A positive Real-Time Elastography (RTE) combined with a Prostate Cancer Gene 3 (PCA3) score above 35 convey a high probability of intermediate- or high-risk prostate cancer in patient admitted for primary prostate biopsy

The mainstay in the diagnosis of prostate cancer (PCa) is biopsy-driven by serum prostate-specific antigen (PSA) and digital rectal examination (DRE). There is really no level of PSA that excludes PCa, and many benign prostatic diseases may cause PSA elevation. The threshold value of PSA for prostate biopsy is arbitrarily chosen, which is dependent on the age of the patient, life expectancy and the size of the prostate. It is well recognized that PSA screening results in both the over-diagnosis and overtreatment of prostate cancer [1‐3]. Furthermore, a lot of men with benign disease are going through prostate biopsy without any beneficial effects. There is also an increase in biopsy-related infections because of antibiotic resistant bacteria, and some of these infections can be lethal [4, 5]. There is a need to better identify those men not harboring PCa to avoid unnecessary biopsies and related complications.

Currently, there is little enthusiasm for population-based PSA screening, and in May 2012 the U.S. Preventive Services Task Force recommended against routine PSA screening [6]. Moreover, European Association of Urology (EAU) Guidelines (2013) do not support programmed mass PSA screening, while recommending early detection in well-informed men [7].

To assist in the decision to perform prostate biopsy, nomograms have been created. The US Food and Drug Administration has approved prostate cancer gene 3 (PCA3) as a predictive test prior to performing a repeat biopsy. PCA3 has shown to enhance the performance of nomograms based on initial biopsy results [8, 9].

Standard systematic prostate biopsy is performed by placing a biopsy needle in 10 to 12 prostate sectors of the peripheral zone under transrectal ultrasound (US) guidance. Cancer in the central or anterior part of the prostate may be overlooked, and insignificant cancer detected with such biopsy regimens [10].

Imaging techniques, specifically advanced US and multiparametric MRI (mpMRI), are evolving, and thereby making it possible to identify areas suspected of harboring PCa [11, 12]. Targeted biopsy guided by RTE detects high-grade cancer, although it misses some significant cancers compared with a systematic 10-core biopsy [13, 14]. mpMRI, together with fusion into real-time US, is practical for targeted biopsy but this approach also misses significant PCa [15].

In a prospective series of patients undergoing radical prostatectomy, the combination of RTE and PCA3 detected 97 % of significant PCa [16]. The present study was undertaken to evaluate prospectively the capability of RTE and PCA 3 to predict clinically significant PCa in patients admitted for initial prostate biopsy.

The study was carried out in the outpatient clinic of the Department of Urology at Haukeland University Hospital from February 2011 to June 2012. The Regional Committee for Medical and Health Research Ethics in Western Norway approved the study.

A total of 127 consecutive patients were included using active inclusion, with only a very small amount of patients declining to participate. The inclusion criteria were a PSA level 3 – 25 ng/ml, age ≤75 years and no prior biopsies within the last five years, in addition to the patients being amenable for radical treatment.

At first, DRE was performed in all patients to determine clinical stage (cT) and to perform the prostatic massage needed before urine sampling. Before further evaluation, the first stray urine was captured and transferred to the transportation tubes needed for the PCA3 analysis. We used Progensa™ PCA3 analysis, and the tests were analyzed at the Fürst Medical Laboratory in Oslo, Norway. After the urine test, all patients were given a single dose of Ciprofloxacin 1 g as an antibiotic prophylaxis. All patients were examined in the left decubital position, with the ultrasound procedures being thoroughly previously described [16]. In brief, all patients were examined using a Hitachi Preirus Ultrasound machine with software for RTE. They were first examined using a V53W transrectal end-fire probe for B-mode evaluation, determination of prostate volume (Pvol), RTE and targeted biopsies. The peripheral zone (PZ) of the prostate was divided in six region of interest (ROI), one at the base, one at the mid prostate and one at the apex on each side. All RTE-reproducible hard lesions of more than 5 mm were allocated to the corresponding ROI. Furthermore, two to four targeted biopsies were taken from suspicious ROIs. A CC531 transrectal simultaneous biplane probe was used for standard systematic biopsies. In the same setting a different urologist blinded for the RTE results performed a 10-core systematic biopsy from the six ROIs. The biopsies were fixated in formaldehyde and analyzed by two uro-pathologists. Total core length, as well as the length of cancer tissue and Gleason grade and score, was separately recorded for each biopsy core.

