# Prostate Cancer Diagnosis by Transurethral Resection of the Prostate Is Associated with Compromised Oncologic Outcomes Post-Prostatectomy

**Authors:** Abdullah Al-Khanaty, Marlon Perera, Brendan Yanada, Melanie Evans, Declan G. Murphy, Damien Bolton, Nathan Papa

PMC · DOI: 10.3390/cancers18040569 · 2026-02-09

## TL;DR

Men diagnosed with prostate cancer during TURP surgery have worse survival outcomes compared to those diagnosed through biopsies.

## Contribution

This study reveals that prostate cancer found during TURP is linked to poorer survival, even after adjusting for key clinical factors.

## Key findings

- TURP-diagnosed patients had 5-year overall survival of 91.2% versus 96.7% for biopsy-diagnosed patients.
- Multivariable analysis showed a 2.33 hazard ratio for TURP-diagnosed patients having worse survival.
- Prostate cancer-specific mortality was higher for TURP-diagnosed patients, though not statistically significant.

## Abstract

Sometimes prostate cancer is found by chance when men have surgery on the prostate to improve urinary symptoms (called TURP), rather than through a planned prostate biopsy. In this study, we looked at men who later had their prostate removed for cancer and compared outcomes between those whose cancer was first found on TURP and those diagnosed by biopsy. We found that men whose prostate cancer was discovered during TURP were more likely to die over time than men diagnosed by biopsy, even after taking into account age, PSA level, and cancer grade. Although prostate cancer-specific deaths were uncommon, the overall survival difference was clear. These results suggest that prostate cancer found incidentally during TURP may behave more aggressively or be harder to fully assess at the time of diagnosis. This is important for patients and doctors when deciding on follow-up and treatment after TURP, and as newer prostate procedures that do not provide tissue for testing become more common.

Background: Following transurethral resection of the prostate (TURP) for lower urinary tract symptoms, incidental diagnosis of prostate cancer occurs in 2–10%. The significance of incidental prostate cancer on TURP compared to diagnosis via traditional diagnostic pathways is unclear. We aimed to compare post-prostatectomy outcomes in patients diagnosed with prostate cancer on TURP and prostate biopsy, using a population-based clinical quality registry. Methods: Data were extracted from the Victorian Prostate Cancer Outcomes Registry (PCOR-Vic). Patients who underwent prostatectomy between September 2008 and September 2020 and who were diagnosed by needle biopsy or TURP were included. The association between diagnosis method and overall survival was examined with Kaplan–Meier plots and the log-rank test. Multivariable Cox proportional hazards regression adjusting for PSA, age, year of surgery, diagnostic Gleason grade group and margin status was also used. Association with prostate cancer-specific mortality was examined with Fine and Gray competing hazards regression including the same covariates as above. Results: In total, 12022 patients met the inclusion criteria, of which 159 (1.3%) were diagnosed on TURP. After a median 58 months follow-up, diagnosis on TURP was associated with poorer 5-year overall survival at 91.2% (84.2–95.0%) compared to diagnosis on needle biopsy at 96.7% (96.2–97.0%), log-rank p = 0.001. Following multivariable adjustment, the hazard ratio of TURP vs. biopsy patients was 2.33 (95%CI: 1.35–4.01). For prostate cancer-specific mortality, there was a similar estimate; however, the 95% confidence interval crossed one, subHR = 2.24 (95% CI: 0.77–6.57). Conclusions: Diagnosis of prostate cancer on TURP was associated with poorer overall survival when compared to men diagnosed on prostate biopsy. These findings have clinical implications given the increased use of photoselective vaporisation of the prostate, which is characterised by the lack of pathologic tissue for assessment.

## Linked entities

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

## Full-text entities

- **Genes:** NPEPPS (aminopeptidase puromycin sensitive) [NCBI Gene 9520] {aka AAP-S, MP100, PSA}, KLK3 (kallikrein related peptidase 3) [NCBI Gene 354] {aka APS, KLK2A1, PSA, hK3}
- **Diseases:** Cancer (MESH:D009369), intraductal carcinoma (MESH:D002285), inflammation (MESH:D007249), injury to (MESH:D014947), bladder outlet obstruction (MESH:D001748), Prostate Cancer (MESH:D011471), fibrosis (MESH:D005355), BPH (MESH:D011470), death (MESH:D003643), peripheral zone tumours (MESH:D010524), bladder malignancy (MESH:D001749), oncologic (MESH:D000072716)
- **Chemicals:** thulium (MESH:D013932), PVP (-), holmium (MESH:D006695)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12939765/full.md

---
Source: https://tomesphere.com/paper/PMC12939765