Internal review board approval (IRB No.: VGHKS19-CT3-13) was granted by a Taiwanese tertiary medical center, the Kaohsiung Veterans General Hospital. All male patients (N=1344) undergoing TRUS prostate biopsies with a 12-core systematic biopsy strategy from 2012 to 2018 were enrolled. The indication for prostate biopsy included an abnormal PSA level (>4 ng/mL) or an abnormal DRE. Each patient would receive DRE and TRUS before the biopsy was performed; prostate volume (PV) was calculated by the ellipsoid formula (length x width x height x π/6). Some patients (53/1344) had multiparametric magnetic resonance imaging (mpMRI) scans on a self-pay basis because the Taiwan National Health Insurance system has not approved the reimbursement of pelvic magnetic resonance imaging (MRI) before prostate biopsy. All prebiopsy mpMRI scans were reported by dedicated urologic radiologists, in agreement with the Prostate Imaging Reporting and Data System, version 2 (PI-RADS v2) [7]. The number of patients who received radical prostatectomy was 137. Consultant pathologists reviewed all biopsies and postprostatectomy specimens.

According to the Rotterdam app, the definition of clinically significant PCa is a tumor stage greater than T2b, or a Gleason biopsy score of ≥7, which is identical to high-risk PCa in the ERSPC risk calculator (ERSPC-RC) [8]. In comparison, the Coral app defined a Gleason biopsy score of ≥7 as high-grade PCa, which originated from the PCPT [2]. In order to use consistent terminology, a Gleason score of ≥7 was defined as high-grade PCa. PSA was designated as the latest total serum PSA level before prostate biopsy.

All patient data were retrospectively collected via electronic medical records. The Rotterdam app accepts input data on age, DRE history and outcome, previous negative biopsy, PSA, PV, volume measure method (TRUS or DRE), TRUS evaluation (normal or abnormal), MRI history, and PI-RADS score. The Coral app requires data on ethnicity (African American, Caucasian, Hispanic, or Other), age, DRE, PSA, family history, and prior biopsy results. Following input data collection, the risks of PCa and high-grade PCa were calculated using the Rotterdam and Coral apps.

Each app customizes its parameters to impose controls or constraints on accepted input values; that is, both the Rotterdam and Coral apps have an input data range for some parameters. For instance, the input PSA range is limited from 0.4-50 ng/mL within the Rotterdam app and 0.3-100 ng/mL within the Coral app. If the patients have prebiopsy MRI scans, there is an age limit between 50 and 75 years. On the contrary, without prebiopsy MRI, both the Rotterdam and Coral apps have no limitation on the input age data. According to the accepted input values from both apps, 197 patients were excluded, either because their PV was <10 or >110 mL (68/197), or their PSA level was <0.4 or >50 ng/mL (118/197), or they underwent prebiopsy MRI at the age of <50 or >75 years (11/197). In addition, 13 more patients with previous positive biopsies (8/13), pathological diagnosis different from adenocarcinoma (3/13), or incomplete data (2/13) were excluded. Details of the inclusion and exclusion process are illustrated in the flow chart in Figure 1.

Statistical analyses were performed utilizing SPSS (version 18; IBM Corp) and R software packages (R Core Team). The Kolmogorov-Smirnov test was used to examine the normality of the distribution of variables. Categorical variables were assessed with the chi-square test. Continuous variables were described as medians and interquartile ranges or means and standard deviations, and compared by the Mann-Whitney U test or the Student independent t test based upon their nonnormal or normal distributions, respectively. The applicability of each PCa risk calculator app in the Taiwanese population cohort was statistically analyzed on the basis of its discrimination, calibration, and clinical utility [9]. Calibration relates to the agreement between the observed and predicted proportion of events; calibration was evaluated graphically utilizing a calibration plot in which the observed probabilities were plotted against the predicted probabilities, enabling assessment of the extent of risk underestimation or overestimation [10]. The statistical significance of miscalibration was examined by the Hosmer-Lemeshow goodness-of-fit test [11].

