in-vivo MRI and fresh specimen ex-vivo MRI. Clinical Radiology. 2014;69(10):e398–e403. doi: 10.1016/j.crad.2014.06.012. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Wolff J. M., Boeckmann W., Mattelaer P., Handt S., Adam G., Jakse G. Determination of prostate gland volume by transrectal ultrasound: Correlation with radical prostatectomy specimens. European Urology. 1995;28(1):10–12. doi: 10.1159/000475012. [DOI] [PubMed] [Google Scholar]
  • 13.Tewari A., Indudhara R., Shino hara K., et al. Comparison of transrectal ultrasound prostatic estimation with magnetic resonance imaging volume estimation and surgical specimen weight in patients with benign prostatic hyperplasia. Journal of Clinical Ultrasound. 1996;24:169–174. doi: 10.1002/(SICI)1097-0096(199605)24:4&#x0003c;169::AID-JCU2&#x0003e;3.0.CO;2-D. [DOI] [PubMed] [Google Scholar]
  • 14.Matthews G. J., Motta J., Fracchia J. A. The accuracy of transrectal ultrasound prostate volume estimation: Clinical correlations. Journal of Clinical Ultrasound. 1996;24(9):501–505. doi: 10.1002/(SICI)1097-0096(199611/12)24:9&#x0003c;501::AID-JCU2&#x0003e;3.0.CO;2-R. [DOI] [PubMed] [Google Scholar]
  • 15.Zlotta A. R., Djavan B., Damoun M., et al. The importance of measuring the prostatic transition zone: An anatomical and radiological study. BJU International. 1999;84(6):661–666. doi: 10.1046/j.1464-410x.1999.00214.x. [DOI] [PubMed] [Google Scholar]
  • 16.Park S. B., Kim J. K., Choi S. H., Noh H. N., Ji E. K., Cho K. S. Prostate volume measurement by TRUS using heights obtained by transaxial and midsagittal scanning: Comparison with specimen volume following radical prostatectomy. Korean Journal of Radiology. 2000;1(2):110–113. doi: 10.3348/kjr.2000.1.2.110. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Freedland S. J., Isaacs W. B., Platz E. A., et al. Prostate size and risk of high-grade, advanced prostate cancer and biochemical progression after radical prostatectomy: A search database study. Journal of Clinical Oncology. 2005;23:7546–7554. doi: 10.1200/JCO.2005.05.525. [DOI] [PubMed] [Google Scholar]
  • 18.Loeb S., Han M., Roehl K. A., Antenor J. A. V., Catalona W. J. Accuracy of prostate weight estimation by digital rectal examination versus transrectal ultrasonography. The Journal of Urology. 2005;173(1):63–65. doi: 10.1097/01.ju.0000145883.01068.5f. [DOI] [PubMed] [Google Scholar]
  • 19.Cabello-Benevente R., Rascon J. J., Monzo J. I., et al. Volume determinations for the whole prostate and of the adenoma by transrectal ultrasound: Correlation with the surgical specimen. Actas Urológicas Españolas. 2006;30(2):175–180. doi: 10.1016/s0210-4806(06)73420-9. [DOI] [PubMed] [Google Scholar]
  • 20.Lee J. S., Chung B. H. Transrectal ultrasound versus magnetic resonance imaging in the estimation of prostate volume as compared with radical prostatectomy specimens. Urologia Internationalis. 2007;78(4):323–327. doi: 10.1159/000100836. [DOI] [PubMed] [Google Scholar]
  • 21.Sajadi K. P., Terris M. K., Hamilton R. J., et al. Body mass index, prostate weight and transrectal ultrasound prostate volume accuracy. The Journal of Urology. 2007;178(3):990–995. doi: 10.1016/j.juro.2007.05.049. [DOI] [PubMed] [Google Scholar]
  • 22.Jeong C. W., Park H. K., Hong S. K., Byun S.-S., Lee H. J., Lee S. E. Comparison of prostate volume measured by transrectal ultrasonography and MRI with the actual prostate volume measured after radical prostatectomy. Urologia Internationalis. 2008;81(2):179–185. doi: 10.1159/000144057. [DOI] [PubMed] [Google Scholar]
  • 23.Rodriguez E., Skarecky D., Narula N., Ahlering T. E. Prostate volume estimation using the ellipsoid formula consistently underestimates actual gland size. The Journal of Urology. 2008;179(2):501–503. doi: 10.1016/j.juro.2007.09.083. [DOI] [PubMed] [Google Scholar]
  • 24.Acer N., Sofikerim M., Ertekin T., Unur E., Çay M., Öztürk F. Assessment of in vivo calculation with ultrasonography compared to physical sections in vitro: a stereological study of prostate volumes. Anatomical Science International. 2011;86(2):78–85. doi: 10.1007/s12565-010-0090-6. [DOI] [PubMed] [Google Scholar]
  • 25.Hong M. K. H., Yao H. H. I., Rzetelski-West K., et al. Prostate weight is the preferred measure of prostate size in radical prostatectomy cohorts. BJU International. 2012;109(S3):57–63. doi: 10.1007/s10147-011-0295-2. [DOI] [PubMed] [Google Scholar]
  • 26.Varkarakis I., Zarkadoulias A., Bourdoumis A., Chatzidarellis E., Antoniou N., Deliveliotis C. Measurement of PSA density by 3 imaging modalities and its correlation with the PSA density of radical prostatectomy specimen. Urologic Oncology: Seminars and Original Investigations. 2013;31(7):1038–1042. doi: 10.1016/j.urolonc.2011.11.033. [DOI] [PubMed] [Google Scholar]