In the statistical analyses, we included not only the results and outcomes of the initial biopsy, but also at least three years of follow-up data for the patients. If there was a clinically persisting suspicion of PCa after the initial biopsies, patients were monitored closely (see Fig. 1). Repeat biopsies were performed in 38 patients within the next six months, while in 24 patients no repeat biopsy was performed. Sixteen patients with benign repeat biopsies went through a mpMRI of the prostate, and in 12 of these we performed targeted biopsies of suspicious areas by TRUS guided biopsies with a “cognitive fusion” of mpMRI. Together with an uro-radiologist, a trained urologist performed such biopsies. All biopsy data were included in the analyses. Among those 24 patients with no repeat biopsy, four patients experienced a normalization of PSA levels at follow-up, six were admitted for TUR-P with a benign pathology, and in 14 patients benign prostatic hyperplasia was assumed as the reason for a slight elevation in PSA level. The medical records for these patients and the registry at our department of pathology were examined in October 2015 to identify whether PCa had been diagnosed since the end of inclusion. The mean observation time for these patients is 46.7 ± 1.5 months (median 44.4, range 41–55). The medical records for the 14 patients with benign repeat biopsies were also examined at the same time, though none have had PCa diagnosed in this period.

In three patients the urine did not contain enough cells for the PCA3 analysis resulting in 124 evaluable patients.

A total of 70 (56 %) patients were diagnosed with PCa, of whom 62 were identified in the initial biopsy setting and eight patients at the repeat biopsy. The inclusion of these eight patients did not alter the diagnostic performance of RTE by ROI as the sensitivity, specificity, PPV and NPV were 43, 84, 49 and 80 %, respectively; the false positive rate was 16 % and the false negative rate 12 %.

According to the European Association of Urology (EAU) risk stratification, there were 21 (30 %) low-, 32 (46 %) intermediate- and 17 (24 %) high-risk cancers [7]. In the eight patients detected with PCa on the repeat biopsies six were low-risk and two were intermediate-risk cancers, there were no high-risk PCa in this group.

The distribution of PSA, PCA3 score, Pvol, age and proportion of positive DRE for all patients and for patients with and without PCa is found in Table 1. The p-values are calculated for the difference between the groups with PCa and without PCa. The clinical stage, biopsy Gleason grade and score and risk stratification according to EAU guidelines are also detailed in Table 1.

RTE was positive in 85 cases and negative in 39 . The average PCA3 score in patients with PCa was significantly higher compared with normal or benign disease (73.6 vs. 26.6, p < 0.001). For PSA, there were no statistical significant differences between those patients with- and those without PCa (9.7 vs. 8.3, p = 0.09).

The sensitivity, specificity, PPV and NPV of RTE by patient, PCA3 at score 35 and the combination of both for any PCa, for intermediate- and high-risk PCa together, and for high-risk PCa alone, are shown in Table 2.

In univariate logistic regression analysis a positive RTE was a highly significant predictor of intermediate- risk and high-risk PCa (Table 3).

Entering PCA3 and RTE in a clinical model encompassing age, PSA and Pvol; PSA, Pvol and PCA3 were independent predictors of intermediate-risk and high-risk PCa while RTE showed a tendency toward significance (Table 3).

The results of the logistic regression analyses were also expressed in a ROC curve that yielded an AUC of 0.826 (0.752-0.899) for the complete model and 0.787 (0.703-0.872) for the clinical model alone (Fig. 2).

To evaluate the clinical impact of the combination of PCA3 and RTE, we utilized the most commonly used cut-off value of 35 for PCA3, and allocated the patients into four groups.

Group 1 included patients for whom both RTE and PCA3 were positive. Patients with a positive RTE and negative PCA3 were put into Group 2, and RTE negative and PCA3 positive patients were allocated to Group 3. Finally, Group 4 encompassed patients negative for RTE, as well as PCA3. Group 1 encompassed 44 patients; 30 had a high- or intermediate-risk PCa, eight a low-risk PCa and six a benign prostate. If both tests were positive, we found a high (86 %) probability of PCa at biopsy. On the other hand, of 23 patients with a PCA3 below 35 and a negative RTE (Group 4), eight patients were diagnosed with PCa, including six with low-risk cancer and two with intermediate-risk cancer, while 15 patients did not have any cancer. There was no high-risk PCa in this group. Omitting a biopsy in this group would imply a 9 % likelihood of missing PCa of clinical importance. In Group 2, 14 patients were diagnosed with cancer and 27 without cancer. There were 16 patients with a PCA3 score equal to or higher than 35 and a negative RTE (Group 3); ten patients had cancer and no cancer was found in the other six. The results achieved from pre-biopsy PCA3 urinary tests and RTE assessments in both Group 1 and Group 4 are informative and may be of benefit in the decision-making process as to whether to perform a biopsy or not.

Out of 70 patients for whom PCa was diagnosed, 27 underwent radical prostatectomy, 27 received external radiotherapy and 16 opted for active surveillance.

There is a changing wind in the way we detect and treat PCa as a consequence of the well-known over-diagnosis and overtreatment of PCa, in addition to the documented increasing rate of post-biopsy infections [4, 5]. There is an ongoing search for new biomarkers and the development of improved methods for identifying clinically significant PCa. Evolving evidences show the benefit of PCA3 in the decision-making process of performing repeat biopsies in men where the initial biopsy is negative.