Discrimination reflects the capacity of a prediction model to differentiate between those with and without an event (any-grade or high-grade PCa) and is quantified utilizing the area under the receiver operating characteristic (ROC) curve (AUC). The AUCs of the Rotterdam and Coral apps were compared using DeLong’s method [12]. As for clinical utility, decision curve analysis was performed to analyze whether both apps were beneficial for clinical decision-making or which app would lead to better decisions. We calculated the net benefit to quantify the clinical utility; different threshold probabilities mean different harm-to-benefit ratios. Net benefit was formulated as the number of true positives subtracted from the proportion of false positives weighted by the odds of the risk threshold probability, and the result was divided by the sample size. By measuring the proportions of net true positives in the models, we could assess whether any model performed better than others and the default strategies of biopsying all or no patients across the reasonable range of risk threshold probabilities [13].

Of 1344 patients undergoing biopsies, 246 (21.7%) patients were diagnosed with PCa; of these 246 patients, 155 (63%) had high-grade PCa, according to the biopsy results. Compared to males with negative biopsies, patients with PCa were significantly older, had higher PSA levels, smaller PVs, more abnormal findings on TRUS and DRE, and higher PI-RADS scores demonstrated on mpMRI (Table 1). Both in the biopsy and prostatectomy cohorts, patients with high-grade PCa had significantly higher PSA, lower PV, and more abnormal findings on TRUS compared to those with low-grade PCa (Table 2). Among 246 diagnoses of PCa, 137 patients underwent radical prostatectomy; based on the postprostatectomy outcomes, 47.2% (25/53) of patients were upgraded to high-grade PCa and 1.2% (1/84) of patients were downgraded to low-grade PCa.

The calibration of both apps was tested with the Hosmer-Lemeshow goodness-of-fit test (Figure 2). Comparing both apps, only the Rotterdam app demonstrated a good calibration (P=.619) for detecting high-grade PCa in the biopsy cohort. Other models were miscalibrated, including all models created from the Coral app.

Both the Rotterdam and Coral apps could significantly predict PCa and high-grade PCa in the biopsy cohort on ROC analysis (Figure 3, a and b). The discriminative capacity for detection of both PCa (AUC: 0.779 vs 0.687; DeLong’s method: P<.001) and high-grade PCa (AUC: 0.862 vs 0.758; P<.001) was significantly better for the Rotterdam app compared to the Coral app. In the prostatectomy cohort, the Rotterdam and Coral apps were not significantly different for predicting high-grade PCa (AUC: 0.857 vs 0.777; P=.128; Figure 3c).

In the decision curve analysis for the biopsy cohort of patients, both apps demonstrated clinical net benefits in the threshold probability range of 10% to 85% for the detection of any PCa. In the detection of high-grade PCa, the Rotterdam and Coral apps provided net benefits in the threshold probability range of 5%-70% and 10%-80%, respectively. In comparing both apps, the net benefit was greater for the Rotterdam app in the prediction of both PCa and high-grade PCa across the range of threshold probabilities from 5%-70% (Figure 4). It seemed that both apps provided net benefits for the detection of high-grade PCa in the prostatectomy cohort (Figure 5). Nevertheless, the prevalence of high-grade PCa in the prostatectomy cohort was very high (79%). With baseline risk being very high, it would be difficult for both apps to push the risk to a level low enough for advice against biopsy. Both apps had higher net benefits when the curves diverged at the threshold probability of about 50%, and therefore, both apps lacked value for the prediction of high-grade PCa in the prostatectomy cohort.