  • 27.Bienz M., Hueber P. A., Al-Hathal N., et al. Accuracy of Transrectal Ultrasonography to Evaluate Pathologic Prostate Weight: Correlation with various prostate size groups. Urology. 2014;84(1):169–174. doi: 10.1016/j.urology.2014.02.022. [DOI] [PubMed] [Google Scholar]
  • 28.Kiliç M., Özdemir A. T., Altinova S., Atmaca A. F., Canda A. E., Balbay M. D. What is the best radiological method to predict the actual weight of the prostate? Turkish Journal of Medical Sciences. 2014;44:31–35. doi: 10.3906/sag-1205-33. [DOI] [PubMed] [Google Scholar]
  • 29.Paterson N. R., Lavallée L. T., Nguyen L. N., et al. Prostate volume estimations using magnetic resonance imaging and transrectal ultrasound compared to radical prostatectomy specimens. Canadian Urological Association Journal. 2016;10(7-8):264–268. doi: 10.5489/cuaj.3236. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Sosna J., Rofsky N. M., Gaston S. M., DeWolf W. C., Lenkinski R. E. Determinations of prostate volume at 3-Tesla using an external phased array coil: Comparisons to pathological specimens. Academic Radiology. 2003;10(8):846–853. doi: 10.1016/S1076-6332(03)00015-1. [DOI] [PubMed] [Google Scholar]
  • 31.Kwon T., Jeong I. G., You D., et al. Effect of prostate size on pathological outcome and biochemical recurrence after radical prostatectomy for prostate cancer: Is it correlated with serum testosterone level? BJU International. 2010;106(5):633–638. doi: 10.1111/j.1464-410X.2009.09182.x. [DOI] [PubMed] [Google Scholar]
  • 32.Bulman J. C., Toth R., Patel A. D., et al. Imaging date: Comparison with radiologist-derived MR imaging and pathologic specimen volumes. Radiology. 2012;262(1):144–151. doi: 10.1148/radiol.11110266. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Turkbey B., Fotin S. V., Huang R. J., et al. Fully automated prostate segmentation on MRI: Comparison with manual segmentation methods and specimen volumes. American Journal of Roentgenology. 2013;201(5):W720–W729. doi: 10.2214/AJR.12.9712. [DOI] [PubMed] [Google Scholar]
  • 34.Karademir I., Shen D., Peng Y., et al. Prostate volumes derived from MRI and volume-adjusted serum prostate-specific antigen: Correlation with Gleason score of prostate cancer. American Journal of Roentgenology. 2013;201(5):1041–1048. doi: 10.2214/AJR.13.10591. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Hong S. K., Poon B. Y., Sjoberg D. D., Scardino P. T., Eastham J. A. Features in men undergoing radical prostatectomy. Urology. 2014;84:153–157. doi: 10.1016/j.urology.2014.04.006. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Le Nobin J., Orczyk C., Deng F.-M., et al. Prostate tumour volumes: Evaluation of the agreement between magnetic resonance imaging and histology using novel co-registration software. BJU International. 2014;114(6):E105–E112. doi: 10.1111/bju.12750. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Chernyak V., Flusberg M., Kurteva T., Ghavamian R., Rozenblit A. M. Accuracy of prostate measurements on MRI with and without an endorectal coil. Clinical Imaging. 2015;39(1):85–88. doi: 10.1016/j.clinimag.2014.09.003. [DOI] [PubMed] [Google Scholar]
  • 38.Mazaheri Y., Goldman D. A., Di Paolo P. L., Akin O., Hricak H. Comparison of prostate volume measured by endorectal coil MRI to prostate specimen volume and mass after radical prostatectomy. Academic Radiology. 2015;22(5):556–562. doi: 10.1016/j.acra.2015.01.003. [DOI] [PubMed] [Google Scholar]
  • 39.Bezinque A., Moriarity A., Farrell C., Peabody H., Noyes S. L., Lane B. R. Determination of prostate volume: A comparison of contemporary methods. Academic Radiology. 2018;25(12):1582–1587. doi: 10.1016/j.acra.2018.03.014. [DOI] [PubMed] [Google Scholar]
  • 40.Osman M., Shebel H., Sankineni S., et al. Whole prostate volume and shape changes with the use of an inflatable and flexible endorectal coil. Radiology Research and Practice. 2014;2014:6. doi: 10.1155/2014/903747.903747 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Bourne R. M., Bailey C., Johnston E. W., et al. Apparatus for histological validation of in vivo and ex vivo magnetic resonance imaging of the human prostate. Frontiers in Oncology. 2017;7 doi: 10.3389/fonc.2017.00047.47 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Anvari A., Halpern E. F., Samir A. E. Essentials of statistical methods for assessing reliability and agreement in quantitative imaging. Academic Radiology. 2017 doi: 10.1016/j.acra.2017.09.010. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Altman D. G., Bland J. M. Assessing agreement between measurement methods. Clinical Chemistry. 2017;63(10):1653–1654. doi: 10.1373/clinchem.2016.268870. [DOI] [PubMed] [Google Scholar]

Articles from Prostate Cancer are provided here courtesy of Wiley

RESOURCES