# Digital rectal exam vs. electronic “digitized” prostate exam

**Authors:** Tabea Borde, Nicole A. Varble, Alexander Kenigsberg, Lindsey A. Hazen, Laetitia Saccenti, Peter A. Pinto, Baris Turkbey, Bradford J. Wood

PMC · DOI: 10.1186/s12894-025-01936-y · BMC Urology · 2025-11-21

## TL;DR

This study finds that digital rectal exams add little value for detecting significant prostate cancer when combined with PSA and MRI.

## Contribution

The study quantifies the limited diagnostic value of DRE in a setting where PSA and mpMRI are already used.

## Key findings

- DRE had low sensitivity (0.17) and moderate specificity (0.92) for detecting clinically significant prostate cancer.
- PSA and PSAD outperformed DRE in predicting csPCa with higher AUC values.
- mpMRI detected all csPCa cases with focal lesions, suggesting it is more reliable than DRE.

## Abstract

The current era of multiparametric prostate MRI (mpMRI) and ultrasound (US)/ MRI fusion has improved early detection of clinically significant prostate cancer (csPCa) while decreasing the number of unnecessary biopsies. Hence, this study aims to define the diagnostic value of pre-biopsy digital rectal examination (DRE) for screening and detection of csPCa, when there is access to mpMRI and prostate-specific antigen (PSA).

This retrospective, single-center study involved 3379 consecutive patients biopsied between 2012 and 2023 using both MRI/US-targeted fusion and systematic approaches. Biopsies were indicated because of elevated PSA levels and/or presence of cancer suspicious lesions on MRI. All patients underwent DRE and mpMRI prior to biopsy. csPCa was defined as Gleason grade group ≥2. Diagnostic performance of DRE for csPCa was compared to PSA and PSA density (PSAD) using receiver operating characteristic curves.

Two thousand one hundred eighty-eight (65%) patients were diagnosed with PCa and 1498 (44%) patients with csPCa. DRE was positive in 410/3379 (12%) patients. 261/410 (64%) DRE positive patients had confirmed csPCa, of which 160/261 (61%) were located in immediate proximity to the rectum. mpMRI was positive for focal lesion(s) in 1494/1498 (100%) csPCa patients. For csPCa detection, DRE had a sensitivity of 0.17, specificity of 0.92, a positive predictive value of 0.63 and a negative predictive value of 0.59. Compared to DRE (AUC 0.55 [CI95% 0.54, 0.56]), PSA (AUC 0.63 [CI95% 0.61, 0.64]) and PSAD (AUC 0.73 [CI95% 0.71, 0.74]) showed better csPCa prediction performance (both p < 0.001).

Pre-biopsy DRE was found to add little to no diagnostic value for the routine diagnostic workflow in a constrained setting when PSA and mpMRI are initial screening tools for patients with suspected csPCa.

The online version contains supplementary material available at 10.1186/s12894-025-01936-y.

## Linked entities

- **Diseases:** prostate cancer (MONDO:0005159)

## Full-text entities

- **Genes:** KLK3 (kallikrein related peptidase 3) [NCBI Gene 354] {aka APS, KLK2A1, PSA, hK3}
- **Diseases:** PCa (MESH:D011471), DRE (MESH:D012002), PSAD (MESH:D011472), pain (MESH:D010146), appendicitis (MESH:D001064), Cancer (MESH:D009369)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

2 references — full list in the complete paper: https://tomesphere.com/paper/PMC12771905/full.md

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Source: https://tomesphere.com/paper/PMC12771905