In this study, we found that the Rotterdam and Coral apps were both applicable to the Taiwanese cohort of patients who had undergone TRUS prostate biopsy, even though these apps were built based on Western populations. In order to externally validate these 2 apps, 3 key statistical measures were used in the assessment of predictive performance. Firstly, most models revealed miscalibration, but the Rotterdam app demonstrated good calibration for the prediction of high-grade PCa in the biopsy cohort. Secondly, the Rotterdam app outperformed the Coral app in its discriminative ability for predicting PCa and high-grade PCa in the biopsy cohort. Thirdly, the Rotterdam app provided greater net benefits than the Coral app to assist in biopsy decision-making. In brief, the Rotterdam app delivered better predictive performance than the Coral app for PCa and high-grade PCa in our Taiwanese population cohort.

To the best of our knowledge, at the stage before PCa is diagnosed, no risk prediction model has ever been validated by the whole prostate specimen. Data from the 137 patients who had undergone radical prostatectomy for any-grade PCa were utilized to evaluate the Rotterdam and Coral apps' predictive capacity for high-grade PCa. Both apps demonstrated fairly good discrimination for predicting high-grade PCa in the prostatectomy cohort and the biopsy cohort. It was implied that after confirmation with postprostatectomy pathology outcomes, both apps still delivered a comparable discriminative ability for predicting high-grade PCa in the present Taiwanese cohort. However, during calibration and decision curve analysis in the prostatectomy cohort, both apps were miscalibrated and revealed few net benefits. This might be explained by the small sample size and different pathology distribution, as there was a higher prevalence of high-grade PCa (79%). Moreover, these apps were built on biopsy cohorts, which are different from the prostatectomy cohort. More patients with radical prostatectomy might need to be enrolled to validate app predictability of high-grade PCa, which would be validated by the whole prostate specimen.

In current clinical practice, most patients with an abnormal PSA level of >4 ng/mL or an abnormal DRE are put forward for biopsy. However, such indications lead to a myriad of unnecessary biopsies and associated complications, such as hematuria, hematospermia, rectal bleeding, acute urinary retention, urinary tract infection, or even sepsis. To increase the accuracy of cancer detection and reduce unnecessary postbiopsy morbidities, several biomarker tests have been developed, including the Prostate Health Index (PHI), percent-free PSA, PCA3, 4K-score, etc [14]. The European Association of Urology (EAU) guidelines suggest an individualized evaluation of PCa risk. Age, family history of PCa, DRE, serum or urine markers, and mpMRI are validated parameters in combination with PSA levels to help predict the risk of PCa [15]. Recently, professionals have formulated a number of PCa risk calculators using some of these useful predictors to improve predictive accuracy, and such multivariable risk approaches have performed better than PSA or DRE alone [10]. Nonetheless, most of them have only been validated in independent cohorts; neither superiority nor global applicability has been shown [16]. De Nunzio et al [4] had validated the Rotterdam and Coral apps' discriminative abilities utilizing a southern European cohort as providing better predictive performance than PSA or DRE; however, the predictability of PCa or high-grade PCa in the Taiwanese population stills needs to be addressed.

It is well known that Gleason upgrading occurs in 32%-49% of patients with initial biopsy of low-grade (Gleason 3+3) PCa at the time of pathological assessment of the whole prostate specimen [14]. Verep et al [17] reviewed 137 patients who were eligible for active surveillance but underwent radical prostatectomy at their institution. The criteria of active surveillance included Gleason 3+3 adenocarcinoma, maximum 2 positive biopsy cores, PSA <10ng/mL, and clinical T-stage equal or less than 2a. Following pathological confirmation, Gleason upgrading was noted in almost half of the patients (49.3%), and upstaging to pT3a occurred in 17 patients (12.5%) [17]. Due to the risks of over-diagnosis and over-treatment for clinically insignificant PCa, active surveillance has become increasingly adopted as a preferred treatment option for patients with low-grade PCa. However, without precise risk stratification, active surveillance might delay the timing of curative treatment for localized PCa, or even increase the risks of lymph node involvement and distant metastasis. Consequently, the accuracy of risk prediction tools has become of paramount importance.

