The use of mpMRI before biopsy in patients with suspected prostate cancer is recommended by current guidelines. Therefore, mpMRI has become an essential milestone in prostate biopsy decisions. It is more sensitive in patients with tumors larger than 6 mm and those with a high Gleason score (2,6-8).
Considering the high imaging quality provided by this method, mpMRI not only assists in decision-making regarding prostate biopsy but can also reveal IEPFs, which can lead to the diagnosis and treatment of these findings. In addition to IEPFs, MRI can also detect the invasion of prostate tumors into adjacent organs and lymphadenopathies (2).
Our study included 1000 patients, and IEPFs were detected in 294 (29.4%) of them. Of these, 51 (14%) were related to the genitourinary system, whereas 312 (86%) were unrelated. In a study conducted by Cutaia et al., which included 647 patients, IEPFs were detected in 52.7% of the cohort (9). In another study by Emekli et al. (10), 426 patients were included, and 49.8% had IEPFs. Similarly, Sherrer et al. (11) worked on the same subject and found that 40% of their 580 participants had IEPFs.
The lower percentage of patients with incidental findings in our study can be ascribed to the fact that our institution is a tertiary referral center and some potential IEPFs might have been treated before undergoing mpMRI at our institution. Additional factors, such as patient demographics, referral patterns, and imaging protocol variations, may also influence the observed rate. These factors should be considered when interpreting the lower detection rate.
Cutaia et al. showed that 322 (69.8%) patients with IEPFs had findings unrelated to the genitourinary system, while 139 (30.2%) had genitourinary system findings (9). In the study by Emekli et al., genitourinary system findings constituted 41.1% (n=132) of all IEPFs detected (10). In a study by Sherrer et al., 51% (n=179) of the 349 IEPFs were unrelated to the genitourinary system, while the remaining were genitourinary system-related (9-11). Our study aligns with the literature, as genitourinary system-unrelated findings were more common than genitourinary system findings.
In line with our analysis, Cutaia et al. categorized IEPFs according to their clinical significance (9). In this study, 355 patients were included in group 1, 94 patients were classified as group 2, and 12 (2.6%) patients were classified as group 3. In contrast, Emekli et al. classified patients into clinically significant and clinically insignificant IEPFs groups (10). The authors reported that 6.9% (n=22) of patients had clinically significant findings.
Since T2 coronal imaging focuses on the prostate in mpMRI performed in accordance with the PI-RADS score, liver and spleen lesions were not detected in our study. Fat-suppressed coronal T2-weighted images can be acquired to detect other organ pathologies. However, these approaches are time-consuming and expensive. Notably, artificial intelligence is a hot topic in mpMRI practice; however, its sensitivity in detecting IEPFs needs to be clarified (12).
In a study by Ediz et al. (13), the PI-RADS scoring system did not contribute to the diagnosis of incidental mp-MRI. This finding aligns with our results, as shown in Table 2, where no relationship was found between the PIRAD scores and IEPFs.
The recent review by Ponsiglione et al. (14) reported a substantially higher overall prevalence of incidental non-prostatic findings on mpMRI in different studies, compared to 29, 4 % in our cohort. This discrepancy may be attributed to differences in institutional imaging protocols, classification criteria, and patient selection criteria. Unlike their pictorial review, which broadly illustrated hepatic, renal, and gastrointestinal findings, our study applied a structured three-tier classification (mild, moderate, severe) and specifically quantified genitourinary IEPFs. Genitourinary lesions were emphasized in our dataset, comprising 13.9% of all incidental findings. Additionally, our exclusion of patients with known metastatic or locally advanced disease may explain the relatively lower detection rate for some non-prostatic findings compared with the broader inclusion criteria in their analysis.
Our study had some strengths and limitations. The main limitations of this study are its retrospective design, single-center data, and relatively limited number of patients included. However, our study is the most extensive series to date, which represents its strength.