Both RTE and mpMRI are capable of identifying PCa that is not visualized on B-mode ultrasound [17, 18].

To the best of our knowledge, the present paper is the first to present prospective data on the combination of pre-biopsy PCA3 and RTE by patient in predicting PCa in an unselected series of men admitted for an initial biopsy.

The most important findings are the high sensitivity as well as NPV in predicting intermediate-risk and high-risk PCa (Table 2). PCA3 and RTE appeared to be of benefit mostly in patients if both parameters were positive or negative. If both parameters are positive, there is good reason to perform a biopsy and there is a high probability of detecting aggressive disease. Additionally, avoiding a biopsy in which PCA3 and RTE are negative carries a small risk of missing patients harboring a clinically significant PCa. In this series we found 32 intermediate-risk PCa and 17 high-risk PCa. By using RTE and PCA3 as selection criteria for performing a biopsy, 23 patients would have been advised against having a biopsy; only two of these patients had intermediate-risk PCa and no patients had high-risk PCa. One could argue that the reduction of unnecessary biopsies is relatively small since only 23 patients (19 %) would have been advised against biopsy. On the other hand, these patients could safely be advised against biopsy, as every reduction of unnecessary biopsies is a step in the right direction in reducing over-diagnosis and overtreatment of low-risk PCa. These findings are in line with our previous study of the combination of PCA3 and RTE in a smaller series of radically operated PCa patients [16].

In the logistic regression analysis PCA3 as well as a positive RTE contributed to the clinical model although RTE achieved a p-value close to significance (0. 068). In a ROC analysis, the full model with PCA3 and RTE achieved an AUC of 0.826. In univariate analysis a positive RTE is a highly significant predictor of PCa.

No definite threshold of PCA3 score has been agreed upon as yet, although a score of 35 is most frequently used as a cut-off value. In our study, we tested two different PCA3 score thresholds of 21 and 35, respectively. A threshold score of 35 provided the most optimal PPV of 80 %, which is the same figure found in a prospective randomized study by Wei et al., using a PCA3 score threshold of 60 in the initial biopsy setting [19]. In our analyses, we utilized a PCA3 score of 35 as the threshold value.

A strength of this study is that it includes histo-pathological data on initial biopsies, repeat biopsies as well as data of further follow-up, including mpMRI targeted biopsies of suspected lesions. No patients in the group diagnosed with a benign disease have been diagnosed with PCa in the period since the study inclusion was closed in June 2012. For all 14 patients with a presumably benign reason for an elevated PSA, both medical records and records for the regional pathology laboratory were checked. We believe that we are as close as possible to the true prevalence of PCa in the study population at the time of the examinations. This makes this study different from other studies investigating PCA3 [8, 20] and RTE [21, 22], in which the performance of these markers has been solely evaluated at the initial biopsy.

In this series of patients, a total of 70 patients were diagnosed with PCa, including 21 who were classified as low-risk and 49 as either high- or intermediate-risk.

Analyzing the group of PCa patients harboring either high- or intermediate-risk PCa, the combination of RTE and PCA3 correctly identified 47 of these patients. That means we correctly identified 96 % of the patients harboring PCa in need of treatment in a pre-biopsy setting. This result may be used to reduce the number of unnecessary biopsies at a small risk of missing PCa in need of treatment.

The present study has some limitations. Firstly, it is a single center, single investigator study. RTE like all US investigations are real-time examinations and are operator dependent and an inter-observer investigation would have been of value. As to the learning curve, it has been shown that after about 30 RTE the novice is achieving comparable results to experienced US operators [23]. Secondly, a relatively small number of patients are included. Thirdly, there is a limited number of patients with high-risk PCa, although the findings are in line with our previously published paper on patients planned for radical prostatectomy [16].

In patients with a positive RTE combined with a PCA3 score above 35 there is a high probability of detecting intermediate- or high-risk PCa. The combination of these markers correctly identified 47 of 49 (96 %) patients in need of a further diagnostic work-up. The high NPV of the combination of PCA3 and RTE makes it possible to avoid some 20 % of the prostate biopsies without missing high-risk PCa. If applied to the upper age group, in which a missing low-risk PCa may be seen as an advantage, the use of RTE and PCA3 may be implemented as pre-biopsy examinations to reduce the number of prostate biopsies.

AUC, area under the curve; CI, confidence interval; DRE, digital rectal examination; EAU, European Association of Urology; mpMRI, multiparametric magnetic resonance imaging; NPV, negative predictive value; PCa, prostate cancer; PCA3, Prostate cancer gene 3; PPV, positive predictive value; PSA, prostate-specific antigen; Pvol, prostate volume; ROC, receiver operating curve; RTE, real-time elastography; TRUS, transrectal ultrasound; US, ultrasound