Mobile health (mHealth) is regarded as a valuable tool to implement patient-centered care, which is in accordance with the individualized risk assessment of PCa recommended by the EAU guidelines. mHealth can provide access to health information, skills, and services, and can also promote positive health behavioral changes to prevent acute and chronic diseases. Real-time monitoring can obtain live data from patients and transmit inputs to a network or a medical app on a smartphone to assist clinical decision-making. Regardless of the environmental circumstances, geographical barriers, and conventional infrastructures, it can share timely information between patients and health personnel, replacing the traditional face-to-face platform of medical care. Nevertheless, to not harm patients, it is pivotal that scientific accuracy, patient safety, and user privacy of mHealth apps be assured [18].

One systematic review that critically appraised PCa risk calculator apps maintained that the Rotterdam Prostate Cancer Risk Calculator and Coral–Prostate Cancer Nomogram Calculator outperformed other apps [3]. The authors utilized the validated user version of the Mobile Application Rating Scale to individually assess and rate 7 apps, including 3 categories of app quality ratings, subjective quality, and perceived impact [19]. Objective characteristics were thoroughly documented and assessed. None of these apps allowed confidentiality, data storage developing trends, or customization. Both the Rotterdam and Coral apps were found to help differentiate low-grade from high-grade PCa, a noteworthy characteristic of patient counseling in active surveillance compared to other curative alternatives.

Mobile technology enables clinicians and patients to download the Rotterdam and Coral apps readily, and the owners can utilize these apps without an internet connection. They both have the advantages of being less time-consuming and more cost-effective, delivering better immediacy, upgradability, and shareability than the original risk calculators. In addition, they are globally available and recommended by the American Urological Association and EAU guidelines to improve prediction and help determine the risk of PCa stratification. Compared with the Coral app, the conspicuous disadvantage of the Rotterdam app is its cost ($1.99 USD). However, it has been proven to reach a wider audience, with availability on both Apple and Android platforms. While the Coral app has merely 1 language choice, the Rotterdam app has 7 different language options, including Chinese, Dutch, English, Estonian, German, Portuguese, and Spanish.

This study was a single-institution retrospective study, and more cohorts from other Taiwanese hospitals are required to confirm the results. Also, the sample size in the prostatectomy cohort was rather small (n= 137). Notwithstanding that, this is the first study validating PCa risk calculators with postprostatectomy pathological outcomes, although the predictive accuracy of both apps for true high-grade PCa could not be completely determined. Further, no PHI data are available in our institution. The PHI is a combination of 3 blood tests measuring different forms of the PSA protein (total PSA, free PSA, and p2PSA) and calculated as (p2PSA/fPSA) × √tPSA. It is one of the predictors listed in the Rotterdam app, although the risks of PCa can still be calculated without PHI data. Few patients underwent mpMRI before biopsy in our cohort; however, mpMRI has emerged as an important prediction tool to identify clinically significant PCa, especially before a repeated biopsy, which has been recommended by the guidelines [14,15]. The Rotterdam app and web-based ERSPC-RC is one of the PCa risk prediction models incorporating mpMRI (PI-RADS 1-5) [20]; nevertheless, the predictor of the PI-RADS used in the Rotterdam app was the first version, and most of our MRI images were graded according to the PI-RADS v2 guidelines. Moreover, the issues of interobserver variability and heterogeneous definitions of abnormality in mpMRI interpretation remain to be explored, and these MRI risk prediction models need to be validated further.

In our external validation study, the Rotterdam and Coral mHealth apps could be applied to the Taiwanese cohort of patients. Following an assessment of calibration, discrimination, and clinical utility, the Rotterdam app outperformed the Coral app for predicting both any-grade PCa and high-grade PCa. The size of the prostatectomy cohort was small; however, both mobile phone apps, to some extent, demonstrated a predictive capacity for true high-grade PCa, confirmed by the whole prostate specimen. As of yet, there is no PCa risk calculator app developed specifically for the Taiwanese population; however, the Rotterdam app might be a good alternative to enhance the predictive accuracy of current methods for detecting PCa and high-grade PCa.