DISCUSSION
The use of mpMRI before biopsy in patients with suspected prostate cancer is recommended by current guidelines. Therefore, mpMRI has become an essential milestone in prostate biopsy decisions. It is more sensitive in patients with tumors larger than 6 mm and those with a high Gleason score (2,6-8).
Considering the high imaging quality provided by this method, mpMRI not only assists in decision-making regarding prostate biopsy but can also reveal IEPFs, which can lead to the diagnosis and treatment of these findings. In addition to IEPFs, MRI can also detect the invasion of prostate tumors into adjacent organs and lymphadenopathies (2).
Our study included 1000 patients, and IEPFs were detected in 294 (29.4%) of them. Of these, 51 (14%) were related to the genitourinary system, whereas 312 (86%) were unrelated. In a study conducted by Cutaia et al., which included 647 patients, IEPFs were detected in 52.7% of the cohort (9). In another study by Emekli et al. (10), 426 patients were included, and 49.8% had IEPFs. Similarly, Sherrer et al. (11) worked on the same subject and found that 40% of their 580 participants had IEPFs.
The lower percentage of patients with incidental findings in our study can be ascribed to the fact that our institution is a tertiary referral center and some potential IEPFs might have been treated before undergoing mpMRI at our institution. Additional factors, such as patient demographics, referral patterns, and imaging protocol variations, may also influence the observed rate. These factors should be considered when interpreting the lower detection rate.
Cutaia et al. showed that 322 (69.8%) patients with IEPFs had findings unrelated to the genitourinary system, while 139 (30.2%) had genitourinary system findings (9). In the study by Emekli et al., genitourinary system findings constituted 41.1% (n=132) of all IEPFs detected (10). In a study by Sherrer et al., 51% (n=179) of the 349 IEPFs were unrelated to the genitourinary system, while the remaining were genitourinary system-related (9-11). Our study aligns with the literature, as genitourinary system-unrelated findings were more common than genitourinary system findings.
In line with our analysis, Cutaia et al. categorized IEPFs according to their clinical significance (9). In this study, 355 patients were included in group 1, 94 patients were classified as group 2, and 12 (2.6%) patients were classified as group 3. In contrast, Emekli et al. classified patients into clinically significant and clinically insignificant IEPFs groups (10). The authors reported that 6.9% (n=22) of patients had clinically significant findings.
Since T2 coronal imaging focuses on the prostate in mpMRI performed in accordance with the PI-RADS score, liver and spleen lesions were not detected in our study. Fat-suppressed coronal T2-weighted images can be acquired to detect other organ pathologies. However, these approaches are time-consuming and expensive. Notably, artificial intelligence is a hot topic in mpMRI practice; however, its sensitivity in detecting IEPFs needs to be clarified (12).
In a study by Ediz et al. (13), the PI-RADS scoring system did not contribute to the diagnosis of incidental mp-MRI. This finding aligns with our results, as shown in Table 2, where no relationship was found between the PIRAD scores and IEPFs.
The recent review by Ponsiglione et al. (14) reported a substantially higher overall prevalence of incidental non-prostatic findings on mpMRI in different studies, compared to 29, 4 % in our cohort. This discrepancy may be attributed to differences in institutional imaging protocols, classification criteria, and patient selection criteria. Unlike their pictorial review, which broadly illustrated hepatic, renal, and gastrointestinal findings, our study applied a structured three-tier classification (mild, moderate, severe) and specifically quantified genitourinary IEPFs. Genitourinary lesions were emphasized in our dataset, comprising 13.9% of all incidental findings. Additionally, our exclusion of patients with known metastatic or locally advanced disease may explain the relatively lower detection rate for some non-prostatic findings compared with the broader inclusion criteria in their analysis.
Our study had some strengths and limitations. The main limitations of this study are its retrospective design, single-center data, and relatively limited number of patients included. However, our study is the most extensive series to date, which represents its strength.